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Raja Brauner

Showing results (81-90 of 96) with videos related to

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Endocrine-Related Cancer|April 1, 2011
Hyperplasia-adenoma sequence in pituitary tumorigenesis related to aryl hydrocarbon receptor interacting protein gene mutationChiara Villa, Maria Stefania Lagonigro, Flavia Magri, et al.
European Journal of Endocrinology|September 13, 2023
Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levelsLuciana Montenegro, Carlos Seraphim, Flávia Tinano, et al.
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.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 22, 2021
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37Housna Zidoune, Laetitia Martinerie, Daisylyn S Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2018
ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signalingAbigail Harris, Pam Siggers, Silvia Corrochano, et al.
Clinical Endocrinology|October 24, 2020
Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohortNicolas Jullien, Alexandru Saveanu, Julia Vergier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 19, 2025
A recurrent splice variant sheds light on 11beta-hydroxylase deficiency in a unique large cohortClément Janot, Delphine Mallet, Alexandre Janin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiencyKyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Human Molecular Genetics|July 5, 2020
TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal lociErica E Davis, Ravikumar Balasubramanian, Zachary A Kupchinsky, et al.
Hormone Research in Paediatrics|July 10, 2017
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org PortalLaura J C Kranenburg, Sam T H Reerds, Martine Cools, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Endocrine-Related Cancer|April 1, 2011
Hyperplasia-adenoma sequence in pituitary tumorigenesis related to aryl hydrocarbon receptor interacting protein gene mutationChiara Villa, Maria Stefania Lagonigro, Flavia Magri, et al.
European Journal of Endocrinology|September 13, 2023
Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levelsLuciana Montenegro, Carlos Seraphim, Flávia Tinano, et al.
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.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 22, 2021
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37Housna Zidoune, Laetitia Martinerie, Daisylyn S Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2018
ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signalingAbigail Harris, Pam Siggers, Silvia Corrochano, et al.
Clinical Endocrinology|October 24, 2020
Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohortNicolas Jullien, Alexandru Saveanu, Julia Vergier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 19, 2025
A recurrent splice variant sheds light on 11beta-hydroxylase deficiency in a unique large cohortClément Janot, Delphine Mallet, Alexandre Janin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiencyKyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Human Molecular Genetics|July 5, 2020
TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal lociErica E Davis, Ravikumar Balasubramanian, Zachary A Kupchinsky, et al.
Hormone Research in Paediatrics|July 10, 2017
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org PortalLaura J C Kranenburg, Sam T H Reerds, Martine Cools, et al.
Pageof 10