Granulomatosis With Polyangiitis
What's New
Last Posted: Nov 28, 2024
- Association between osteoprotegerin and RANKL single nucleotide polymorphisms and destructive rhinosinusitis in patients with granulomatosis with polyangiitis.
Marília A D Furquim, et al. BMC rheumatology 2024 0 (1) 63 - Polymorphisms of the SERPINA1 gene are associated with higher mortality in a Brazilian cohort of ANCA-associated vasculitis patients.
Henrique Ayres Mayrink Giardini, et al. Clinics (Sao Paulo, Brazil) 2024 0 100524 - HLA sequencing identifies novel associations and suggests clinical relevance of DPB1*04:01 in ANCA-associated Granulomatosis with polyangiitis.
Sabyasachi Senapati, et al. Gene 2023 0 148024 - Seasonal influence on development of anti-neutrophil cytoplasmic antibody-associated vasculitis: a retrospective cohort study conducted at multiple institutions in Japan (J-CANVAS).
Yusuke Yoshida, et al. The Journal of rheumatology 2023 0 - Identifying shared genetic architecture between rheumatoid arthritis and other conditions: a phenome-wide association study with genetic risk scores.
Harrison G Zhang, et al. EBioMedicine 2023 0 104581 - Human Leukocyte Antigen Genotyping of Idiopathic Subglottic Stenosis.
Rohlfing Matthew L, et al. The Laryngoscope 2023 0 - Rheumatoid factor false positivity in patients with ANCA-associated vasculitis not having medical conditions producing rheumatoid factor.
Moon Jae-Seung, et al. Clinical rheumatology 2017 0 (10) 2771-2779 - Is granulomatosis with polyangiitis in Asia different from the West?
Naidu Godasi S R S N K, et al. International journal of rheumatic diseases 2018 0 90-94 - Cancer development in Korean patients with ANCA-associated vasculitis: a single centre study.
Yoo Juyoung, et al. Clinical and experimental rheumatology 2018 0 (2) 73-77 - FCGR3B polymorphism predicts relapse risk in eosinophilic granulomatosis with polyangiitis.
Alberici Federico, et al. Rheumatology (Oxford, England) 2020 0 (11) 3563-3566
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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
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