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Maya B Lodish

Showing results (41-50 of 61) with videos related to

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Pediatric Research|April 20, 2017
Pediatric Cushing disease: disparities in disease severity and outcomes in the Hispanic and African-American populationsAlexandra Gkourogianni, Ninet Sinaii, Sharon H Jackson, et al.
Hormone Research in Paediatrics|November 22, 2017
Failure to Thrive in the Context of Carney ComplexAmit Tirosh, Adi Auerbach, Belen Bonella, et al.
Endocrine-Related Cancer|October 24, 2012
Bone mineral density in children and young adults with neurofibromatosis type 1Maya B Lodish, Urania Dagalakis, Ninet Sinaii, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2019
Large Genomic Aberrations in Corticotropinomas Are Associated With Greater AggressivenessChristina Tatsi, Nathan Pankratz, John Lane, et al.
The Journal of Clinical Endocrinology and Metabolism|May 22, 2020
The Association of ARMC5 with the Renin-Angiotensin-Aldosterone System, Blood Pressure, and Glycemia in African AmericansJoshua J Joseph, Xiaofei Zhou, Mihail Zilbermint, et al.
Journal of the Endocrine Society|December 8, 2018
Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic LocusGiampaolo Trivellin, Erin Sharwood, Hadia Hijazi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 8, 2014
Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigationFabio R Faucz, Mihail Zilbermint, Maya B Lodish, et al.
Journal of the Endocrine Society|December 22, 2017
Corticotropinoma as a Component of Carney ComplexLaura C Hernández-Ramírez, Christina Tatsi, Maya B Lodish, et al.
The Journal of Clinical Endocrinology and Metabolism|June 5, 2019
Germline USP8 Mutation Associated With Pediatric Cushing Disease and Other Clinical Features: A New SyndromeMichal Cohen, Rebecca Persky, Rachel Stegemann, et al.
Endocrine-Related Cancer|April 27, 2010
Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of ZuckerkandlMaya B Lodish, Karen T Adams, Thanh T Huynh, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Pediatric Research|April 20, 2017
Pediatric Cushing disease: disparities in disease severity and outcomes in the Hispanic and African-American populationsAlexandra Gkourogianni, Ninet Sinaii, Sharon H Jackson, et al.
Hormone Research in Paediatrics|November 22, 2017
Failure to Thrive in the Context of Carney ComplexAmit Tirosh, Adi Auerbach, Belen Bonella, et al.
Endocrine-Related Cancer|October 24, 2012
Bone mineral density in children and young adults with neurofibromatosis type 1Maya B Lodish, Urania Dagalakis, Ninet Sinaii, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2019
Large Genomic Aberrations in Corticotropinomas Are Associated With Greater AggressivenessChristina Tatsi, Nathan Pankratz, John Lane, et al.
The Journal of Clinical Endocrinology and Metabolism|May 22, 2020
The Association of ARMC5 with the Renin-Angiotensin-Aldosterone System, Blood Pressure, and Glycemia in African AmericansJoshua J Joseph, Xiaofei Zhou, Mihail Zilbermint, et al.
Journal of the Endocrine Society|December 8, 2018
Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic LocusGiampaolo Trivellin, Erin Sharwood, Hadia Hijazi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 8, 2014
Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigationFabio R Faucz, Mihail Zilbermint, Maya B Lodish, et al.
Journal of the Endocrine Society|December 22, 2017
Corticotropinoma as a Component of Carney ComplexLaura C Hernández-Ramírez, Christina Tatsi, Maya B Lodish, et al.
The Journal of Clinical Endocrinology and Metabolism|June 5, 2019
Germline USP8 Mutation Associated With Pediatric Cushing Disease and Other Clinical Features: A New SyndromeMichal Cohen, Rebecca Persky, Rachel Stegemann, et al.
Endocrine-Related Cancer|April 27, 2010
Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of ZuckerkandlMaya B Lodish, Karen T Adams, Thanh T Huynh, et al.
Pageof 7