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The Journal of Clinical Endocrinology and Metabolism
|
April 8, 2003
The effect of cessation of growth hormone (GH) therapy on bone mineral accretion in GH-deficient adolescents at the completion of linear growth
W M Drake, P V Carroll, K T Maher, et al.
BMC Pediatrics
|
December 24, 2013
Growth and metabolic outcome in adolescents born preterm (GROWMORE): follow-up protocol for the Newcastle Preterm Birth GRowth study (PTBGS)
Claire L Wood, Robert J Tinnion, S Murthy Korada, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 31, 2007
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility
Alison Sutherland, Jocelyn Davies, Catherine J Owen, et al.
European Journal of Endocrinology
|
August 12, 2025
Leptin and adiponectin in children and young persons with congenital adrenal hyperplasia
Irina A Bacila, Neil R Lawrence, Sabah Alvi, et al.
European Journal of Endocrinology
|
September 15, 2021
The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series
Min Sun, Jonathan W Mueller, Lorna C Gilligan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 13, 2023
Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia-UK Nationwide Multicenter Assessment
Neil Richard Lawrence, Irina Bacila, Jeremy Dawson, et al.
European Journal of Endocrinology
|
August 24, 2022
Health status of children and young persons with congenital adrenal hyperplasia in the UK (CAH-UK): a cross-sectional multi-centre study
Irina Bacila, Neil Richard Lawrence, Sundus Mahdi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 23, 2021
Adjuvant Rituximab-Exploratory Trial in Young People With Graves Disease
Tim D Cheetham, Michael Cole, Mario Abinun, et al.
Leukemia
|
March 10, 2015
A tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant clone
C N Hahn, D M Ross, J Feng, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency
Kyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 103) with videos related to
Sort By:
Page
of 11
The Journal of Clinical Endocrinology and Metabolism
|
April 8, 2003
The effect of cessation of growth hormone (GH) therapy on bone mineral accretion in GH-deficient adolescents at the completion of linear growth
W M Drake, P V Carroll, K T Maher, et al.
BMC Pediatrics
|
December 24, 2013
Growth and metabolic outcome in adolescents born preterm (GROWMORE): follow-up protocol for the Newcastle Preterm Birth GRowth study (PTBGS)
Claire L Wood, Robert J Tinnion, S Murthy Korada, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 31, 2007
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility
Alison Sutherland, Jocelyn Davies, Catherine J Owen, et al.
European Journal of Endocrinology
|
August 12, 2025
Leptin and adiponectin in children and young persons with congenital adrenal hyperplasia
Irina A Bacila, Neil R Lawrence, Sabah Alvi, et al.
European Journal of Endocrinology
|
September 15, 2021
The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series
Min Sun, Jonathan W Mueller, Lorna C Gilligan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 13, 2023
Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia-UK Nationwide Multicenter Assessment
Neil Richard Lawrence, Irina Bacila, Jeremy Dawson, et al.
European Journal of Endocrinology
|
August 24, 2022
Health status of children and young persons with congenital adrenal hyperplasia in the UK (CAH-UK): a cross-sectional multi-centre study
Irina Bacila, Neil Richard Lawrence, Sundus Mahdi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 23, 2021
Adjuvant Rituximab-Exploratory Trial in Young People With Graves Disease
Tim D Cheetham, Michael Cole, Mario Abinun, et al.
Leukemia
|
March 10, 2015
A tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant clone
C N Hahn, D M Ross, J Feng, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency
Kyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Page
of 11