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Results: 10

Authors: KLEIN C HALEVY A GANDELMANMARTON R HALPERN Z WEISSGARTEN J AVERBUKH Z ARLAZOROFF A
Citation: C. Klein et al., NERVE-CONDUCTION ABNORMALITIES IN THE ARMS OF PATIENTS WITH ARTERIOVENOUS-FISTULA, Renal failure, 18(1), 1996, pp. 85-89

Authors: THEITLER J MARTONGANDELMAN R KLEIN C JOSSIPHOV J ARLAZOROFF A
Citation: J. Theitler et al., CHRONIC VARICELLA-ZOSTER-VIRUS ENCEPHALITIS IN AN ELDERLY PATIENT, La Presse medicale, 25(15), 1996, pp. 718-719

Authors: CHAPMAN J ARLAZOROFF A GOLDFARB LG CERVENAKOVA L NEUFELD MY WERBER E HERBERT M BROWN P GAJDUSEK DC KORCZYN AD
Citation: J. Chapman et al., FATAL INSOMNIA IN A CASE OF FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH THE CODON 200(LYS) MUTATION, Neurology, 46(3), 1996, pp. 758-761

Authors: POLLAK L KLEIN C GILADI R KERTESZ J ARLAZOROFF A
Citation: L. Pollak et al., PROGRESSIVE DETERIORATION OF BRAIN-STEM AUDITORY-EVOKED POTENTIALS INCREUTZFELDT-JAKOB-DISEASE - CLINICAL AND ELECTROENCEPHALOGRAPHIC CORRELATION, Clinical EEG electroencephalography, 27(2), 1996, pp. 95-99

Authors: MARTON R GOTLIEBSTEIMATSKY T KLEIN C ARLAZOROFF A
Citation: R. Marton et al., ACUTE HERPES-SIMPLEX ENCEPHALITIS - CLINICAL-ASSESSMENT AND PROGNOSTIC DATA, Acta neurologica Scandinavica, 93(2-3), 1996, pp. 149-155

Authors: MARTON R GOTLIEBSTEMATSKY T KLEIN C LAHAT E ARLAZOROFF A
Citation: R. Marton et al., MILD FORM OF ACUTE HERPES-SIMPLEX ENCEPHALITIS IN CHILDHOOD, Brain & development, 17(5), 1995, pp. 360-361

Authors: POLLAK L KLEIN C TIEDER M ARLAZOROFF A
Citation: L. Pollak et al., THERAPY-RESISTANT SEIZURES IN PSEUDOHYPOPARATHYROIDISM - A CASE-REPORT, Journal of pediatric endocrinology & metabolism, 8(3), 1995, pp. 209-211

Authors: LAHAT E AVITAL E BARR J BERKOVITCH M ARLAZOROFF A ALADJEM M
Citation: E. Lahat et al., BAEP STUDIES IN CHILDREN WITH ATTENTION-DEFICIT DISORDER, Developmental Medicine and Child Neurology, 37(2), 1995, pp. 119-123

Authors: ARLAZOROFF A CHAPMAN J NEUFELD MY WERBER E KORCZYN AD GOLDFARB LG BROWN P GAJDUSEK DC GAMBETTI P
Citation: A. Arlazoroff et al., FATAL INSOMNIA IN A CASE OF FAMILIAL CREUTZFELDT-JAKOB-DISEASE (CJD) WITH THE CODON 200(LYS) MUTATION, Neurology, 44(4), 1994, pp. 10000219-10000219

Authors: CHAPMAN J BROWN P GOLDFARB LG ARLAZOROFF A GAJDUSEK DC KORCZYN AD
Citation: J. Chapman et al., CLINICAL HETEROGENEITY AND UNUSUAL PRESENTATIONS OF CREUTZFELDT-JAKOB-DISEASE IN JEWISH PATIENTS WITH THE PRNP CODON 200 MUTATION, Journal of Neurology, Neurosurgery and Psychiatry, 56(10), 1993, pp. 1109-1112
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