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1079 related items for PubMed ID: 23910690

  • 1. Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients.
    Köker MY, Camcıoğlu Y, van Leeuwen K, Kılıç SŞ, Barlan I, Yılmaz M, Metin A, de Boer M, Avcılar H, Patıroğlu T, Yıldıran A, Yeğin O, Tezcan I, Sanal Ö, Roos D.
    J Allergy Clin Immunol; 2013 Nov; 132(5):1156-1163.e5. PubMed ID: 23910690
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  • 3. Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease.
    Yu G, Hong DK, Dionis KY, Rae J, Heyworth PG, Curnutte JT, Lewis DB.
    Clin Immunol; 2008 Aug; 128(2):117-26. PubMed ID: 18625437
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  • 5. Mutations of chronic granulomatous disease in Turkish families.
    Köker MY, Sanal O, De Boer M, Tezcan I, Metin A, Ersoy F, Roos D.
    Eur J Clin Invest; 2007 Jul; 37(7):589-95. PubMed ID: 17576211
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  • 10. Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort.
    Baris HE, Ogulur I, Akcam B, Kiykim A, Karagoz D, Saraymen B, Akgun G, Eltan SB, Aydemir S, Akidagi Z, Bentli E, Nain E, Kasap N, Baser D, Altintas DU, Camcioglu Y, Yesil G, Ozen A, Koker MY, Karakoc-Aydiner E, Baris S.
    J Allergy Clin Immunol Pract; 2020 Jul; 8(10):3525-3534.e1. PubMed ID: 32736065
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  • 12. Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease.
    Badalzadeh M, Tajik S, Fazlollahi MR, Houshmand M, Fattahi F, Alizadeh Z, Movahedi M, Adab Z, Khotaei GT, Hamidieh AA, Heidarnazhad H, Pourpak Z.
    Int J Immunogenet; 2017 Dec; 44(6):314-321. PubMed ID: 28941186
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  • 13. Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience.
    El Hawary R, Meshaal S, Deswarte C, Galal N, Abdelkawy M, Alkady R, Elaziz DA, Freiberger T, Ravcukova B, Litzman J, Bustamante J, Boutros J, Gaafar T, Elmarsafy A.
    J Clin Immunol; 2016 Aug; 36(6):610-8. PubMed ID: 27222152
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  • 14. A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.
    van de Vosse E, van Wengen A, van Geelen JA, de Boer M, Roos D, van Dissel JT.
    J Hum Genet; 2009 Jun; 54(6):313-6. PubMed ID: 19329991
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  • 15. Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91(phox) resulting in the rare X91(+) variant of chronic granulomatous disease.
    Boog B, Quach A, Costabile M, Smart J, Quinn P, Singh H, Gold M, Booker G, Choo S, Hii CS, Ferrante A.
    Hum Mutat; 2012 Mar; 33(3):471-5. PubMed ID: 22125116
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  • 16. A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran.
    Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Zandieh F, Khandan S, Pourpak Z.
    Iran J Allergy Asthma Immunol; 2016 Oct; 15(5):426-429. PubMed ID: 27917630
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  • 17. X-linked chronic granulomatous disease: first report of mutations in patients of Argentina.
    Barese C, Copelli S, Zandomeni R, Oleastro M, Zelazko M, Rivas EM.
    J Pediatr Hematol Oncol; 2004 Oct; 26(10):656-60. PubMed ID: 15454837
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  • 18. Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease.
    Köker MY, van Leeuwen K, de Boer M, Celmeli F, Metin A, Ozgür TT, Tezcan I, Sanal O, Roos D.
    Eur J Clin Invest; 2009 Apr; 39(4):311-9. PubMed ID: 19292887
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  • 19. Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells.
    Bionda C, Li XJ, van Bruggen R, Eppink M, Roos D, Morel F, Stasia MJ.
    Hum Genet; 2004 Oct; 115(5):418-27. PubMed ID: 15338276
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  • 20. [Molecular aspects of chronic granulomatous disease. "the NADPH oxidase complex"].
    Morel F.
    Bull Acad Natl Med; 2007 Feb; 191(2):377-90; discussion 390-2. PubMed ID: 17969555
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