Sanal O - Search Results

1

Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations.

Köker MY, Sanal O, van Leeuwen K, de Boer M, Metin A, Patiroğlu T, Ozgür TT, Tezcan I, Roos D. Köker MY, et al. Among authors: sanal o. Eur J Clin Invest. 2009 Oct;39(10):942-51. doi: 10.1111/j.1365-2362.2009.02195.x. Epub 2009 Jul 17. Eur J Clin Invest. 2009. PMID: 19624736

2

Thirty years of primary immunodeficiencies in Turkey.

Sanal O, Tezcan I. Sanal O, et al. Ann N Y Acad Sci. 2011 Nov;1238:15-23. doi: 10.1111/j.1749-6632.2011.06242.x. Ann N Y Acad Sci. 2011. PMID: 22129049

3

Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family.

Köker MY, Sanal O, de Boer M, Tezcan I, Metin A, Tan C, Ersoy F, Roos D. Köker MY, et al. Among authors: sanal o. Eur J Clin Invest. 2006 Apr;36(4):257-64. doi: 10.1111/j.1365-2362.2006.01619.x. Eur J Clin Invest. 2006. PMID: 16620288

4

Mutations of chronic granulomatous disease in Turkish families.

Köker MY, Sanal O, De Boer M, Tezcan I, Metin A, Ersoy F, Roos D. Köker MY, et al. Among authors: sanal o. Eur J Clin Invest. 2007 Jul;37(7):589-95. doi: 10.1111/j.1365-2362.2007.01828.x. Eur J Clin Invest. 2007. PMID: 17576211

5

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. Köker MY, et al. Among authors: sanal o. Eur J Clin Invest. 2009 Apr;39(4):311-9. doi: 10.1111/j.1365-2362.2009.02093.x. Eur J Clin Invest. 2009. PMID: 19292887

6

Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.

Turul-Ozgür T, Türkkani-Asal G, Tezcan I, Köker MY, Metin A, Yel L, Ersoy F, Sanal O. Turul-Ozgür T, et al. Among authors: sanal o. Turk J Pediatr. 2010 Nov-Dec;52(6):576-81. Turk J Pediatr. 2010. PMID: 21428188

7

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients.

Cağdaş D, Ozgür TT, Asal GT, Tezcan I, Metin A, Lambert N, de Saint Basile G, Sanal O. Cağdaş D, et al. Among authors: sanal o. Eur J Pediatr. 2012 Oct;171(10):1527-31. doi: 10.1007/s00431-012-1765-x. Epub 2012 Jun 19. Eur J Pediatr. 2012. PMID: 22711375

8

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. Köker MY, et al. Among authors: sanal o. J Allergy Clin Immunol. 2013 Nov;132(5):1156-1163.e5. doi: 10.1016/j.jaci.2013.05.039. Epub 2013 Jul 31. J Allergy Clin Immunol. 2013. PMID: 23910690

9

Chronic granulomatous disease presenting with hypogammaglobulinemia.

Hanoglu D, Ozgür TT, Ayvaz D, Köker MY, Sanal O. Hanoglu D, et al. Among authors: sanal o. J Investig Allergol Clin Immunol. 2011;21(4):310-2. J Investig Allergol Clin Immunol. 2011. PMID: 21721378 Free article.

10

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

Sanal O, Ersoy F, Tezcan I, Metin A, Yel L, Ménasché G, Gürgey A, Berkel I, de Saint Basile G. Sanal O, et al. J Clin Immunol. 2002 Jul;22(4):237-43. doi: 10.1023/a:1016045026204. J Clin Immunol. 2002. PMID: 12148598

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