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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Sapho Syndrome[original query]
Single-nucleotide polymorphisms p53 G72C and Mdm2 T309G in patients with psoriasis, psoriatic arthritis, and SAPHO syndrome.
Rheumatology international 2010 Aug 30 (10): 1273-6.
Assmann Gunter, Wagner Annette D, Monika Mueller, Pfoehler Claudia, Pfreundschuh Michael, Tilgen Wolfgang, Roemer Kla
Genetic susceptibility factors in a cohort of 38 patients with SAPHO syndrome: a study of PSTPIP2, NOD2, and LPIN2 genes.
The Journal of rheumatology 2010 Feb 37 (2): 401-9.
Hurtado-Nedelec Margarita, Chollet-Martin Sylvie, Chapeton Diana, Hugot Jean-Pierre, Hayem Gilles, Gérard Bénédic
Different Contributions of CDKAL1, KIF21B, and LRRK2/MUC19 Polymorphisms to SAPHO Syndrome, Rheumatoid Arthritis, Ankylosing Spondylitis, and Seronegative Spondyloarthropathy.
Genetic testing and molecular biomarkers 2016 Dec .
Li Nan, Ma Junfen, Li Kai, Guo Changlong, Ming Lia
Association analysis of interleukin-23 receptor SNPs and SAPHO syndrome in Chinese people.
International journal of rheumatic diseases 2019 Nov .
Guo Changlong, Li Chen, Han Feifei, Gao Jianen, Ma
Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome. GWAS Catalog
Frontiers in cell and developmental biology 2021 9 643644.
Cai Ruikun, Dong Yichao, Fang Mingxia, Fan Yuxuan, Cheng Zian, Zhou Yue, Gao Jianen, Han Feifei, Guo Changlong, Ma
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