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kw.\*:("Syndrome d'Omenn")

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Results 1 to 25 of 31

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First reported case of Omenn syndrome in a patient with reticular dysgenesisHENDERSON, Lauren A; FRUGONI, Francesco; HOPKINS, Gregory et al.Journal of allergy and clinical immunology. 2013, Vol 131, Num 4, pp 1227-1230, issn 0091-6749, 4 p.Article

Treatment with cyclosporin A in a patient with Omenn's syndromeMEYER-BAHLBURG, A; HAAS, J-P; HAASE, R et al.Archives of disease in childhood. 2002, Vol 87, Num 3, pp 231-233, issn 0003-9888, 3 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's syndrome : lessons from a red babyKATUGAMPOLA, R. P; MORGAN, G; KHETAN, R et al.Clinical and experimental dermatology (Print). 2008, Vol 33, Num 4, pp 425-428, issn 0307-6938, 4 p.Article

Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implicationsMARRELLA, Veronica; POLIANI, Pietro L; TRAGGIAI, Elisabetta et al.Blood. 2012, Vol 120, Num 5, pp 1005-1014, issn 0006-4971, 10 p.Article

RAG mutations in severe combined immunodeficiency and Omenn's syndromeSCHWARZ, K; VILLA, A.Immunology and allergy clinics of North America. 2000, Vol 20, Num 1, issn 0889-8561, xii, 129-142 [15 p.]Article

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

Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutationsMATANGKASOMBUT, Ponpan; PICHAVANT, Muriel; NOTARANGELO, Luigi D et al.Blood. 2008, Vol 111, Num 1, pp 271-274, issn 0006-4971, 4 p.Article

Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndromeVAN TIL, Niek P; SARWARI, Roya; CASSANI, Barbara et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 4, pp 1116-1123, issn 0091-6749, 8 p.Article

Decrease of Skin Infiltrating and Circulating CCR10 + T Cells Coincides with Clinical Improvement after Topical Tacrolimus in Omenn SyndromeFAAIJ, Claudia M; ANNELS, Nicola E; RUIGROK, Geertje et al.Journal of investigative dermatology. 2010, Vol 130, Num 1, pp 308-311, issn 0022-202X, 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

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

Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndromeLUIGI POLIANI, Pietro; FACCHETTI, Fabio; RAVANINI, Maria et al.Blood. 2009, Vol 114, Num 1, pp 105-108, issn 0006-4971, 4 p.Article

Saving the red baby : Successful allogeneic cord blood transplantation in Omenn syndromeSCHÖNBERGER, Stefan; OTT, Hagen; DILLOO, Dagmar et al.Clinical immunology (Orlando, Fla. Print). 2009, Vol 130, Num 3, pp 259-263, issn 1521-6616, 5 p.Article

Variability of clinical and laboratory features among patients with ribonuclease mitochondrial RNA processing endoribonuclease gene mutationsKAVADAS, Fotini D; GILIANI, Silvia; YIPING GU et al.Journal of allergy and clinical immunology. 2008, Vol 122, Num 6, pp 1178-1184, issn 0091-6749, 7 p.Article

From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient familyMARTINEZ-MARTINEZ, Laura; VAZQUEZ-ORTIZ, Marta; GONZALEZ-SANTESTEBAN, Cecilia et al.Pediatric allergy and immunology. 2012, Vol 23, Num 7, pp 660-666, issn 0905-6157, 7 p.Article

More than just SCID-The phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2NIEHUES, Tim; PEREZ-BECKER, Ruy; SCHUETZ, Catharina et al.Clinical immunology (Orlando, Fla. Print). 2010, Vol 135, Num 2, pp 183-192, issn 1521-6616, 10 p.Article

Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: The Primary Immune Deficiency Treatment Consortium experienceSHEARER, William T; DUNN, Elizabeth; PAI, Sung-Yun et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 4, pp 1092-1098, issn 0091-6749, 7 p.Article

Clinical characteristics and molecular analysis of three Chinese children with Omenn syndromeZHANG, Zhi-Yong; ZHAO, Xiao-Dong; JIANG, Li-Ping et al.Pediatric allergy and immunology. 2011, Vol 22, Num 5, pp 482-487, issn 0905-6157, 6 p.Article

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