Esenboga S - Search Results

1

An infant with ZAP-70 deficiency with disseminated mycobacterial disease.

Esenboga S, Ayvaz DC, Cetinkaya PG, van der Burg M, Tezcan İ. Esenboga S, et al. J Clin Immunol. 2016 Feb;36(2):103-6. doi: 10.1007/s10875-015-0229-2. Epub 2015 Dec 28. J Clin Immunol. 2016. PMID: 26707786 No abstract available.

2

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: esenboga s. 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.

3

CVID Associated with Systemic Amyloidosis.

Esenboga S, Çagdas Ayvaz D, Saglam Ayhan A, Peynircioglu B, Sanal O, Tezcan I. Esenboga S, et al. Case Reports Immunol. 2015;2015:879179. doi: 10.1155/2015/879179. Epub 2015 Aug 4. Case Reports Immunol. 2015. PMID: 26346511 Free PMC article.

4

Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD.

Esenboga S, Emiralioglu N, Cagdas D, Erman B, De Boer M, Oguz B, Kiper N, Tezcan İ. Esenboga S, et al. J Clin Immunol. 2017 Apr;37(3):269-272. doi: 10.1007/s10875-017-0376-8. Epub 2017 Feb 21. J Clin Immunol. 2017. PMID: 28224353

5

Characteristics of drug-induced anaphylaxis in children and adolescents.

Cavkaytar O, Karaatmaca B, Cetinkaya PG, Esenboga S, Arik Yilmaz E, Sahiner UM, Sekerel BE, Soyer O. Cavkaytar O, et al. Among authors: esenboga s. Allergy Asthma Proc. 2017 Sep 1;38(5):56-63. doi: 10.2500/aap.2017.38.4064. Allergy Asthma Proc. 2017. PMID: 28814352

6

Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis.

Taşkıran EZ, Sönmez HE, Ayvaz DÇ, Koşukcu C, Batu ED, Esenboğa S, Topaloğlu R, Orhan D, Bilginer Y, Alikaşifoğlu M, Özen S, Tezcan İ. Taşkıran EZ, et al. Among authors: esenboga s. Clin Immunol. 2018 Feb;187:92-94. doi: 10.1016/j.clim.2017.10.010. Epub 2017 Nov 7. Clin Immunol. 2018. PMID: 29107076 No abstract available.

7

Clinical and genetic features of the patients with X-Linked agammaglobulinemia from Turkey: Single-centre experience.

Esenboga S, Cagdas D, Ozgur TT, Gur Cetinkaya P, Turkdemir LM, Sanal O, VanDerBurg M, Tezcan I. Esenboga S, et al. Scand J Immunol. 2018 Mar;87(3). doi: 10.1111/sji.12647. Scand J Immunol. 2018. PMID: 29424453 Free article.

8

A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly.

Esenboga S, Çagdas D, Oguz B, Bajin I, Aydin B, Akyuz C, Tezcan I. Esenboga S, et al. J Pediatr Hematol Oncol. 2018 Apr;40(3):248-251. doi: 10.1097/MPH.0000000000001101. J Pediatr Hematol Oncol. 2018. PMID: 29432311 No abstract available.

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: esenboga s. 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

Two siblings with PRKDC defect who presented with cutaneous granulomas and review of the literature.

Esenboga S, Akal C, Karaatmaca B, Erman B, Dogan S, Orhan D, Boztug K, Ayvaz D, Tezcan İ. Esenboga S, et al. Clin Immunol. 2018 Dec;197:1-5. doi: 10.1016/j.clim.2018.08.002. Epub 2018 Aug 16. Clin Immunol. 2018. PMID: 30121298 Review.

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