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Maya Lodish

Showing results (51-60 of 70) with videos related to

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The Journal of Allergy and Clinical Immunology|June 5, 2021
Cushing syndrome and glucocorticoids: T-cell lymphopenia, apoptosis, and rescue by IL-21SuJin Hwang, Christina Tatsi, Hye Sun Kuehn, et al.
Endocrine-Related Cancer|March 11, 2016
Screening for GPR101 defects in pediatric pituitary corticotropinomasGiampaolo Trivellin, Ricardo R Correa, Maria Batsis, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 5, 2011
Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutationsKathryn S King, Tamara Prodanov, Vitaly Kantorovich, et al.
European Journal of Pediatrics|January 23, 2016
A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothersMarie Helene Schernthaner-Reiter, David Adams, Giampaolo Trivellin, et al.
Endocrine-Related Cancer|August 19, 2016
Growth hormone and risk for cardiac tumors in Carney complexW Patricia Bandettini, Alexander S Karageorgiadis, Ninet Sinaii, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Characteristics of Pediatric vs Adult Pheochromocytomas and ParagangliomasChristina Pamporaki, Barbora Hamplova, Mirko Peitzsch, et al.
European Journal of Nuclear Medicine and Molecular Imaging|December 6, 2017
Superiority of <sup>68</sup>Ga-DOTATATE over <sup>18</sup>F-FDG and anatomic imaging in the detection of succinate dehydrogenase mutation (SDHx )-related pheochromocytoma and paraganglioma in the pediatric populationAbhishek Jha, Alexander Ling, Corina Millo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 1, 2017
Outcomes of Children and Adolescents with Advanced Hereditary Medullary Thyroid Carcinoma Treated with VandetanibIra L Kraft, Srivandana Akshintala, Yuelin Zhu, et al.
The New England Journal of Medicine|June 3, 2024
Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal HyperplasiaKyriakie Sarafoglou, Mimi S Kim, Maya Lodish, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

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Pageof 7
The Journal of Allergy and Clinical Immunology|June 5, 2021
Cushing syndrome and glucocorticoids: T-cell lymphopenia, apoptosis, and rescue by IL-21SuJin Hwang, Christina Tatsi, Hye Sun Kuehn, et al.
Endocrine-Related Cancer|March 11, 2016
Screening for GPR101 defects in pediatric pituitary corticotropinomasGiampaolo Trivellin, Ricardo R Correa, Maria Batsis, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 5, 2011
Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutationsKathryn S King, Tamara Prodanov, Vitaly Kantorovich, et al.
European Journal of Pediatrics|January 23, 2016
A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothersMarie Helene Schernthaner-Reiter, David Adams, Giampaolo Trivellin, et al.
Endocrine-Related Cancer|August 19, 2016
Growth hormone and risk for cardiac tumors in Carney complexW Patricia Bandettini, Alexander S Karageorgiadis, Ninet Sinaii, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Characteristics of Pediatric vs Adult Pheochromocytomas and ParagangliomasChristina Pamporaki, Barbora Hamplova, Mirko Peitzsch, et al.
European Journal of Nuclear Medicine and Molecular Imaging|December 6, 2017
Superiority of <sup>68</sup>Ga-DOTATATE over <sup>18</sup>F-FDG and anatomic imaging in the detection of succinate dehydrogenase mutation (SDHx )-related pheochromocytoma and paraganglioma in the pediatric populationAbhishek Jha, Alexander Ling, Corina Millo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 1, 2017
Outcomes of Children and Adolescents with Advanced Hereditary Medullary Thyroid Carcinoma Treated with VandetanibIra L Kraft, Srivandana Akshintala, Yuelin Zhu, et al.
The New England Journal of Medicine|June 3, 2024
Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal HyperplasiaKyriakie Sarafoglou, Mimi S Kim, Maya Lodish, et al.
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