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E Hershkovitz

Showing results (1-10 of 38) with videos related to

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Harefuah|May 1, 1991
[Potassium permanganate poisoning in infancy]E Hershkovitz, Z Weizman
Hormone Research|August 3, 2004
The childhood component of the ICP model is appropriate for growth analysis of short Israeli childrenY Limony, E Leiberman, E Hershkovitz
Orphanet Journal of Rare Diseases|November 26, 2020
Incidence of inherited metabolic disorders in southern Israel: a comparison between consanguinity and non-consanguinity communitiesG Hazan, E Hershkovitz, O Staretz-Chacham
European Radiology|June 23, 2001
Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disordersG Blinder, J Corat-Simon, E Hershkovitz
Israel Journal of Medical Sciences|November 1, 1996
Status epilepticus following intravenous N-acetylcysteine therapyE Hershkovitz, Z Shorer, A Levitas, et al.
Prenatal Diagnosis|September 1, 1996
Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)R Parvari, E Hershkovitz, R Carmi, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Continuous glucose monitoring in children with glycogen storage disease type IE Hershkovitz, A Rachmel, H Ben-Zaken, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
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 ArabR Parvari, S Moses, E Hershkovitz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 1, 1995
Thyrotropin secreting pituitary adenoma associated with hypopituitarism and diabetes insipidus in an adolescent boyM Phillip, E Hershkovitz, P Kornmehl, et al.
Hormone Research|July 1, 1996
Short-term growth hormone therapy increases serum lipoprotein (a) levels in normal short children without growth hormone deficiencyE Hershkovitz, E Leiberman, Y Limony, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Harefuah|May 1, 1991
[Potassium permanganate poisoning in infancy]E Hershkovitz, Z Weizman
Hormone Research|August 3, 2004
The childhood component of the ICP model is appropriate for growth analysis of short Israeli childrenY Limony, E Leiberman, E Hershkovitz
Orphanet Journal of Rare Diseases|November 26, 2020
Incidence of inherited metabolic disorders in southern Israel: a comparison between consanguinity and non-consanguinity communitiesG Hazan, E Hershkovitz, O Staretz-Chacham
European Radiology|June 23, 2001
Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disordersG Blinder, J Corat-Simon, E Hershkovitz
Israel Journal of Medical Sciences|November 1, 1996
Status epilepticus following intravenous N-acetylcysteine therapyE Hershkovitz, Z Shorer, A Levitas, et al.
Prenatal Diagnosis|September 1, 1996
Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)R Parvari, E Hershkovitz, R Carmi, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Continuous glucose monitoring in children with glycogen storage disease type IE Hershkovitz, A Rachmel, H Ben-Zaken, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
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 ArabR Parvari, S Moses, E Hershkovitz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 1, 1995
Thyrotropin secreting pituitary adenoma associated with hypopituitarism and diabetes insipidus in an adolescent boyM Phillip, E Hershkovitz, P Kornmehl, et al.
Hormone Research|July 1, 1996
Short-term growth hormone therapy increases serum lipoprotein (a) levels in normal short children without growth hormone deficiencyE Hershkovitz, E Leiberman, Y Limony, et al.
Pageof 4