Polyarteritis Nodosa
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Last Posted: Mar 08, 2023
- Polyarteritis nodosa: lessons from 25 years of experience.
Sönmez Hafize Emine, et al. Clinical and experimental rheumatology 2018 0 (2) 52-56 - Comorbidities in familial Mediterranean fever: analysis of 2000 genetically confirmed patients.
Balc?-Peynircio?lu Banu, et al. Rheumatology (Oxford, England) 2019 0 (6) 1372-1380 - A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2.
Özen Seza, et al. The Journal of rheumatology 2019 0 (1) 117-125 - Association of Vasculitis and Familial Mediterranean Fever.
Abbara Salam, et al. Frontiers in immunology 2019 0 763 - Identification of Novel Adenosine Deaminase 2 Gene Variants and Varied Clinical Phenotype in Pediatric Vasculitis.
Gibson Kristen M, et al. Arthritis & rheumatology (Hoboken, N.J.) 2019 0 (10) 1747-1755 - Cardiovascular Sequelae and Genetics of Familial Mediterranean Fever: A Literature Review.
Malik Jahanzeb, et al. Pulse (Basel, Switzerland) 2021 0 (3-4) 78-85 - Risk of venous thromboembolism among patients with vasculitis: a systematic review and meta-analysis.
Ungprasert Patompong, et al. Clinical rheumatology 2016 8 - Cutaneous polyarteritis nodosa
From NCATS Genetic and Rare Diseases Information Center - Polyarteritis nodosa
From NCATS Genetic and Rare Diseases Information Center - HLA-DR in Brazilian patients with polyarteritis nodosa (PAN) and microscopic polyangiitis (MPA).
de Lira Freire A, et al. Disease markers 2009 7 (3) 3
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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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