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Items: 1 to 50 of 110

1.

Predictable and Unusual Adverse Effects of Immunosuppression in Pediatric Liver Transplant Patients.

Öztürk H, Ekşi Bozbulut N, Sarı S, Eğritaş Gürkan Ö, Sözen H, Sapmaz A, Dalgıç A, Dalgıç B.

Exp Clin Transplant. 2019 Jan;17(Suppl 1):230-233. doi: 10.6002/ect.MESOT2018.P81.

2.

Portal Hypertensive Biliopathy as a Cause of Severe Cholestasis in Children With Congenital Hepatic Fibrosis.

Dalgıç A, Sarı S, Sözen MH, Gürcan Kaya N, Dalgıç B.

Exp Clin Transplant. 2019 Jan;17(Suppl 1):223-225. doi: 10.6002/ect.MESOT2018.P79.

3.

The Frequency of Lysosomal Acid Lipase Deficiency in Children With Unexplained Liver Disease.

Kuloglu Z, Kansu A, Selbuz S, Kalaycı AG, Şahin G, Kirsaclioglu CT, Demirören K, Dalgıç B, Kasırga E, Önal Z, İşlek A; National LAL-D Study Group.

J Pediatr Gastroenterol Nutr. 2019 Mar;68(3):371-376. doi: 10.1097/MPG.0000000000002224.

PMID:
30540705
4.

High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease.

Koca S, Tümer L, Okur İ, Erten Y, Bakkaloğlu S, Biberoğlu G, Kasapkara Ç, Küçükçongar A, Dalgıç B, Oktar SÖ, Öner Y, Atalay T, Cemri M, Çiftçi B, Topçu B, Hasanoğlu A, Ezgü F.

Gene. 2019 Mar 1;687:280-288. doi: 10.1016/j.gene.2018.11.054. Epub 2018 Nov 20.

PMID:
30468909
5.

Urinary 24-hour copper excretion at the time of diagnosis in children with Wilson's disease.

Aksu AÜ, Sarı S, Gürkan ÖE, Dalgıç B.

Acta Gastroenterol Belg. 2018 Jul-Sep;81(3):410-414.

PMID:
30350530
6.

The effect of Helicobacter pylori eradication on functional dyspepsia in Turkish children.

Ünlüsoy Aksu A, Yılmaz G, Eğritaş Gürkan Ö, Sarı S, Dalgıç B.

Helicobacter. 2018 Aug;23(4):e12497. doi: 10.1111/hel.12497. Epub 2018 Jun 6.

PMID:
29873438
7.

Correction to: Molecular characterization of a human group C rotavirus detected first in Turkey.

Mitui MT, Bozdayi G, Dalgic B, Bostanci I, Nishizono A, Ahmed K.

Virus Genes. 2018 Aug;54(4):621. doi: 10.1007/s11262-018-1572-1.

PMID:
29774496
8.

Prototheca zopfii Colitis in Inherited CARD9 Deficiency.

Sari S, Dalgic B, Muehlenbachs A, DeLeon-Carnes M, Goldsmith CS, Ekinci O, Jain D, Keating MK, Vilarinho S.

J Infect Dis. 2018 Jul 2;218(3):485-489. doi: 10.1093/infdis/jiy198.

9.

Tacrolimus-Induced Autoimmune Hemolytic Anemia in a Previously Reported Child With History of Thrombocytopenia Following Liver Transplant.

Kaya Z, Egritas O, Dalgic B.

Exp Clin Transplant. 2018 Jun;16(3):355-356. doi: 10.6002/ect.2017.0289. Epub 2018 Apr 9. No abstract available.

10.

Intestinal Failure and Aberrant Lipid Metabolism in Patients With DGAT1 Deficiency.

van Rijn JM, Ardy RC, Kuloğlu Z, Härter B, van Haaften-Visser DY, van der Doef HPJ, van Hoesel M, Kansu A, van Vugt AHM, Thian M, Kokke FTM, Krolo A, Başaran MK, Kaya NG, Aksu AÜ, Dalgıç B, Ozcay F, Baris Z, Kain R, Stigter ECA, Lichtenbelt KD, Massink MPG, Duran KJ, Verheij JBGM, Lugtenberg D, Nikkels PGJ, Brouwer HGF, Verkade HJ, Scheenstra R, Spee B, Nieuwenhuis EES, Coffer PJ, Janecke AR, van Haaften G, Houwen RHJ, Müller T, Middendorp S, Boztug K.

Gastroenterology. 2018 Jul;155(1):130-143.e15. doi: 10.1053/j.gastro.2018.03.040. Epub 2018 Mar 29.

11.

Evaluation of malnutrition development risk in hospitalized children.

Beser OF, Cokugras FC, Erkan T, Kutlu T, Yagci RV; TUHAMAR Study Group.

Nutrition. 2018 Apr;48:40-47. doi: 10.1016/j.nut.2017.10.020. Epub 2017 Nov 29.

12.

Cow`s milk protein allergy awareness and practice among Turkish pediatricians: A questionnaire-survey.

Yüce A, Dalgıç B, Çullu-Çokuğraş F, Çokuğraş H, Kansu A, Alptekin-Sarıoğlu A, Şekerel BE.

Turk J Pediatr. 2017;59(3):233-243. doi: 10.24953/turkjped.2017.03.002.

13.

Fibrinogen Gamma Chain Mutations Provoke Fibrinogen and Apolipoprotein B Plasma Deficiency and Liver Storage.

Callea F, Giovannoni I, Sari S, Guldal E, Dalgic B, Akyol G, Sogo T, Al-Hussaini A, Maggiore G, Bartuli A, Boldrini R, Francalanci P, Bellacchio E.

Int J Mol Sci. 2017 Dec 15;18(12). pii: E2717. doi: 10.3390/ijms18122717.

14.

EVALUATION OF HUMAN LEUKOCYTE ANTIGEN CLASS I AND II ANTIGENS IN HELICOBACTER PYLORI-POSITIVE PEDIATRIC PATIENTS WITH ACTIVE GASTRITIS AND DUODENAL ULCER.

Gönen S, Sari S, Kandur Y, Dalgiç B, Söylemezoğlu O.

Arq Gastroenterol. 2017 Dec;54(4):297-299. doi: 10.1590/s0004-2803.201700000-62. Epub 2017 Oct 2.

15.

Multiple Presentations of LRBA Deficiency: a Single-Center Experience.

Kostel Bal S, Haskologlu S, Serwas NK, Islamoglu C, Aytekin C, Kendirli T, Kuloglu Z, Yavuz G, Dalgic B, Siklar Z, Kansu A, Ensari A, Boztug K, Dogu F, Ikinciogullari A.

J Clin Immunol. 2017 Nov;37(8):790-800. doi: 10.1007/s10875-017-0446-y. Epub 2017 Sep 27.

PMID:
28956255
16.

A novel fibrinogen gamma chain mutation (c.1096C>G; p.His340Asp), fibrinogen Ankara, causing hypofibrinogenaemia and hepatic storage.

Callea F, Giovannoni I, Sari S, Aksu AU, Esendagly G, Dalgic B, Boldrini R, Akyol G, Francalanci P, Bellacchio E.

Pathology. 2017 Aug;49(5):534-537. doi: 10.1016/j.pathol.2017.03.007. Epub 2017 Jun 30. No abstract available.

PMID:
28673429
17.

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

Ozen A, Comrie WA, Ardy RC, Domínguez Conde C, Dalgic B, Beser ÖF, Morawski AR, Karakoc-Aydiner E, Tutar E, Baris S, Ozcay F, Serwas NK, Zhang Y, Matthews HF, Pittaluga S, Folio LR, Unlusoy Aksu A, McElwee JJ, Krolo A, Kiykim A, Baris Z, Gulsan M, Ogulur I, Snapper SB, Houwen RHJ, Leavis HL, Ertem D, Kain R, Sari S, Erkan T, Su HC, Boztug K, Lenardo MJ.

N Engl J Med. 2017 Jul 6;377(1):52-61. doi: 10.1056/NEJMoa1615887. Epub 2017 Jun 28.

18.

Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention.

Kotlarz D, Egritas Gurkan O, Haskologlu ZS, Ekinci O, Aksu Unlusoy A, Gürcan Kaya N, Puchalka J, Klein C, Dalgic B.

World J Gastrointest Pathophysiol. 2017 May 15;8(2):87-92. doi: 10.4291/wjgp.v8.i2.87.

19.

Iron Overload in the Liver of 2 Children: Nonalcoholic Steatohepatitis and Juvenile Hemochromatosis.

Ünlüsoy Aksu A, Caleffi A, Pietrangelo A, Sari S, Eğritaş Gürkan Ö, Demirtaş Z, Yilmaz G, Dalgiç B.

J Pediatr Hematol Oncol. 2017 Aug;39(6):466-469. doi: 10.1097/MPH.0000000000000752.

PMID:
28067690
20.

Consensus statement on diagnosis, treatment and follow-up of cow's milk protein allergy among infants and children in Turkey.

Kansu A, Yüce A, Dalgıç B, Şekerel BE, Çullu-Çokuğraş F, Çokuğraş H.

Turk J Pediatr. 2016;58(1):1-11.

21.

Favorable Response to Sirolimus in a Child With Blue Rubber Bleb Nevus Syndrome in the Gastrointestinal Tract.

Ünlüsoy Aksu A, Sari S, Eğritaş Gürkan Ö, Dalgiç B.

J Pediatr Hematol Oncol. 2017 Mar;39(2):147-149. doi: 10.1097/MPH.0000000000000681.

PMID:
27820137
22.

ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment.

Vilarinho S, Sari S, Mazzacuva F, Bilgüvar K, Esendagli-Yilmaz G, Jain D, Akyol G, Dalgiç B, Günel M, Clayton PT, Lifton RP.

Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):11289-11293. Epub 2016 Sep 19.

23.

Classification chaos in coeliac disease: Does it really matter?

Özakıncı H, Kırmızı A, Savaş B, Kalkan Ç, Soykan İ, Çetinkaya H, Kuloğlu Z, Kansu A, Gürkan ÖE, Dalgıç B, Şentürk Z, Ensari A.

Pathol Res Pract. 2016 Dec;212(12):1174-1178. doi: 10.1016/j.prp.2016.08.012. Epub 2016 Sep 3.

PMID:
27637158
24.

Aspartate aminotransferase-to-platelet ratio index in children with cholestatic liver diseases to assess liver fibrosis.

Ünlüsoy Aksu A, Sarı S, Yılmaz G, Eğritaş Gürkan Ö, Demirtaş Z, Dalgıç B.

Turk J Pediatr. 2015 Sep-Oct;57(5):492-7.

PMID:
27411417
25.

Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension.

Vilarinho S, Sari S, Yilmaz G, Stiegler AL, Boggon TJ, Jain D, Akyol G, Dalgic B, Günel M, Lifton RP.

Hepatology. 2016 Jun;63(6):1977-86. doi: 10.1002/hep.28499. Epub 2016 Mar 31.

26.

Chanarin-Dorfman syndrome: a novel mutation in a Turkish girl.

Ünlüsoy-Aksu A, Sarı S, Eğritaş-Gürkan Ö, Dalgıç B.

Turk J Pediatr. 2015 May-Jun;57(3):300-3.

PMID:
26701953
27.

A Successful HSCT in a Girl with Novel LRBA Mutation with Refractory Celiac Disease.

Sari S, Dogu F, Hwa V, Haskologlu S, Dauber A, Rosenfeld R, Polat M, Kuloglu Z, Kansu A, Dalgic B, Ikinciogullari A.

J Clin Immunol. 2016 Jan;36(1):8-11. doi: 10.1007/s10875-015-0220-y. Epub 2015 Dec 19. No abstract available.

PMID:
26686526
28.

Partial Hepatectomy for the Resistant Fasciola Hepatica Infection in a Child.

Belgin G, S KY, H T, A ÖP, B D, A D, G Y.

APSP J Case Rep. 2015 Sep 1;6(3):27. eCollection 2015 Sep-Dec.

29.

Mutant neurogenin-3 in a Turkish boy with congenital malabsorptive diarrhea.

Ünlüsoy Aksu A, Eğritaş Gürkan Ö, Sarı S, Demirtaş Z, Türkyılmaz C, Poyraz A, Dalgıç B.

Pediatr Int. 2016 May;58(5):379-382. doi: 10.1111/ped.12783. Epub 2015 Nov 6.

PMID:
26541772
30.

Rare disorders can be an underlying cause of cyclic vomiting: Familial Mediterranean fever, Helicobacter pylori gastritis, and cavernous transformation of the portal vein.

Egritaş Gürkan Ö, Ünlüsoy Aksu A, Demirtaş Z, Dalgıç B.

Turk J Gastroenterol. 2015 Nov;26(6):461-7. doi: 10.5152/tjg.2015.0015. Epub 2015 Oct 26.

31.

Fibrinogen storage disease and cirrhosis associated with hypobetalipoproteinemia owing to fibrinogen Aguadilla in a Turkish child.

Sari S, Yilmaz G, Gonul II, Dalgic B, Akyol G, Giovannoni I, Francalanci P, Callea F.

Liver Int. 2015 Dec;35(12):2501-5. doi: 10.1111/liv.12914. Epub 2015 Aug 18.

PMID:
26176881
32.

A case with rare type of congenital disorder of glycosylation: PGM1-CDG.

Küçükçongar A, Tümer L, Ezgü FS, Kasapkara ÇS, Jaeken J, Matthijs G, Rymen D, Dalgiç B, Bıdecı A, Hasanoğlu A.

Genet Couns. 2015;26(1):87-90. No abstract available.

PMID:
26043514
33.

Yield of coeliac screening in abdominal pain-associated functional gastrointestinal system disorders.

Kansu A, Kuloğlu Z, Demir A, Yaman A; Turkish Celiac Study Group.

J Paediatr Child Health. 2015 Nov;51(11):1066-70. doi: 10.1111/jpc.12929. Epub 2015 Jun 3.

PMID:
26041019
34.

Megabulbus in endoscopy; suspect for superior mesenteric artery syndrome in children.

Eğritaş Ö, Demiroğullari B, Dalgıç B.

Turk J Gastroenterol. 2015 Mar;26(2):186-8. doi: 10.5152/tjg.2015.4221.

35.

An insight into the relationships between prohepcidin, iron deficiency anemia, and interleukin-6 values in pediatric Helicobacter pylori gastritis.

Emiralioglu N, Yenicesu I, Sari S, Egritas O, Poyraz A, Pasaoglu OT, Celik B, Dalgic B.

Eur J Pediatr. 2015 Jul;174(7):903-10. doi: 10.1007/s00431-014-2482-4. Epub 2015 Jan 9.

PMID:
25567795
36.

Successful treatment of Paecilomyces variotii peritonitis in a liver transplant patient.

Polat M, Kara SS, Tapısız A, Demirtaş Z, Sarı S, Kalkancı A, Tezer H, Dalgıç B.

Mycopathologia. 2015 Apr;179(3-4):317-20. doi: 10.1007/s11046-014-9854-1. Epub 2014 Dec 23.

PMID:
25534477
37.

A complication to be aware of: hyperkalaemia following propranolol therapy for an infant with intestinal haemangiomatozis.

Belen B, Oguz A, Okur A, Dalgic B.

BMJ Case Rep. 2014 May 19;2014. pii: bcr2014203746. doi: 10.1136/bcr-2014-203746.

38.

Immune thrombocytopenic purpura in a liver transplant patient.

Ünlüsoy Aksu A, Eğritaş Gürkan Ö, Sarı S, Yenicesu İ, Dalgıç B.

Exp Clin Transplant. 2014 Mar;12 Suppl 1:175-7.

39.

Chylous ascites after a living-donor liver graft, effectively treated in a child with octreotide.

Ünlüsoy Aksu A, Demirtaş Z, Eğritaş Gürkan Ö, Dalgıç B, Sözen H, Dalgıç A.

Exp Clin Transplant. 2014 Mar;12 Suppl 1:173-4.

40.

Relation between ghrelin level and treatment response in functional constipation.

Gürkan OE, Dalgıç B, Bideci A.

Turk J Gastroenterol. 2013;24(6):515-20.

41.

Resolution of inflammatory colitis with pegfilgrastim treatment in a case of severe congenital neutropenia due to glucose 6 phosphatase catalytic subunit-3 deficiency.

Kaya Z, Eğritaş O, Albayrak M, Göçün PU, Koçak U, Dalgiç B, Gürsel T.

J Pediatr Hematol Oncol. 2014 Jul;36(5):e316-8. doi: 10.1097/MPH.0000000000000079.

PMID:
24322501
42.

Colonic lymphoid nodular hyperplasia in childhood: causes of familial Mediterranean fever need extra attention.

Gurkan OE, Yilmaz G, Aksu AU, Demirtas Z, Akyol G, Dalgic B.

J Pediatr Gastroenterol Nutr. 2013 Dec;57(6):817-21. doi: 10.1097/MPG.0b013e3182a9083b.

PMID:
24280993
43.

Jejunal stricture in a premature infant: Is cytomegalovirus the causative pathogen or a superinfection?

Unlüsoy Aksu A, Sarı S, Karabulut R, Ekinci O, Dalgıç B.

Turk J Gastroenterol. 2013;24(3):273-6.

44.

Eosinophilic esophagitis and anaphylaxis due to cow's milk in an infant.

Topal E, Eğritaş O, Arga M, Sarı S, Poyraz A, Bakırtaş A, Dalgıç B.

Turk J Pediatr. 2013 Mar-Apr;55(2):222-5.

PMID:
24192687
45.

An unusual cause of acute abdomen in an adolescent with concurrent disease.

Kandur Y, Bakkaloglu SA, Gonul II, Yenicesu I, Akkan K, Dalgic B.

Pediatr Nephrol. 2015 Mar;30(3):433-7. doi: 10.1007/s00467-013-2649-7. Epub 2013 Oct 17. No abstract available.

PMID:
24132540
46.

Complete Genome Sequence of an MLB2 Astrovirus from a Turkish Child with Diarrhea.

Mitui MT, Bozdayi G, Matsumoto T, Dalgic B, Nishizono A, Ahmed K.

Genome Announc. 2013 Aug 15;1(4). pii: e00619-13. doi: 10.1128/genomeA.00619-13.

47.

Comparison of double balloon enteroscopy in adults and children.

Gurkan OE, Karakan T, Dogan I, Dalgic B, Unal S.

World J Gastroenterol. 2013 Aug 7;19(29):4726-31. doi: 10.3748/wjg.v19.i29.4726.

48.

Gastrointestinal mucosal involvement without amyloidosis in children with familial Mediterranean fever.

Gurkan OE, Dalgic B.

J Pediatr Gastroenterol Nutr. 2013 Sep;57(3):319-23. doi: 10.1097/MPG.0b013e318295fc65.

PMID:
23591909
49.

Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort.

Martín MG, Lindberg I, Solorzano-Vargas RS, Wang J, Avitzur Y, Bandsma R, Sokollik C, Lawrence S, Pickett LA, Chen Z, Egritas O, Dalgic B, Albornoz V, de Ridder L, Hulst J, Gok F, Aydoğan A, Al-Hussaini A, Gok DE, Yourshaw M, Wu SV, Cortina G, Stanford S, Georgia S.

Gastroenterology. 2013 Jul;145(1):138-148. doi: 10.1053/j.gastro.2013.03.048. Epub 2013 Apr 2.

50.

Esophagitis and widespread aphthous ulcerations in gastric mucosa in an infant with familial Mediterranean fever.

Gurkan OE, Fidan K, Dalgic B.

J Pediatr Gastroenterol Nutr. 2014 Jul;59(1):e11-3. doi: 10.1097/MPG.0b013e3182906d8f. No abstract available.

PMID:
23492736

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