Tan C - Search Results

1

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: tan c. 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

2

The role of human leucocyte antigens in children with hydatid disease: their association with clinical condition and prognosis.

Yalcin E, Kiper N, Tan C, Ozcelik U, Dogru D, Cobanoglu N, Kose M, Pekcan S, Aslan AT, Ersoy F. Yalcin E, et al. Among authors: tan c. Parasitol Res. 2010 Mar;106(4):795-800. doi: 10.1007/s00436-009-1719-z. Epub 2010 Jan 29. Parasitol Res. 2010. PMID: 20111876

3

Increased availability of family donors for hematopoietic stem cell transplantation in a population with increased incidence of consanguinity.

Balcı YI, Tavil B, Tan CS, Ozgur TT, Bulum B, Cetin M, Balcı M, Yalcın S, Tezcan I, Uckan D. Balcı YI, et al. Clin Transplant. 2011 May-Jun;25(3):475-80. doi: 10.1111/j.1399-0012.2010.01310.x. Epub 2010 Jul 14. Clin Transplant. 2011. PMID: 20636407

4

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype.

Mesci L, Ozdag H, Yel L, Ozgur TT, Tan C, Sanal O. Mesci L, et al. Among authors: tan c. Int J Immunogenet. 2011 Jun;38(3):209-13. doi: 10.1111/j.1744-313X.2010.00989.x. Epub 2011 Jan 4. Int J Immunogenet. 2011. PMID: 21199394

5

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma.

Topaloglu R, Taskiran EZ, Tan C, Erman B, Ozaltin F, Sanal O. Topaloglu R, et al. Among authors: tan c. Clin Rheumatol. 2012 Jul;31(7):1123-6. doi: 10.1007/s10067-012-1978-4. Epub 2012 May 11. Clin Rheumatol. 2012. PMID: 22576477

6

Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS.

Tan Ç, Özgül RK, Çağdaş Ayvaz D, Tezcan İ, Sanal Ö. Tan Ç, et al. Turk J Pediatr. 2015 Mar-Apr;57(2):141-5. Turk J Pediatr. 2015. PMID: 26690594

7

Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients.

Tan Ç, Çağdaş-Ayvaz D, Metin A, Keskin Ö, Tezcan İ, Sanal Ö. Tan Ç, et al. Turk J Pediatr. 2016;58(4):356-361. doi: 10.24953/turkjped.2016.04.002. Turk J Pediatr. 2016. PMID: 28276206 Free article.

8

Tumor necrosis factor α-308 G/A and interleukin 1 β-511 C/T gene polymorphisms in patients with scarring acne.

Akoglu G, Tan C, Ayvaz DC, Tezcan I. Akoglu G, et al. Among authors: tan c. J Cosmet Dermatol. 2019 Feb;18(1):395-400. doi: 10.1111/jocd.12558. Epub 2018 Apr 19. J Cosmet Dermatol. 2019. PMID: 29675912

9

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.

Cagdas D, Gur Cetinkaya P, Karaatmaca B, Esenboga S, Tan C, Yılmaz T, Gümüş E, Barış S, Kuşkonmaz B, Ozgur TT, Bali P, Santisteban I, Orhan D, Yüce A, Cetinkaya D, Boztug K, Hershfield M, Sanal O, Tezcan İ. Cagdas D, et al. Among authors: tan c. J Clin Immunol. 2018 May;38(4):484-493. doi: 10.1007/s10875-018-0496-9. Epub 2018 May 9. J Clin Immunol. 2018. PMID: 29744787

10

Effects of oral prophylaxis including tongue cleaning on halitosis and gingival inflammation in gingivitis patients-a randomized controlled clinical trial.

Acar B, Berker E, Tan Ç, İlarslan YD, Tekçiçek M, Tezcan İ. Acar B, et al. Among authors: tan c. Clin Oral Investig. 2019 Apr;23(4):1829-1836. doi: 10.1007/s00784-018-2617-5. Epub 2018 Sep 13. Clin Oral Investig. 2019. PMID: 30218226 Clinical Trial.

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