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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.
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.
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.
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.
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.
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.
The New England Journal of Medicine|February 3, 2007
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosisLinda M Scott, Wei Tong, Ross L Levine, et al.
European Journal of Nuclear Medicine and Molecular Imaging|December 6, 2017
Superiority of 68Ga-DOTATATE over 18F-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.
American Journal of Physiology. Endocrinology and Metabolism|March 8, 2002
Nomenclature of the GLUT/SLC2A family of sugar/polyol transport facilitatorsHans-Georg Joost, Graeme I Bell, James D Best, et al.
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