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Pediatric Research
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April 20, 2017
Pediatric Cushing disease: disparities in disease severity and outcomes in the Hispanic and African-American populations
Alexandra Gkourogianni, Ninet Sinaii, Sharon H Jackson, et al.
Hormone Research in Paediatrics
|
November 22, 2017
Failure to Thrive in the Context of Carney Complex
Amit Tirosh, Adi Auerbach, Belen Bonella, et al.
Endocrine-Related Cancer
|
October 24, 2012
Bone mineral density in children and young adults with neurofibromatosis type 1
Maya 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 Aggressiveness
Christina 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 Americans
Joshua 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 Locus
Giampaolo 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 investigation
Fabio R Faucz, Mihail Zilbermint, Maya B Lodish, et al.
Journal of the Endocrine Society
|
December 22, 2017
Corticotropinoma as a Component of Carney Complex
Laura 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 Syndrome
Michal 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 Zuckerkandl
Maya B Lodish, Karen T Adams, Thanh T Huynh, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Pediatric Research
|
April 20, 2017
Pediatric Cushing disease: disparities in disease severity and outcomes in the Hispanic and African-American populations
Alexandra Gkourogianni, Ninet Sinaii, Sharon H Jackson, et al.
Hormone Research in Paediatrics
|
November 22, 2017
Failure to Thrive in the Context of Carney Complex
Amit Tirosh, Adi Auerbach, Belen Bonella, et al.
Endocrine-Related Cancer
|
October 24, 2012
Bone mineral density in children and young adults with neurofibromatosis type 1
Maya 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 Aggressiveness
Christina 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 Americans
Joshua 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 Locus
Giampaolo 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 investigation
Fabio R Faucz, Mihail Zilbermint, Maya B Lodish, et al.
Journal of the Endocrine Society
|
December 22, 2017
Corticotropinoma as a Component of Carney Complex
Laura 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 Syndrome
Michal 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 Zuckerkandl
Maya B Lodish, Karen T Adams, Thanh T Huynh, et al.
Page
of 7