Carcinoid Tumor
What's New
Last Posted: Apr 04, 2023
- Fully-Automated detection of small bowel carcinoid tumors in CT scans using deep learning.
Seung Yeon Shin et al. Medical physics 2023 - [Not Available].
Vialon Magaly, et al. Annales d'endocrinologie 2019 0 S19-S28 - Artificial intelligence-augmented analysis of contemporary procedural, mortality, and cost trends in carcinoid heart disease in a large national cohort with a focus on the "forgotten pulmonic valve".
Dominique J Monlezun et al. Frontiers in cardiovascular medicine 2023 91071138 - Local Coverage Determination (LCD): Diagnostic and Therapeutic Colonoscopy (L34213)
The U.S. Centers for Medicare & Medicaid Services - Local Coverage Determination (LCD): Diagnostic and Therapeutic Colonoscopy (L36868)
The U.S. Centers for Medicare & Medicaid Services - Local Coverage Determination (LCD): Genomic Sequence Analysis Panels in the Treatment of Solid Organ Neoplasms (L37810)
The U.S. Centers for Medicare & Medicaid Services - Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.
Georgitsi Marianthi, et al. The Journal of clinical endocrinology and metabolism 2007 8 (8) 3321-5 - Carcinoid tumor
From NCATS Genetic and Rare Diseases Information Center - Carcinoid tumor childhood
From NCATS Genetic and Rare Diseases Information Center - A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.
Walsh Kyle M, et al. Endocrine-related cancer 2011 2 (1) 171-80
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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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