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Brain : a Journal of Neurology|October 1, 1990
Congenital myasthenia associated with facial malformations in Iraqi and Iranian Jews. A new genetic syndromeY Goldhammer, I Blatt, M Sadeh, et al.Journal of Child Neurology|June 27, 2000
Common peroneal neuropathy due to surfingN Watemberg, S Amsel, M Sadeh, et al.Postgraduate Medical Journal|March 1, 1992
Adult metachromatic leukodystrophy with an unusual relapsing-remitting courseM Sadeh, A Kuritzky, E Ben-David, et al.Brain : a Journal of Neurology|February 1, 1993
Vacuolar myopathy sparing the quadricepsM Sadeh, N Gadoth, H Hadar, et al.Pediatric Neurology|November 27, 1998
Lissencephaly associated with congenital hypomyelinating and axonal neuropathyA Nissenkorn, S Weintraub, M Sadeh, et al.The Journal of Dermatological Treatment|May 16, 2009
Occlusive therapy in atopic dermatitis: overviewSabrina J Braham, Rupa Pugashetti, John Koo, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1972
Subacute spongiform encephalopathy and its relation to Jakob-Creutzfeldt disease: report on six casesY Goldhammer, J J Bubis, I Sarova-Pinhas, et al.Clinical Neurology and Neurosurgery|April 20, 2001
Benign intracranial hypertension: correlation of cerebral blood flow with disease severityM Lorberboym, Y Lampl, A Kesler, et al.Human Genetics|May 1, 1996
A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth diseaseR Navon, B Seifried, N S Gal-On, et al.Pediatric Neurology|October 1, 1995
Cerebral calcinosis and learning disabilities in hypoparathyroidism: a cause and effect or a coincidence?A Shuper, A Zeharia, L Korenreich, et al.Pageof 14