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Showing results (671-680 of 717) with videos related to

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Science Translational Medicine|December 18, 2024
The pharmacological basis for nonpeptide agonism of the GLP-1 receptor by orforglipronKyle W Sloop, Amy L Cox, David B Wainscott, et al.
Bioorganic & Medicinal Chemistry Letters|March 13, 2013
Discovery of SAR184841, a potent and long-lasting inhibitor of 11β-hydroxysteroid dehydrogenase type 1, active in a physiopathological animal model of T2DOlivier Venier, Cécile Pascal, Alain Braun, et al.
Journal of Medical Genetics|October 27, 2017
Contribution of de novo and mosaic <i>TP53</i> mutations to Li-Fraumeni syndromeMariette Renaux-Petel, Françoise Charbonnier, Jean-Christophe Théry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2022
Genome Alert!: A standardized procedure for genomic variant reinterpretation and automated gene-phenotype reassessment in clinical routineKevin Yauy, François Lecoquierre, Stéphanie Baert-Desurmont, et al.
European Journal of Human Genetics : EJHG|December 5, 2013
Development of primary early-onset colorectal cancers due to biallelic mutations of the FANCD1/BRCA2 geneEmilie Degrolard-Courcet, Joanna Sokolowska, Marie-Martine Padeano, et al.
Human Mutation|June 25, 2019
Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutationsEnzo Cohen, Sabrina Belkacem, Soumeya Fedala, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2025
Digenic Inheritance Mode in Congenital Hypothyroidism due to Thyroid Dysgenesis: HYPOTYGEN translational cohort studyAthanasia Stoupa, Dulanjalee Kariyawasam, Fabienne Jabot-Hanin, et al.
Annales D'Endocrinologie|August 14, 2023
Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)Thierry Brue, Haïfa Rahabi, Abdoulaye Barry, et al.
JAMA Network Open|April 14, 2022
Characterization of Depressive Symptoms Trajectories After Breast Cancer Diagnosis in Women in FranceCécile Charles, Aurélie Bardet, Alicia Larive, et al.
European Journal of Endocrinology|December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric populationYasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
Pageof 72

Showing results (671-680 of 717) with videos related to

Sort By:
Pageof 72
Science Translational Medicine|December 18, 2024
The pharmacological basis for nonpeptide agonism of the GLP-1 receptor by orforglipronKyle W Sloop, Amy L Cox, David B Wainscott, et al.
Bioorganic & Medicinal Chemistry Letters|March 13, 2013
Discovery of SAR184841, a potent and long-lasting inhibitor of 11β-hydroxysteroid dehydrogenase type 1, active in a physiopathological animal model of T2DOlivier Venier, Cécile Pascal, Alain Braun, et al.
Journal of Medical Genetics|October 27, 2017
Contribution of de novo and mosaic <i>TP53</i> mutations to Li-Fraumeni syndromeMariette Renaux-Petel, Françoise Charbonnier, Jean-Christophe Théry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2022
Genome Alert!: A standardized procedure for genomic variant reinterpretation and automated gene-phenotype reassessment in clinical routineKevin Yauy, François Lecoquierre, Stéphanie Baert-Desurmont, et al.
European Journal of Human Genetics : EJHG|December 5, 2013
Development of primary early-onset colorectal cancers due to biallelic mutations of the FANCD1/BRCA2 geneEmilie Degrolard-Courcet, Joanna Sokolowska, Marie-Martine Padeano, et al.
Human Mutation|June 25, 2019
Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutationsEnzo Cohen, Sabrina Belkacem, Soumeya Fedala, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2025
Digenic Inheritance Mode in Congenital Hypothyroidism due to Thyroid Dysgenesis: HYPOTYGEN translational cohort studyAthanasia Stoupa, Dulanjalee Kariyawasam, Fabienne Jabot-Hanin, et al.
Annales D'Endocrinologie|August 14, 2023
Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)Thierry Brue, Haïfa Rahabi, Abdoulaye Barry, et al.
JAMA Network Open|April 14, 2022
Characterization of Depressive Symptoms Trajectories After Breast Cancer Diagnosis in Women in FranceCécile Charles, Aurélie Bardet, Alicia Larive, et al.
European Journal of Endocrinology|December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric populationYasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
Pageof 72