Literature DB >> 15235788

[Classification and diagnosis of immunodeficiency syndromes].

K Warnatz1, H-H Peter.   

Abstract

Primary immunodeficiency diseases of the adult are rare disorders, but often lead to serious consequences. Therefore an early diagnosis is critical. The variety in the clinical presentation, the complexity of the immune system and the ongoing discovery of new defects render it a difficult area for the involved physician. Due to the often imprecise complaint of a weak immune system the primary task is the identification of patients with true immunodeficiency. Subsequently, the immune defect needs to be identified in collaboration with a center for immunodeficiency disorders. The diagnostic procedure is dependent on the pattern of infections and follows a defined series of steps. This procedure should prevent costly diagnostic evaluation when not indicated, and also prevent the delayed diagnosis of patients with manifest immunodeficiency disease.

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Mesh:

Year:  2004        PMID: 15235788     DOI: 10.1007/s00108-004-1239-y

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  60 in total

Review 1.  Molecular basis of IgG subclass deficiency.

Authors:  Q Pan; L Hammarström
Journal:  Immunol Rev       Date:  2000-12       Impact factor: 12.988

Review 2.  TAP deficiency syndrome.

Authors:  S D Gadola; H T Moins-Teisserenc; J Trowsdale; W L Gross; V Cerundolo
Journal:  Clin Exp Immunol       Date:  2000-08       Impact factor: 4.330

Review 3.  IgA deficiency.

Authors:  P D Burrows; M D Cooper
Journal:  Adv Immunol       Date:  1997       Impact factor: 3.543

4.  Adenosine deaminase deficiency in adults.

Authors:  H Ozsahin; F X Arredondo-Vega; I Santisteban; H Fuhrer; P Tuchschmid; W Jochum; A Aguzzi; H M Lederman; A Fleischman; J A Winkelstein; R A Seger; M S Hershfield
Journal:  Blood       Date:  1997-04-15       Impact factor: 22.113

5.  Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry.

Authors:  H Kanegane; S Tsukada; T Iwata; T Futatani; K Nomura; J Yamamoto; T Yoshida; K Agematsu; A Komiyama; T Miyawaki
Journal:  Clin Exp Immunol       Date:  2000-06       Impact factor: 4.330

Review 6.  The genetic background of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy and its autoimmune disease components.

Authors:  Arndt Vogel; Christian P Strassburg; Petra Obermayer-Straub; Georg Brabant; Michael P Manns
Journal:  J Mol Med (Berl)       Date:  2002-02-05       Impact factor: 4.599

Review 7.  ZAP-70 and defects of T-cell receptor signaling.

Authors:  M E Elder
Journal:  Semin Hematol       Date:  1998-10       Impact factor: 3.851

8.  Persistent activation of the tumor necrosis factor system in a subgroup of patients with common variable immunodeficiency--possible immunologic and clinical consequences.

Authors:  P Aukrust; E Lien; A K Kristoffersen; F Müller; C J Haug; T Espevik; S S Frøland
Journal:  Blood       Date:  1996-01-15       Impact factor: 22.113

9.  Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects.

Authors:  B Piqueras; C Lavenu-Bombled; L Galicier; F Bergeron-van der Cruyssen; L Mouthon; S Chevret; P Debré; C Schmitt; E Oksenhendler
Journal:  J Clin Immunol       Date:  2003-09       Impact factor: 8.317

Review 10.  The human model: a genetic dissection of immunity to infection in natural conditions.

Authors:  Jean-Laurent Casanova; Laurent Abel
Journal:  Nat Rev Immunol       Date:  2004-01       Impact factor: 53.106

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