Historical Perspectives in the Diagnosis and Treatment of Primary Immune Deficiencies

Author:

Ballow Mark

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Immunology and Allergy

Reference12 articles.

1. Bruton O (1968) The discovery of agammaglobulinemia. In: Bergsman D, Good RA (eds) Birth defects original article series. National Foundation of the March of Dimes, Sanibel Island, pp 2–3

2. Bruton O, Apt L, Gitlin D, Janeway C (1952) Absence of serum gamma globulins. Am J Dis Child 84:632–636, abstract

3. Hitzig W, Biro Z, Bosch H, Huser H (1958) Agammaglobulinemia and alymphocytosis with atrophy of lymphatic tissue. Helv Paediatr Acta 13:551–585

4. Bousfiha A, Jeddane L, Ailal F, Herz W, Conley M, Cunningham-Rundles C et al (2013) A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. J Clin Immunol 33(6):1078–1087

5. Boyle J, Buckley R (2007) Population prevalence of diagnosed primary immunodeficiency diseases in the United States. J Clin Immunol 27:497–502

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