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Nick J Shaw

Showing results (21-30 of 25) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|July 6, 2021
Zoledronic Acid vs Placebo in Pediatric Glucocorticoid-induced Osteoporosis: A Randomized, Double-blind, Phase 3 TrialLeanne M Ward, Anup Choudhury, Nathalie Alos, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Diabetes|June 29, 2004
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneityValérie Senée, Krishna M Vattem, Marc Delépine, et al.
American Journal of Human Genetics|September 29, 2009
PPIB mutations cause severe osteogenesis imperfectaFleur S van Dijk, Isabel M Nesbitt, Eline H Zwikstra, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
The Journal of Clinical Endocrinology and Metabolism|July 6, 2021
Zoledronic Acid vs Placebo in Pediatric Glucocorticoid-induced Osteoporosis: A Randomized, Double-blind, Phase 3 TrialLeanne M Ward, Anup Choudhury, Nathalie Alos, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Diabetes|June 29, 2004
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneityValérie Senée, Krishna M Vattem, Marc Delépine, et al.
American Journal of Human Genetics|September 29, 2009
PPIB mutations cause severe osteogenesis imperfectaFleur S van Dijk, Isabel M Nesbitt, Eline H Zwikstra, et al.
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