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Neurology|December 1, 1993
An Israeli family with Gerstmann-Sträussler-Scheinker disease manifesting the codon 102 mutation in the prion protein geneY Goldhammer, R Gabizon, Z Meiner, 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.European Neurology|January 1, 1986
Does prolonged use of diphenylhydantoin predispose to pulmonary sarcoidosis?I Rubinstein, G L Baum, Y Hiss, et al.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.Neurochirurgia|March 1, 1976
Trans-sphenoidal surgical approach in pituitary apoplexyI Z Kosary, J Braham, R Tadmor, et al.Neurology|September 1, 1994
The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutationJ Chapman, J Ben-Israel, Y Goldhammer, et al.Archives of Neurology|April 1, 1982
Basal encephalocele associated with suprasellar epidermoid cystM Sadeh, Y Goldhammer, I Shacked, 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.Epilepsia|September 1, 1991
Treatment of porphyric convulsions with magnesium sulfateM Sadeh, I Blatt, G Martonovits, et al.Ophthalmology|July 1, 1986
Sixth nerve palsy and unilateral Horner's syndromeI Gutman, S Levartovski, Y Goldhammer, et al.Pageof 71