Literature DB >> 20042230

Laboratory evaluation of primary immunodeficiencies.

João B Oliveira1, Thomas A Fleisher.   

Abstract

Primary immunodeficiencies are congenital disorders caused by defects in different elements of the immune system. Affected patients usually present clinically with recurrent infections, severe infections, or both, as well as autoimmune phenomena that are associated with many of these disorders. Early diagnosis is essential for referral to specialized care centers and the prompt initiation of appropriate therapy. In this article the authors describe a general approach for the investigation of the most common primary immunodeficiencies, outlining the typical clinical symptoms and most appropriate laboratory investigations. Copyright 2010 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.

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Year:  2009        PMID: 20042230      PMCID: PMC3412511          DOI: 10.1016/j.jaci.2009.08.043

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  60 in total

1.  STAT3 mutations in the hyper-IgE syndrome.

Authors:  Steven M Holland; Frank R DeLeo; Houda Z Elloumi; Amy P Hsu; Gulbu Uzel; Nina Brodsky; Alexandra F Freeman; Andrew Demidowich; Joie Davis; Maria L Turner; Victoria L Anderson; Dirk N Darnell; Pamela A Welch; Douglas B Kuhns; David M Frucht; Harry L Malech; John I Gallin; Scott D Kobayashi; Adeline R Whitney; Jovanka M Voyich; James M Musser; Cristina Woellner; Alejandro A Schäffer; Jennifer M Puck; Bodo Grimbacher
Journal:  N Engl J Med       Date:  2007-09-19       Impact factor: 91.245

2.  The EUROclass trial: defining subgroups in common variable immunodeficiency.

Authors:  Claudia Wehr; Teemu Kivioja; Christian Schmitt; Berne Ferry; Torsten Witte; Efrem Eren; Marcela Vlkova; Manuel Hernandez; Drahomira Detkova; Philip R Bos; Gonke Poerksen; Horst von Bernuth; Ulrich Baumann; Sigune Goldacker; Sylvia Gutenberger; Michael Schlesier; Florence Bergeron-van der Cruyssen; Magali Le Garff; Patrice Debré; Roland Jacobs; John Jones; Elizabeth Bateman; Jiri Litzman; P Martin van Hagen; Alessandro Plebani; Reinhold E Schmidt; Vojtech Thon; Isabella Quinti; Teresa Espanol; A David Webster; Helen Chapel; Mauno Vihinen; Eric Oksenhendler; Hans Hartmut Peter; Klaus Warnatz
Journal:  Blood       Date:  2007-09-26       Impact factor: 22.113

Review 3.  Complement deficiencies and systemic lupus erythematosus.

Authors:  Lennart Truedsson; Anders A Bengtsson; Gunnar Sturfelt
Journal:  Autoimmunity       Date:  2007-12       Impact factor: 2.815

Review 4.  Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders.

Authors:  Alexandra H Filipovich
Journal:  Immunol Allergy Clin North Am       Date:  2008-05       Impact factor: 3.479

Review 5.  Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

Authors:  Kathleen E Sullivan
Journal:  Immunol Allergy Clin North Am       Date:  2008-05       Impact factor: 3.479

Review 6.  Congenital neutropenia syndromes.

Authors:  Kaan Boztug; Karl Welte; Cornelia Zeidler; Christoph Klein
Journal:  Immunol Allergy Clin North Am       Date:  2008-05       Impact factor: 3.479

7.  Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study.

Authors:  Baldassarre Martire; Roberto Rondelli; Annarosa Soresina; Claudio Pignata; Teresa Broccoletti; Andrea Finocchi; Paolo Rossi; Marco Gattorno; Marco Rabusin; Chiara Azzari; Rosa M Dellepiane; Maria C Pietrogrande; Antonino Trizzino; Paolo Di Bartolomeo; Silvana Martino; Luigi Carpino; Fausto Cossu; Franco Locatelli; Rita Maccario; Paolo Pierani; Maria C Putti; Achille Stabile; Luigi D Notarangelo; Alberto G Ugazio; Alessandro Plebani; Domenico De Mattia
Journal:  Clin Immunol       Date:  2007-11-26       Impact factor: 3.969

8.  Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome.

Authors:  Joshua D Milner; Jason M Brenchley; Arian Laurence; Alexandra F Freeman; Brenna J Hill; Kevin M Elias; Yuka Kanno; Christine Spalding; Houda Z Elloumi; Michelle L Paulson; Joie Davis; Amy Hsu; Ava I Asher; John O'Shea; Steven M Holland; William E Paul; Daniel C Douek
Journal:  Nature       Date:  2008-03-12       Impact factor: 49.962

Review 9.  Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.

Authors:  D Moraes-Vasconcelos; B T Costa-Carvalho; T R Torgerson; H D Ochs
Journal:  J Clin Immunol       Date:  2008-02-09       Impact factor: 8.317

Review 10.  Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells.

Authors:  Troy R Torgerson; Hans D Ochs
Journal:  J Allergy Clin Immunol       Date:  2007-10       Impact factor: 10.793

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  28 in total

1.  A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside.

Authors:  Ahmed Aziz Bousfiha; Leïla Jeddane; Fatima Ailal; Waleed Al Herz; Mary Ellen Conley; Charlotte Cunningham-Rundles; Amos Etzioni; Alain Fischer; Jose Luis Franco; Raif S Geha; Lennart Hammarström; Shigeaki Nonoyama; Hans D Ochs; Chaim M Roifman; Reinhard Seger; Mimi L K Tang; Jennifer M Puck; Helen Chapel; Luigi D Notarangelo; Jean-Laurent Casanova
Journal:  J Clin Immunol       Date:  2013-05-09       Impact factor: 8.317

Review 2.  Laboratory diagnosis of primary immunodeficiencies.

Authors:  Bradley A Locke; Trivikram Dasu; James W Verbsky
Journal:  Clin Rev Allergy Immunol       Date:  2014-04       Impact factor: 8.667

Review 3.  Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update.

Authors:  E de Vries
Journal:  Clin Exp Immunol       Date:  2012-01       Impact factor: 4.330

4.  Proteomics plus genomics approaches in primary immunodeficiency: the case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.

Authors:  D Zennaro; E Scala; D Pomponi; E Caprini; D Arcelli; E Gambineri; G Russo; A Mari
Journal:  Clin Exp Immunol       Date:  2012-01       Impact factor: 4.330

5.  Profile of the patients who present to immunology outpatient clinics because of frequent infections.

Authors:  Sonay Aldırmaz; Esra Yücel; Ayça Kıykım; Haluk Çokuğraş; Necla Akçakaya; Yıldız Camcıoğlu
Journal:  Turk Pediatri Ars       Date:  2014-09-01

6.  Differing Performance of the Warning Signs for Immunodeficiency in the Diagnosis of Pediatric Versus Adult Patients in a Two-Center Tertiary Referral Population.

Authors:  Jaclyn A Bjelac; Jennifer R Yonkof; James Fernandez
Journal:  J Clin Immunol       Date:  2019-01-04       Impact factor: 8.317

Review 7.  Role of siglecs and related glycan-binding proteins in immune responses and immunoregulation.

Authors:  Bruce S Bochner; Nives Zimmermann
Journal:  J Allergy Clin Immunol       Date:  2015-01-13       Impact factor: 10.793

8.  Primary Immunodeficiency Diseases in Oman: 10-Year Experience in a Tertiary Care Hospital.

Authors:  Salem Al-Tamemi; Shafiq Ur Rehman Naseem; Nabila Al-Siyabi; Ibtisam El-Nour; Abdulhakim Al-Rawas; David Dennison
Journal:  J Clin Immunol       Date:  2016-10-03       Impact factor: 8.317

9.  Diagnostic and Management Errors in an Immunodeficient Patient with Pneumococcal Pneumonia with Bacteraemia due to Incorrect Assessment of the Patient's Immune Status.

Authors:  Takahiro Ito; Yukinori Harada; Taro Shimizu
Journal:  Eur J Case Rep Intern Med       Date:  2021-04-26

Review 10.  Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency.

Authors:  Emily S J Edwards; Julian J Bosco; Samar Ojaimi; Robyn E O'Hehir; Menno C van Zelm
Journal:  Cell Mol Immunol       Date:  2020-08-17       Impact factor: 11.530

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