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Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1985
Retinitis pigmentosa and early onset myopathy: a case reportN Gadoth, T Treves, A Kuritzky, et al.Israel Journal of Medical Sciences|February 1, 1979
Cat-scratch disease presenting as status epilepticus. A case reportN Gadoth, A Oren, A Keynan, et al.Israel Journal of Medical Sciences|August 1, 1984
1H and 31P nuclear magnetic resonance spectroscopy of erythrocyte extracts in myotonic muscular dystrophyN Gadoth, J Grinblat, H Shvo, et al.Journal of the American Academy of Dermatology|August 1, 1988
Electromyographic abnormalities in patients undergoing long-term therapy with etretinateM David, E Hodak, M Sandbank, et al.Journal of Pediatric Ophthalmology and Strabismus|November 1, 1981
Cyclic esotropia with minimal brain dysfunctionN Gadoth, Z Dickerman, M Lerman, et al.Cytogenetics and Cell Genetics|January 1, 1978
A homologous tandem translocation [45,XX,-13,-13,+t(13;13) (q12;q34)]M M Cohen, Y Rosen, N Gadoth, et al.Brain & Development|January 1, 1991
Three modality evoked potentials in Charcot-Marie-Tooth disease (HMSN-1)N Gadoth, C R Gordon, N Bleich, et al.Neurology|July 1, 1994
Machado-Joseph (Azorean) disease in a Yemenite Jewish family in IsraelH Goldberg-Stern, R D'jaldetti, E Melamed, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Vestibulo-ocular arreflexia in families with spinocerebellar ataxia type 3 (Machado-Joseph disease)C R Gordon, V Joffe, G Vainstein, et al.Brain : a Journal of Neurology|February 1, 1993
Vacuolar myopathy sparing the quadricepsM Sadeh, N Gadoth, H Hadar, et al.Pageof 16