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Clinical Endocrinology|July 9, 2024
Resource use and costs of transitioning from paediatric to adult care for patients with chronic endocrine diseaseDaniela Choukair, Janna Mittnacht, Dorothea Treiber, et al.
Hormone Research in Paediatrics|February 1, 2014
Guanine nucleotide-binding protein α subunit hypofunction in children with short stature and disproportionate shortening of the 4th and 5th metacarpalsIoana Monica Inta, Daniela Choukair, Sebastian Bender, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short statureGudrun A Rappold, Maki Fukami, Beate Niesler, et al.
International Journal of Neonatal Screening|March 6, 2021
Guideline Adherence and Registry Recruitment of Congenital Primary Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (HypoDok)Julia Thomann, Sascha R Tittel, Egbert Voss, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism - experiences from the DGKED/AQUAPE study group for quality improvement in GermanyJohanna Hammersen, Markus Bettendorf, Walter Bonfig, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 28, 2006
Prevalence of autoantibodies associated with thyroid and celiac disease in Ullrich-Turner syndrome in relation to adult height after growth hormone treatmentMarkus Bettendorf, Helmuth G Doerr, Berthold P Hauffa, et al.
Clinical Endocrinology|May 1, 2012
Identification and management of poor response to growth-promoting therapy in children with short staturePeter Bang, S Faisal Ahmed, Jesús Argente, et al.
European Journal of Pediatrics|March 26, 2021
Predictors of transient congenital primary hypothyroidism: data from the German registry for congenital hypothyroidism (AQUAPE "HypoDok")Nicola Matejek, Sascha R Tittel, Holger Haberland, et al.
American Journal of Hypertension|June 14, 2015
Blood Pressure in a Large Cohort of Children and Adolescents With Classic Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase DeficiencyWalter Bonfig, Friedrich-Wilhelm Roehl, Stefan Riedl, et al.
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