Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Hyperplasia and HLA-C[original query] |
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| Human leukocyte antigen class II alleles in white Brazilian patients with celiac disease. Journal of pediatric gastroenterology and nutrition 2000 Oct 31 (4): 391-4. Silva E M, Fernandes M I, Galvão L C, Sawamura R, Donadi E |
| HLA class II genotypes in Mexican Mestizo patients with myasthenia gravis. European journal of neurology : the official journal of the European Federation of Neurological Societies 2003 Nov 10 (6): 707-10. García-Ramos G, Téllez-Zenteno J F, Zapata-Zúñiga M, Yamamoto-Furusho J K, Ruiz-Morales J A, Villarreal-Garza C, Vargas-Alarcón G, Estañol B, Llorente L, Granados |
| The prevalence, molecular analysis and HLA typing of late-onset 21-hydroxylase deficiency in Turkish woman with hirsutism and polycystic ovary. Endocrine journal 2004 Feb 51 (1): 31-6. Yarman S, Dursun A, Oguz F, Alagol F |
| [Analysis of the association of HLA-DQ1 alleles with mutation of the 21-hydroxylase gene in patients with congenital adrenal hyperplasia]. Genetika 2004 Jan 40 (1): 97-101. Osinovskaia N S, Ivashchenko T E, Baranov V |
| Association of HLA-DR4 (DRB1*0404) with human papillomavirus infection in patients with focal epithelial hyperplasia. Archives of dermatology 2004 Oct 140 (10): 1227-31. García-Corona Cristina, Vega-Memije Elisa, Mosqueda-Taylor Adalberto, Yamamoto-Furusho Jesús K, Rodríguez-Carreón Alma A, Ruiz-Morales Jorge A, Salgado Norma, Granados Jul |
| HLA class II and class I polymorphism in Venezuelan patients with myasthenia gravis. Human immunology 2004 Jan 65 (1): 54-9. Fernández-Mestre Mercedes T, Vargas Vivian, Montagnani Silvia, Cotúa Maritza, Ogando Violeta, Layrisse Zul |
| Distribution of the V281L mutation of the CYP21 gene in Israeli congenital adrenal hyperplasia patients and its association with HLA- B14. Pediatric endocrinology reviews : PER 2006 Aug 3 Suppl 3 447-50. Israel Shoshana, Weinrib Limor, Weintrob Naomi, Miller Kerem, Brautbar Cha |
| The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency. Molecular genetics and metabolism 2009 May 97 (1): 75-9. Lee Yann-Jinn, Tsai Li-Ping, Niu Dau-Ming, Shu San-Ging, Chao Mei-Chyn, Lee Hsien-Hsiu |
| CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles. European journal of endocrinology / European Federation of Endocrine Societies 2014 Dec 171 (6): 743-50. Brønstad Ingeborg, Skinningsrud Beate, Bratland Eirik, Løvås Kristian, Undlien Dag, Sverre Husebye Eystein, Wolff Anette Susanne B |
| Associations between HLA-A\B\DRB1 polymorphisms and risks of vulvar lichen sclerosus or squamous cell hyperplasia of the vulva. Genetics and molecular research : GMR 2015 14 (4): 15962-71. Liu G L, Cao F L, Zhao M Y, Shi J, Liu S |
| Immunogenetics of prostate cancer and benign hyperplasia--the potential use of an HLA-G variant as a tag SNP for prostate cancer risk. HLA : immune response genetics 2016 Feb 87 (2): 79-88. Zambra F M B, Biolchi V, de Cerqueira C C S, Brum I S, Castelli E C, Chies J A |
| Human Leucocyte Antigen B50 Is Associated with Conversion to Generalized Myasthenia Gravis in Patients with Pure Ocular Onset. Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2017 26 (1): 71-77. Tiftikcioglu Bedile Irem, Uludag Irem Fatma, Zorlu Yasar, Pirim ?brahim, Sener Ufuk, Tokucoglu Figen, Korucuk Melt |
| Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population. HLA 2016 Oct . Grubic Z, Maskalan M, Stingl Jankovic K, Zvecic S, Dumic Kubat K, Krnic N, Zunec R, Ille J, Kusec V, Dumic |
| Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians. Genetics in medicine : official journal of the American College of Medical Genetics 2017 11 19 (11): 1276-1279. Hannah-Shmouni Fady, Morissette Rachel, Sinaii Ninet, Elman Meredith, Prezant Toni R, Chen Wuyan, Pulver Ann, Merke Deborah |
| Revisiting the association of HLA alleles and haplotypes with CYP21A2 mutations in a large cohort of patients with congenital adrenal hyperplasia. Gene 2018 11 687 30-34. Jayakrishnan Rahul, Lao Qizong, Adams Sharon D, Ward William W, Merke Deborah |
| Issues with the Detection of Large Genomic Rearrangements in Molecular Diagnosis of 21-Hydroxylase Deficiency. Molecular diagnosis & therapy 2019 Jul . Concolino Pao |
| Refractory myasthenia gravis: Characteristics of a portuguese cohort. Muscle & nerve 2019 5 60 (2): 188-191. Santos Ernestina, Bettencourt Andreia, Duarte Sara, Gabriel Denis, Oliveira Vanessa, da Silva Ana Martins, Costa Paulo Pinho, Lopes Carlos, Gonçalves Guilherme, da Silva Berta Martins, Leite Maria Isab |
| Study of Human Leukocyte Antigen (HLA) in 13 cases of familial frontal fibrosing alopecia: CYP21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA-A*33:01; B*14:02; C*08:02 as a genetic marker. The Australasian journal of dermatology 2019 Jan . Porriño-Bustamante María Librada, López-Nevot Miguel Ángel, Aneiros-Fernández José, Casado-Ruiz Jorge, García-Linares Susana, Pedrinacci-Rodríguez Susana, García-Lora Elena, Martín-Casares María Antonia, Fernández-Pugnaire María Antonia, Arias-Santiago Salvad |
| The Weight of HLA-DPA1 rs3077 Single Nucleotide Polymorphism in Prostate Cancer, a Multicenter Study. Prostate cancer 2021 5 2021 5539851. Alenzi Mohammed Jayed, Ghazy Amany A, Taha Diaa-Eld |
| GENOMIC AND EPIGENOMIC PREDICTORS FOR VARIOUS CLINICAL PHENOTYPES OF MYASTHENIA GRAVIS. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2021 74 (3 cz 1): 475-480. Klimova Elena M, Drozdova Larisa A, Lavinskaya Elena V, Minukhin Dmitriy V, Kudrevych Iryna O, Kudrevych Oleksandr |
| HLA-DQB1*05:02, *05:03, and *03:01 alleles as risk factors for myasthenia gravis in a Spanish cohort. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 May . Salvado Maria, Caro Jose Luis, Garcia Cecilia, Rudilla Francesc, Zalba-Jadraque Laura, Lopez Eva, Sanjuan Elia, Gamez Josep, Vidal-Taboada Jose Manu |
| Congenital Adrenal Hyperplasia and Human Leukocyte Antigen B: A Meta-Analysis. Cureus 2023 4 15 (3): e35900. Thibaut Dylan, Walter Madison R, McGonegal Courtney, Daniel Ryan, Goodman Jer |
- Page last reviewed:Feb 1, 2024
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