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Andrew Dauber

Showing results (31-40 of 144) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|February 15, 2017
Novel germline mutation (Leu512Met) in the thyrotropin receptor gene (TSHR) leading to sporadic non-autoimmune hyperthyroidismStephanie A Roberts, Jennifer E Moon, Andrew Dauber, et al.
The Journal of Clinical Endocrinology and Metabolism|September 19, 2021
Clinical Utility of Anti-Mullerian Hormone in PediatricsRoopa Kanakatti Shankar, Tazim Dowlut-McElroy, Andrew Dauber, et al.
The Journal of Pediatrics|September 15, 2012
Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorderAndrew Dauber, Joan Stoler, Eliana Hechter, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 21, 2013
Acquired hypothyroidism in an infant related to excessive maternal iodine intake: food for thoughtDaniel E Shumer, Jamie E Mehringer, Lewis E Braverman, et al.
Hormone Research in Paediatrics|January 21, 2016
Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 DeficiencyChristiaan de Bruin, Zerrin Orbak, Melissa Andrew, et al.
Hormone Research in Paediatrics|July 5, 2017
Two Siblings with a Mutation in CCDC8 Presenting with Mild Short Stature: A Case of 3-M SyndromeLihong Liao, Hoong-Wei Gan, Vivian Hwa, et al.
Clinical Endocrinology|December 29, 2019
Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding proteinAnkur Rughani, Dongsheng Zhang, Kanimozhi Vairamani, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 6, 2019
A Novel Homozygous Mutation of the Acid-Labile Subunit <i>(IGFALS)</i> Gene in a Male AdolescentŞükran Poyrazoğlu, Vivian Hwa, Firdevs Baş, et al.
The Journal of Pediatrics|April 26, 2021
Racial and Ethnic Disparities in the Investigation and Treatment of Growth Hormone DeficiencyColin P Hawkes, Hareesh Gunturi, Andrew Dauber, et al.
Journal of the Endocrine Society|November 6, 2024
Treatment of Short Stature in Aggrecan-deficient Patients With Recombinant Human GH: 3-year ResponseGajanthan Muthuvel, Andrew Dauber, Eirene Alexandrou, et al.
Pageof 15

Showing results (31-40 of 144) with videos related to

Sort By:
Pageof 15
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 15, 2017
Novel germline mutation (Leu512Met) in the thyrotropin receptor gene (TSHR) leading to sporadic non-autoimmune hyperthyroidismStephanie A Roberts, Jennifer E Moon, Andrew Dauber, et al.
The Journal of Clinical Endocrinology and Metabolism|September 19, 2021
Clinical Utility of Anti-Mullerian Hormone in PediatricsRoopa Kanakatti Shankar, Tazim Dowlut-McElroy, Andrew Dauber, et al.
The Journal of Pediatrics|September 15, 2012
Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorderAndrew Dauber, Joan Stoler, Eliana Hechter, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 21, 2013
Acquired hypothyroidism in an infant related to excessive maternal iodine intake: food for thoughtDaniel E Shumer, Jamie E Mehringer, Lewis E Braverman, et al.
Hormone Research in Paediatrics|January 21, 2016
Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 DeficiencyChristiaan de Bruin, Zerrin Orbak, Melissa Andrew, et al.
Hormone Research in Paediatrics|July 5, 2017
Two Siblings with a Mutation in CCDC8 Presenting with Mild Short Stature: A Case of 3-M SyndromeLihong Liao, Hoong-Wei Gan, Vivian Hwa, et al.
Clinical Endocrinology|December 29, 2019
Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding proteinAnkur Rughani, Dongsheng Zhang, Kanimozhi Vairamani, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 6, 2019
A Novel Homozygous Mutation of the Acid-Labile Subunit <i>(IGFALS)</i> Gene in a Male AdolescentŞükran Poyrazoğlu, Vivian Hwa, Firdevs Baş, et al.
The Journal of Pediatrics|April 26, 2021
Racial and Ethnic Disparities in the Investigation and Treatment of Growth Hormone DeficiencyColin P Hawkes, Hareesh Gunturi, Andrew Dauber, et al.
Journal of the Endocrine Society|November 6, 2024
Treatment of Short Stature in Aggrecan-deficient Patients With Recombinant Human GH: 3-year ResponseGajanthan Muthuvel, Andrew Dauber, Eirene Alexandrou, et al.
Pageof 15