Hematopoietic stem cell transplantation in Omenn syndrome : a single-center experienceMAZZOLARI, E; MOSHOUS, D; PORTA, F et al.Bone marrow transplantation (Basingstoke). 2005, Vol 36, Num 2, pp 107-114, issn 0268-3369, 8 p.Article

Omenn's syndromeNAZZARI, G; DRAGO, F; CROVATO, F et al.International journal of dermatology. 1997, Vol 36, Num 2, pp 141-144, issn 0011-9059Article

Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disordersWADA, T; TAKEI, K; YACHIE, A et al.Clinical and experimental immunology (Print). 2000, Vol 119, Num 1, pp 148-155, issn 0009-9104Article

Omenn syndrome due to ARTEMIS mutationsEGE, Markus; YUNMEI MA; MANFRAS, Burkhard et al.Blood. 2005, Vol 105, Num 11, pp 4179-4186, issn 0006-4971, 8 p.Article

Omenn syndrome. A case report of a successful, heterologous bone marrow transplantationCAVALLI, R; RESTANO, L; CAMBIAGHI, S et al.EJD. European journal of dermatology. 1997, Vol 7, Num 1, pp 12-14, issn 1167-1122Article

Omenn syndrome in an infant with IL7RA gene mutationGILIANI, Silvia; BONFIM, Carmen; DE SAINT BASILE, Genevieve et al.The Journal of pediatrics. 2006, Vol 148, Num 2, pp 272-274, issn 0022-3476, 3 p.Article

Omenn's syndrome occurring in patients without mutations in recombination activating genesGENNERY, Andrew R; HODGES, Elizabeth; WILLIAMS, Anthony P et al.Clinical immunology (Orlando, Fla. Print). 2005, Vol 116, Num 3, pp 246-256, issn 1521-6616, 11 p.Article

Bone marrow transplantation without conditioning regimen in omenn syndrome : A case reportMELLOULI, Fethi; TORJMEN, Lamia; KSOURI, Habib et al.Pediatric transplantation. 2007, Vol 11, Num 8, pp 922-926, issn 1397-3142, 5 p.Article

Omenn syndrome: a case report and review of literatureHSU, Chia-Chi; YU-YUN LEE, Julia; CHAO, Sheau-Chiou et al.Zhōnghuá pífūkē yīxué zázhì. 2011, Vol 29, Num 2, pp 50-54, issn 1027-8117, 5 p.Article

Omenn syndrome : A disorder of Rag1 and Rag2 genesVILLA, A; SANTAGATA, S; BOZZI, F et al.Journal of clinical immunology. 1999, Vol 19, Num 2, pp 87-97, issn 0271-9142Article

What syndrome is this ?RICCI, G; PATRIZI, A; SPECCHIA, F et al.Pediatric dermatology. 1997, Vol 14, Num 1, pp 49-52, issn 0736-8046Conference Paper

Omenn syndrome : Inflammation in leaky severe combined immunodeficiencyVILLA, Anna; NOTARANGELO, Luigi D; ROIFMAN, Chaim M et al.Journal of allergy and clinical immunology. 2008, Vol 122, Num 6, pp 1082-1086, issn 0091-6749, 5 p.Article

Mutations in the RNA component of rnase mitochondrial RNA processing might cause Omenn syndromeROIFMAN, Chaim M; YIPING GU; COHEN, Amos et al.Journal of allergy and clinical immunology. 2006, Vol 117, Num 4, pp 897-903, issn 0091-6749, 7 p.Article

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiencyWADA, Taizo; TOMA, Tomoko; YACHIE, Akihiro et al.Blood. 2005, Vol 106, Num 6, pp 2099-2101, issn 0006-4971, 3 p.Article

GvHD-associated cytokine polymorphisms do not associate with omenn syndrome rather than T-B-SCID in patients with defects in RAG genesHAQ, Iram J; STEINBERG, Laura J; HOENIG, Manfred et al.Clinical immunology (Orlando, Fla. Print). 2007, Vol 124, Num 2, pp 165-169, issn 1521-6616, 5 p.Article

Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infectionDALAL, Ilan; TABORI, Uri; BIELORAI, Bela et al.Clinical immunology (Orlando, Fla. Print). 2005, Vol 115, Num 1, pp 70-73, issn 1521-6616, 4 p.Article

Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiencyGRUBER, Tanja A; SHAH, Ami J; HERNANDEZ, Michelle et al.Pediatric transplantation. 2009, Vol 13, Num 2, pp 244-250, issn 1397-3142, 7 p.Article

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiencyYU NEE LEE; FRUGONI, Francesco; HENDERSON, Lauren A et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 4, pp 1099-1108, issn 0091-6749, 10 p.Article

Analysis of mutations and recombination activity in RAG-deficient patientsASAI, Erika; WADA, Taizo; MURAMATSU, Hideki et al.Clinical immunology (Orlando, Fla. Print). 2011, Vol 138, Num 2, pp 172-177, issn 1521-6616, 6 p.Article

Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire developmentXIAOMIN YU; ALMEIDA, Jorge R; MILNER, Joshua D et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 4, pp 1109-1115, issn 0091-6749, 7 p.Article

Defect of regulatory T cells in patients with Omenn syndromeCASSANI, Barbara; POLIANI, Pietro Luigi; FACCHETTI, Fabio et al.Journal of allergy and clinical immunology. 2010, Vol 125, Num 1, pp 209-216, issn 0091-6749, 8 p.Article

Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cellsSOMECH, Raz; SIMON, Amos J; LEV, Atar et al.Journal of allergy and clinical immunology. 2009, Vol 124, Num 4, pp 793-800, issn 0091-6749, 8 p.Article

Primary immune deficiencies with aberrant IgE productionOZCAN, Esra; NOTARANGELO, Luigi D; GEHA, Raif S et al.Journal of allergy and clinical immunology. 2008, Vol 122, Num 6, pp 1054-1062, issn 0091-6749, 9 p.Article

The genetic and biochemical basis of Omenn syndromeSANTAGATA, Sandro; VILLA, Anna; SOBACCHI, Cristina et al.Immunological reviews. 2000, Vol 178, pp 64-74, issn 0105-2896Article

Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B- SCID or Omenn syndromeDALAL, Ilan; TASHER, Diana; SOMECH, Raz et al.Clinical immunology (Orlando, Fla. Print). 2011, Vol 140, Num 3, pp 284-290, issn 1521-6616, 7 p.Article