Lista de obras -

A comparison of fentanyl with tramadol during propofol-based deep sedation for pediatric upper endoscopy

artículo científico publicado en 2011

A variant Muckle-Wells syndrome with a novel mutation in CIAS1 gene responding to anakinra.

artículo científico publicado en 2007

Acute pancreatitis: a rare presenting feature of Henoch Schonlein purpura

scientific article published on 01 March 2008

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

artículo científico publicado en 2015

Analbuminemia Zonguldak: Case report and mutational analysis

artículo científico publicado en 2008

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

artículo científico publicado en 2015

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

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

artículo científico publicado en 2016

Cholecystitis, pancreatitis and hemobilia: a serious trilogy after liver biopsy

scientific article published on 01 August 2010

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

artículo científico publicado en 2014

Classification chaos in coeliac disease: Does it really matter?

artículo científico publicado en 2016

Clinicopathological dissociation in isolated esophageal eosinophilia

scientific article published on 01 December 2014

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

artículo científico publicado en 2013

Colonic phasic motor activity is stronger in patients with repaired anorectal malformations than patients with severe colonic dismotility

artículo científico publicado en 2010

Comparison of double balloon enteroscopy in adults and children

artículo científico publicado en 2013

Congenital chloride diarrhea misdiagnosed as Bartter syndrome

scientific article published on 01 June 2011

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

artículo científico publicado en 2013

Diagnostic Yield of Next-generation Sequencing in Very Early-onset Inflammatory Bowel Diseases: A Multicentre Study

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Duplication 4q associated with chronic cholestatic changes in liver biopsy

artículo científico publicado en 2010

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome

artículo científico publicado en 2018

Early but prolonged gallbladder hydrops in a 7-month-old girl with Kawasaki syndrome: Report of a case

artículo científico publicado en 2007

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

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Food‐induced immediate response of the esophagus in pediatric eosinophilic esophagitis

artículo científico publicado en 2023

Gastrointestinal mucosal involvement without amyloidosis in children with familial Mediterranean fever

artículo científico publicado en 2013

Gastrointestinal ulceration in celiac disease

artículo científico publicado en 2013

Granulomatous hepatitis, perihepatic lymphadenopathies, and autoantibody positivity: an unusual association in a child with hepatitis C.

artículo científico publicado en 2008

Gray hair and acrodermatitis enteropathica-like dermatitis: an unexpected presentation of cystic fibrosis

artículo científico publicado en 2011

Hepatoportal sclerosis in childhood: some presenting with cholestatic features (a re-evaluation of 12 children)

artículo científico publicado en 2011

Immune thrombocytopenic purpura in a liver transplant patient

artículo científico publicado en 2014

Infantile colitis as a novel presentation of familial Mediterranean fever responding to colchicine therapy

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Is familial Mediterranean fever a possible cofactor for Budd-Chiari syndrome?

artículo científico publicado en 2009

Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy

artículo científico publicado en 2012

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Normal defecation pattern, frequency of constipation and factors related to constipation in Turkish children 0-6 years old.

artículo científico publicado en 2011

Novel mutations in TTC37 associated with tricho-hepato-enteric syndrome

article

Platelet usage trends in a tertiary care hospital - Could it be less and less expensive?

artículo científico publicado en 2012

Pleural effusion: always innocent?

artículo científico publicado en 2008

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

scientific article published on 01 January 2019

Prevalence of Celiac disease in Turkish children with type 1 diabetes mellitus and their non-diabetic first-degree relatives

artículo científico publicado en 2010

Prevalence of celiac disease in Turkish children with autoimmune thyroiditis

artículo científico publicado en 2008

Prevalence of celiac disease in healthy Turkish school children

artículo científico publicado en 2011

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

artículo científico publicado en 2015

Relation between ghrelin level and treatment response in functional constipation

artículo científico publicado en 2013

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

artículo científico publicado en 2014

SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.

artículo científico publicado en 2012

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

artículo científico publicado en 2018

The diagnosis and outcomes of persistent diarrhea in infants aged 0-24 months--a Turkish cohort study.

artículo científico publicado en 2011

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

artículo científico publicado en 2018

The familial Mediterranean fever (MEFV) gene may be a modifier factor of inflammatory bowel disease in infancy.

artículo científico publicado en 2007

The first experience of eosinophilic esophagitis in Turkish children.

artículo científico publicado en 2012

Tricho-hepato-enteric syndrome presenting with mild colitis

Two cases of esophageal eosinophilia: eosinophilic esophagitis or gastro-esophageal reflux disease?

artículo científico publicado en 2014

Lista de obras de

A comparison of fentanyl with tramadol during propofol-based deep sedation for pediatric upper endoscopy

A variant Muckle-Wells syndrome with a novel mutation in CIAS1 gene responding to anakinra.

Acute pancreatitis: a rare presenting feature of Henoch Schonlein purpura

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

Analbuminemia Zonguldak: Case report and mutational analysis

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

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

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

Cholecystitis, pancreatitis and hemobilia: a serious trilogy after liver biopsy

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

Classification chaos in coeliac disease: Does it really matter?

Clinicopathological dissociation in isolated esophageal eosinophilia

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

Colonic phasic motor activity is stronger in patients with repaired anorectal malformations than patients with severe colonic dismotility

Comparison of double balloon enteroscopy in adults and children

Congenital chloride diarrhea misdiagnosed as Bartter syndrome

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

Diagnostic Yield of Next-generation Sequencing in Very Early-onset Inflammatory Bowel Diseases: A Multicentre Study

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

Duplication 4q associated with chronic cholestatic changes in liver biopsy

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome

Early but prolonged gallbladder hydrops in a 7-month-old girl with Kawasaki syndrome: Report of a case

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

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

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

Food‐induced immediate response of the esophagus in pediatric eosinophilic esophagitis

Gastrointestinal mucosal involvement without amyloidosis in children with familial Mediterranean fever

Gastrointestinal ulceration in celiac disease

Granulomatous hepatitis, perihepatic lymphadenopathies, and autoantibody positivity: an unusual association in a child with hepatitis C.

Gray hair and acrodermatitis enteropathica-like dermatitis: an unexpected presentation of cystic fibrosis

Hepatoportal sclerosis in childhood: some presenting with cholestatic features (a re-evaluation of 12 children)

Immune thrombocytopenic purpura in a liver transplant patient

Infantile colitis as a novel presentation of familial Mediterranean fever responding to colchicine therapy

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

Is familial Mediterranean fever a possible cofactor for Budd-Chiari syndrome?

Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy

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

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

Normal defecation pattern, frequency of constipation and factors related to constipation in Turkish children 0-6 years old.

Novel mutations in TTC37 associated with tricho-hepato-enteric syndrome

Platelet usage trends in a tertiary care hospital - Could it be less and less expensive?

Pleural effusion: always innocent?

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

Prevalence of Celiac disease in Turkish children with type 1 diabetes mellitus and their non-diabetic first-degree relatives

Prevalence of celiac disease in Turkish children with autoimmune thyroiditis

Prevalence of celiac disease in healthy Turkish school children

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

Relation between ghrelin level and treatment response in functional constipation

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

SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.

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

The diagnosis and outcomes of persistent diarrhea in infants aged 0-24 months--a Turkish cohort study.

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

The familial Mediterranean fever (MEFV) gene may be a modifier factor of inflammatory bowel disease in infancy.

The first experience of eosinophilic esophagitis in Turkish children.

Tricho-hepato-enteric syndrome presenting with mild colitis

Two cases of esophageal eosinophilia: eosinophilic esophagitis or gastro-esophageal reflux disease?

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