J. P. Newman

发表

Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.

V. Meiner, M. Macarov, M. Zeigler, 2007, Journal of intellectual disability research : JIDR.

Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.

R. Rozen, V. Meiner, S. Korman, 2014, JAMA Neurology.

Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.

S. Klebe, A. Durr, N. Elleuch, 2006, Archives of neurology.

A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced β-glucocerebrosidase activity

V. Meiner, O. Abramsky, O. Kakhlon, 2014, Journal of the Neurological Sciences.

Successful parathyroidectomy improves cognition in patients with primary hyperparathyroidism: A prospective study in a tertiary medical center and comprehensive review of the literature

H. Mazeh, A. Szalat, J. P. Newman, 2022, Frontiers in Endocrinology.

Early clinical heterogeneity in choreoacanthocytosis.

A. Monaco, N. Gadoth, L. Fananapazir, 2005, Archives of neurology.

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

J. Gomori, Z. Meiner, D. Ekstein, 2003, Journal of Neurology.

Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.

O. Schueler‐Furman, J. Gomori, M. Harel, 2015, Brain : a journal of neurology.

Lipoid proteinosis with bilateral amygdalae calcifications, headache, and cognitive impairments

D. Arkadir, J. Gomori, I. Lerer, 2013, Neurology.

Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.

R. Rozen, V. Meiner, S. Korman, 2014, JAMA neurology.