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E Hershkovitz

Showing results (31-40 of 38) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 1996
An early rise in urine N-telopeptide predicts the growth response of normal prepubertal short children to growth hormone therapyM Phillip, E Hershkovitz, Y Limoni, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1993
Luteinizing hormone-releasing hormone antagonists interfere with autocrine and paracrine growth stimulation of MCF-7 mammary cancer cells by insulin-like growth factorsE Hershkovitz, M Marbach, E Bosin, et al.
American Journal of Medical Genetics|June 22, 2000
Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studiesS Shatzky, S Moses, J Levy, et al.
Hormone Research|October 22, 2009
Effects of a twelve-week randomized intervention of exercise and/or diet on weight loss and weight maintenance, and other metabolic parameters in obese preadolescent childrenS Shalitin, L Ashkenazi-Hoffnung, M Yackobovitch-Gavan, et al.
American Journal of Medical Genetics|October 23, 1997
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studiesR Parvari, K J Lei, N Bashan, et al.
American Journal of Human Genetics|April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23B Annabi, H Hiraiwa, B C Mansfield, et al.
Clinical Genetics|August 31, 2016
Mitochondrial epileptic encephalopathy, 3-methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutationsM A Shahrour, O Staretz-Chacham, D Dayan, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 1996
An early rise in urine N-telopeptide predicts the growth response of normal prepubertal short children to growth hormone therapyM Phillip, E Hershkovitz, Y Limoni, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1993
Luteinizing hormone-releasing hormone antagonists interfere with autocrine and paracrine growth stimulation of MCF-7 mammary cancer cells by insulin-like growth factorsE Hershkovitz, M Marbach, E Bosin, et al.
American Journal of Medical Genetics|June 22, 2000
Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studiesS Shatzky, S Moses, J Levy, et al.
Hormone Research|October 22, 2009
Effects of a twelve-week randomized intervention of exercise and/or diet on weight loss and weight maintenance, and other metabolic parameters in obese preadolescent childrenS Shalitin, L Ashkenazi-Hoffnung, M Yackobovitch-Gavan, et al.
American Journal of Medical Genetics|October 23, 1997
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studiesR Parvari, K J Lei, N Bashan, et al.
American Journal of Human Genetics|April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23B Annabi, H Hiraiwa, B C Mansfield, et al.
Clinical Genetics|August 31, 2016
Mitochondrial epileptic encephalopathy, 3-methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutationsM A Shahrour, O Staretz-Chacham, D Dayan, et al.
Pageof 4