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Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype

Inflammatory bowel diseases, 2015-01, Vol.21 (1), p.40-47

2015

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A Rare Contiguous Gene Deletion Leading to Trichothiodystrophy Type 4 and Glutaric Aciduria Type 3

Molecular syndromology, 2023-04, Vol.14 (2), p.136-142

2023

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Co-Occurring Atypical Galactosemia and Wilson Disease

Molecular syndromology, 2022-12, Vol.13 (5), p.454-458

2022

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Evaluation of the Effectiveness of Using Handgrip Strength in Determining Malnutrition in Adolescents

Topics in clinical nutrition, 2023-10, Vol.38 (4), p.336-345

2023

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Duodenal bulb biopsy in the diagnostic work-up of coeliac disease

Virchows Archiv : an international journal of pathology, 2020-10, Vol.477 (4), p.507-515

2020

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Neonatal ichthyosis-sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature

Clinical dysmorphology, 2023-04, Vol.32 (2), p.88-91

2023

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Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient

Clinical dysmorphology, 2023-01, Vol.32 (1), p.25-28

2023

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Early-onset inflammatory bowel disease and common variable immunodeficiency–like disease caused by IL-21 deficiency

Journal of allergy and clinical immunology, 2014-06, Vol.133 (6), p.1651-1659.e12

2014

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Turkish Validity-Reliability Study of the Celiac Disease-Specific Pediatric Quality of Life Scale

The Turkish Journal of Gastroenterology, 2022-03, Vol.33 (3), p.248-256

2022

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Diagnostic Workup and Micronutrient Deficiencies in Children With Failure to Thrive Without Underlying Diseases

Nutrition in clinical practice, 2019-08, Vol.34 (4), p.581-588

2019

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Assessment of cows milk‐related symptom scoring awareness tool in young Turkish children

Journal of paediatrics and child health, 2020-11, Vol.56 (11), p.1799-1805

2020

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Current Trends in Tolerance Induction in Cow's Milk Allergy: From Passive to Proactive Strategies

Frontiers in pediatrics, 2019-09, Vol.7, p.372-372

2019

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The frequency of Duchenne muscular dystrophy/Becker muscular dystrophy and Pompe disease in children with isolated transaminase elevation: results from the observational VICTORIA study

Frontiers in pediatrics, 2023-09, Vol.11, p.1272177-1272177

2023

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A rare cause of hepatomegaly in the childhood: Lysosomal acid lipase deficiency

The Turkish journal of gastroenterology, 2018-07, Vol.29 (4), p.518-519

2018

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Tacrolimus toxicity-related chorea in an infant after liver transplantation

Acute and Critical Care, 2022, 37(3), , pp.477-479

2022

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Cyclosporine-associated thrombotic microangiopathy and thrombocytopenia-associated multiple organ failure: a case successfully treated with therapeutic plasma exchange

Journal of pediatric hematology/oncology, 2014-03, Vol.36 (2), p.e88-e90

2014

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An infant with severe refractory Crohn’s disease and homozygous MEFV mutation who dramatically responded to colchicine

Rheumatology international, 2012-03, Vol.32 (3), p.783-785

2012

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Celiac disease: presentation of 109 children

Yonsei Medical Journal, 2009, 50(5), , pp.617-623

2009

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Can partially hydrolyzed guar gum be an alternative to lactulose in treatment of childhood constipation?

The Turkish journal of gastroenterology, 2010-12, Vol.21 (4), p.360-364

2010

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Congenital multisegmental lymphatic dysplasia with systemic involvement: a case report

Clinical dysmorphology, 2016-10, Vol.25 (4), p.174-177

2016

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A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia

Journal of clinical immunology, 2016-05, Vol.36 (4), p.370-373

2016

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Carotid intima-media thickness and arterial stiffness as early markers of atherosclerosis in pediatric celiac disease

Turkish journal of pediatrics, 2016, Vol.58 (2), p.172-179

2016

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Change of Helicobacter pylori prevalence in a decade among children undergoing endoscopy

Turkish journal of pediatrics, 2016-11, Vol.58 (6), p.579-582

2016

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Valproic Acid-Induced Acute Pancreatitis and Multiorgan Failure in a Child

Pediatric emergency care, 2013-05, Vol.29 (5), p.659-661

2013

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Proteinuria in a Crohn’s disease patient: Answers

Pediatric nephrology (Berlin, West), 2015-09, Vol.30 (9), p.1435-1436

2015

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Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype

A Rare Contiguous Gene Deletion Leading to Trichothiodystrophy Type 4 and Glutaric Aciduria Type 3

Co-Occurring Atypical Galactosemia and Wilson Disease

Evaluation of the Effectiveness of Using Handgrip Strength in Determining Malnutrition in Adolescents

Duodenal bulb biopsy in the diagnostic work-up of coeliac disease

Neonatal ichthyosis-sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature

Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient

Early-onset inflammatory bowel disease and common variable immunodeficiency–like disease caused by IL-21 deficiency

Turkish Validity-Reliability Study of the Celiac Disease-Specific Pediatric Quality of Life Scale

Diagnostic Workup and Micronutrient Deficiencies in Children With Failure to Thrive Without Underlying Diseases

Assessment of cows milk‐related symptom scoring awareness tool in young Turkish children

Current Trends in Tolerance Induction in Cow's Milk Allergy: From Passive to Proactive Strategies

The frequency of Duchenne muscular dystrophy/Becker muscular dystrophy and Pompe disease in children with isolated transaminase elevation: results from the observational VICTORIA study

A rare cause of hepatomegaly in the childhood: Lysosomal acid lipase deficiency

Tacrolimus toxicity-related chorea in an infant after liver transplantation

Cyclosporine-associated thrombotic microangiopathy and thrombocytopenia-associated multiple organ failure: a case successfully treated with therapeutic plasma exchange

An infant with severe refractory Crohn’s disease and homozygous MEFV mutation who dramatically responded to colchicine

Celiac disease: presentation of 109 children

Can partially hydrolyzed guar gum be an alternative to lactulose in treatment of childhood constipation?

Congenital multisegmental lymphatic dysplasia with systemic involvement: a case report

A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia

Carotid intima-media thickness and arterial stiffness as early markers of atherosclerosis in pediatric celiac disease

Change of Helicobacter pylori prevalence in a decade among children undergoing endoscopy

Valproic Acid-Induced Acute Pancreatitis and Multiorgan Failure in a Child

Proteinuria in a Crohn’s disease patient: Answers

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