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5. [Primary deficiencies in antibody synthesis. I. Hypogammaglobulinemia]. García-Tamayo F Bol Med Hosp Infant Mex; 1983 Apr; 40(4):179-87. PubMed ID: 6347219 [No Abstract] [Full Text] [Related]
6. Recurrent bacteremia and multifocal lower limb cellulitis due to Helicobacter-like organisms in a patient with X-linked hypogammaglobulinemia. Gerrard J; Alfredson D; Smith I Clin Infect Dis; 2001 Nov; 33(10):E116-8. PubMed ID: 11595979 [TBL] [Abstract][Full Text] [Related]
7. Myofibroblastic tumor of the lower lip in a patient with X-linked hypogammaglobulinemia and isolated growth hormone deficiency: a case report. Imanguli MM; Karai LJ; Shanti RM; Stewart DM; Brahim JS J Oral Maxillofac Surg; 2007 Jun; 65(6):1219-22. PubMed ID: 17517309 [No Abstract] [Full Text] [Related]
8. Additional polymorphisms useful in linkage analysis for X-linked agammaglobulinemia. Parolini O; Conley ME Immunodeficiency; 1993; 4(1-4):217-9. PubMed ID: 8167704 [No Abstract] [Full Text] [Related]
9. Regulatory mechanisms immunoglobulin synthesis in patients with X-linked and common variable immunodeficiency with hypogammaglobulinemia. Gajl-Peczalska K; Mizerski J; Chartrand S; Kersey J; Page A Mater Med Pol; 1981; 13(3):159-64. PubMed ID: 7345260 [No Abstract] [Full Text] [Related]
10. Systemic amyloidosis-induced diarrhea in sex-linked agammaglobulinemia. Meysman M; Debeuckelaer S; Reynaert H; Schoors DF; Dehou MF; Van Camp B Am J Gastroenterol; 1993 Aug; 88(8):1275-7. PubMed ID: 8338101 [No Abstract] [Full Text] [Related]
11. X-linked agammaglobulinemia and isolated growth hormone deficiency. Arslan D; Patiroğlu T; Kendirci M; Kurtoğlu S Turk J Pediatr; 1998; 40(4):609-12. PubMed ID: 10028873 [TBL] [Abstract][Full Text] [Related]
12. Electrophysiological findings in X-linked myopathy with excessive autophagy. Jääskeläinen SK; Juel VC; Udd B; Villanova M; Liguori R; Minassian BA; Falck B; Niemi P; Kalimo H Ann Neurol; 2002 May; 51(5):648-52. PubMed ID: 12112116 [TBL] [Abstract][Full Text] [Related]
13. [On grave mesenchymopathies in infants. Description of a new clinical form: myoarthropathic mesenchymopathy with endomyocardial sclerohyalinosis, immune deficit and congenital chromosome aberrations]. Tîrnoveanu G; Dobrescu G; Harmanschi A; Cighir R; Gheorghiu C; Anastasiu V; Mitescu G Pediatria (Bucur); 1971; 20(6):505-15. PubMed ID: 4112141 [No Abstract] [Full Text] [Related]
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