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Scientific Reports|April 17, 2022
Accuracy and self-validation of automated bone age determinationD D Martin, A D Calder, M B Ranke, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 16, 2010
Metacarpal thickness, width, length and medullary diameter in children--reference curves from the First Zürich Longitudinal StudyD D Martin, C Heckmann, O G Jenni, et al.The Journal of Clinical Endocrinology and Metabolism|April 1, 1995
Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysisG Binder, M B RankeJournal of Pediatric Endocrinology & Metabolism : JPEM|August 1, 2007
The course of neonatal cholestasis in congenital combined pituitary hormone deficiencyG Binder, D D Martin, I Kanther, et al.The Journal of Clinical Endocrinology and Metabolism|November 7, 2003
Cortical bone density is normal in prepubertal children with growth hormone (GH) deficiency, but initially decreases during GH replacement due to early bone remodelingR Schweizer, D D Martin, C P Schwarze, et al.The Journal of Clinical Endocrinology and Metabolism|January 14, 2000
Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormoneG Binder, C P Schwarze, M B RankeHormone Research|August 18, 2001
Radiological signs of Leri-Weill dyschondrosteosis in Turner syndromeG Binder, H Fritsch, R Schweizer, et al.The Journal of Clinical Endocrinology and Metabolism|November 18, 2005
The d3-growth hormone (GH) receptor polymorphism is associated with increased responsiveness to GH in Turner syndrome and short small-for-gestational-age childrenG Binder, F Baur, R Schweizer, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Nested polymerase chain reaction study of 53 cases with Turner's syndrome: is cytogenetically undetected Y mosaicism common?G Binder, A Koch, E Wajs, et al.The Journal of Clinical Endocrinology and Metabolism|June 30, 2005
PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndromeG Binder, K Neuer, M B Ranke, et al.Pageof 29