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11 in total

1. Clinical characteristics and mutation analysis of X-linked severe combined immunodeficiency in China.

Authors: Cui Zhang; Zhi-Yong Zhang; Jun-Feng Wu; Xue-Mei Tang; Xi-Qiang Yang; Li-Ping Jiang; Xiao-Dong Zhao
Journal: World J Pediatr Date: 2011-11-21 Impact factor: 2.764

2. Failure in antigen responses by T cells from patients with common variable immunodeficiency (CVID).

Authors: A J Stagg; M Funauchi; S C Knight; A D Webster; J Farrant
Journal: Clin Exp Immunol Date: 1994-04 Impact factor: 4.330

3. Interleukin-2 receptor gamma-chain mutations in severe combined immunodeficiency with B-lymphocytes.

Authors: I Tsuge; H Matsuoka; T Abe; Y Kamachi; S Torii
Journal: Eur J Pediatr Date: 1996-12 Impact factor: 3.183

Review 4. A syndrome of primary combined immunodeficiency with microcephaly, cerebellar hypoplasia, growth failure and progressive pancytopenia.

Authors: F Berthet; R Caduff; U B Schaad; H Roten; P Tuchschmid; E Boltshauser; R A Seger
Journal: Eur J Pediatr Date: 1994-05 Impact factor: 3.183

Review 5. Molecular and genetic basis of X-linked immunodeficiency disorders.

Authors: J M Puck
Journal: J Clin Immunol Date: 1994-03 Impact factor: 8.317

6. X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.

Authors: I Tsuge; H Matsuoka; T Abe; Y Kamachi; S Torii
Journal: Eur J Pediatr Date: 1993-11 Impact factor: 3.183

7. A double-blind, placebo-controlled, crossover therapy study with natural human IL-2 (nhuIL-2) in combination with regular intravenous gammaglobulin (IVIG) infusions in 10 patients with common variable immunodeficiency (CVID).

Authors: J A Rump; A Jahreis; M Schlesier; S Stecher; H H Peter
Journal: Clin Exp Immunol Date: 1997-11 Impact factor: 4.330

8. Defects in antigen-driven lymphocyte responses in common variable immunodeficiency (CVID) are due to a reduction in the number of antigen-specific CD4+ T cells.

Authors: M Funauchi; J Farrant; C Moreno; A D Webster
Journal: Clin Exp Immunol Date: 1995-07 Impact factor: 4.330

9. A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population.

Authors: Concepción Núñez; Raquel López-Mejías; Alfonso Martínez; M Cruz García-Rodríguez; Miguel Fernández-Arquero; Emilio G de la Concha; Elena Urcelay
Journal: BMC Med Genet Date: 2006-03-15 Impact factor: 2.103

10. HLA-A and -B alleles and haplotypes in 240 index patients with common variable immunodeficiency and selective IgG subclass deficiency in central Alabama.

Authors: James C Barton; Luigi F Bertoli; Ronald T Acton
Journal: BMC Med Genet Date: 2003-06-12 Impact factor: 2.103