S. Gottlieb

发表

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.

D. Stephan, E. Puffenberger, J. Parod, 2006, The New England journal of medicine.

Ganglioside GM 3 is essential for the structural integrity and function of cochlear hair cells

K. Strauss, A. Suzuki, J. Inokuchi, 2015 .

Ganglioside GM3 is essential for the structural integrity and function of cochlear hair cells.

K. Strauss, A. Suzuki, J. Inokuchi, 2015, Human molecular genetics.

Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier.

E. Puffenberger, K. Strauss, K. Aoki, 2019, Molecular genetics and metabolism.

Acute Hemorrhagic Leukoencephalitis: Recovery and Reversal of Magnetic Resonance Imaging Findings in a Child

N. Rosman, S. Gottlieb, Carolyn A. Bernstein, 1997, Journal of child neurology.

Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.

Peter B Crino, David A Ramsay, David W Craig, 2007, Brain : a journal of neurology.

Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant

E. Puffenberger, K. Strauss, K. Millen, 2016, American journal of human genetics.

Central nervous system hemangiomatosis in early childhood.

N. Rosman, S. Gottlieb, D. M. Capin, 1997, Pediatric neurology.

Stroke in Children After Blunt Intraoral Trauma: Use of Magnetic Resonance Angiography as a Noninvasive Diagnostic Tool

N. Rosman, S. Gottlieb, R. Stich, 1996, Journal of child neurology.