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1989 2
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1993 3
1994 3
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1996 3
1997 5
1998 3
1999 1
2000 3
2001 2
2002 3
2004 1
2005 3
2006 1
2007 2
2008 2
2009 1
2011 1
2013 2
2014 1
2015 2
2016 2
2017 4
2018 3
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2024 1

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Page 1
X-linked severe combined immunodeficiency.
Conley ME. Conley ME. Clin Immunol Immunopathol. 1991 Nov;61(2 Pt 2):S94-9. doi: 10.1016/s0090-1229(05)80043-1. Clin Immunol Immunopathol. 1991. PMID: 1934618 Review.
X-Linked Severe Combined Immunodeficiency and Hepatoblastoma: A Case Report and Review of Literature.
Diaz-Parra S, Lozano-Sanchez G, Escobosa-Sanchez O, Moreno-Perez D, Morales-Martinez A, Armengol-Niell C, Acha-Garcia T. Diaz-Parra S, et al. J Pediatr Hematol Oncol. 2018 Aug;40(6):e348-e349. doi: 10.1097/MPH.0000000000001133. J Pediatr Hematol Oncol. 2018. PMID: 29620683 Review.
Severe combined immunodeficiency is an inherited disease with profoundly defective T cells, B cells, and natural killer cells. X-linked severe combined immunodeficiency is the most common form. ...This case is the first report which describes an …
Severe combined immunodeficiency is an inherited disease with profoundly defective T cells, B cells, and natural killer cells. X-l …
Gene therapy of X-linked severe combined immunodeficiency.
Cavazzana-Calvo M, Hacein-Bey-Abina S, Fischer A. Cavazzana-Calvo M, et al. Curr Opin Allergy Clin Immunol. 2002 Dec;2(6):507-9. doi: 10.1097/00130832-200212000-00005. Curr Opin Allergy Clin Immunol. 2002. PMID: 14752333 Review.
This review addresses several questions in the light of the results recently obtained by a gene therapy trial for the treatment of X-linked severe combined immunodeficiency. This primary immunodeficiency, characterized by a complete absence of T …
This review addresses several questions in the light of the results recently obtained by a gene therapy trial for the treatment of X- …
Carrier detection of the X-linked primary immunodeficiency diseases using X-chromosome inactivation analysis.
Winkelstein JA, Fearon E. Winkelstein JA, et al. J Allergy Clin Immunol. 1990 Jun;85(6):1090-7. doi: 10.1016/0091-6749(90)90055-9. J Allergy Clin Immunol. 1990. PMID: 2191994 Review.
Carrier detection of three of the X-linked primary immunodeficiency diseases (X-linked agammaglobulinemia, X-linked severe combined immunodeficiency disease, and the Wiskott-Aldrich syndrome) is possible by analyzing patterns of X-chromosome ina …
Carrier detection of three of the X-linked primary immunodeficiency diseases (X-linked agammaglobulinemia, X-linked severe …
The molecular basis of X-linked severe combined immunodeficiency: defective cytokine receptor signaling.
Leonard WJ. Leonard WJ. Annu Rev Med. 1996;47:229-39. doi: 10.1146/annurev.med.47.1.229. Annu Rev Med. 1996. PMID: 8712778 Review.
X-linked severe combined immunodeficiency (XSCID) is an inherited disease characterized by profoundly diminished cell-mediated and humoral immunity. ...
X-linked severe combined immunodeficiency (XSCID) is an inherited disease characterized by profoundly dim …
Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.
Sener S, Basaran O, Batu ED, Atalay E, Esenboga S, Cagdas D, Kuskonmaz BB, Bilginer Y, Ozaltin F, Oguz B, Duzova A, Tezcan I, Ozen S. Sener S, et al. Clin Rheumatol. 2022 Sep;41(9):2883-2892. doi: 10.1007/s10067-022-06295-9. Epub 2022 Jul 20. Clin Rheumatol. 2022. PMID: 35854168 Review.
A 14-year-old patient had lipopolysaccharide-sensitive beige-like anchor (LRBA) deficiency, and a 16-year-old had X-linked severe combined immunodeficiency (X-linked SCID). During the follow-up, they developed findings suggestive of vasculitides …
A 14-year-old patient had lipopolysaccharide-sensitive beige-like anchor (LRBA) deficiency, and a 16-year-old had X-linked …
X chromosome linked immunodeficiency.
Schwaber J, Rosen FS. Schwaber J, et al. Immunodefic Rev. 1990;2(3):233-51. Immunodefic Rev. 1990. PMID: 1981831 Review.
X-linked chronic granulomatous disease and Wiskott-Aldrich syndrome map to loci on the short arm of the X chromosome; X-linked severe combined immunodeficiency, X-linked agammaglobulinemia, X-linked immunodeficiency with hyper-IgM, and X-linked …
X-linked chronic granulomatous disease and Wiskott-Aldrich syndrome map to loci on the short arm of the X chromosome; X-linked …
Clinical characteristics and mutation analysis of X-linked severe combined immunodeficiency in China.
Zhang C, Zhang ZY, Wu JF, Tang XM, Yang XQ, Jiang LP, Zhao XD. Zhang C, et al. World J Pediatr. 2013 Feb;9(1):42-7. doi: 10.1007/s12519-011-0330-4. Epub 2011 Nov 21. World J Pediatr. 2013. PMID: 22105576
X-linked severe combined immunodeficiency (X-SCID) is a rare, life-threatening immune disorder, caused by mutations of the gene for the gamma-chain (gammac) of the interleukin-2 receptor, IL2RG. ...
X-linked severe combined immunodeficiency (X-SCID) is a rare, life-threatening immune disorder, caused by …
78 results