Henoch-schonlein Purpura
What's New
Last Posted: May 04, 2024
- Association between polymorphism at codon 469 of the ICAM-1 gene and Henoch-Schönlein purpura in an Iranian cohort.
Shima Salehi, et al. Nucleosides, nucleotides & nucleic acids 2024 0 1-8 - Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children.
Yang Ruan, et al. Heliyon 2024 0 (8) e29469 - Association of Interleukin-2 Gene Polymorphism with Henoch-schönlein Purpura Nephritis.
Jiajia Cao, et al. Iranian journal of allergy, asthma, and immunology 2023 0 (3) 319-326 - Angiotensin-converting enzyme insertion/deletion gene polymorphism and Henoch-Schonlein purpura nephritis risk in children: a meta-analysis.
Pan Yan, et al. Polish journal of pathology : official journal of the Polish Society of Pathologists 2023 0 (1) 29-35 - 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 - Risk factors associated with IgA vasculitis with nephritis (Henoch-Schönlein purpura nephritis) progressing to unfavorable outcomes: A meta-analysis.
Shi Dongmei, et al. PloS one 2019 0 (10) e0223218 - MEFV gene mutations in children with Henoch-Schönlein purpura and their correlations-do mutations matter?
Cakici Evrim Kargin, et al. Clinical rheumatology 2019 0 (7) 1947-1952 - Cardiovascular Sequelae and Genetics of Familial Mediterranean Fever: A Literature Review.
Malik Jahanzeb, et al. Pulse (Basel, Switzerland) 2021 0 (3-4) 78-85 - The Association Between the PTPN22 C1858T Variant and Vasculitis: A Meta-analysis Update with Trial Sequential Analysis.
Lee Young Ho, et al. Genetic testing and molecular biomarkers 2022 0 (10) 492-500 - HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study.
Koskela Mikael, et al. Pediatric nephrology (Berlin, Germany) 2021 2
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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
- Page last updated:May 07, 2024
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