Artan R - Search Results

1

Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype.

Serwas NK, Kansu A, Santos-Valente E, Kuloğlu Z, Demir A, Yaman A, Gamez Diaz LY, Artan R, Sayar E, Ensari A, Grimbacher B, Boztug K. Serwas NK, et al. Among authors: artan r. Inflamm Bowel Dis. 2015 Jan;21(1):40-7. doi: 10.1097/MIB.0000000000000266. Inflamm Bowel Dis. 2015. PMID: 25479458

2

Comparison of two different regimens of combined interferon-alpha2a and lamivudine therapy in children with chronic hepatitis B infection.

Kansu A, Doğanci T, Akman SA, Artan R, Kuyucu N, Kalayci AG, Dikici B, Dalgiç B, Selimoğlu A, Kasirga E, Ozkan TB, Kuloğlu Z, Aydoğdu S, Boşnak M, Ertekin V, Tanir G, Haspolat K, Girgin N, Yağci RV. Kansu A, et al. Among authors: artan r. Antivir Ther. 2006;11(2):255-61. Antivir Ther. 2006. PMID: 16640106 Clinical Trial.

3

Percutaneous endoscopic gastrostomy in children: Is early feeding safe?

Islek A, Sayar E, Yilmaz A, Artan R. Islek A, et al. Among authors: artan r. J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):659-62. doi: 10.1097/MPG.0b013e3182a0d171. J Pediatr Gastroenterol Nutr. 2013. PMID: 23799454 Clinical Trial.

4

Chromogranin-A staining reveals enteric anendocrinosis in unexplained congenital diarrhea.

Sayar E, Yilmaz A, Islek A, Elpek GO, Flanagan SE, Artan R. Sayar E, et al. Among authors: artan r. J Pediatr Gastroenterol Nutr. 2013 Oct;57(4):e21. doi: 10.1097/MPG.0b013e3182560f26. J Pediatr Gastroenterol Nutr. 2013. PMID: 24084374 No abstract available.

5

Extremely rare cause of congenital diarrhea: enteric anendocrinosis.

Sayar E, Islek A, Yilmaz A, Akcam M, Flanagan SE, Artan R. Sayar E, et al. Among authors: artan r. Pediatr Int. 2013 Oct;55(5):661-3. doi: 10.1111/ped.12169. Pediatr Int. 2013. PMID: 24134759

6

Langerhans cell histiocytosis in IPEX syndrome: possible role for natural regulatory T cells?

Sayar E, Uygun DF, Islek A, Hazar-Sayar E, Akkaya B, Vignoli M, Gambineri E, Yesilipek MA, Artan R. Sayar E, et al. Among authors: artan r. Pediatr Allergy Immunol. 2014 Oct;25(6):601-3. doi: 10.1111/pai.12219. Epub 2014 Mar 16. Pediatr Allergy Immunol. 2014. PMID: 24628744 No abstract available.

7

Novel mutation in the CLDN1 gene in a Turkish family with neonatal ichthyosis sclerosing cholangitis (NISCH) syndrome.

Kirchmeier P, Sayar E, Hotz A, Hausser I, Islek A, Yilmaz A, Artan R, Fischer J. Kirchmeier P, et al. Among authors: artan r. Br J Dermatol. 2014 Apr;170(4):976-8. doi: 10.1111/bjd.12724. Br J Dermatol. 2014. PMID: 24641442 No abstract available.

8

A rare outcome of iron deficiency and pica: Rapunzel syndrome in a 5-year-old child iron deficiency and pica.

Islek A, Sayar E, Yılmaz A, Boneval C, Artan R. Islek A, et al. Among authors: artan r. Turk J Gastroenterol. 2014 Feb;25(1):100-2. doi: 10.5152/tjg.2014.4051. Turk J Gastroenterol. 2014. PMID: 24918141 Free article.

9

Islek A, Inci A, Sayar E, Yilmaz A, Uzun OC, Artan R. Islek A, et al. Among authors: artan r. J Pediatr Gastroenterol Nutr. 2016 Apr;62(4):e35-7. doi: 10.1097/MPG.0000000000000478. J Pediatr Gastroenterol Nutr. 2016. PMID: 25000356 No abstract available.

10

Microvillus inclusion disease associated with necrotizing enterocolitis in a premature infant.

Sayar E, Kalay S, Yilmaz A, Oztekin O, Islek A, Elpek GO, Kalay Z, Tezel G, Artan R. Sayar E, et al. Among authors: artan r. AJP Rep. 2014 Nov;4(2):e61-4. doi: 10.1055/s-0034-1370353. Epub 2014 May 12. AJP Rep. 2014. PMID: 25452882 Free PMC article.

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