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Clinical Endocrinology|January 5, 2000
Growth response to rhIGF-I 80 microg/kg twice daily in children with growth hormone insensitivity syndrome: relationship to severity of clinical phenotypeC Azcona, M A Preece, S J Rose, et al.Hormone Research|January 5, 1999
Catch-up growth after childhood-onset substitution in primary hypothyroidism: is it a guide towards optimal growth hormone treatment in idiopathic growth hormone deficiency?M B Ranke, C P Schwarze, K Mohnike, et al.Journal of Medical Genetics|October 21, 2005
Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domainT Eggermann, N Schönherr, E Meyer, et al.Hormone Research|January 18, 2007
Age at growth hormone therapy start and first-year responsiveness to growth hormone are major determinants of height outcome in idiopathic short statureMichael B Ranke, Anders Lindberg, David A Price, et al.Hormone Research|September 11, 2002
Normal progression of testicular size in boys with idiopathic short stature and isolated growth hormone deficiency treated with growth hormone: experience from the KIGSA C Lindgren, P Chatelain, A Lindberg, et al.Hormone Research|May 18, 2001
Transient pseudohypoaldosteronism with complex malformation of internal genitalia. A case reportD I Iliev, U R Petruch, M B Ranke, et al.Hormone Research in Paediatrics|July 16, 2011
Short children with low birth weight born either small for gestational age or average for gestational age show similar growth response and changes in insulin-like growth factor-1 to growth hormone treatment during the first prepubertal yearM B Ranke, D D Martin, S Ehehalt, et al.Annales De Genetique|May 20, 2000
Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literatureS Mergenthaler, H A Wollmann, B Burger, et al.Acta Endocrinologica|June 1, 1993
Insulin-like growth factors (IGF) I and II and IGF binding proteins 1, 2 and 3 during low-dose growth hormone (GH) infusion and sequential euglycemic and hypoglycemic glucose clamps: studies in GH-deficient patientsJ O Jørgensen, W F Blum, N Horn, et al.Hormone Research in Paediatrics|September 18, 2010
Normal-weight 14-year-old girl with acanthosis nigricans and markedly increased hepatic steatosis: evidence for the important role of ectopic fat deposition in the pathogenesis of insulin resistance in childhood and adolescenceFabian Springer, Huu Phuc Nguyen, Jürgen Machann, et al.Pageof 177