Nirit D. Carmi

Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features

P. May, R. Krause, S. Haas, 2017, Brain : a journal of neurology.

Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2016, Journal of child neurology.

Human Placental Derived Mesenchymal Stromal Cells (MSC) Grown in 3D-Culture (PLX-I), Promotes Engraftment of Human Umbilical Cord Blood (hUCB) Derived CD34+ Cells in NOD/SCID Mice.

A. Nagler, A. Kadouri, E. Horwitz, 2007 .

Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype

R. Gershoni-baruch, E. Dagan, E. Friedman, 2002, European Journal of Human Genetics.

Age-related changes in upper airway muscles morphological and oxidative properties

R. Coleman, M. Odeh, A. Oliven, 2001, Experimental Gerontology.

Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome?

K. Bhatia, D. Lev, W. Dobyns, 2020, American journal of medical genetics. Part A.

Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep.

E. Leshinsky‐Silver, D. Lev, Y. Anikster, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.