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2. GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes. Haq IJ; Steinberg LJ; Hoenig M; van der Burg M; Villa A; Cant AJ; Middleton PG; Gennery AR Clin Immunol; 2007 Aug; 124(2):165-9. PubMed ID: 17572155 [TBL] [Abstract][Full Text] [Related]
3. Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders. Wada T; Takei K; Kudo M; Shimura S; Kasahara Y; Koizumi S; Kawa-Ha K; Ishida Y; Imashuku S; Seki H; Yachie A Clin Exp Immunol; 2000 Jan; 119(1):148-55. PubMed ID: 10606976 [TBL] [Abstract][Full Text] [Related]
4. Omenn syndrome: a lack of tolerance on the background of deficient lymphocyte development and maturation. Hönig M; Schwarz K Curr Opin Rheumatol; 2006 Jul; 18(4):383-8. PubMed ID: 16763459 [TBL] [Abstract][Full Text] [Related]
5. Mutations in the RNA component of RNase mitochondrial RNA processing might cause Omenn syndrome. Roifman CM; Gu Y; Cohen A J Allergy Clin Immunol; 2006 Apr; 117(4):897-903. PubMed ID: 16630949 [TBL] [Abstract][Full Text] [Related]
6. Recombination activating gene and its defects. Villa A; Sobacchi C; Vezzoni P Curr Opin Allergy Clin Immunol; 2001 Dec; 1(6):491-5. PubMed ID: 11964731 [TBL] [Abstract][Full Text] [Related]
7. Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome. Corneo B; Moshous D; Güngör T; Wulffraat N; Philippet P; Le Deist FL; Fischer A; de Villartay JP Blood; 2001 May; 97(9):2772-6. PubMed ID: 11313270 [TBL] [Abstract][Full Text] [Related]
8. Bone marrow transplantation in severe combined immunodeficiency: potential and current limitations. Friedrich W; Knobloch C; Greher J; Hartmann W; Peter HH; Goldmann SF; Kleihauer E Immunodeficiency; 1993; 4(1-4):315-22. PubMed ID: 8167725 [No Abstract] [Full Text] [Related]
9. Novel RAG1 mutation in a case of severe combined immunodeficiency. Zhang J; Quintal L; Atkinson A; Williams B; Grunebaum E; Roifman CM Pediatrics; 2005 Sep; 116(3):e445-9. PubMed ID: 16061569 [TBL] [Abstract][Full Text] [Related]
10. Long-term outcomes of nonconditioned patients with severe combined immunodeficiency transplanted with HLA-identical or haploidentical bone marrow depleted of T cells with anti-CD6 mAb. Patel NC; Chinen J; Rosenblatt HM; Hanson IC; Brown BS; Paul ME; Abramson SL; Ritz J; Shearer WT J Allergy Clin Immunol; 2008 Dec; 122(6):1185-93. PubMed ID: 19084111 [TBL] [Abstract][Full Text] [Related]
11. Omenn syndrome: a rare case of neonatal erythroderma. Puzenat E; Rohrlich P; Thierry P; Girardin P; Taghian M; Ouachee M; Plouvier E; Fischer A; Humbert P; Aubin F Eur J Dermatol; 2007; 17(2):137-9. PubMed ID: 17337397 [TBL] [Abstract][Full Text] [Related]
12. Successful treatment of autoimmune hemolytic anemia with rituximab in a child with severe combined immunodeficiency following nonidentical T-cell-depleted bone marrow transplantation. Bonduel M; Zelazko M; Figueroa C; Magaldi G; Rossi J; del Pozo A Bone Marrow Transplant; 2005 Apr; 35(8):819-21. PubMed ID: 15750606 [No Abstract] [Full Text] [Related]
18. Identification of anti-herpes simplex virus antibody-producing B cells in a patient with an atypical RAG1 immunodeficiency. Kumaki S; Villa A; Asada H; Kawai S; Ohashi Y; Takahashi M; Hakozaki I; Nitanai E; Minegishi M; Tsuchiya S Blood; 2001 Sep; 98(5):1464-8. PubMed ID: 11520796 [TBL] [Abstract][Full Text] [Related]