Castleman Disease
What's New
Last Posted: Mar 04, 2023
- Paraneoplastic pemphigus: a clinical, laboratorial, and therapeutic overview.
Maruta Celina Wakisaka, et al. Anais brasileiros de dermatologia 2019 0 (4) 388-398 - Mediterranean fever gene variants modify clinical phenotypes of idiopathic multi-centric Castleman disease.
Endo Yushiro, et al. Clinical and experimental immunology 2021 0 (1) 91-98 - This med student was given last rites before finding a treatment that saved his life. His method could help millions
R Pryor, CNN, September 14, 2019 - Quantitative analysis of a rare disease network's international contact database and E-repository provides insights into biobanking in the electronic consent era.
Suarez Alexander et al. Orphanet journal of rare diseases 2019 Jul 14(1) 173 - Novel insights and therapeutic approaches in idiopathic multicentric Castleman disease.
Fajgenbaum David C et al. Hematology. American Society of Hematology. Education Program 2018 Nov 2018(1) 318-325 - Human herpesvirus 6, 7, and 8 in solid organ transplantation: Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice.
Pellett Madan Rebecca et al. Clinical transplantation 2019 Mar e13518 - Interleukin-6 receptor polymorphism is prevalent in HIV-negative Castleman Disease and is associated with increased soluble interleukin-6 receptor levels.
Stone K, et al. PloS one 2013 2 (1) 1 - Castleman disease
From NCATS Genetic and Rare Diseases Information Center - Multicentric Castleman Disease
From NCATS Genetic and Rare Diseases Information Center - Unicentric Castleman disease
From NCATS Genetic and Rare Diseases Information Center
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About Rare Diseases PHGKB
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 the CDC Office of Public Health Genomics 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, 2023
- Page last updated:Jun 07, 2023
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