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Acta Endocrinologica|October 1, 1989
Serum GH binding protein activities identifies the heterozygous carriers for Laron type dwarfismZ Laron, B Klinger, B Erster, et al.
Journal of Endocrinological Investigation|November 5, 2003
Identification of two novel mutations in the human growth hormone receptor geneO Shevah, P Borrelli, M Rubinstein, et al.
Lancet (London, England)|November 19, 1988
Effect of acute administration of insulin-like growth factor I in patients with Laron-type dwarfismZ Laron, B Klinger, B Erster, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 24, 2005
The intellectual capacity of patients with Laron syndrome (LS) differs with various molecular defects of the growth hormone receptor gene. Correlation with CNS abnormalitiesO Shevah, L Kornreich, A Galatzer, et al.
Cellular and Molecular Life Sciences : CMLS|January 20, 2009
Cell migration to the chemokine CXCL8: paxillin is activated and regulates adhesion and cell motilityE Cohen-Hillel, R Mintz, T Meshel, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|August 1, 1995
Cryptococcal meningitis in a child with hyperimmunoglobulin E syndromeB Z Garty, B Wolach, S Ashkenazi, et al.
Pediatric Emergency Care|October 26, 1999
Management of children with aseptic meningitis in the emergency departmentY Waisman, Y Lotem, M Hemmo, et al.
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