Pemphigus
What's New
Last Posted: Jan 30, 2024
- Genetic Association and Differential RNA Expression of Histone (De)Acetylation-Related Genes in Pemphigus Foliaceus-A Possible Epigenetic Effect in the Autoimmune Response.
Maiara Sulzbach Denardin, et al. Life (Basel, Switzerland) 2024 0 (1) - Whole-exome sequencing reveals the genomic profile and IL6ST mutations as a prognostic biomarker of paraneoplastic pemphigus associated unicentric Castleman disease.
Sai Wang, et al. The Journal of investigative dermatology 2023 0 - HLA class II antigens in Croatian patients with pemphigus vulgaris and their correlation with anti-desmoglein antibodies.
Ines Lakoš Juki?, et al. Frontiers in immunology 2023 0 1200992 - Two Novel and a Recurrent ATP2C1 Mutations in Chinese Population with Hailey-Hailey Disease.
Deng Zhang, et al. Clinical, cosmetic and investigational dermatology 2023 0 1545-1548 - Patient genetics shape the autoimmune response in the blistering skin disease pemphigus vulgaris.
Baker John, et al. Frontiers in immunology 2023 0 1064073 - HLA class II alleles of susceptibility and protection in Brazilian and Dutch pemphigus foliaceus.
de Sena Nogueira Maehara L, et al. The British journal of dermatology 2017 0 (3) e212-e214 - Relationship between pemphigus and American tegumentary leishmaniasis: insights from serological and genetic profiles.
Walsh Priscilla, et al. Transactions of the Royal Society of Tropical Medicine and Hygiene 2017 0 (8) 345-353 - Comorbid autoimmune diseases in patients with pemphigus: a nationwide case-control study in Taiwan.
Chiu Yun-Wen, et al. European journal of dermatology : EJD 2017 0 (4) 375-381 - NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a Chinese man with pemphigus vulgaris.
Yan W, et al. The British journal of dermatology 2017 0 (1) e40-e41 - Azathioprine-induced myelosuppression in two pemphigus vulgaris patients with homozygous polymorphism of NUDT15.
Shih Yen-Chi, et al. The Journal of dermatology 2018 0 (2) e59-e61 - Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of "Fogo Selvagem" Pemphigus Foliaceus.
Oliveira Luana Caroline, et al. Frontiers in immunology 2019 0 2585 - Paraneoplastic pemphigus: a clinical, laboratorial, and therapeutic overview.
Maruta Celina Wakisaka, et al. Anais brasileiros de dermatologia 2019 0 (4) 388-398 - Pemphigus vulgaris in two pairs of siblings from two unrelated Italian families: Human leukocyte antigen genotypes, ST18 mutation and immunological profile.
Fania Luca, et al. The Journal of dermatology 2020 0 (2) 211-214 - Novel HLA alleles associated with pemphigus vulgaris in Indian population detected by DNA microarray analysis.
Handa Sanjeev, et al. Indian journal of dermatology, venereology and leprology 2021 0 (6) 867-869 - Unsuspected Associations of Variants within the Genes NOTCH4 and STEAP2-AS1 Uncovered by a GWAS in Endemic Pemphigus Foliaceus.
Augusto Danillo G, et al. The Journal of investigative dermatology 2021 0 (11) 2741-2744 - Evaluation of X chromosome inactivation in endemic Tunisian pemphigus foliaceus.
Abida Olfa, et al. Molecular genetics & genomic medicine 2022 0 (12) e2080 - Allele frequency and the associations of HLA-DRB1 and HLA-DQB1 polymorphisms with pemphigus subtypes and disease severity.
Le Thanh Thai Van, et al. Medicine 2022 0 (7) e28855 - Association of MIF gene polymorphisms with pemphigus vulgaris: a case-control study with comprehensive review of the literature.
Gupta Parikshaa, et al. International journal of clinical and experimental pathology 2021 0 (11) 1080-1089 - Evaluation of Comorbidities in Patients with Autoimmune Bullous Diseases: A Retrospective Study.
Karabay Ezgi Akta?, et al. Sisli Etfal Hastanesi tip bulteni 2020 0 (4) 302-306 - Update on fogo selvagem, an endemic form of pemphigus foliaceus.
Aoki Valeria, et al. The Journal of dermatology 2015 0 (1) 18-26
More
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 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 01, 2024
- Content source: