Combined immunodeficiency in the United States and Kuwait: Comparison of patients' characteristics and molecular diagnosis

Author:

Al-Herz Waleed,Notarangelo Luigi D.,Sadek Ali,Buckley Rebecca,Akhter Javeed,Ballas Zuhair K.,Ballow Mark,Bonilla Francisco A.,Chen Karin,Cheng Laurence E.,Cunningham-Rundles Charlotte,Garabedian Elizabeth,Haddad Élie,Kleiner Gary,Ochs Hans D.,Patel Niraj,Secord Elizabeth A.,Seroogy Christine,Sullivan Kathleen,Uygungil Burcin

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference25 articles.

1. Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency;Al-Herz;Front. Immunol.,2014

2. Positive family history, infection, low absolute lymphocyte count (ALC) and absent thymic shadow: diagnostic clues for severe combined immunodeficiency (SCID);McWilliams;J. Allergy Clin. Immunol. Pract.,2015

3. Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency;Felgentreff;Clin. Immunol.,2011

4. Defining combined immunodeficiency;Roifman;J. Allergy Clin. Immunol.,2012

5. The natural history of children with severe combined immunodeficiency: baseline features of the first fifty patients of the primary immune deficiency treatment consortium prospective study 6901;Dvorak;J. Clin. Immunol.,2013

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