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E Hershkovitz

Showing results (21-30 of 38) with videos related to

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Journal of Inherited Metabolic Disease|May 19, 1998
Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientR Parvari, J Shen, E Hershkovitz, et al.
European Journal of Pediatrics|February 14, 1998
Increase of serum lipoprotein (a) levels during growth hormone therapy in normal short childrenE Hershkovitz, O Belotserkovsky, Y Limony, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Carnitine-acylcarnitine translocase deficiency: identification of a novel molecular defect in a Bedouin patientD Galron, O S Birk, A Kazanovitz, et al.
Journal of Inherited Metabolic Disease|September 4, 2009
Total oxidant-scavenging capacities of plasma from glycogen storage disease type Ia patients as measured by cyclic voltammetry, FRAP and luminescence techniquesE Koren, J Lipkin, A Klar, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Once versus twice daily injections of growth hormone in children with idiopathic short statureM Phillip, E Hershkovitz, O Belotserkovsky, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patientsR Parvari, S Moses, J Shen, et al.
Biochemical and Biophysical Research Communications|August 17, 1999
Lipoamide dehydrogenase deficiency due to a novel mutation in the interface domainE Shany, A Saada, D Landau, et al.
Early Human Development|June 21, 1995
Differences in cord serum retinol concentrations by ethnic origin in the Negev (southern Israel)R Gorodischer, B Sarov, E Gazala, et al.
Hormone Research|March 4, 1998
Serum insulin-like growth factors I and II are not affected by undernutrition in children with nonorganic failure to thriveM Phillip, E Hershkovitz, H Rosenblum, et al.
Israel Journal of Medical Sciences|May 1, 1995
The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patientsE Hershkovitz, S Shalitin, J Levy, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|May 19, 1998
Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientR Parvari, J Shen, E Hershkovitz, et al.
European Journal of Pediatrics|February 14, 1998
Increase of serum lipoprotein (a) levels during growth hormone therapy in normal short childrenE Hershkovitz, O Belotserkovsky, Y Limony, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Carnitine-acylcarnitine translocase deficiency: identification of a novel molecular defect in a Bedouin patientD Galron, O S Birk, A Kazanovitz, et al.
Journal of Inherited Metabolic Disease|September 4, 2009
Total oxidant-scavenging capacities of plasma from glycogen storage disease type Ia patients as measured by cyclic voltammetry, FRAP and luminescence techniquesE Koren, J Lipkin, A Klar, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Once versus twice daily injections of growth hormone in children with idiopathic short statureM Phillip, E Hershkovitz, O Belotserkovsky, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patientsR Parvari, S Moses, J Shen, et al.
Biochemical and Biophysical Research Communications|August 17, 1999
Lipoamide dehydrogenase deficiency due to a novel mutation in the interface domainE Shany, A Saada, D Landau, et al.
Early Human Development|June 21, 1995
Differences in cord serum retinol concentrations by ethnic origin in the Negev (southern Israel)R Gorodischer, B Sarov, E Gazala, et al.
Hormone Research|March 4, 1998
Serum insulin-like growth factors I and II are not affected by undernutrition in children with nonorganic failure to thriveM Phillip, E Hershkovitz, H Rosenblum, et al.
Israel Journal of Medical Sciences|May 1, 1995
The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patientsE Hershkovitz, S Shalitin, J Levy, et al.
Pageof 4