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Journal Abstract Search

229 related items for PubMed ID: 17650836

  • 1. Selective IgM deficiency and 22q11.2 deletion syndrome.
    Kung SJ, Gripp KW, Stephan MJ, Fairchok MP, McGeady SJ.
    Ann Allergy Asthma Immunol; 2007 Jul; 99(1):87-92. PubMed ID: 17650836
    [Abstract] [Full Text] [Related]

  • 2. Clinical and immunological features in IgM deficiency.
    Yel L, Ramanuja S, Gupta S.
    Int Arch Allergy Immunol; 2009 Jul; 150(3):291-8. PubMed ID: 19494527
    [Abstract] [Full Text] [Related]

  • 3. Selective immunoglobulin M deficiency presenting with recurrent impetigo: a case report and review of the literature.
    Belgemen T, Suskan E, Dogu F, Ikinciogullari A.
    Int Arch Allergy Immunol; 2009 Jul; 149(3):283-8. PubMed ID: 19218822
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  • 4. Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome).
    Finocchi A, Di Cesare S, Romiti ML, Capponi C, Rossi P, Carsetti R, Cancrini C.
    Pediatr Allergy Immunol; 2006 Aug; 17(5):382-8. PubMed ID: 16846458
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  • 6. Selective IgM deficiency: a case study.
    Endoh M, Kaneshige H, Tomino Y, Nomoto Y, Sakai H, Arimori S.
    Tokai J Exp Clin Med; 1981 Jul; 6(3):327-31. PubMed ID: 7303010
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  • 7. Immunologic defects in 22q11.2 deletion syndrome.
    McLean-Tooke A, Barge D, Spickett GP, Gennery AR.
    J Allergy Clin Immunol; 2008 Aug; 122(2):362-7, 367.e1-4. PubMed ID: 18485468
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  • 9. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
    Morava E, Masszi G, Czakó M, Tóth G, Melegh B, Kosztolányi G.
    Orv Hetil; 2000 Aug 20; 141(34):1873-5. PubMed ID: 11006712
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  • 10. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S, Kolialexi A, Fryssira H, Galla-Voumvouraki A, Salavoura K, Kanariou M, Tsangaris GT, Kanavakis E, Mavrou A.
    In Vivo; 2004 Aug 20; 18(5):603-8. PubMed ID: 15523900
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  • 11. Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G, Devriendt K, Swillen A, Rommel N, Vogels A, Eyskens B, Gewillig M, Feenstra L, Fryns JP.
    Genet Couns; 1999 Aug 20; 10(1):3-9. PubMed ID: 10191424
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  • 12. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
    Ford LC, Sulprizio SL, Rasgon BM.
    Laryngoscope; 2000 Mar 20; 110(3 Pt 1):362-7. PubMed ID: 10718420
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  • 13. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec 20; 35(4):248-51. PubMed ID: 23834556
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  • 14. The deletions of 22q11--the Portuguese experience.
    Gaspar IM, Lourenço MT, Reis MI, Soares MA, Nogueira G, Ferreira F, Feijóo MJ.
    Genet Couns; 1999 Dec 20; 10(1):51-7. PubMed ID: 10191429
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  • 15. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
    Pinquier C, Héron D, de Carvalho W, Lazar G, Mazet P, Cohen D.
    Encephale; 2001 Dec 20; 27(1):45-50. PubMed ID: 11294038
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  • 16. 22q11 deletion syndrome and limb anomalies: report on two Brazilian patients.
    Kokitsu-Nakata NM, Guion-Almeida ML, Richieri-Costa A.
    Cleft Palate Craniofac J; 2008 Sep 20; 45(5):561-6. PubMed ID: 18788865
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  • 17. Coexistent yellow nail syndrome and selective antibody deficiency.
    Bokszczanin A, Levinson AI.
    Ann Allergy Asthma Immunol; 2003 Nov 20; 91(5):496-500. PubMed ID: 14692436
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  • 18. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
    Gerkes EH, Hordijk R, Dijkhuizen T, Sival DA, Meiners LC, Sikkema-Raddatz B, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2010 Nov 20; 53(5):344-6. PubMed ID: 20553986
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