Pheochromocytoma
What's New
Last Posted: Jun 18, 2024
- Prenatal exome sequencing for morphologically normal fetus: Should we be doing it?
Zhi Gao et al. Prenat Diagn 2024 - Germline genetic variants in pheochromocytoma/paraganglioma: single-center experience.
José V Lima et al. Endocr Oncol 2023 3(1) e220091 - Artificial intelligence with a deep learning network for the quantification and distinction of functional adrenal tumors based on contrast-enhanced CT images.
Parehe Alimu et al. Quant Imaging Med Surg 2023 13(4) 2675-2687 - Metastatic pheochromocytoma and paraganglioma: Somatostatin receptor 2 expression, genetics and therapeutic responses.
Alessa Fischer et al. The Journal of clinical endocrinology and metabolism 2023 - Genetic Testing for Adrenal Tumors-What the Contemporary Surgeon Should Know.
Maria F Bates et al. Surgical oncology clinics of North America 2023 32(2) 303-313 - Genetic study in pheochromocytoma ¿is it possible to stratify the risk of hereditary pheochromocytoma?
Marta Araujo-Castro et al. Neuroendocrinology 2023 - An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes.
Schwartz Alison et al. Frontiers in oncology 2022 12942741 - Mutational Profile and Potential Molecular Therapeutic Targets of Pheochromocytoma.
Ma Xiaosen et al. Frontiers in endocrinology 2022 13921645 - Surveillance improves outcomes for carriers of SDHB pathogenic variants: a multi-center study.
Davidoff Dahlia F et al. The Journal of clinical endocrinology and metabolism 2022 - Universal Germline Panel Testing for Individuals with Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield.
Horton Carolyn et al. The Journal of clinical endocrinology and metabolism 2022
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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