Non-thermal microwave/lower frequency electromagnetic fields (EMFs) act via voltage-gated calcium channel (VGCC) activation. Calcium channel blockers block EMF effects and several types of additional evidence confirm this mechanism. Low intensity microwave EMFs have been proposed to produce neuropsychiatric effects, sometimes called microwave syndrome, and the focus of this review is whether these are indeed well documented and consistent with the known mechanism(s) of action of such EMFs. VGCCs occur in very high densities throughout the nervous system and have near universal roles in release of neurotransmitters and neuroendocrine hormones. Soviet and Western literature shows that much of the impact of non-thermal microwave exposures in experimental animals occurs in the brain and peripheral nervous system, such that nervous system histology and function show diverse and substantial changes. These may be generated through roles of VGCC activation, producing excessive neurotransmitter/neuroendocrine release as well as oxidative/nitrosative stress and other responses. Excessive VGCC activity has been shown from genetic polymorphism studies to have roles in producing neuropsychiatric changes in humans. Two U.S. government reports from the 1970s to 1980s provide evidence for many neuropsychiatric effects of non-thermal microwave EMFs, based on occupational exposure studies. 18 more recent epidemiological studies, provide substantial evidence that microwave EMFs from cell/mobile phone base stations, excessive cell/mobile phone usage and from wireless smart meters can each produce similar patterns of neuropsychiatric effects, with several of these studies showing clear dose–response relationships. Lesser evidence from 6 additional studies suggests that short wave, radio station, occupational and digital TV antenna exposures may produce similar neuropsychiatric effects. Among the more commonly reported changes are sleep disturbance/insomnia, headache, depression/depressive symptoms, fatigue/tiredness, dysesthesia, concentration/attention dysfunction, memory changes, dizziness, irritability, loss of appetite/body weight, restlessness/anxiety, nausea, skin burning/tingling/dermographism and EEG changes. In summary, then, the mechanism of action of microwave EMFs, the role of the VGCCs in the brain, the impact of non-thermal EMFs on the brain, extensive epidemiological studies performed over the past 50 years, and five criteria testing for causality, all collectively show that various non-thermal microwave EMF exposures produce diverse neuropsychiatric effects.


Excessive calcium effects
Oxidative/nitrosative stress
Low-intensity microwave electromagnetic fields

Chemicals having roles:


Nitric oxide (NO)

Oxido nitrite (peroxynitrite)

1. Introduction

Microwave syndrome (Hocking, 2001, Johnson Liakouris, 1998), a combination of various neuropsychiatric symptoms originally described in persons with occupational exposures to microwave frequency EMFs, has been disputed largely because of the lack of an apparent mechanism for generating these symptoms. It is reported to often include such symptoms as fatigue, headache, insomnia, dysesthesia (impaired sensation), irritability, lack of concentration and other symptoms (Hocking, 2001, Johnson Liakouris, 1998). Similar but more extensive combinations of symptoms have been reported following occupational exposures in two U.S. government reports from the 1970s/1980s (Naval Medical Research Institute Research Report, 1971, Raines, 1981) and following environmental exposures as described in two more recent reviews (Khurana et al., 2010, Levitt and Lai, 2010).

The goal here is not just to review the epidemiology, however, but more importantly to consider the issue of possible physiological mechanism(s). Hennekens and Buring (1989), on p. 40 in their textbook Epidemiology in Medicine state “The belief in the existence of a cause and effect relationship is enhanced if there is a known or postulated biologic mechanism by which the exposure might reasonably alter risk of developing disease.” It is of critical importance therefore to assess possible biological mechanism before considering the epidemiological evidence.

Accordingly, this paper considers the mechanism by which low intensity microwave EMFs impact the cells of our bodies, how that mechanism may be predicted to impact the nervous system, evidence for such impact from experimental animal studies, genetic polymorphism evidence for that mechanism acting in humans to produce neuropsychiatric effects and finally, the epidemiological evidence for such effects in human populations with repeated low level microwave EMF exposure. Consideration of each of these types of evidence influences the overall interpretation presented in this paper.

2. Microwave/lower frequency EMFs act to activate voltage-gated calcium channels

In 24 different studies reviewed earlier (Pall, 2013) and two additional studies (Li et al., 2014, Lisi et al., 2006), microwave and lower frequency low intensity EMF effects were blocked or greatly lowered by calcium channel blockers, agents thought to be specific for blocking voltage-gated calcium channels (VGCCs). In these 26 studies, a total of 5 distinct types of channel blockers were used, with each type having a distinct structure and binding to a distinct site, such that it is essentially certain that these must be acting by blocking VGCCs, which is their only known common property. In each of these 26 studies, each of the responses studied, were blocked or greatly lowered by calcium channel blockers, showing that VGCC activation has roles in producing a wide variety of EMF effects. There is a large literature on changes in calcium fluxes and in calcium signaling following microwave EMF exposure (partially reviewed in Walleczek, 1992, Adey, 1993); each of these, including calcium efflux changes, can be explained as being due to VGCC activation, again suggesting a widespread role of VGCC activation in producing biological responses to EMFs. Pilla (2012) showed that pulsed microwave field exposure, produced an almost instantaneous increase in calcium/calmodulin-dependent nitric oxide (NO) signaling, providing strong evidence that these fields can produce an almost instantaneous VGCC activation. It is likely, that these EMFs act directly on the voltage sensor of the VGCCs to produce VGCC activation (Pall, 2015) with the voltage sensor being exquisitely sensitive to these EMFs because of its physical properties and location in the plasma membrane.

EMFs have been proposed to act to produce a wide variety of responses in the cell, via downstream effects of VGCC activation (Pall, 2013, Pall, 2014, Pall, 2015), including elevated intracellular calcium [Ca2+]i, excessive calcium and nitric oxide signaling and also excessive peroxynitrite, free radicals and oxidative stress.

VGCC activation has been shown to have a universal or near-universal role in the release of neurotransmitters in the brain and also in the release of hormones by neuroendocrine cells (Berridge, 1998, Dunlap et al., 1995, Wheeler et al., 1994), with such release being produced by calcium signaling. There are high densities of diverse VGCCs occurring in neurons throughout the nervous system. Both the high VGCC density and their function in neurotransmitter and neuroendocrine release throughout the nervous system suggests that the nervous system is likely to be highly sensitive to low intensity EMFs.

3. Genetic polymorphism studies

Genetic polymorphism studies are powerful tools for looking at the roles of specific proteins in human populations. In Table 1, a series of genetic polymorphism studies have been performed that show that an alleleproducing increased expression of the gene encoding the channel of the main L-type VGCC in the brain, produces diverse neuropsychiatric effects. These studies clearly show that excess L-type VGCC activity can cause neuropsychiatric effects. They also predict, therefore, that increased VGCC activity produced by microwave EMFs may be able to also produce widespread neuropsychiatric effects.

Table 1. Influence of genetic polymorphism of the CACNA1C in producing diverse neuropsychiatric effects.

4. Histological and functional changes in central nervous system (CNS) and peripheral nervous system (PNS) in animals exposed to microwave EMFs

The most extensive literature on histological and functional changes in animals is from the Soviet literature from the 1950s/1960s with additional Western literature from the same time period. Both Soviet and non-Soviet literature were reviewed in an English language Publication by Tolgskaya and Gordon (1973). This publication is, therefore, the main focus of this section. That publication was divided into thermal and non-thermal exposure studies, with the non-thermal studies which occupy the majority of the text (pp. 53–137) being of sole interest here.

These were all derived from the Tolgskaya and Gordon (1973) review and page numbers listed are page numbers from that document. All refer to changes produced by non-thermal exposures in the nervous system of experimental animals, with most being in rats.

This discussion scrolls down through Table 2.

Table 2. Histological and functional changes in brain function in animals following exposure to non-thermal microwave EMFs.

The majority of the histological changes seen in these mostly rodent studies, are seen in the nervous system, despite its being less than 2% of the rodent cell mass. There are statements made that the nervous system, both central and peripheral, is the most highly sensitive tissue to these non-thermal microwave and lower frequency EMFs. Following the nervous system in sensitivity are the myocardium and the testis; myocardial cells are known to have very high densities of VGCCs with especially high densities in the pacemaker cells and the testis is known to have high densities specifically of the T-type VGCCs. Pulsed EMFs are more active in producing histological changes in the brain than are non-pulsed fields, in two studies reviewed; there is a much larger literature showing that in most cases pulsed fields are more biologically active (Pall, 2015, Pangopoulos et al., 2013, Belyaev, 2015).

A wide variety of brain and peripheral nervous system tissues show histological changes following non-thermal exposures. Among the important tissues impacted are the hypothalamus and pituitary gland, where both show similar patterns of changes in neuroendocrine activities. There Is an initial increase in neuroendocrine activity (this may be produced directly by VGCC stimulation of secretion), followed over time by “exhaustion” of neuroendocrine activity (this may be produced by tissue damage produced from long term intracellular calcium [Ca2+]i elevation).

There are widespread histological changes produced in neuronal and neuroendocrine tissues. These were repeatedly reported to be largely reversible on cessation of EMF exposure. They become, however, irreversible when exposure is extended in time. There are changes in EEGactivity, which may be an easily measurable monitor of neurological damage.

In a summary statement, Tolgskaya and Gordon (1973) state, “This does not confirm the view, so widely held in the past among Soviet investigators and still maintained to a large extent even at the present time in the West, that the action of microwaves is entirely thermal.”

While there were many studies of brain impact of non-thermal EMFs performed in the 1950s/60s that make the information content of Tolgskaya and Gordon (1973) quite high, there is also a substantial recent literature on brain effects of non-thermal microwave EMF exposures (see, for example: Ammari et al., 2008a, Ammari et al., 2008b, Bas et al., 2009, Brillaud et al., 2007, Carballo-Quintás et al., 2011, Eberhardt et al., 2008, Dasdag et al., 2009, Dasdag et al., 2012, Grafström et al., 2008, Kumlin et al., 2007, López-Martín et al., 2006, Mausset-Bonnefont et al., 2004, Odaci et al., 2008, Rağbetli et al., 2010, Salford et al., 2003, Sonmez et al., 2010).

5. Older epidemiological reviews and other related studies

Two U.S. Government reports each listed many apparent neuropsychiatric effects of microwave/radiofrequency EMFs and a third recognized the role of non-thermal effects on our bodies, but had only a little consideration of neuropsychiatric effects.

The earliest to these was a Naval Medical Research Institute (NMRI) Research Report (1971) which listed 40 apparent neuropsychiatric changes produced by non-thermal exposures including: 5 central/peripheral nervous system (NS) changes, 9 CNS effects, 4 autonomic system effects, 17 psychological disorders, 4 behavioral changes and 2 misc. effects. This NMRI report also provided a supplementary document listing over 2300 citations documenting these and other effects of microwave exposures in humans and in animals.

The Raines (1981) NASA report reviewed extensive literature based on occupational exposures to non-thermal microwave EMFs, with that literature coming from U.S., Western European and Eastern European studies. There are no obvious differences in the literature coming from these different regions. Based on multiple studies, Raines (1981) reports 19 neuropsychiatric effects to be associated with occupational microwave/radiofrequency EMFs.

The Bolen (1994) report put out by the Rome Laboratory of the U.S. Air Force, acknowledged the role of non-thermal effects of microwave EMFs on humans. This report states in the Conclusion section that “Experimental evidence has shown that exposure to low intensity radiation can have a profound effect on biological processes. The nonthermal effects of RF/MW radiation exposure are becoming important measures of biological interaction of EM fields.” Clearly Bolen (1994) rejects the claim that only thermal effects occur. Bolen (1994) discusses a specific non-thermal neuropsychiatric effect, where anesthetized animals are awakened when the head is irradiated with microwave EMFs. This suggests a similar mechanism to that acting in humans where such EMFs produce insomnia (see below).

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6. Specific epidemiological studies on neuropsychiatric effects of microwave EMFs

There are 26 different epidemiological studies described in Table 3. Although 4 of these only studied a single neuropsychiatric effect, 22 of these each provide substantial evidence for the pattern described in the earlier U.S. reports, that a wide range of neuropsychiatric effects are produced by exposure to various non-thermal microwave frequency EMFs. Perhaps the most important of these 26 is the Santini et al. (2003) study of people living near cell phone base stations.

Table 3. Neuropsychiatric symptoms apparently produced by exposure to various electromagnetic fields.

There are three recent studies on the generation of headache during or shortly following long mobile phone calls (listed under Chu et al., 2011 in Table 3). The timing of development of these headaches and the finding that they occur on the ipsilateral side of the head, the side receiving much higher EMF exposure during the call, both argue strongly that these headaches are caused by the long mobile phone calls. Such causality was concluded earlier by Frey (1998) based on earlier studies and is now still more strongly documented.

7. Criteria for assessing causality in epidemiological studies

It is important to consider the different criteria that allow one to judge whether a cause and effect relationship is justified by the studies listed in Table 3 and the individual studies cited in Raines (1981). There are five such criteria that should be considered in making that judgment (see pp. 39–43 in Hennekens and Buring, 1989):

Strength of Association: Is there a strong correlation between exposure and the neuropsychiatric symptoms? There clearly is for several studies cited in Raines (1981). One example is the Dwyer and Leeper (1978) study (see Table 3) where there is a large increase in symptoms and where that increase is greater with longer occupational exposure. Another example is the Lerner (1980) study of 1300 microwave workers, where workers with relatively low exposure levels had an approximate doubling of neurological complaints and where those with substantially higher exposure levels had an approximate tripling of neurological complaints over controls. Sadcikova (1974) found that 7 of 8 neuropsychiatric symptoms studied, showed a statistically significant rise in prevalence with longer occupational exposure (see Table 3). Sadcikova (1974), also found that microwave workers had increases of 3 to over 10-fold in: feeling of heaviness in the head; tiredness; irritability; sleepiness; partial loss of memory; and skin sensitivity. There is also a strong association where important new exposures occur – this is clearly the case with all of the studies of people living near cell/mobile phone base stations, listed in Table 3 and also with the two studies of people who become exposed to radiation from smart meters. The studies listed in Table 3under Chu et al. (2011) (see also Chia et al., 2000, Oftedal et al., 2000) are of a special type. Here people making very long (over 1 h) cell/mobile phone calls develop headaches an hour or more following the initiation of the long call. So these occur within a specific time range following initiation of these long calls, such that headache would only occur very infrequently in that time frame by chance. So here again, there is a strong association. While there is no question that many of these studies show high strength of association, it is also clear that it is becoming progressively more difficult to do these studies. As exposures become almost universal in countries around the world, it is getting difficult if not impossible to find good negative controls. There may be a similar problem in doing animal studies, such that it may be necessary to raise animals in Faraday cages in order to avoid exposures that would otherwise occur as a consequence of our near ubiquitous EMFs.

Biological credibility is extremely strong here, with three aspects of the biology predicting that these low intensity fields cause widespread neuropsychiatric effects. This was discussed above and is reconsidered in the following section.

Consistency within the different epidemiological studies and with other types of studies. The epidemiological studies listed in Table 3 and also those showing neuropsychiatric effects that were cited in Raines (1981) have been performed in many different countries with different cultures. They have been performed in multiple countries in Western Europe, Eastern Europe, the Middle East and in East Asia, as well as in the U.S. and Australia. They are, therefore, not limited to one or two cultural contexts. This is deemed, therefore, an important indicator of causality. We also have a surprising consistency of apparent neuropsychiatric effects of different fields, including various occupational exposures and exposures to cell/mobile phone base stations, exposure to the phones themselves, exposure to smart meter pulses, and other EMFs (see Table 3). Pulsation patterns, frequencies and exact intensities may produce various biological responses (Pall, 2015, Pangopoulos et al., 2013, Belyaev, 2015) so it is a bit surprising that we have as much consistency as we do have across different types of exposures. We also have consistency with the biology discussed in the previous section. Because elevated VGCC activity produced by genetic polymorphism (Table 1) produces diverse neuropsychiatric effects, it is not surprising that elevation of VGCC activity produced by microwave EMF exposure apparently also produces diverse neuropsychiatric effects. Similarly because non-thermal EMF exposures produce widespread changes in brain structure and function in animals (Tolgskaya and Gordon, 1973), it is not surprising that the neuropsychiatric symptoms, which are produced as a consequence of brain dysfunction are produced by such EMFs.

Time sequence: It is clear that the all of these effects follow exposure in the various studies that have been published. In some studies, it is also clear that longer occupational exposure times produce increased symptom prevalence. These include Dwyer and Leeper (1978) and Baranski and Edelwejn (1975). These observations all support a causal relationship between exposure to EMF and the development of neuropsychiatric symptoms.

Dose–response relationship: It is assumed, here, that biological effects have a positive correlation with the intensity of the apparent causal stressor. This is not necessarily true of EMF effects, because it has been shown that there are “window effects” where specific intensities have larger biological effects, than do either lower or higher intensities (Pall, 2015, Pangopoulos et al., 2013, Belyaev, 2015). Nevertheless, where different intensities were studied in these epidemiological studies, they do show the dose–response relationship assumed here including Altpeter et al. (2000), Dwyer and Leeper (1978), Eger and Jahn (2010), Lerner (1980), Navarro et al. (2003), Oberfeld et al. (2004), Salama and Abou El Naga (2004), Santini et al. (2003) and Thomée et al. (2011). Thus these data do fit well to the assumed dose–response relationship, found in most causal roles. The Altpeter et al. (2000)study showed a special type of evidence for causality: during a 3-day period when the broadcasting tower was turned off, the melatonin levels recovered to near-normal levels. The studies of headache occurrence on prolonged cell/mobile phone calls (typically well over one hour) listed under Chu et al. (2011) in Table 3 also suggest the assumed dose–response relationship (see also Chia et al., 2000, Oftedal et al., 2000 and earlier citations listed in Frey, 1998). Because such headaches only occur with prolonged cell/mobile phone calls, these studies also provide evidence for a dose–response relationship because low doses are ineffective. Furthermore these same studies provide evidence for such a dose–response relationship from another type of observation. Because the headaches occur predominantly on the ipsilateral side of the head which receives much higher EMF exposure intensity, rather than on the contralateral side of the head, which receives much lower intensities, this provides an additional type of evidence for the predicted dose–response relationship.

While the evidence is convincing that the various neuropsychiatric apparent consequences of microwave EMF exposure are in fact caused by such exposures, there may be somewhat more controversy about another EMF-neuropsychiatric linkage. Havas et al. (2010) have reported a similar list of neuropsychiatric symptoms in electromagnetic hypersensitivity (EHS) patients. They found that each of the following symptoms were common in EHS: poor short term memory; difficulty of concentration; eye problems; sleep disorder; feeling unwell; headache; dizziness; tinnitus; chronic fatigue; tremors; body pain; difficulty speaking; tingling sensation in feet or hands; difficulty writing; difficulty walking; migraine. The similarity of these symptoms to the most commonly found symptoms following non-thermal microwave EMF exposures (Table 3), suggests that EHS is a genuine sensitivity to EMFs. In the bottom row in Table 2, sensitivities were found in rodent studies following non-thermal exposure that suggest a possible animal model for the study of EHS. Each of these EHS-related issues needs to be followed up experimentally.

8. Discussion and conclusions

In the previous section, each of the five criteria for assessing whether an epidemiological association is causal, were considered. Those five are (Hennekens and Buring, 1989): (1) strength of association; (2) biological credibility; (3) consistency; (4) time sequence; (5) dose–response relationship. Each of these five provide strong support for causality such that the combination of all five provides compelling evidence for causality. Low-intensity microwave frequency EMFs do cause diverse neuropsychiatric symptoms. While each of these five is important here, the one that is most important is the criterion of biological credibility.

Three related sets of biological observations each predict that low-intensity microwave EMFs produce widespread neuropsychiatric effects:


Such EMFs act via activation of VGCCs, acting through the VGCC voltage sensor which is predicted to be exquisitely sensitive to these EMFs (Pall, 2015). VGCCs occur in high densities throughout the nervous system and have essential roles throughout the nervous system in releasing neurotransmitters and neuroendocrine hormones. These properties predict, therefore, that these low intensity non-thermal microwave EMFs cause widespread changes in the nervous system, causing, in turn, diverse neuropsychiatric effects.


Elevated VGCC activity, produced by an allele of the CACNA1C gene which encodes the channel of the main L-type VGCC in the brain, produces various neuropsychiatric effects (Table 1). This predicts, that low intensity non-thermal microwave frequency EMFs which also produce elevated L-type and other VGCC activity, therefore produce widespread neuropsychiatric effects.


Studies reviewed in the Tolgskaya and Gordon, 1973 publication (Table 2) have shown that the cells of the mammalian nervous system show high sensitivity to various non-thermal microwave and lower frequency EMFs, being apparently more sensitive than any other organ in the body of rodents. These studies predict that the human nervous system is likely to be similarly sensitive to these EMFs, predicting, therefore, widespread neuropsychiatric effects in humans.

We not only have biological credibility but also more importantly, each of these distinct but interrelated biological considerations predicts that low-intensity, non-thermal microwave EMFs produce widespread neuropsychiatric effects. That common prediction is verified by extensive data summarized in citations provided by the Naval Medical Research Institute Research Report (June 1971), data provided by The Raines (1981)NASA report, and by 26 epidemiological studies summarized in Table 3.

The most commonly reported neuropsychiatric symptoms from these studies are summarized in Table 4.

Table 4. Commonly reported neuropsychiatric symptoms following microwave EMF exposure.

A total of 22 different studies described in Table 3 were used for data for this table, but not 4 others that only assessed a single neuropsychiatric end point. The Altpeter study which only assessed sleep disturbance/melatonin depletion and the three studies listed under Chu et al. which only assessed headache occurrence following long cell phone calls, listed in Table 3 were not included. Because many of the studies only assessed from 3 to 7 specific symptoms, it is not surprising that the numbers of studies reporting a specific symptom fall far below 22. Where several symptom descriptions were included under one heading, such as dysesthesia, if a study had more than one of these symptom descriptions, it was only counted once.

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All the symptoms listed in Table 4 should be considered established parts of microwave syndrome (Hocking, 2001, Johnson Liakouris, 1998). Even if the statistical significance in each study was of the lowest statistical significance (p < .05) one would expect only 1 positive study to occur at random out of the 22 studies included here. Because many individual symptoms were not surveyed in many individual studies, the expectation is substantially lower than that. Each of these, having shown positive results in 5 or more studies are highly unlikely, therefore, to have occurred by chance. Stong statistical significance is also seen for individual neuropsychiatric effects reported to have p < 0.001 in the Eger and Jahn (2010) and Oto et al. (1994) studies (see Table 3).

EEG changes may well be part of microwave syndrome, as well. While none of the studies described in Table 3 measured EEGs, six studies of human occupational exposure cited in the Raines (1981) showed EEG changes (Baranski and Edelwejn, 1975, Bise, 1978, Dumanskij and Shandala, 1974, Lerner, 1980, Sheppard and Eisenbud, 1977). Murbach et al. (2014) cited 10 human studies in support of their statement that “the most consistently reported effects (of mobile phone use) in various studies conducted by different laboratories are changes in the electroencephalogram (EEG) power spectrum.” Three recent studies (Lustenberger et al., 2013, Schmid et al., 2012a, Schmid et al., 2012b) and several earlier studies cited in Wagner et al. (1998) have each shown EEG changes in sleeping humans exposed to non-thermal pulsed microwave fields. Two recent studies showed EEG changes in persons exposed to Wi-Fi fields (Maganioti et al., 2010, Papageorgiou et al., 2011). Lai (1997) described 8 animal studies showing changes in EEG patterns in animals exposed to non-thermal EMFs and three additional animal studies were described in Tolgskaya and Gordon (1973). With the exception of the 6 studies cited in the second sentence in this paragraph, all of these are direct experimental studies which are not, therefore, susceptible to the questions of causality that can be raised about epidemiological studies. It is the author’s view that future studies should consider studying EEG changes as an objectively measurable assessment of brain physiology and that before and after increased exposure studies should be considered when a new EMF source is to be introduced into human populations. While such studies must be done carefully, given the complexity of EEGs, even very small numbers of individuals may produce highly statistically significant results in well designed studies analyzed with paired t-tests.

One of the citations from the previous paragraph, Bise (1978) reviewed earlier studies of low level microwave frequency exposures in humans and concluded that such EMFs produced the following neuropsychiatric effects: headache, fatigue, irritability, dizziness, loss of appetite, sleepiness, sweating, difficulty of concentration, memory loss, depression, emotional instability, dermographism, tremor, hallucinations and insomnia. The strong similarity of this list from 37 years ago and the list in Table 4 should be noted. The Bise (1978) list is based on occupational exposure studies whereas the current list in Table 4 is based primarily on EMF exposures from cell/mobile phone base stations, from heavy cell phone usage and from smart meters, three types of exposures that did not exist in 1978. The strong similarity between the Bise (1978) list and the current one 37 years later alone produces a compelling argument that the 11 neuropsychiatric effects found on both lists are caused by exposure to multiple types of low-intensity microwave EMFs.

The pattern of evidence is compelling in support of the earlier statement of Levitt and Lai (2010) that “the primary questions now involve specific exposure parameters, not the reality of complaints or attempts to attribute such complaints to psychosomatic causes, malingering or beliefs in paranormal phenomena.”

We can barely imagine how the combinations of neuropsychiatric effects, including those in Table 4, will influence human behavior and social interactions, now that the majority of the human populations on earth are exposed to ever increasing intensities and diversity of microwave frequency EMFs. You may recall that three of the occupational exposure studies cited in (Raines, 1981 showed increasing prevalence of neuropsychiatric symptoms with years of exposure to consistent patterns of EMF exposure intensities (Dwyer and Leeper, 1978, Sadcikova, 1974, Baranski and Edelwejn, 1975). With ever increasing exposures in human populations, we have no idea what the consequences of these ever increasing exposures will be.

Conflict of interest

The author declares no conflict of interest.


Abdel-Rassoul et al., 2007
G. Abdel-Rassoul, O.A. El-Fateh, M.A. Salem, A. Michael, F.Farahat, M.A. El-Batanouny, E. SalemNeurobehavioral effects among inhabitants around mobile phone stations
Neurotoxicology, 28 (2007), pp. 434-440
Adey, 1993
W.R. AdeyBiological effects of electromagnetic fields
J. Cell. Biochem., 51 (1993), pp. 410-416
Al-Khlaiwi and Meo, 2004
T. Al-Khlaiwi, S.A. MeoAssociation of mobile phone radiation with fatigue, headache, dizziness, tension and sleep disturbance in Saudi population
Saudi Med. J., 25 (2004), pp. 732-736
Altpeter et al., 2000
E. Altpeter, M. Battaglia, A. Bader, D. Pluger, C.E. Minder, T. AbelinTen Years Experience with Epidemiological Research in the Vicinity of the Short-Wave Broadcasting Area Schwarzenburg: What does the Story Tell Us?
Ammari et al., 2008a
M. Ammari, E. Brillaud, C. Gamez, A. Lecomte, M. Sakly, H.Abdelmelek, R. de SezeEffect of a chronic GSM 900 MHz exposure on glia in the rat brain
Biomed. Pharmacother., 62 (2008), pp. 273-281
Ammari et al., 2008b
M. Ammari, A. Lecomte, M. Sakly, H. Abdelmelek, R. de-SezeExposure to GSM 900 MHz electromagnetic fields affects cerebral cytochrome c oxidase activity
Toxicology, 250 (2008), pp. 70-74
Baranski and Edelwejn, 1975
S. Baranski, Z. EdelwejnExperimental morphologic and electroencephalographic studies of microwave effects on the nervous system
Ann. N. Y. Acad. Sci., 47 (1975), pp. 109-116
Bas et al., 2009
O. Bas, E. Odaci, S. Kaplan, N. Acer, K. Ucok, S. Colakoglu900 MHz electromagnetic field exposure affects qualitative and quantitative features of hippocampal pyramidal cells in the adult female rat
Brain Res., 1265 (2009), pp. 178-185
Belyaev, 2015
I. BelyaevBiophysical mechanisms for nonthermal microwave effects
Marko S. Markov (Ed.), Electromagnetic Fields in Biology and Medicine, CRC Press, New York (2015), pp. 49-67
Berridge, 1998
M.J. BerridgeNeuronal calcium signaling
Neuron, 21 (1998), pp. 13-26
Bhat et al., 2012
S. Bhat, D.T. Dao, C.E. Terrillion, M. Arad, R.J. Smith, N.M. Soldatov, T.D.GouldCACNA1C (Cav1.2) in the pathophysiology of psychiatric disease
Prog. Neurobiol., 99 (2012), pp. 1-14
Bigos et al., 2010
K.L. Bigos, V.S. Mattay, J.H. Callicott, R.E. Straub, R. Vakkalanka, B.Kolachana, T.M. Hyde, B.K. Lipska, J.E. Kleinman, D.R. WeinbergerGenetic variation in CACNA1C affects brain circuitries related to mental illness
Arch. Gen. Psychiatry, 67 (2010), pp. 939-945
Bise, 1978
W. BiseLow power radio-frequency and microwave effects on human electroencephalogram and behavior
Physiol. Chem. Phys., 10 (1978), pp. 387-398
Bolen, 1994
S.M. BolenRadiofrequency/Microwave Radiation Biological Effects and Safety Standards: A Review
AD-A282 886, Rome Laboratory, U.S. Air Force Material Command, Griffiss Air Force Base, New York (1994)
Bortkiewicz et al., 2004
A. Bortkiewicz, M. Zmyslony, A. Szyjkowska, E. GadzickaSubjective symptoms reported by people living in the vicinity of cellular phone base stations: review
Med. Pr., 55 (2004), pp. 345-351
Bortkiewicz et al., 2012
A. Bortkiewicz, E. Gadzicka, A. Szyjkowska, P. Politański, P. Mamrot, W. Szymczak, M. ZmyślonySubjective complaints of people living near mobile phone base stations in Poland
Int. J. Occup. Med. Environ. Health, 25 (2012), pp. 31-40
Brillaud et al., 2007
E. Brillaud, A. Piotrowski, R. de SezeEffect of an acute 900 MHz GSM exposure on glia in the rat brain: a time-dependent study
Toxicology, 238 (2007), pp. 23-33
Carballo-Quintás et al., 2011
M1 Carballo-Quintás, I. Martínez-Silva, C. Cadarso-Suárez, M.Alvarez-Figueiras, F.J. Ares-Pena, E. López-MartínA study of neurotoxic biomarkers, c-fos and GFAP after acute exposure to GSM radiation at 900 MHz in the picrotoxin model of rat brains
Neurotoxicology, 32 (2011), pp. 478-494
Chia et al., 2000
S.E. Chia, H.P. Chia, J.S. TanPrevalence of headache among handheld cellular telephone users in Singapore: a community study
Environ. Health Perspect., 108 (2000), pp. 1059-1062
Chu et al., 2011
M.K. Chu, H.G. Song, C. Kim, B.C. LeeClinical features of headache associated with mobile phone use: a cross-sectional study in university students
BMC Neurol., 11 (2011, September), p. 115, 10.1186/1471-2377-11-115
Conrad, 2013
R.H. ConradSmart Meter Health Effects Survey and Report
Dasdag et al., 2009
S. Dasdag, M.Z. Akdag, E. Ulukaya, A.K. Uzunlar, A.R. OcakEffect of mobile phone exposure on apoptotic glial cells and status of oxidative stress in rat brain
Electromagn. Biol. Med., 28 (2009), pp. 342-354
Dasdag et al., 2012
S. Dasdag, M.Z. Akdag, G. Kizil, M. Kizil, D.U. Cakir, B. YokusEffect of 900 MHz radio frequency radiation on beta amyloid protein, protein carbonyl, and malondialdehyde in the brain
Electromagn. Biol. Med., 31 (2012), pp. 67-74
Dasdag et al., 1992
S. Dasdag, K. Balci, M.S. Celik, S. Batun, A. Kaplan, Z. Bolaman, S.Tekes, Z. AkdagNeurologic and biochemical findings and CD4/CD8 ratio in people occupationally exposed to RF and microwave
Biotechnol. Biotechnol. Equip., 6 (4) (1992), pp. 37-39
Dumanskij and Shandala, 1974
J.D. Dumanskij, M.G. ShandalaThe biologic action and hygienic significance of electromagnetic fields of super-high and ultrahigh frequencies in densely populated areas
P. Czerski, et al. (Eds.), Effects and Health Hazards of Microwave Radiation, Proceedings of an International Symposium, Warsaw15–18 October 1973 (1974)
Dunlap et al., 1995
K. Dunlap, J.L. Luebke, T.J. TurnerExocytic Ca++ channels in the mammalian central nervous system
Neuroscience, 18 (1995), pp. 89-98
Dwyer and Leeper, 1978
M.J. Dwyer, D.B. LeeperA Current Literature Report on the Carcinogenic Properties of Ionizing and Nonionizing Radiation
DHEW Publication (NIOSH) (1978), pp. 78-134
Eberhardt et al., 2008
J.L. Eberhardt, B.R. Persson, A.E. Brun, L.G. Salford, L.O. MalmgrenBlood–brain barrier permeability and nerve cell damage in rat brain 14 and 28 days after exposure to microwaves from GSM mobile phones
Electromagn. Biol. Med., 27 (2008), pp. 215-229
Eger and Jahn, 2010
H. Eger, M. JahnSpecific symptoms and radiation from mobile basis stations in Selbitz, Bavaria, Germany: evidence for dose–effect relationship
Umw. – Med. Ges., 23 (2010), pp. 130-139
Frey, 1998
A.H. FreyHeadaches from cellular telephones: are they real and what are the implications?
Environ. Health Perspect., 106 (1998), pp. 101-103
Grafström et al., 2008
G. Grafström, H. Nittby, A. Brun, L. Malmgren, B.R. Persson, L.G.Salford, J. EberhardtHistopathological examinations of rat brains after long-term exposure to GSM-900 mobile phone radiation
Brain Res. Bull., 77 (2008), pp. 257-263
Havas et al., 2010
M. Havas, J. Marrongelle, B. Pollner, E. Kelley, C.R.G. Rees, L. TullyProvocation study using heart rate variability shows microwave radiation from 2.4 GHz phone affects autonomic nervous system
Eur. J. Oncol. Libr., 5 (2010), pp. 273-300
Hennekens and Buring, 1989
C.H. Hennekens, J.E. BuringEpidemiology in Medicine
Little Brown and Co., Boston (1989)
Hocking, 2001
B. HockingMicrowave sickness: a reappraisal
Occup. Med., 51 (2001), pp. 66-69
Johnson Liakouris, 1998
A.G. Johnson LiakourisRadiofrequency (RF) sickness in the Lilienfeld study: an effect of modulated microwaves?
Arch. Environ. Health, 53 (1998), pp. 226-228
Khan, 2008
M.M. KhanAdverse effects of excessive mobile phone use
Int. J. Occup. Med. Environ. Health, 21 (2008), pp. 289-293
Khurana et al., 2010
V.G. Khurana, L. Hardell, J. Everaert, A. Bortkiewicz, M. Carlberg, M.AhonenEpidemiological evidence for a health risk from mobile phone base stations
Int. J. Occup. Environ. Health, 16 (2010), pp. 263-267
Kolodynskii and Kolodinska, 1996
A.A. Kolodynskii, V.V. KolodinskaMotor and psychological functions of school children living in the area of the Skrunda Radio Location Station in Latvia
Sci. Total Environ., 180 (1996), pp. 87-93
Krug et al., 2010
A. Krug, V. Nieratschker, V. Markov, S. Krach, A. Jansen, K. Zerres, T.Eggermann, T. Stöcker, N.J. Shah, J. Treutlein, T.W. Mühleisen, T. Kircher
Neuroimage, 49 (2010), pp. 1831-1836
Krug et al., 2014
A. Krug, S.H. Witt, H. Backes, B. Dietsche, V. Nieratschker, N.J. Shah, M.M.Nöthen, M. Rietschel, T. KircherA genome-wide supported variant in CACNA1C influences hippocampal activation during episodic memory encoding and retrieval
Eur. Arch. Psychiatry Clin. Neurosci., 264 (2014), pp. 103-110
Kumlin et al., 2007
T. Kumlin, H. Iivonen, P. Miettinen, A. Juvonen, T. van Groen, L. Puranen, R. Pitkäaho, J. Juutilainen, H. TanilaMobile phone radiation and the developing brain: behavioral and morphological effects in juvenile rats
Radiat. Res., 168 (2007), pp. 471-479
Lai, 1997
H. LaiNeurological effects of radiofrequency electromagnetic radiation relating to wireless communication technology
Paper presented at the IBC-UK Conference: “Mobile Phones – Is There a Health Risk?” (1997)
Lamech, 2014
F. LamechSelf-reporting of symptom development from exposure to radiofrequency fields of wireless smart meters in Victoria, Australia: a case series
Altern. Ther. Health Med., 20 (2014), pp. 28-39
Lerner, 1980
E.J. LernerRF radiation: biological effects
IEEE Spectr., 17 (December) (1980), pp. 51-59
Levitt and Lai, 2010
B.B. Levitt, H. LaiBiological effects from exposure to electromagnetic radiation emitted by cell towers base stations and other antenna arrays
Environ. Rev., 18 (2010), pp. 369-395
Li et al., 2014
Y. Li, X. Yan, J. Liu, L. Li, X. Hu, H. Sun, J. TianPulsed electromagnetic field enhances brain-derived neurotrophic factor expression through L-type voltage-gated calcium channel- and Erk-dependent signaling pathways in neonatal rat dorsal root ganglion neurons
Neurochem. Int., 75 (2014), pp. 96-104
Lisi et al., 2006
A. Lisi, M. Ledda, E. Rosola, D. Pozzi, E. D’Emilia, L. Giuliani, A. Foletti, A.Modesti, S.J. Morris, S. GrimaldiExtremely low frequency electromagnetic field exposure promotes differentiation of pituitary corticotrope-derived AtT20 D16V cells
Bioelectromagnetics, 27 (2006), pp. 641-651
López-Martín et al., 2006
E. López-Martín, J.L. Relova-Quinteiro, R. Gallego-Gómez, M.Peleteiro-Fernández, F.J. Jorge-Barreiro, F.J. Ares-PenaGSM radiation triggers seizures and increases cerebral c-Fos positivity in rats pretreated with subconvulsive doses of picrotoxin
Neurosci. Lett., 398 (2006), pp. 139-144
Lustenberger et al., 2013
C. Lustenberger, M. Murbach, R. Dürr, M.R. Schmid, N. Kuster, P.Achermann, R. HuberStimulation of the brain with radiofrequency electromagnetic field pulses affects sleep-dependent performance improvement
Brain Stimul., 6 (2013), pp. 805-811
Maganioti et al., 2010
A.E. Maganioti, C.C. Papageorgiou, C.D. Hountala, M.A. Kyprianou, A.D. Rabavilas, G.N. Papadimitriou, C.N. CapsalisWi-Fi electromagnetic fields exert gender related alterations of EEG
6th International Workshop on Biological Effects of Electromagnetic Fields, Bodrun, Turkey, October (2010)
Mausset-Bonnefont et al., 2004
A.L. Mausset-Bonnefont, H. Hirbec, X. Bonnefont, A. Privat, J. Vignon, R. de SezeAcute exposure to GSM 900 MHz electromagnetic fields induces glial reactivity and biochemical modifications in the rat brain
Neurobiol. Dis., 17 (2004), pp. 445-454
Murbach et al., 2014
M. Murbach, E. Neufeld, M. Christopoulou, P. Achermann, N. KusterModeling of EEG electrode artifacts and thermal ripples in human radiofrequency exposure studies
Bioelectromagnetics, 35 (2014), pp. 273-283
Naval Medical Research Institute Research Report, 1971
Naval Medical Research Institute Research ReportBiobliography of Reported Biological Phenomena (“Effects”) and Clinical Manifestations Attributed to Microwave and Radio-Frequency Radiation. Report No. 2 Revised
(1971, June)
Navarro et al., 2003
G. Navarro, J. Segure, M. Porteles, Gomez PerrettaThe microwave syndrome: study in Spain
Electromag. Biol. Med., 22 (2003), pp. 161-169
Oberfeld et al., 2004
G. Oberfeld, A.E. Navarro, M. Portoles, C. Maestu, C. Gomez-PerrettaThe microwave syndrome: further aspects of a Spanish study
Odaci et al., 2008
E. Odaci, O. Bas, S. KaplanEffects of prenatal exposure to a 900 MHz electromagnetic field on the dentate gyrus of rats: a stereological and histopathological study
Brain Res., 1238 (2008), pp. 224-249
Oftedal et al., 2000
G. Oftedal, J. Wilén, M. Sandström, K.H. MildSymptoms experienced in connection with mobile phone use
Occup. Med. (Lond.), 50 (2000), pp. 237-245
Oto et al., 1994
R. Oto, Z. Akdag, S. Dasdag, Y. CelikEvaluation of psychologic parameters in people occupationally exposed to radiofrequencies and microwave
Biotechnol. Biotechnol. Equip., 8 (4) (1994), pp. 71-74
Pall, 2013
M.L. PallElectromagnetic fields act via activation of voltage-gated calcium channels to produce beneficial or adverse effects
J. Cell. Mol. Med., 17 (2013), pp. 958-965
Pall, 2014
M.L. PallElectromagnetic field activation of voltage-gated calcium channels: role in therapeutic effects
Electromagn. Biol. Med., 33 (2014), p. 251
Pall, 2015
M.L. PallReview: scientific evidence contradicts findings and assumptions of Canadian safety panel 6: microwaves act through voltage-gated calcium channel activation to induce biological impacts a non-thermal levels, supporting a paradigm shift for microwave/lower frequency electromagnetic field action
Rev. Environ. Health, 30 (2015), pp. 99-116
Pangopoulos et al., 2013
D.J. Pangopoulos, O. Johansson, G.L. CarloEvaluation of specific absorption rate as a dosimetric quantity for electromagnetic fields bioeffects
PLOS ONE, 8 (6) (2013), p. e62663
Papageorgiou et al., 2011
C.C. Papageorgiou, C.D. Hountala, A.E. Maganioti, M.A.Kyprianou, A.D. Rabavilas, G.N. Papadimitriou, C.N. CapsalisEffects of wi-fi signals on the p300 component of event-related potentials during an auditory hayling task
J. Integr. Neurosci., 10 (2011), pp. 189-202
Pilla, 2012
A.A. PillaElectromagnetic fields instantaneously modulate nitric oxide signaling in challenged biological systems
Biochem. Biophys. Res. Commun., 426 (2012), pp. 330-333
Rağbetli et al., 2010
MC1 Rağbetli, A. Aydinlioğlu, N. Koyun, C. Rağbetli, S. Bektas, S.OzdemirThe effect of mobile phone on the number of Purkinje cells: a stereological study
Int. J. Radiat. Biol., 86 (2010), pp. 548-554
Raines, 1981
J.K. RainesElectromagnetic Field Interactions with the Human Body: Observed Effects and Theories
National Aeronautics and Space Adminstration, NASA CR 166661, Greenbelt, Maryland (1981, April)
Sadcikova, 1974
M.N. SadcikovaClinical manifestations of reactions to microwave radiation in various occupational groups
P. Czerski (Ed.), Biological Effects and Health Hazards of Microwave Radiation. Proceedings of the International Symposium, Warsaw 13–18 October 1973, Polish Med Publishers, Warsaw (1974), pp. 261-267
Salama and Abou El Naga, 2004
O.E. Salama, R.M. Abou El NagaCellular phones: are they detrimental?
J. Egypt. Public Health Assoc., 79 (2004), pp. 197-223
Salford et al., 2003
L.G. Salford, A.E. Brun, J.L. Eberhardt, L. Malmgren, B.R. PerssonNerve cell damage in mammalian brain after exposure to microwaves from GSM mobile phones
Environ. Health Perspect., 111 (2003), pp. 881-883
Santini et al., 2003
R. Santini, P. Santini, P. Le Ruz, J.M. Danze, M. SeigneSurvey of people living in the vicinity of cellular phone base stations
Electromagn. Biol. Med., 22 (2003), pp. 41-49
Schmid et al., 2012a
M.R. Schmid, S.P. Loughran, S.J. Regel, M. Murbach, A. Bratic Grunauer, T. Rusterholz, A. Bersagliere, N. Kuster, P. AchermannSleep EEG alterations: effects of different pulse-modulated radio frequency electromagnetic fields
J. Sleep Res., 21 (2012), pp. 50-58
Schmid et al., 2012b
M.R. Schmid, M. Murbach, C. Lustenberger, M. Maire, N. Kuster, P.Achermann, S.P. LoughranSleep EEG alterations: effects of pulsed magnetic fields versus pulse-modulated radio frequency electromagnetic fields
J. Sleep Res., 21 (2012), pp. 620-629
Schüz et al., 2009
J. Schüz, G. Waldemar, J.H. Olsen, C. JohansenRisks for central nervous system diseases among mobile phone subscribers: a Danish retrospective cohort study
PLoS ONE, 4 (2) (2009), p. e4389, 10.1371/journal.pone.0004389
Sheppard and Eisenbud, 1977
A.R. Sheppard, M. EisenbudBiological Effects of Electric and Magnetic Fields of Extremely Low Frequency
New York University Press, New York (1977)
Söderqvist et al., 2008
F. Söderqvist, M. Carlberg, L. HardellUse of wireless telephones and self-reported health symptoms: a population-based study among Swedish adolescents aged 15–19 years
Environ. Health, 7 (May) (2008), p. 18, 10.1186/1476-069X-7-18
Soeiro-de-Souza et al., 2012
M.G. Soeiro-de-Souza, M.C. Otaduy, C.Z. Dias, D.S. Bio, R.Machado-Vieira, R.A. MorenoThe impact of the CACNA1C risk allele on limbic structures and facial emotions recognition in bipolar disorder subjects and healthy controls
J. Affect. Disord., 141 (2012), pp. 94-101
Sonmez et al., 2010
O.F. Sonmez, E. Odaci, O. Bas, S. KaplanPurkinje cell number decreases in the adult female rat cerebellum following exposure to 900 MHz electromagnetic field
Brain Res., 1356 (2010), pp. 95-101
Tesli et al., 2013
M. Tesli, K.C. Skatun, O.T. Ousdal, A.A. Brown, C. Thoresen, I. Agartz, I.Melle, S. Djurovic, J. Jensen, O.A. AndreassenCACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls
PLOS ONE, 8 (2) (2013), p. e56970, 10.1371/journal.pone.0056970
Thimm et al., 2011
M. Thimm, T. Kircher, T. Kellermann, V. Markov, S. Krach, A. Jansen, K.Zerres, T. Eggermann, T. Stöcker, N.J. Shah, M.M. Nöthen, M. Rietschel, S.H. Witt, K.Mathiak, A. KrugEffects of a CACNA1C genotype on attention networks in healthy individuals
Psychol. Med., 41 (2011), pp. 1551-1561
Thomée et al., 2011
S. Thomée, A. Härenstam, M. HagbergMobile phone use and stress, sleep disturbances, and symptoms of depression among young adults – a prospective cohort study
BMC Public Health, 11 (January) (2011), p. 66, 10.1186/1471-2458-11-66
Tolgskaya and Gordon, 1973
M.S. Tolgskaya, Z.V. GordonPathological Effects of Radio Waves
(B. Haigh, Trans.)
Consultants Bureau, New York/London (1973), p. 146
Wagner et al., 1998
P. Wagner, J. Röschke, K. Mann, W. Hiller, C. FrankHuman sleep under the influence of pulsed radiofrequency electromagnetic fields: a polysomnographic study using standardized conditions
Bioelectromagnetics, 19 (1998), pp. 199-202
Waldmann-Selsam et al., 2009
C. Waldmann-Selsam, C. Aschermann, M. KernWarning against adverse health effects from the operation of digital broadcast television stations (DVB-T): letter from 3 German physicians to the U.S. President and Congress
Walleczek, 1992
J. WalleczekElectromagnetic field effects on cells of the immune system: the role of calcium signaling
FASEB J., 6 (1992), pp. 3177-3185
Wheeler et al., 1994
D.B. Wheeler, A. Randall, R.W. TsienRoles of N-type and Q-type channels in supporting hippocampal synaptic transmission
Science, 264 (1994), pp. 107-111