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Seminara

Showing results (511-520 of 642) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 13, 2024
Contributions of Common Genetic Variants to Constitutional Delay of Puberty and Idiopathic Hypogonadotropic HypogonadismMargaret F Lippincott, Evan C Schafer, Anna A Hindman, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delayJ C Achermann, W X Gu, T J Kotlar, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2011
Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadismJanne Tornberg, Gerasimos P Sykiotis, Kimberly Keefe, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2019
Hypothalamic Reproductive Endocrine Pulse Generator Activity Independent of Neurokinin B and Dynorphin SignalingMargaret F Lippincott, Silvia León, Yee-Ming Chan, et al.
The Journal of Clinical Endocrinology and Metabolism|January 7, 2011
Expanding the phenotype and genotype of female GnRH deficiencyNatalie D Shaw, Stephanie B Seminara, Corrine K Welt, et al.
The Journal of Allergy and Clinical Immunology. Global|March 17, 2025
Multicenter food protein-induced enterocolitis syndrome (FPIES) data collection: Leveraging a REDCap FPIES registry for improved clinical outcomesAnkona Banerjee, J Andrew Bird, Amy M Scurlock, et al.
Clinical Genetics|November 22, 2008
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndromeM C J Jongmans, C M A van Ravenswaaij-Arts, N Pitteloud, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2013
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypesFlavia Amanda Costa-Barbosa, Ravikumar Balasubramanian, Kimberly W Keefe, et al.
The New England Journal of Medicine|January 21, 2011
A genetic basis for functional hypothalamic amenorrheaLisa M Caronia, Cecilia Martin, Corrine K Welt, et al.
Human Molecular Genetics|October 12, 2013
Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIPChang-He Shi, Jonathan C Schisler, Carrie E Rubel, et al.
Pageof 65

Showing results (511-520 of 642) with videos related to

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Pageof 65
The Journal of Clinical Endocrinology and Metabolism|March 13, 2024
Contributions of Common Genetic Variants to Constitutional Delay of Puberty and Idiopathic Hypogonadotropic HypogonadismMargaret F Lippincott, Evan C Schafer, Anna A Hindman, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delayJ C Achermann, W X Gu, T J Kotlar, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2011
Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadismJanne Tornberg, Gerasimos P Sykiotis, Kimberly Keefe, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2019
Hypothalamic Reproductive Endocrine Pulse Generator Activity Independent of Neurokinin B and Dynorphin SignalingMargaret F Lippincott, Silvia León, Yee-Ming Chan, et al.
The Journal of Clinical Endocrinology and Metabolism|January 7, 2011
Expanding the phenotype and genotype of female GnRH deficiencyNatalie D Shaw, Stephanie B Seminara, Corrine K Welt, et al.
The Journal of Allergy and Clinical Immunology. Global|March 17, 2025
Multicenter food protein-induced enterocolitis syndrome (FPIES) data collection: Leveraging a REDCap FPIES registry for improved clinical outcomesAnkona Banerjee, J Andrew Bird, Amy M Scurlock, et al.
Clinical Genetics|November 22, 2008
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndromeM C J Jongmans, C M A van Ravenswaaij-Arts, N Pitteloud, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2013
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypesFlavia Amanda Costa-Barbosa, Ravikumar Balasubramanian, Kimberly W Keefe, et al.
The New England Journal of Medicine|January 21, 2011
A genetic basis for functional hypothalamic amenorrheaLisa M Caronia, Cecilia Martin, Corrine K Welt, et al.
Human Molecular Genetics|October 12, 2013
Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIPChang-He Shi, Jonathan C Schisler, Carrie E Rubel, et al.
Pageof 65