Total oxidant-scavenging capacities of plasma from glycogen storage disease type Ia patients as measured by cyclic voltammetry, FRAP and luminescence techniquesKOREN, E; LIPKIN, J; KLAR, A et al.Journal of inherited metabolic disease. 2009, Vol 32, Num 5, pp 651-659, issn 0141-8955, 9 p.Article

Blood lipids and endothelial function in glycogen storage disease type IIIHERSHKOVITZ, E; DONALD, A; MULLEN, M et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 8, pp 891-898, issn 0141-8955Article

Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)PARVARI, R; HERSHKOVITZ, E; CARMI, R et al.Prenatal diagnosis. 1996, Vol 16, Num 9, pp 862-865, issn 0197-3851Article

Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientPARVARI, R; SHEN, J; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1998, Vol 21, Num 2, pp 141-148, issn 0141-8955Article

Status epilepticus following intravenous N-acetylcysteine therapyHERSHKOVITZ, E; SHORER, Z; LEVITAS, A et al.Israel journal of medical sciences. 1996, Vol 32, Num 11, pp 1102-1104, issn 0021-2180Conference Paper

RFLPs for linkage analysis in families with glycogen storage disease type IIIMISHORI-DERY, A; BASHAN, N; MOSES, S et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 2, pp 207-210, issn 0141-8955Article

Carnitine-acylcarnitine translocase deficiency: Identification of a novel molecular defect in a Bedouin patientGALRON, D; BIRK, O. S; KAZANOVITZ, A et al.Journal of inherited metabolic disease. 2004, Vol 27, Num 2, pp 267-273, issn 0141-8955, 7 p.Article

Continuous glucose monitoring in children with glycogen storage disease type IHERSHKOVITZ, E; RACHMEL, A; BEN-ZAKEN, H et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 8, pp 863-869, issn 0141-8955Article

High prevalence of thyroxine-binding globulin deficiency among Bedouin infants in Southern IsraelHERSHKOVITZ, E; LEIBERMAN, E; REFETOFF, S et al.Israel journal of medical sciences. 1995, Vol 31, Num 8, pp 500-502, issn 0021-2180Conference Paper

Luteinizing hormone-releasing hormone antagonists interfere with autocrine and paracrine growth stimulation of MCF-7 mammary cancer cells by insulin-like growth factorsHERSHKOVITZ, E; MARBACH, M; BOSIN, E et al.The Journal of clinical endocrinology and metabolism. 1993, Vol 77, Num 4, pp 963-968, issn 0021-972XArticle

Adrenal insufficiency after achalasia in the triple-A syndrome. EditorialPHILLIP, M; HERSHKOVITZ, E; SCHULMAN, H et al.Clinical pediatrics. 1996, Vol 35, Num 2, pp 99-102, issn 0009-9228Article

Once versus twice daily injections of growth hormone in children with idiopathic short staturePHILLIP, M; HERSHKOVITZ, E; BELOTSERKOVSKY, O et al.Acta paediatrica (Oslo). 1998, Vol 87, Num 5, pp 518-520, issn 0803-5253Article

Glycogen storage disease type 1a in Israel : Biochemical, clinical, and mutational studiesPARVARI, R; LEI, K.-J; BASHAN, N et al.American journal of medical genetics. 1997, Vol 72, Num 3, pp 286-290, issn 0148-7299Article

Differences in cord serum retinol concentrations by ethnic origin in the Negev (Southern Israel)GORODISCHER, R; SAROV, B; GAZALA, E et al.Early human development. 1995, Vol 42, Num 2, pp 123-130, issn 0378-3782Article

The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay : a report of six patientsHERSHKOVITZ, E; SHALITIN, S; LEVY, J et al.Israel journal of medical sciences. 1995, Vol 31, Num 5, pp 293-297, issn 0021-2180Article

Prenatal ultrasonic diagnosis of nonhypertrophic pyloric stenosis associated with intestinal malrotationHERSHKOVITZ, E; STEINER, Z; SHINWELL, E. S et al.Journal of clinical ultrasound. 1993, Vol 22, Num 1, pp 52-54, issn 0091-2751Article

Controlling activated surface diffusion by external fieldsTALKNER, P; HERSHKOVITZ, E; POLLAK, E et al.Surface science. 1999, Vol 437, Num 1-2, pp 198-206, issn 0039-6028Article

Multiple hops in multidimensional activated surface diffusionHERSHKOVITZ, E; TALKNER, P; POLLAK, E et al.Surface science. 1999, Vol 421, Num 1-2, pp 73-88, issn 0039-6028Article

Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43PARVARI, R; HERSHKOVITZ, E; KANIS, A et al.American journal of human genetics. 1998, Vol 63, Num 1, pp 163-169, issn 0002-9297Article

Increase of serum lipoprotein (a) levels during growth hormone therapy in normal short childrenHERSHKOVITZ, E; BELOTSERKOVSKY, O; LIMONY, Y et al.European journal of pediatrics. 1998, Vol 157, Num 1, pp 4-7, issn 0340-6199Article

The gene for glycogen-storage disease type 1b maps to chromosome 11q23ANNABI, B; HIRAIWA, H; FRYMAN, M et al.American journal of human genetics. 1998, Vol 62, Num 2, pp 400-405, issn 0002-9297Article

Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim ArabPARVARI, R; MOSES, S; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 1, pp 21-27, issn 0141-8955Article