Paragangliomas 2
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Last Posted: Feb 02, 2024
- Succinate dehydrogenase mutations in head and neck paragangliomas: A systematic review and meta-analysis of individual patients' data.
Elizabeth S Koh, et al. Head & neck 2024 0 - Outcomes of systemic treatment according to germline mutational status in patients with metastatic pheochromocytoma and paraganglioma.
Young-Gyu Park, et al. Clinical genitourinary cancer 2024 0 - Local recurrence and metastatic disease in pheochromocytomas and sympathetic paragangliomas.
Marta Araujo-Castro, et al. Frontiers in endocrinology 2023 0 1279828 - The Natural History of Observed SDHx-Related Head and Neck Paragangliomas Using Three-Dimensional Volumetric Tumor Analysis.
Evan L Tooker, et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2023 0 - Genotype-phenotype associations in paragangliomas of the temporal bone in a multi-ethnic cohort.
Simon I Angeli, et al. Acta oto-laryngologica 2023 0 1-7 - Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients with Paraganglioma.
Fagundes Gustavo F C, et al. The Journal of clinical endocrinology and metabolism 2023 0 - SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas.
Manotas María Carolina, et al. Frontiers in genetics 2023 0 999329 - Serum succinate/fumarate ratio in paraganglioma/pheochromocytoma patients attending an endocrine oncogenetic unit.
Bancel Léo-Paul, et al. The Journal of clinical endocrinology and metabolism 2023 0 - The SDHD:p.H102R Variant Is Frequent in Russian Patients with Head and Neck Paragangliomas and Associated with Loss of 11p15.5 Region and Hypermethylation of H19-DMR.
Snezhkina Anastasiya, et al. International journal of molecular sciences 2023 0 (1) - Clinical management of pheochromocytoma and paraganglioma in Singapore: missed opportunities for genetic testing.
Chew Winston Hong Wern, et al. Molecular genetics & genomic medicine 2017 0 (5) 602-607
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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
- Page last updated:May 03, 2024
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