Resolution of Sleep Paralysis by Weak Electromagnetic Fields in a Patient with Multiple Sclerosis

References

• Aldegunde M., Miguez I., Veira J. Effects of pinealectomy on regional brain serotonin metabolism. International Journal of Neuroscience 1985; 26: 9–13
   PubMed Web of Science ®Google Scholar
• Aldrich M. S. Narcolepsy. Neurology 1992; 42(suppl 6)34–43
   PubMedGoogle Scholar
• Aldrich M. S. The neurobiology of narcolepsy-cataplexy. Progress in Neurobiology 1993; 41: 533–541
   PubMed Web of Science ®Google Scholar
• Anderson E. G., Proudfit H. K. The functional role of the bulbospinal serotonergic nervous system. Serotonin neurotransmission and behavior, B. L. Jacobs, A. Gelperin. MIT Press, London 1981; 307–308
   Google Scholar
• Anton-Tay F., Chou C., Anton S., Wurtman R. J. Brain serotonin concentration: elevation following intraperitoneal administration of melatonin. Science 1968; 162: 277–278
   PubMed Web of Science ®Google Scholar
• Baldissera F., Broggi G., Mancia M. Monosynaptic and polysynaptic spinal reflexes during physiological sleep and wakefulness. Archives of Italian Biology 1966; 104: 112–133
   PubMedGoogle Scholar
• Barasi S., Roberts M. H. T. The action of 5-hydroxytryptamine antagonists and precursors on bulbospinal facilitation of spinal reflexes. Brain Research 1973; 52: 385–388
   PubMed Web of Science ®Google Scholar
• Barinaga M. How scary things get that way. Science 1992; 258: 887–888
   PubMed Web of Science ®Google Scholar
• Baumgarten H. G., Lachenmayer L. Anatomical features and physiological properties of central serotonin neurons. Pharmacopsychiatrie 1985; 18: 180–187
   PubMed Web of Science ®Google Scholar
• Bawin S. M., Adey W. R. Sensitivity of calcium binding in cerebral tissue to weak environmental electric fields oscillating at low frequency. Proceedings of the National Academy of Sciences, USA 1976; 73: 1999–2003
   PubMed Web of Science ®Google Scholar
• Blackman C. F., Shawnee B. G., Kinney S., Joines W. T., House D. E. Effects of ELF fields on calcium-ion efflux from brain tissue in vitro. Radiation Research 1982; 92: 510–520
   PubMed Web of Science ®Google Scholar
• Berg O., Hanley J. Narcolepsy in two cases of multiple sclerosis. Acta Neurologica Scandinavica 1963; 39: 252–257
   PubMed Web of Science ®Google Scholar
• Besset A. Effect of antidepressants on human sleep. Advances in Biosciences 1978; 21: 141–148
   PubMedGoogle Scholar
• Birkeland A. J. Plasma melatonin levels and nocturnal transitions between sleep and wakefulness. Neuroendocrinology 1982; 34: 126–131
   PubMed Web of Science ®Google Scholar
• Brickner R. M., Simon D. J. Emotional stress in relation to attacks of multiple sclerosis. Association for Research in Nervous Disorders Proceedings 1950; 28: 143–146
   PubMedGoogle Scholar
• Buckingham R. L., Radulovacki M. 5-hydroxyindoleacetic acid in cerebrospinal fluid: an indicator of slow wave sleep. Brain Research 1975; 99: 440–443
   PubMed Web of Science ®Google Scholar
• Cardinali D. P. Changes in hypothalamic neurotransmitter uptake following pinealectomy, superior cervical ganglionectomy or melatonin administration to rats. Neuroendocrinology 1975; 19: 91–95
   PubMed Web of Science ®Google Scholar
• Chase M. H., McGinty D. J., Sterman M. B. Cyclic variations in the amplitude of a brainstem reflex during sleep and wakefulness. Experientia 1968; 24: 47–48
   PubMedGoogle Scholar
• Chelmicka-Schorr E., Arnason B. G. Nervous system-immune system interactions and their role in multiple sclerosis. Annals of Neurology 1994; 36: S29–S32, suppl
   Google Scholar
• Clark C. M., Fleming J. A., Li D., Oger J., Klonoff H., Paty D. Sleep disturbance, depression, and lesion site in multiple sclerosis. Archives of Neurology 1992; 49: 641–643
   PubMedGoogle Scholar
• Claveria L. E., Curzon G., Harrison M. J. G., Kantamaneni B. D. Amine metabolites in the cerebrospinal fluid of patients with disseminated sclerosis. Journal of Neurology, Neurosurgery and Psychiatry 1974; 37: 715–718
   PubMed Web of Science ®Google Scholar
• Culebras A. Clinical handbook of sleep disorders. Butterworth-Heinemann, Boston 1996; 328–329
   Google Scholar
• Dafny N. Electrophysiological evidence of photic, acoustic, and central input to the pineal body and hypothalamus. Experimental Neurology 1977; 55: 449–457
   PubMed Web of Science ®Google Scholar
• Dafny N. Two photic pathways contribute to pineal evoked responses. Life Sciences 1980; 26: 737–742
   PubMed Web of Science ®Google Scholar
• Daniels L. E. Narcolepsy. Medicine (Baltimore) 1934; 13: 1–122
   Google Scholar
• Davidson D., Pullar I. A., Mawdsley C., Kinloch N., Yates M. Monoamine metabolites in cerebrospinal fluid in multiple sclerosis. Journal of Neurology, Neurosurgery and Psychiatry 1977; 40: 741–745
   PubMed Web of Science ®Google Scholar
• Demaine C., Semm P. The avian pineal gland as an independent magnetic sensor. Neurscience Letters 1985; 62: 119–122
   PubMed Web of Science ®Google Scholar
• Ebadi M. Regulation of the synthesis of melatonin and its significance to neuroendocrinology. The pineal gland, R. J. Reiter. Raven Press, New York 1984; 1–37
   Google Scholar
• Eleftheriou B. E. The neurobiology of the amygdala. Plenum Press, New York 1972; 11–18
   Google Scholar
• Franklin G., Nelson L., Haeton R. Stress and its relationship to acute exacerbation in MS. Journal of Neurological Rehabilitation 1988; 2: 7–11
   Google Scholar
• Gschwend J. Der Haltetonus der Katze im Schlaf. Brain Research 1970; 22: 29–45
   PubMed Web of Science ®Google Scholar
• Glenn L. L., Foutz A. S., Dement W. C. Membrane potential of spinal motoneurons during natural sleep in the cat. Sleep 1978; 1: 199–204
   PubMedGoogle Scholar
• Grant I., Brown G., Harris T. Severely threatening events and marked life difficulties preceding onset or exacerbation of MS. Journal of Neurology Neurosurgery and Psychiatry 1989; 52: 8–13
   PubMed Web of Science ®Google Scholar
• Guilleminault C. Cataplexy. Narcolepsy, C. Guilleminault, W. C. Dement, P. Passauant. Spectrum Publications. Inc., New York 1976; 125–143
   Google Scholar
• Guilleminault C., Wilson R. A., Dement W. C. A study on cataplexy. Archives of Neurology 1974; 31: 255–261
   PubMedGoogle Scholar
• Halgren E. The amygdala contribution to emotion and memory: current studies in humans. The amygdaloid complex, Y. Ben-Ari. Elsevier, New York 1981; 345–408
   Google Scholar
• Hansen T., Birkeland A. J., Lingiaerde O. Melatonin and sleep in man: a preliminary report. Sleep research, R. G. Priest, A. Pletscher, J. Ward. University Park Press, Baltimore 1978; 43–44
   Google Scholar
• Isaacson R. L. The limbic system. Plenum, New York 1982; 325
   Google Scholar
• Jacobs B. L. Serotonin and behavior: emphasis on motor control. Journal of Clinical Psychiatry 1991; 52(12 (suppl))17–23
   PubMedGoogle Scholar
• Jacobs B. L. Serotonin, motor activity and depression-related disorders. American Scientist 1994; 82: 456–463
   Web of Science ®Google Scholar
• Jacobs B. L., Trulson M. E. Dreams, hallucinations, and psychosis- the serotonin connection. Trends in Neurosciences 1979; 11: 276–280
   Web of Science ®Google Scholar
• Jacobs B. L., Fornal C. A. 5-HT and motor control: a hypothesis. Trends in Neurosciences 1993; 16: 346–352
   PubMed Web of Science ®Google Scholar
• Jacobs B. L., Heym J., Trulson M. E. Behavioral and physiological correlates of brain serotonergic unit activity. Journal of Physiology (Paris) 1981; 77: 431–436
   PubMedGoogle Scholar
• Johansson B., Roos B. E. 5-hydroxyindoleacetic acid in cerebrospinal fluid of patients with neurological diseases. European Neurology 1974; 11: 37–45
   PubMed Web of Science ®Google Scholar
• Jones B. E. Paradoxical sleep and its chemical/structural substrates in the brain. Neuroscience 1991; 40: 637–656
   PubMed Web of Science ®Google Scholar
• Jouvet M., Delorme F. Locus coeruleus et sommeil paradoxal. CR Society of Biology 1965; 159: 895–899
   Google Scholar
• Jouvet M. Biogenic amines and the states of sleep. Science 1969; 163: 32–34
   PubMed Web of Science ®Google Scholar
• Kawakami M., Yamaoka S., Yamaguchi T. Influence of light and hormones upon circadian rhythm of EEG slow-wave and paradoxial sleep. Advanes in climatic physiology, S. Itoh, K. Ogata, H. Yoshimura. Shoin, Tokyo 1972; 349–366
   Google Scholar
• Kelly D. D. Sleep'and dreaming. Principles of neural science3rd Edition, E. R. Kandel, J. H. Schwartz, T. M. Jessell. Elsevier, New York 1991; 792
   Google Scholar
• Klein D. C., Smoot R., Weller J. L., Higa S., Markey S. P., Creed G. J., Jacobowitz D. M. Lesions of the paraventricular nucleus area of the hypothalamus disrupt the suprachiasmatic-spinal cord circuit in the melatonin rhythm generating system. Brain Research Bulletin 1983; 10: 647–652
   PubMed Web of Science ®Google Scholar
• Kovacevic R., Rudulovacki M. Monoamine changes in the brain of cats during slow-wave sleep. Science 1976; 193: 1025–1027
   PubMed Web of Science ®Google Scholar
• Leo G. J., Rao S. M., Bernardin L. Sleep disturbance in multiple sclerosis. Neurology 1991; 41(suppl 1)727
   Google Scholar
• Lhermitte J. Le sommeil et les narcolepsies. Progress Medicale 1930; 22: 962–975
   Google Scholar
• Lynch H. J., Deng M. H. Pineal responses to stress. Journal of Neural Transmission 1986; 21: 461–173, suppl
   Google Scholar
• Mahowald M. W., Schenck C. H. Dissociated states of wakefulness and sleep. Neurology 1992; 42(suppl 6)44–52
   PubMedGoogle Scholar
• McGinty D. J., Harper R. M. Dorsal raphe neurons: depression of firing during sleep in cats. Brain Research 1973; 101: 569–575
   Web of Science ®Google Scholar
• Mess B., Ruzsas C., Trentini G. P. Pineal mechanisms regulating reproduction in seasona and nonseasonal breeders: a comparative survey. Neuroendocrinology Letters 1984; 6: 253–259
   Google Scholar
• Miguez J. M., Martin F., Aldegunde M. Differential effects of pinealectomy on amyg dala and hippocampus serotonin metabolism. Journal of Pineal Research 1991a; 10: 100–103
   PubMed Web of Science ®Google Scholar
• Miguez J. M., Martin F., Aldegunde M. Long-term pinealectomy alters hypothalamic serotonin metabolism in the rat. Journal of Pineal Research 1991b; 11: 75–79
   PubMed Web of Science ®Google Scholar
• Miguez J. M., Martin F. J., Aldegunde M. Effects of single doses and daily melatonin treatments on serotonin metabolism in rat brain regions. Journal of Pineal Research 1994; 17: 170–176
   PubMed Web of Science ®Google Scholar
• Montplaisir J., Godbout R. Zimelidine: a new treatment for cataplexy. Abstract 4th International Congress of Sleep Research. Bologna, Italy 1983; 332
   Google Scholar
• Montplaisir J., Godbout R. Serotoninergic reuptake mechanisms in the control of cataplexy. Sleep 1986; 9: 280–284
   PubMed Web of Science ®Google Scholar
• Morales F., Chase M. H. Post-synaptic control of lumbar motoneurons excitability during active sleep in the chronic cat. Brain Research 1981; 225: 279–295
   PubMed Web of Science ®Google Scholar
• Moszkowska A., Kordon C., Ebels I. Biochemical fractions and mechanisms involved in the pineal modulation of pituitary gonadotropin release. The pineal gland, G. E. W. Wolstenholme, J. Knigh. Churchill-Livingstone, London 1971; 241–258
   Google Scholar
• Mouret J., Coindet J., Chouvet G. Effet de la pinealectomie sur les etats et rythmes de sommeil du rat male. Brain Research 1974; 81: 97–105
   PubMedGoogle Scholar
• Parkes J. D. Sleep and its disorders. W. B. Saunders, London 1985; 294
   Google Scholar
• Passouant P., Baldy-Molinier M., Aussilloux Ch. Etat de mal cataplectique au cours d'une maladie de Gelineau, influence de la clomipramine. Revue Neurologique 1970; 123: 56–60
   PubMed Web of Science ®Google Scholar
• Pavel S., Goldstein R., Petrescu M. Vasotocin, melatonin and narcolepsy: possible involvement of the pineal gland in its pathophysiological mechanisms. Peptides 1980; 1: 281–284
   PubMed Web of Science ®Google Scholar
• Pazo J. H. Effects of melatonin on spontaneous and evoked neuronal activity in the mesencephalic reticular formation. Brain Research Bulletin 1979; 4: 725–730
   PubMed Web of Science ®Google Scholar
• Pierpaoli W., Maestroni G. J. M. Melatonin: a principal neuroimmunoregulatory and anti-stress hormone: its anti-aging effect. Immunology Letters 1987; 16: 355–362
   PubMed Web of Science ®Google Scholar
• Pompeiano O. The neurophysiological mechanisms of the postural and motor events during desynchronized sleep. Research Publications of the Association of Nervous and Mental Disease 1967; 45: 351–423
   Google Scholar
• Relkin R. The pineal gland. New England Journal of Medicine 1966; 214: 944–949
   Google Scholar
• Romijn H. J. The pineal, a tranquillizing organ?. Life Sciences 1978; 23: 2257–2274
   PubMed Web of Science ®Google Scholar
• Roth B. Narcolepsy and hypersomnia. S. Karger, Basel 1980
   Google Scholar
• Ruzsas C. Functional Relationships between pineal gland and habenular complex. Fundamentals and clinics in pineal research, G. P. Trentini, C. De Gaetani, P. Pevet. Raven Press, New York 1987; 257–270
   Google Scholar
• Sakai K. Some anatomical and physiological properties of ponto-mesencephalic tegmental neurons. The reticular formation revisited, J. A. Hobson, M. A. B. Brazier. Raven Press, New York 1980; 427–447
   Google Scholar
• Sakai K. Executive mechanisms of paradoxical sleep. Archives of Italian Biology 1988; 126: 239–257
   PubMedGoogle Scholar
• Sandyk R. Successful treatment of multiple sclerosis with magnetic fields. International Journal of Neuroscience 1992; 66: 237–250
   PubMed Web of Science ®Google Scholar
• Sandyk R. Rapid normalization of visual evoked potentials by picotesla range magnetic fields in chronic progressive multiple sclerosis. International Journal of Neuroscience 1994; 11: 243–259
   Google Scholar
• Sandyk R. Chronic relapsing multiple sclerosis: a case of rapid recovery by application of weak electromagnetic fields. International Journal of Neuroscience 1995a; 82: 223–242
   PubMed Web of Science ®Google Scholar
• Sandyk R. Long term beneficial effects of weak electromagnetic fields in multiple sclerosis. International Journal of Neuroscience 1995b; 83: 45–57
   PubMed Web of Science ®Google Scholar
• Sandyk R. The pineal gland, cataplexy, and multiple sclerosis. International Journal of Neuroscience 1995c; 83: 153–163
   PubMed Web of Science ®Google Scholar
• Sandyk R. Resolution of partial cataplexy in multiple sclerosis by treatment with weak electromagnetic fields. International Journal of Neuroscience 1996a; 84: 157–164
   PubMed Web of Science ®Google Scholar
• Sandyk R. Treatment with electromagnetic fields alters the clinical course of chronic progressive multiple sclerosis: a case report. International Journal of Neuroscience 1996b; 88: 75–82
   PubMed Web of Science ®Google Scholar
• Sandyk R., Awerbuch G. I. Nocturnal plasma melatonin and alpha-melanocyte stimulating hormone levels during exacerbation of multiple sclerosis. International Journal of Neuroscience 1992; 67: 173–186
   PubMed Web of Science ®Google Scholar
• Sandyk R., Awerbuch G. I. Nocturnal melatonin secretion in multiple sclerosis patients with affective disorders. International Journal of Neuroscience 1993; 68: 227–240
   PubMed Web of Science ®Google Scholar
• Sandyk R., Dann L. C. Weak electromagnetic fields attenuate tremor in multiple sclerosis. International Journal of Neuroscience 1994; 79: 199–212
   PubMed Web of Science ®Google Scholar
• Sandyk R., Dann L. C. Resolution of Lhermitte's sign in multiple sclerosis by treatment with weak electromagnetic fields. International Journal of Neuroscience 1995; 81: 215–224
   PubMed Web of Science ®Google Scholar
• Sandyk R., Derpapas K. Magnetic fields normalize visual and brainstem auditory evoked potentials in multiple sclerosis. International Journal of Neuroscience 1993a; 68: 241–253
   PubMedGoogle Scholar
• Sandyk R., Derpapas K. Successful treatment of an acute exacerbation of multiple sclerosis by external magnetic fields. International Journal of Neuroscience 1993b; 70: 97–105
   PubMedGoogle Scholar
• Sandyk R., Iacono R. P. Resolution of longstanding symptoms of multiple sclerosis by application of picotesla range magnetic fields. International Journal of Neuroscience 1993; 70: 255–269
   PubMed Web of Science ®Google Scholar
• Schrader H., Goltlibsen O. B., Slomedial G. M. Multiple sclerosis and narcolepsy/cataplexy in a monozygotic twin. Neurology 1980; 30: 105–108
   PubMed Web of Science ®Google Scholar
• Scrinia L. An etiology of narcolepsy-cataplexy and a proposed cataplexy neuromechanism. International Journal of Neuroscience 1981; 15: 69–86
   PubMedGoogle Scholar
• Semm P. Neurobiological investigations on the magnetic sensitivity of the pineal gland in rodents and pigeons. Comparative Biochemistry and Physiology 1983; 76A: 683–689
   Web of Science ®Google Scholar
• Shapiro W. R. Treatment of cataplexy with clomipramine. Archives of Neurology 1975; 32: 653–656
   PubMedGoogle Scholar
• Sibley W. A. Therapeutic claims in multiple sclerosis. Demos Publications, New York 1992; 15
   Google Scholar
• Smale L., Cassone V. M., Moore R. Y., Mortin L. P. Paraventricular nucleus projections mediating pineal melatonin and gonadal responses to photoperiod in the hamster. Brain Research Bulletin 1989; 22: 263–269
   PubMed Web of Science ®Google Scholar
• Smith A. R., Kappers J. A. Effect of pinealectomy, gonadectomy, pCPA and pineal extracts on the rat parvocellular neurosecretory hypothalamic system: a fluorescence histochemical investigation. Brain Research 1975; 86: 353–371
   PubMed Web of Science ®Google Scholar
• Sonninen V., Riekkinen P., Rinne U. K. Acid monoamine metabolites in cerebrospinal fluid in multiple sclerosis. Neurology 1973; 23: 760–763
   PubMed Web of Science ®Google Scholar
• Stehle J., Vanecek J., Vollrath L. Effects of melatonin on spontaneous electrical activity of neurons in rat suprachiasmatic nuclei: an in vitro iontophoretic study. Journal of Neural Transmission 1989; 78: 173–177
   PubMed Web of Science ®Google Scholar
• Steriade M. Basic mechanisms of sleep generation. Neurology 1992; 42(suppl 6)9–18
   PubMedGoogle Scholar
• Tima L., Trentini G. P., Mess B. Effect of serotonin on ovulation induced by pinealectomy in anovulatory frontal deafferented rats. Neuroendocrinology 1973; 12: 149–152
   PubMedGoogle Scholar
• Trulson M., Jacobs B. L. Raphe unit activity in freely moving cats: correlation with level of behavioral arousal. Brain Research 1979; 163: 135–150
   PubMed Web of Science ®Google Scholar
• Trulson M., Jacobs B. L., Morrison A. R. Raphe unit activity during REM sleep in normal cats and in pontine lesioned cats displaying REM sleep without atonia. Brain Research 1981; 226: 75–91
   PubMed Web of Science ®Google Scholar
• Vizioli R. Les bases neurophysiologiques de la cataplexie. Electroencephalography & Clinical Neurophysiology 1964; 16: 191–193
   PubMedGoogle Scholar
• Warren S., Greenhill S., Warren K. Emotional stress and the development of MS: case-control evidence of a relationship. Journal of Chronic Disease 1982; 35: 821–831
   PubMedGoogle Scholar
• Wendel O. T., Waterbury L. D., Pearce L. A. Increase in monoamine concentration in rat brain following melatonin administration. Experientia 1974; 30: 1167–1168
   PubMedGoogle Scholar
• Welker H. A., Semm P., Willig R. P., Commentz J. C., Wiltschko W., Vollrath L. Effects of an artificial magnetic field on serotonin N-acetyltransferase activity and melatonin content of the rat pineal gland. Experimental Brain Research 1983; 50: 426–132
   PubMed Web of Science ®Google Scholar
• Wilson B. W., Chess E. K., Anderson L. E. 60-Hz electric-field effects on pineal melatonin rhythms: time course for onset and recovery. Bioelectromagnetics 1986; 7: 239–242
   PubMed Web of Science ®Google Scholar
• Wilson B. W., Stevens R. G., Anderson L. E. Neuroendocrine mediated effects of electromagnetic field exposure: possible role of the pineal gland. Life Sciences 1989; 45: 1319–1332
   PubMed Web of Science ®Google Scholar
• Wilson B. W., Stevens R. G., Anderson L. E. Effects of electromagnetic field exposure on neuroendocrine function. Electromagnetic fields and circadian rhythmicity, M. C. Moore-Ede, S. S. Campbell, R. J. Reiter. Birkhauser, Boston 1992; 29–50
   Google Scholar
• Wyatt R. J., Neff N. H., Vaughan T., Frantz J., Ommaya A. Ventricular fluid 5-hydroxyindolacetic acid concentrations during human sleep. Advances in biochemicalpsychopharmacology, E. Costa, P. Greengard. Raven Press, New York 1974; vol. 11: 193–197
   Google Scholar
• Yanowski J., Witcher J., Adler N., Markey S. P., Klein D. C. Stimulation of the paraventricular nucleus area of the hypothalamus elevates urinary 6-hydroxymelatonin during daytime. Brain Research Bulletin 1987; 19: 129–133
   PubMed Web of Science ®Google Scholar
• Yates C. A., Herbert J. Differential circadian rhythms in pineal and hypothalamic 5-HT induced by artificial photoperiods or melatonin. Nature 1976; 262: 219–220
   PubMed Web of Science ®Google Scholar
• Younger D. S., Pedley T. A., Thorpy M. J. Multiple sclerosis and narcolepsy: possible similar genetic susceptibility. Neurology 1991; 41: 447–148
   PubMed Web of Science ®Google Scholar