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Maya B Lodish

Showing results (51-60 of 61) with videos related to

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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 5, 2010
SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumorsJosé Gaal, Constantine A Stratakis, J Aidan Carney, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 3, 2019
Optical Imaging Technology: A Useful Tool to Identify Remission in Cushing Disease After SurgeryAli Afshari, Margaret Keil, Charalampos Lyssikatos, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 15, 2019
Correction: Optical Imaging Technology: A Useful Tool to Identify Remission in Cushing Disease After SurgeryAli Afshari, Margaret Keil, Charalampos Lyssikatos, et al.
European Journal of Endocrinology|May 1, 2015
Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentationsMaya B Lodish, Bo Yuan, Isaac Levy, et al.
The Journal of Clinical Endocrinology and Metabolism|October 8, 2014
Ectopic adrenocorticotropic hormone and corticotropin-releasing hormone co-secreting tumors in children and adolescents causing cushing syndrome: a diagnostic dilemma and how to solve itAlexander S Karageorgiadis, Georgios Z Papadakis, Juliana Biro, et al.
Endocrine|May 8, 2019
CRH stimulation improves <sup>18</sup>F-FDG-PET detection of pituitary adenomas in Cushing's diseaseJacqueline Boyle, Nicholas J Patronas, James Smirniotopoulos, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort StudyNicholas E Khan, Andrew J Bauer, Kris Ann P Schultz, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2015
Primary Aldosteronism and ARMC5 VariantsMihail Zilbermint, Paraskevi Xekouki, Fabio R Faucz, et al.
Frontiers in Endocrinology|July 28, 2020
Rare Germline <i>DICER1</i> Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?Idoia Martínez de LaPiscina, Laura C Hernández-Ramírez, Nancy Portillo, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 5, 2010
SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumorsJosé Gaal, Constantine A Stratakis, J Aidan Carney, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 3, 2019
Optical Imaging Technology: A Useful Tool to Identify Remission in Cushing Disease After SurgeryAli Afshari, Margaret Keil, Charalampos Lyssikatos, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 15, 2019
Correction: Optical Imaging Technology: A Useful Tool to Identify Remission in Cushing Disease After SurgeryAli Afshari, Margaret Keil, Charalampos Lyssikatos, et al.
European Journal of Endocrinology|May 1, 2015
Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentationsMaya B Lodish, Bo Yuan, Isaac Levy, et al.
The Journal of Clinical Endocrinology and Metabolism|October 8, 2014
Ectopic adrenocorticotropic hormone and corticotropin-releasing hormone co-secreting tumors in children and adolescents causing cushing syndrome: a diagnostic dilemma and how to solve itAlexander S Karageorgiadis, Georgios Z Papadakis, Juliana Biro, et al.
Endocrine|May 8, 2019
CRH stimulation improves <sup>18</sup>F-FDG-PET detection of pituitary adenomas in Cushing's diseaseJacqueline Boyle, Nicholas J Patronas, James Smirniotopoulos, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort StudyNicholas E Khan, Andrew J Bauer, Kris Ann P Schultz, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2015
Primary Aldosteronism and ARMC5 VariantsMihail Zilbermint, Paraskevi Xekouki, Fabio R Faucz, et al.
Frontiers in Endocrinology|July 28, 2020
Rare Germline <i>DICER1</i> Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?Idoia Martínez de LaPiscina, Laura C Hernández-Ramírez, Nancy Portillo, et al.
Pageof 7