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The Journal of Clinical Endocrinology and Metabolism
|
December 16, 2017
Ezh2 Mutations Found in the Weaver Overgrowth Syndrome Cause a Partial Loss of H3K27 Histone Methyltransferase Activity
Julian C Lui, Kevin M Barnes, Lijin Dong, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 29, 2025
Effect of Vosoritide therapy on IGF-I and Endogenous C-type Natriuretic Peptide in Hypochondroplasia
Roopa Kanakatti Shankar, Despoina M Galetaki, Anqing Zhang, et al.
The Journal of Pediatrics
|
October 23, 2019
Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome
Eirene Alexandrou, Catalina Cabrera-Salcedo, Guillaume Labilloy, et al.
Molecular Genetics & Genomic Medicine
|
November 14, 2025
Living With Hypochondroplasia: A Qualitative Exploration of Children's and Caregivers' Experiences, Challenges, and Unmet Needs
Elisabeth M Oehrlein, Reni Pekala, Stacie Cavallaro, et al.
European Journal of Endocrinology
|
January 22, 2020
Anthropometric and biochemical correlates of PAPP-A2, free IGF-I, and IGFBP-3 in childhood
Masanobu Fujimoto, Jane C Khoury, Philip R Khoury, et al.
Hormone Research in Paediatrics
|
March 6, 2019
Growth Hormone Improves Short-Term Growth in Patients with Temple Syndrome
Diana S Brightman, Oluwakemi Lokulo-Sodipe, Beverly A Searle, et al.
Hormone Research in Paediatrics
|
October 20, 2024
Phase 2 Trial of Vosoritide Use in Patients with Hypochondroplasia: A Pharmacokinetic/Pharmacodynamic Analysis
Despoina Galetaki, Anqing Zhang, Yulan Qi, et al.
Journal of the Endocrine Society
|
June 19, 2026
Clinical burden of classic congenital adrenal hyperplasia and glucocorticoid-related complications: a claims analysis
Hyunwoo Kim, Vivian H Lin, Ron S Newfield, et al.
Endocrinology
|
April 13, 2019
Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation
Masanobu Fujimoto, Melissa Andrew, Lihong Liao, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 25, 2011
Genetic defect in CYP24A1, the vitamin D 24-hydroxylase gene, in a patient with severe infantile hypercalcemia
Andrew Dauber, Thutrang T Nguyen, Etienne Sochett, et al.
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of 15
Search research articles
Search
Showing results (71-80 of 144) with videos related to
Sort By:
Page
of 15
The Journal of Clinical Endocrinology and Metabolism
|
December 16, 2017
Ezh2 Mutations Found in the Weaver Overgrowth Syndrome Cause a Partial Loss of H3K27 Histone Methyltransferase Activity
Julian C Lui, Kevin M Barnes, Lijin Dong, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 29, 2025
Effect of Vosoritide therapy on IGF-I and Endogenous C-type Natriuretic Peptide in Hypochondroplasia
Roopa Kanakatti Shankar, Despoina M Galetaki, Anqing Zhang, et al.
The Journal of Pediatrics
|
October 23, 2019
Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome
Eirene Alexandrou, Catalina Cabrera-Salcedo, Guillaume Labilloy, et al.
Molecular Genetics & Genomic Medicine
|
November 14, 2025
Living With Hypochondroplasia: A Qualitative Exploration of Children's and Caregivers' Experiences, Challenges, and Unmet Needs
Elisabeth M Oehrlein, Reni Pekala, Stacie Cavallaro, et al.
European Journal of Endocrinology
|
January 22, 2020
Anthropometric and biochemical correlates of PAPP-A2, free IGF-I, and IGFBP-3 in childhood
Masanobu Fujimoto, Jane C Khoury, Philip R Khoury, et al.
Hormone Research in Paediatrics
|
March 6, 2019
Growth Hormone Improves Short-Term Growth in Patients with Temple Syndrome
Diana S Brightman, Oluwakemi Lokulo-Sodipe, Beverly A Searle, et al.
Hormone Research in Paediatrics
|
October 20, 2024
Phase 2 Trial of Vosoritide Use in Patients with Hypochondroplasia: A Pharmacokinetic/Pharmacodynamic Analysis
Despoina Galetaki, Anqing Zhang, Yulan Qi, et al.
Journal of the Endocrine Society
|
June 19, 2026
Clinical burden of classic congenital adrenal hyperplasia and glucocorticoid-related complications: a claims analysis
Hyunwoo Kim, Vivian H Lin, Ron S Newfield, et al.
Endocrinology
|
April 13, 2019
Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation
Masanobu Fujimoto, Melissa Andrew, Lihong Liao, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 25, 2011
Genetic defect in CYP24A1, the vitamin D 24-hydroxylase gene, in a patient with severe infantile hypercalcemia
Andrew Dauber, Thutrang T Nguyen, Etienne Sochett, et al.
Page
of 15