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Quoted phrase not found in phrase index: "Agammaglobulinemia 8, autosomal dominant"
Page 1
Humoral immunodeficiencies: conferred risk of infections and benefits of immunoglobulin replacement therapy.
Gernez Y, Baker MG, Maglione PJ. Gernez Y, et al. Transfusion. 2018 Dec;58 Suppl 3(Suppl 3):3056-3064. doi: 10.1111/trf.15020. Transfusion. 2018. PMID: 30536429 Free PMC article. Review.
In fact, the most common PID diseases worldwide are antibody deficiencies and include common variable immunodeficiency, congenital agammaglobulinemia, hyper-IgM syndrome, specific antibody deficiency, and Good syndrome. ...Moreover, the infection trends in some patients wi …
In fact, the most common PID diseases worldwide are antibody deficiencies and include common variable immunodeficiency, congenital agamma …
Bronchiectasis diagnosed after renal transplantation: a retrospective multicenter study.
Dury S, Colosio C, Etienne I, Anglicheau D, Merieau E, Caillard S, Rivalan J, Thervet E, Essig M, Babinet F, Subra JF, Toubas O, Rieu P, Launois C, Perotin-Collard JM, Lebargy F, Deslée G; Spiesser group. Dury S, et al. BMC Pulm Med. 2015 Nov 7;15:141. doi: 10.1186/s12890-015-0133-9. BMC Pulm Med. 2015. PMID: 26545860 Free PMC article.
RESULTS: Forty-six patients were included (mean age 58.2 years, 52.2 % men). Autosomal dominant polycystic kidney disease (32.6 %) was the main underlying renal disease. ...Hypogammaglobulinemia was observed in 46.9 % patients. Bronchiectasis was usually extensive ( …
RESULTS: Forty-six patients were included (mean age 58.2 years, 52.2 % men). Autosomal dominant polycystic kidney disease (32. …