Literature DB >> 6600917

Familial hypogammaglobulinemia. Genetic linkage with alpha 1-antitrypsin deficiency.

N D Phung, R J Harbeck, C Helbling-Muntges.   

Abstract

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Year:  1983        PMID： 6600917     DOI： 10.1001/archinte.143.3.575

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN： 0003-9926


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  4 in total

Review 1.  alpha-1-Antitrypsin and the pathogenesis of emphysema.

Authors:  R A Stockley
Journal:  Lung       Date:  1987       Impact factor: 2.584

2.  A preliminary assessment of alpha-1 antitrypsin S and Z deficiency allele frequencies in common variable immunodeficiency patients with and without bronchiectasis.

Authors:  M E Sansom; B L Ferry; Z P M C Sherrell; H M Chapel
Journal:  Clin Exp Immunol       Date:  2002-12       Impact factor: 4.330

3.  Alpha-1 Antitrypsin Deficiency and Pulmonary Morbidity in Patients with Primary Immunodeficiency Disease: A Single-Center Experience.

Authors:  Georg Evers; Arik Bernard Schulze; Michael Thrull; Jan-Philipp Hering; Christoph Schülke; Rainer Wiewrodt; Helmut Wittkowski; Lars Henning Schmidt; Michael Mohr
Journal:  Can Respir J       Date:  2020-05-27       Impact factor: 2.409

4.  A rare case of alpha 1-antitrypsin deficiency associated with hypogammaglobulinemia and recurrent pulmonary thrombosis.

Authors:  Raghav Gupta; Srilekha Sridhara; John A Wood
Journal:  Ann Thorac Med       Date:  2014-01       Impact factor: 2.219
  4 in total

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