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Anne Barlier

Showing results (161-170 of 166) with videos related to

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The New England Journal of Medicine|December 4, 2014
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutationGiampaolo Trivellin, Adrian F Daly, Fabio R Faucz, et al.
Endocrine-Related Cancer|July 19, 2015
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patientsLiliya Rostomyan, Adrian F Daly, Patrick Petrossians, et al.
Medrxiv : the Preprint Server for Health Sciences|March 18, 2026
Familial medullary thyroid carcinoma secondary to an <i>SLC30A9</i> intragenic deletion and translation reinitiationDonato Iacovazzo, Federica Begalli, Oniz Suleyman, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2010
Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative studyAdrian F Daly, Maria A Tichomirowa, Patrick Petrossians, et al.
Annales D'Endocrinologie|March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.
Annales D'Endocrinologie|May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.
Pageof 17

Showing results (161-170 of 166) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 166 results.
The New England Journal of Medicine|December 4, 2014
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutationGiampaolo Trivellin, Adrian F Daly, Fabio R Faucz, et al.
Endocrine-Related Cancer|July 19, 2015
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patientsLiliya Rostomyan, Adrian F Daly, Patrick Petrossians, et al.
Medrxiv : the Preprint Server for Health Sciences|March 18, 2026
Familial medullary thyroid carcinoma secondary to an <i>SLC30A9</i> intragenic deletion and translation reinitiationDonato Iacovazzo, Federica Begalli, Oniz Suleyman, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2010
Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative studyAdrian F Daly, Maria A Tichomirowa, Patrick Petrossians, et al.
Annales D'Endocrinologie|March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.
Annales D'Endocrinologie|May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.
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