310 related articles for article (PubMed ID: 18822103)
1. Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency.
Gruber TA; Shah AJ; Hernandez M; Crooks GM; Abdel-Azim H; Gupta S; McKnight S; White D; Kapoor N; Kohn DB
Pediatr Transplant; 2009 Mar; 13(2):244-50. PubMed ID: 18822103
[TBL] [Abstract][Full Text] [Related]
2. Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infection.
Dalal I; Tabori U; Bielorai B; Golan H; Rosenthal E; Amariglio N; Rechavi G; Toren A
Clin Immunol; 2005 Apr; 115(1):70-3. PubMed ID: 15870023
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. RAG-dependent primary immunodeficiencies.
Sobacchi C; Marrella V; Rucci F; Vezzoni P; Villa A
Hum Mutat; 2006 Dec; 27(12):1174-84. PubMed ID: 16960852
[TBL] [Abstract][Full Text] [Related]
5. Relative CD4 lymphopenia and a skewed memory phenotype are the main immunologic abnormalities in a child with Omenn syndrome due to homozygous RAG1-C2633T hypomorphic mutation.
McCusker C; Hotte S; Le Deist F; Hirschfeld AF; Mitchell D; Nguyen VH; Gagnon R; Mazer B; Turvey SE; Jabado N
Clin Immunol; 2009 Jun; 131(3):447-55. PubMed ID: 19246248
[TBL] [Abstract][Full Text] [Related]
6. Defining combined immunodeficiency.
Roifman CM; Somech R; Kavadas F; Pires L; Nahum A; Dalal I; Grunebaum E
J Allergy Clin Immunol; 2012 Jul; 130(1):177-83. PubMed ID: 22664165
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia.
Alsmadi O; Al-Ghonaium A; Al-Muhsen S; Arnaout R; Al-Dhekri H; Al-Saud B; Al-Kayal F; Al-Saud H; Al-Mousa H
BMC Med Genet; 2009 Nov; 10():116. PubMed ID: 19912631
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome.
Tabori U; Mark Z; Amariglio N; Etzioni A; Golan H; Biloray B; Toren A; Rechavi G; Dalal I
Clin Genet; 2004 Apr; 65(4):322-6. PubMed ID: 15025726
[TBL] [Abstract][Full Text] [Related]
11. Three faces of recombination activating gene 1 (RAG1) mutations.
Patiroglu T; Akar HH; Van Der Burg M
Acta Microbiol Immunol Hung; 2015 Dec; 62(4):393-401. PubMed ID: 26689875
[TBL] [Abstract][Full Text] [Related]
12. A variant of SCID with specific immune responses and predominance of gamma delta T cells.
Ehl S; Schwarz K; Enders A; Duffner U; Pannicke U; Kühr J; Mascart F; Schmitt-Graeff A; Niemeyer C; Fisch P
J Clin Invest; 2005 Nov; 115(11):3140-8. PubMed ID: 16211094
[TBL] [Abstract][Full Text] [Related]
13. Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome.
Dalal I; Tasher D; Somech R; Etzioni A; Garti BZ; Lev D; Cohen S; Somekh E; Leshinsky-Silver E
Clin Immunol; 2011 Sep; 140(3):284-90. PubMed ID: 21624848
[TBL] [Abstract][Full Text] [Related]
14. More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2.
Niehues T; Perez-Becker R; Schuetz C
Clin Immunol; 2010 May; 135(2):183-92. PubMed ID: 20172764
[TBL] [Abstract][Full Text] [Related]
15. Recombinase-activating gene 1 immunodeficiency: different immunological phenotypes in three siblings.
Pasic S; Djuricic S; Ristic G; Slavkovic B
Acta Paediatr; 2009 Jun; 98(6):1062-4. PubMed ID: 19243569
[TBL] [Abstract][Full Text] [Related]
16. [Clinical phenotype and gene diagnostic analysis of Omenn syndrome].
Wang YQ; Cui YX; Feng J
Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):64-8. PubMed ID: 23527934
[TBL] [Abstract][Full Text] [Related]
17. Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cells.
Somech R; Simon AJ; Lev A; Dalal I; Spirer Z; Goldstein I; Nagar M; Amariglio N; Rechavi G; Roifman CM
J Allergy Clin Immunol; 2009 Oct; 124(4):793-800. PubMed ID: 19767069
[TBL] [Abstract][Full Text] [Related]
18. Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency.
Wada T; Toma T; Okamoto H; Kasahara Y; Koizumi S; Agematsu K; Kimura H; Shimada A; Hayashi Y; Kato M; Yachie A
Blood; 2005 Sep; 106(6):2099-101. PubMed ID: 15845893
[TBL] [Abstract][Full Text] [Related]
19. A novel splice-site mutation in the common gamma chain (gammac) gene IL2RG results in X-linked severe combined immunodeficiency with an atypical NK+ phenotype.
Ginn SL; Smyth C; Wong M; Bennetts B; Rowe PB; Alexander IE
Hum Mutat; 2004 May; 23(5):522-3. PubMed ID: 15108287
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
