Cagdas D - Search Results

1

Differential diagnosis of primary immunodeficiency in patients with BCGitis and BCGosis: A single-centre study.

Soyak Aytekin E, Keskin A, Tan C, Yalçın E, Dogru D, Ozcelik U, Kiper N, Tezcan I, Cagdas D. Soyak Aytekin E, et al. Among authors: cagdas d. Scand J Immunol. 2021 Oct;94(4):e13084. doi: 10.1111/sji.13084. Epub 2021 Jul 28. Scand J Immunol. 2021. PMID: 34780073 Free article.

2

Community-acquired pneumonia and parapneumonic effusions in developing countries.

Seçmeer G, Ciftçi AO, Kanra G, Ceyhan M, Kara A, Cengiz AB, Kiper N, Haliloğlu M, Ozçelik U, Cağdaş DN. Seçmeer G, et al. Turk J Pediatr. 2008 Jan-Feb;50(1):51-7. Turk J Pediatr. 2008. PMID: 18365592

3

Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation.

Çağdaş D, Özgür TT, Asal GT, Revy P, De Villartay JP, van der Burg M, Sanal Ö, Tezcan I. Çağdaş D, et al. Pediatr Transplant. 2012 Aug;16(5):E167-71. doi: 10.1111/j.1399-3046.2011.01491.x. Epub 2011 Apr 27. Pediatr Transplant. 2012. PMID: 21535335

4

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. 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

5

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia.

Serwas NK, Cagdas D, Ban SA, Bienemann K, Salzer E, Tezcan I, Borkhardt A, Sanal O, Boztug K. Serwas NK, et al. Among authors: cagdas d. Blood. 2014 Jul 24;124(4):655-7. doi: 10.1182/blood-2014-03-564930. Blood. 2014. PMID: 25061172 Free PMC article. No abstract available.

6

A novel mutation in leukocyte adhesion deficiency type II/CDGIIc.

Cagdas D, Yilmaz M, Kandemir N, Tezcan I, Etzioni A, Sanal Ö. Cagdas D, et al. J Clin Immunol. 2014 Nov;34(8):1009-14. doi: 10.1007/s10875-014-0091-7. Epub 2014 Sep 21. J Clin Immunol. 2014. PMID: 25239688

7

Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion.

Yılmaz M, Çağdaş D, Grandin V, Altıntaş DU, Tezcan İ, de Saint Basile G, Sanal Ö. Yılmaz M, et al. Among authors: cagdas d. Pediatr Allergy Immunol. 2014 Dec;25(8):817-9. doi: 10.1111/pai.12285. Epub 2014 Oct 31. Pediatr Allergy Immunol. 2014. PMID: 25283056 No abstract available.

8

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R.

Erman B, Bilic I, Hirschmugl T, Salzer E, Çagdas D, Esenboga S, Akcoren Z, Sanal O, Tezcan I, Boztug K. Erman B, et al. Among authors: cagdas d. Haematologica. 2015 Jun;100(6):e216-9. doi: 10.3324/haematol.2014.120980. Epub 2015 Mar 13. Haematologica. 2015. PMID: 25769540 Free PMC article. No abstract available.

9

Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation.

Ünal Ş, Tezcan İ, Güçer Ş, Boyraz MS, Çağdaş D, Uçkan Çetinkaya D. Ünal Ş, et al. Among authors: cagdas d. Turk J Haematol. 2015 Dec;32(4):378-9. doi: 10.4274/tjh.2014.0475. Epub 2015 Apr 27. Turk J Haematol. 2015. PMID: 25912830 Free PMC article. No abstract available.

10

Detection of parasites in children with chronic diarrhea.

Maçin S, Kaya F, Çağdaş D, Hizarcioglu-Gulsen H, Saltik-Temizel IN, Tezcan İ, Demir H, Ergüven S, Akyön Y. Maçin S, et al. Among authors: cagdas d. Pediatr Int. 2016 Jun;58(6):531-3. doi: 10.1111/ped.12959. Pediatr Int. 2016. PMID: 27322863

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