R. Amit

Fatal familial infantile glycogen storage disease: Multisystem phosphofructokinase deficiency

Y. Shapira, N. Bashan, S. Sofer, 1992, Muscle & nerve.

Familial Ataxia with Extreme Difference in Age of Clinical Onset

Y. Shapira, R. Amit, G. Granit, 1986, Neuropediatrics.

Acute, severe, central and peripheral nervous system combined demyelination.

Y. Shapira, M. Aker, M. Aker, 1986, Pediatric neurology.

Vitamin E deficiency in Werdnig‐Hoffmann disease

Y. Shapira, Eliezer Rachmilewitz, R. Amit, 1981, Annals of neurology.

Blockage of eye-closure-generated generalized paroxysms by mental activity

D. Amit, Y. Amit, R. Amit, 2006, Journal of Pediatric Neurology.

Benign focal epilepsy of childhood: individual and intrafamilial multifocality of spikes.

R. Amit, 1987, Clinical EEG.

Ring 18 chromosome with mental retardation, hemidysmorphism, and mitochondrial encephalomyopathy.

G. Kohn, A. Gutman, V. Barash, 1988, Pediatric neurology.