Zamir Shorer
Soroka Medical Center(IL)
Publications by Year
Research Areas
Epilepsy research and treatment, Hereditary Neurological Disorders, Pharmacological Effects and Toxicity Studies, Mitochondrial Function and Pathology, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy(2006)194 cited
- → Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9(2008)188 cited
- → Demyelinating Peripheral Neuropathy in Merosin-Deficient Congenital Muscular Dystrophy(1995)171 cited
- → CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy(2012)164 cited
- → Melatonin Effect on Seizures in Children with Severe Neurologic Deficit Disorders(2001)149 cited
- → Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: Genetic heterogeneity, novel mutations in theTRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies(2000)135 cited
- → Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ(2008)134 cited
- → Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations(2010)125 cited
- → SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome(2017)101 cited
- → Outcome of infants with unilateral Sturge-Weber syndrome and early onset seizures(2000)87 cited