Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 17 (of 17 Records) |
Query Trace: Autoimmune Hemolytic Anemia[original query] |
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CTLA-4 exon 1 polymorphism in patients with autoimmune blood disorders. American journal of hematology 2003 Feb 72 (2): 147-9. Pavkovic Marica, Georgievski Borce, Cevreska Lidija, Spiroski Mirko, Efremov Dimitar |
TP53 gene mutation, an unfavorable prognostic factor for malignant lymphomas in autoimmune diseases. Oncology 2005 69 (2): 175-83. Hoshida Y, Hongyo T, Xu JX, Sasaki T, Tomita Y, Nomura T, Aozasa K |
Association between -174 interleukin-6 gene polymorphism and biological response to rituximab in several systemic autoimmune diseases. DNA and cell biology 2012 Sep 31 (9): 1486-91. Robledo Gema, Dávila-Fajardo Cristina Lucía, Márquez Ana, Ortego-Centeno Norberto, Callejas Rubio José Luis, de Ramón Garrido Enrique, Sánchez-Román Julio, García-Hernández Francisco J, Ríos-Fernández Raquel, González-Escribano Maria Francisca, Camps García Maria Teresa, Castillo Palma Maria Jesús, Ayala Maria Del Mar, Martín Javi |
Polymorphisms in NAT2 (N-acetyltransferase 2) gene in patients with systemic lupus erythematosus. Revista brasileira de reumatologia 0 56 (6): 521-529. Santos Elaine Cristina Lima Dos, Pinto Amanda Chaves, Klumb Evandro Mendes, Macedo Jacyara Maria Bri |
CB2-63 polymorphism and immune-mediated diseases associated with HCV chronic infection. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2016 Jul . Coppola Nicola, Zampino Rosa, Bellini Giulia, Stanzione Maria, Capoluongo Nicolina, Marrone Aldo, Macera Margherita, Adinolfi Luigi Elio, Giudice Emanuele Miraglia Del, Gentile Ivan, Sagnelli Evangelista, Rossi Frances |
Tumor necrosis factor gene polymorphisms in adult patients with autoimmune hemolytic anemia. International journal of laboratory hematology 2017 Jan . Pavkovic M, Petlichkovski A, Angelovic R, Genadieva-Stavric S, Cevreska L, Stojanovic |
Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations. Clinical immunology (Orlando, Fla.) 2018 1 188 52-57. Besnard Caroline, Levy Eva, Aladjidi Nathalie, Stolzenberg Marie-Claude, Magerus-Chatinet Aude, Alibeu Olivier, Nitschke Patrick, Blanche Stéphane, Hermine Olivier, Jeziorski Eric, Landman-Parker Judith, Leverger Guy, Mahlaoui Nizar, Michel Gérard, Pellier Isabelle, Suarez Felipe, Thuret Isabelle, de Saint-Basile Geneviève, Picard Capucine, Fischer Alain, Neven Bénédicte, Rieux-Laucat Frédéric, Quartier Pierre, |
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes. Blood 2019 Apr . Hadjadj Jérôme, Aladjidi Nathalie, Fernandes Helder, Leverger Guy, Magérus-Chatinet Aude, Mazerolles Fabienne, Stolzenberg Marie-Claude, Jacques Sidonie, Picard Capucine, Rosain Jérémie, Fourrage Cécile, Hanein Sylvain, Zarhrate Mohammed, Pasquet Marlène, Abou Chahla Wadih, Barlogis Vincent, Bertrand Yves, Pellier Isabelle, Colomb Bottollier Elodie, Fouyssac Fanny, Blouin Pascale, Thomas Caroline, Cheikh Nathalie, Dore Eric, Pondarre Corinne, Plantaz Dominique, Jeziorski Eric, Millot Frédéric, Garcelon Nicolas, Ducassou Stéphane, Perel Yves, Leblanc Thierry, Neven Bénédicte, Fischer Alain, Rieux-Laucat Frédéric, |
NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series. Drug metabolism and personalized therapy 2020 8 35 (4): . Devasia Anup J, Illangeswaran Raveen Stephen Stallon, Raj Infencia Xavier, George Biju, Balasubramanian Poonkuzha |
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: A systematic review. Autoimmunity reviews 2020 4 19 (6): 102526. Park Jae Hyon, Lee Keum Hwa, Jeon Bokyoung, Ochs Hans D, Lee Joon Suk, Gee Heon Yung, Seo Seeun, Geum Dongil, Piccirillo Ciriaco A, Eisenhut Michael, van der Vliet Hans J, Lee Jiwon M, Kronbichler Andreas, Ko Younhee, Shin Jae |
Autoimmune Lymphoproliferative Syndrome in Children with Nonmalignant Organomegaly, Chronic Immune Cytopenia, and Newly Diagnosed Lymphoma. Turkish journal of haematology : official journal of Turkish Society of Haematology 2020 12 38 (2): 145-150. Kaya Zühre, I??k Melek, Oruklu Nihan, Kirkiz Serap, Ba?r?aç?k Emin Ümit, Allende Luis M., Díaz-Madroñero María J., Ruiz-García Raquel, P?narl? Faruk Güçlü, Göçün Uyar P?nar, Koçak Ülk |
Revisiting Autoimmunity in Chronic Lymphocytic Leukemia: Prognostic Value of Positive Direct Antiglobulin Test in a Retrospective Study and Literature Review. Journal of blood medicine 2021 4 12 225-234. Ahmed Shimaa A, Abdallah Ghada E M, Aly Mai M, Abdelsalam Eman M Nagiub, Mohammed Saleh Mostafa |
Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7R? Chain. Frontiers in immunology 2022 4 13 867837. Mansour Rana, Bsat Yasmin El, Fadel Anthony, El-Orfali Youmna, Noun Dolly, Tarek Nidale, Kabbara Nabil, Abboud Miguel, Massaad Michel |
STEREOTYPED CASES IN UKRAINIAN COHORT OF CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS DEPENDING ON THE IONIZING RADIATION EXPOSURE. Problemy radiatsiinoi medytsyny ta radiobiolohii 2022 12 27 307-323. Bilous N I, Abramenko I V, Chumak A A, Dyagil I S, Martina Z |
Rare Case of Hemolytic Anemia and Distal Renal Tubular Acidosis in an adult due to Homozygous SLC4A1 Mutation. Indian journal of nephrology 2023 7 33 (3): 209-212. Wasiyeeullah Shaikh, Lohitaksha Suratkal, Abhay Bha |
Cytokine polymorphisms in patients with autoimmune hemolytic anemia. Frontiers in immunology 2023 11 14 1221582. Anna Zaninoni, Bruno Fattizzo, Loredana Pettine, Cristina Vercellati, Anna P Marcello, Wilma Barcelli |
Evaluating the prevalence of inborn errors of immunity in adults with chronic immune thrombocytopenia or Evans syndrome. Blood advances 2023 10 . Debbie Jiang, Kira Maria Rosenlind, Sarah K Baxter, Terry Gernsheimer, Suleyman Gulsuner, Eric Allenspach, Sioban B Ke |
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