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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.
The Journal of Clinical Investigation|May 1, 1991
A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan originP C White, J Dupont, M I New, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1988
11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosisA Rösler, N Weshler, E Leiberman, et al.
Hormone Research|January 1, 1982
Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyA Rösler, E Leiberman, J Sack, et al.
The Journal of Pediatrics|August 1, 1994
Effect of long-term growth hormone therapy on bone age and pubertal maturation in boys with and without classic growth hormone deficiencyZ Zadik, S Chalew, A Zung, et al.
American Journal of Medical Genetics|March 4, 2000
Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiencyE Leiberman, D Pesler, R Parvari, et al.
Archives of Disease in Childhood|September 1, 1996
Spontaneous growth in idiopathic short stature. European Study GroupL T Rekers-Mombarg, J M Wit, G G Massa, et al.
The Journal of Pediatrics|April 17, 1998
Growth hormone therapy with three dosage regimens in children with idiopathic short stature. European Study Group Participating InvestigatorsL T Rekers-Mombarg, G G Massa, J M Wit, et al.
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