Publications by authors named "Turgay Coskun"

100Publications

Creatine Transporter Deficiency Presenting as Autism Spectrum Disorder.

Pediatrics 2020 11;146(5)

Pediatric Neurology, Department of Pediatrics and.

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http://dx.doi.org/10.1542/peds.2019-3460DOI Listing
November 2020

Glutaric aciduria type 1: Genetic and phenotypic spectrum in 53 patients.

Eur J Med Genet 2020 Nov 7;63(11):104032. Epub 2020 Aug 7.

Hacettepe University Faculty of Medicine, Division of Pediatric Metabolism, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2020.104032DOI Listing
November 2020

Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delay.

Turk J Pediatr 2020 ;62(3):474-478

Divisions of Pediatric Nutrition and Metabolism, Hacettepe University Faculty of Medicine, Ankara.

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http://dx.doi.org/10.24953/turkjped.2020.03.015DOI Listing
January 2020

Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review.

Am J Med Genet A 2020 07 7;182(7):1608-1614. Epub 2020 Apr 7.

Department of Pediatrics, Metabolism Unit, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.61590DOI Listing
July 2020

Oral health status of children with phenylketonuria.

J Pediatr Endocrinol Metab 2020 Mar;33(3):361-365

Department of Pediatric Dentistry, Faculty of Dentistry, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1515/jpem-2019-0439DOI Listing
March 2020

Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department.

Eur J Pediatr 2020 Jul 11;179(7):1107-1114. Epub 2020 Feb 11.

Division of Pediatric Metabolism, Department of Pediatrics, Hacettepe University Ihsan Dogramaci Children's Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1007/s00431-020-03602-xDOI Listing
July 2020

Genotypes and estimated prevalence of phosphomannomutase 2 deficiency in Turkey differ significantly from those in Europe.

Am J Med Genet A 2020 04 25;182(4):705-712. Epub 2020 Jan 25.

Faculty of Medicine, Department of Pediatrics, Division of Pediatric Metabolism, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.61488DOI Listing
April 2020

Caring for a Child with Phenylketonuria: Parental Experiences from a Eurasian Country.

J Dev Behav Pediatr 2020 04;41(3):195-202

Departments of Pediatrics, Pediatric Metabolism, Biostatistics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1097/DBP.0000000000000748DOI Listing
April 2020

The effectiveness of enzyme replacement therapy on cardiac findings in patients with mucopolysaccharidosis.

J Pediatr Endocrinol Metab 2019 Oct;32(10):1049-1053

Division of Pediatric Metabolism, Hacettepe University, Medical Faculty, Ankara, Turkey.

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http://dx.doi.org/10.1515/jpem-2019-0293DOI Listing
October 2019

Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency.

Pediatr Neurol 2019 10 28;99:69-75. Epub 2019 Jun 28.

Division of Pediatric Metabolism, Hacettepe University Children's Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.pediatrneurol.2019.06.015DOI Listing
October 2019

Imaging liver nodules in tyrosinemia type-1: A retrospective review of 16 cases in a tertiary pediatric hospital.

Eur J Radiol 2019 Jul 23;116:41-46. Epub 2019 Apr 23.

Department of Radiology, Hacettepe University School of Medicine Ankara, Turkey.

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http://dx.doi.org/10.1016/j.ejrad.2019.04.016DOI Listing
July 2019

Do not Miss Rare and Treatable Cause of Early-Onset Hemolytic Uremic Syndrome: Cobalamin C Deficiency.

Nephron 2019 28;142(3):258-263. Epub 2019 May 28.

Division of Pediatric Metabolic Diseases, Department of Pediatrics, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1159/000497822DOI Listing
June 2020

Cognitive and behavioral impairment in mild hyperphenylalaninemia.

Turk J Pediatr 2018 ;60(6):617-624

Departments of Pediatric Metabolism, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.24953/turkjped.2018.06.001DOI Listing
January 2018

Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder.

Turk J Pediatr 2016 ;58(1):94-96

Pediatric Metabolic Diseases Unit, Department of Pediatrics, Hacettepe University Faculy of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.24953/turkjped.2016.01.014DOI Listing
June 2017

Partial hydatidiform mole in a phenylketonuria patient treated with sapropterin dihydrochloride.

Gynecol Endocrinol 2017 Jan 29;33(1):19-20. Epub 2016 Nov 29.

a Division of Pediatric Metabolism , Department of Pediatrics, Faculty of Medicine, Hacettepe University , Ankara , Turkey.

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http://dx.doi.org/10.1080/09513590.2016.1247796DOI Listing
January 2017

Screening for mucopolysaccharidoses in the Turkish population: Analytical and clinical performance of an age-range specific, dye-based, urinary glycosaminoglycan assay.

Clin Chim Acta 2017 Jan 15;464:72-78. Epub 2016 Nov 15.

Department of Medical Biochemistry, Faculty of Medicine, Hacettepe University, Ankara, Turkey; Clinical Pathology Laboratory, Hacettepe University Hospitals, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.cca.2016.11.015DOI Listing
January 2017

Evaluation and identification of IDUA gene mutations in Turkishpatients with mucopolysaccharidosis type I.

Turk J Med Sci 2016 Feb 17;46(2):404-8. Epub 2016 Feb 17.

Department of Biology, Faculty of Science and Arts, Aksaray University, Aksaray, Turkey.

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http://dx.doi.org/10.3906/sag-1411-160DOI Listing
February 2016

Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation.

Turk J Pediatr 2015 Jul-Aug;57(4):388-393

Division of Pediatric Metabolism, Department of Pediatrics Faculty of Medicine, Hacettepe University, Ankara, Turkey.

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February 2017

Conventional and advanced MR imaging in infantile Refsum disease.

Turk J Pediatr 2015 May-Jun;57(3):294-9

Divisions of Pediatric Nutrition and Metabolism, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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August 2016

Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four.

Turk J Pediatr 2015 May-Jun;57(3):213-8

Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

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August 2016

A case of fucosidosis type II: diagnosed with dysmorphological and radiological findings.

Turk J Pediatr 2014 Jul-Aug;56(4):430-3

Division of Medical Genetics, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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March 2016

Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screening.

Eur J Pediatr 2015 Aug 11;174(8):1077-84. Epub 2015 Mar 11.

Faculty of Science and Arts, Department of Biology, Aksaray University, Aksaray, Turkey,

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http://dx.doi.org/10.1007/s00431-015-2509-5DOI Listing
August 2015

Fundus autofluorescence and optical coherence tomography findings in glutathione synthetase deficiency.

J AAPOS 2015 Feb;19(1):80-2

Division of Metabolism and Nutrition, Department of Pediatrics, Hacettepe University Faculty of Medicine, 06100 Ankara, Turkey.

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http://dx.doi.org/10.1016/j.jaapos.2014.09.014DOI Listing
February 2015

Phenotypic and genotypic spectrum of Turkish patients with isovaleric acidemia.

Eur J Med Genet 2014 Oct 8;57(10):596-601. Epub 2014 Sep 8.

Hacettepe University, Faculty of Medicine, Department of Pediatrics, Metabolism Unit, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2014.08.006DOI Listing
October 2014

Mucopolysaccharidosis: Otolaryngologic findings, obstructive sleep apnea and accumulation of glucosaminoglycans in lymphatic tissue of the upper airway.

Int J Pediatr Otorhinolaryngol 2014 Jun 27;78(6):944-9. Epub 2014 Mar 27.

Department of Pediatrics, Section of Metabolic Disorders, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.ijporl.2014.03.021DOI Listing
June 2014

Cobalamin C defect: a patient of late-onset type with homozygous p.R132* mutation.

Turk J Pediatr 2013 Nov-Dec;55(6):633-6

Division of Hacettepe University Faculty of Medicine, Ankara, Turkey, and 3University Children's Hospital, Basel, Switzerland.

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August 2014

Serum alpha-fetoprotein levels in neonatal cholestasis.

Turk J Pediatr 2013 Mar-Apr;55(2):152-7

Division of Pediatric Gastroenterology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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December 2013

Pregnancy and lactation outcomes in a Turkish patient with lysinuric protein intolerance.

JIMD Rep 2014 20;13:33-6. Epub 2013 Oct 20.

Division of Metabolism, Department of Pediatrics, Hacettepe University, İhsan Doğramacı Children's Hospital, Ankara, Turkey,

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http://dx.doi.org/10.1007/8904_2013_259DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110330PMC
July 2014

Galactosemia in the Turkish population with a high frequency of Q188R mutation and distribution of Duarte-1 and Duarte-2 variations.

J Hum Genet 2013 Oct 8;58(10):675-8. Epub 2013 Aug 8.

1] Metabolism Unit, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey [2] Institute of Child Health, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1038/jhg.2013.76DOI Listing
October 2013

Detection of other inborn errors of metabolism in hyperphenylalaninemic babies picked up on narrow-spectrum screening programs.

Turk J Pediatr 2012 Jul-Aug;54(4):409-12

Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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August 2013

Genetic basis of hyperlysinemia.

Orphanet J Rare Dis 2013 Apr 9;8:57. Epub 2013 Apr 9.

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Academic Medical Center, University of Amsterdam, Meibergdreef 9, Amsterdam, AZ 1105, The Netherlands.

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http://dx.doi.org/10.1186/1750-1172-8-57DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626681PMC
April 2013

Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance.

Gene 2013 Jun 28;521(2):293-5. Epub 2013 Mar 28.

Metabolism Unit, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.gene.2013.03.033DOI Listing
June 2013

A rare galactosemia complication: vitreous hemorrhage.

JIMD Rep 2012 11;5:89-93. Epub 2011 Dec 11.

Neonatology Unit, Hacettepe University Ihsan Dogramaci Children's Hospital, 06100, Ankara, Turkey,

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http://dx.doi.org/10.1007/8904_2011_103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509908PMC
February 2013

Vanishing White Matter With Hepatomegaly and Hypertriglyceridemia Attacks.

J Child Neurol 2013 Nov 18;28(11):1509-1512. Epub 2012 Sep 18.

1Department of Pediatrics, Hacettepe University, Division of Metabolism and Nutrition, Ankara, Turkey.

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http://dx.doi.org/10.1177/0883073812458711DOI Listing
November 2013

A Patient With Pyruvate Carboxylase Deficiency and Nemaline Rods on Muscle Biopsy.

J Child Neurol 2013 Nov 10;28(11):1505-1508. Epub 2012 Sep 10.

1Department of Pediatrics, Division of Metabolism and Nutrition, Fellow of Metabolism, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1177/0883073812458710DOI Listing
November 2013

Microarray based mutational analysis of patients with methylmalonic acidemia: identification of 10 novel mutations.

Mol Genet Metab 2012 Aug 1;106(4):419-23. Epub 2012 Jun 1.

Metabolism Unit, Department of Pediatrics, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.ymgme.2012.05.014DOI Listing
August 2012

When do we need to perform a diagnostic lumbar puncture for neurometabolic diseases? Positive yield and retrospective analysis from a tertiary center.

Turk J Pediatr 2012 Jan-Feb;54(1):52-8

Unit of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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April 2012

Home visits in phenylketonuria: a 12-month longitudinal study.

Turk J Pediatr 2011 Mar-Apr;53(2):149-53

Department of Nutrition and Dietetics, Faculty of Health Science, Ankara, Turkey.

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November 2011

Gyrate atrophy of the choroid and retina: a case report.

Turk J Pediatr 2011 Jan-Feb;53(1):94-6

Karaman State Hospital, Karaman, Turkey.

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June 2011

A novel mutation in the DGUOK gene in a Turkish newborn with mitochondrial depletion syndrome.

Turk J Pediatr 2011 Jan-Feb;53(1):79-82

Unit of Metabolism, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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June 2011

Zinc supplementation and TNF-α levels in vaccinated cardiac patients.

J Trace Elem Med Biol 2011 Apr 22;25(2):85-90. Epub 2011 Apr 22.

Unit of Social Pediatrics, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.jtemb.2011.03.002DOI Listing
April 2011

Antihyperlipidemic agents cause a decrease in von Willebrand factor levels in pediatric patients with familial hyperlipidemia.

J Pediatr Endocrinol Metab 2010 Aug;23(8):765-71

Hacettepe University Faculty of Medicine Department ofPediatrics, 06100, Ankara, Turkey.

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http://dx.doi.org/10.1515/jpem.2010.126DOI Listing
August 2010

The urinary cotinine levels of infants and the determinants.

Turk J Pediatr 2010 May-Jun;52(3):294-300

Dr. Sami Ulus Children's and Maternity Training and Research Hospital, Ankara, Turkey.

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September 2010

The relationship between vitamin D receptor gene polymorphisms and bone density, osteocalcin level and growth in adolescents.

J Pediatr Endocrinol Metab 2010 May;23(5):491-6

Health Ministry Ankara Diskapi Children's Hospital, Infancy Service, Turkey.

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http://dx.doi.org/10.1515/jpem.2010.080DOI Listing
May 2010

L-2-hydroxyglutaric aciduria and brain tumors.

Authors:
Turgay Coşkun

J Pediatr Hematol Oncol 2010 May;32(4):339-40; author reply 340

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http://dx.doi.org/10.1097/MPH.0b013e3181d74596DOI Listing
May 2010

Maternal and environmental determinants of breast-milk mercury concentrations.

Turk J Pediatr 2010 Jan-Feb;52(1):1-9

Department of Pediatrics, Hacettepe University, Faculty of Medicine, Ankara, Turkey.

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May 2010

3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures.

Turk J Pediatr 2009 Nov-Dec;51(6):587-92

Unit of Metabolism and Nutrition, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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March 2010

Molecular genetics of maple syrup urine disease in the Turkish population.

Turk J Pediatr 2009 Mar-Apr;51(2):97-102

Department of General Pediatrics, Heinrich-Heine University, Düsseldorf, Germany.

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June 2009

Effect of passive smoking on growth and infection rates of breast-fed and non-breast-fed infants.

Pediatr Int 2009 Jun 26;51(3):352-8. Epub 2008 Nov 26.

Department of Pediatrics, Keçiören Training and Research Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1111/j.1442-200X.2008.02757.xDOI Listing
June 2009

Two new cases with Pearson syndrome and review of Hacettepe experience.

Turk J Pediatr 2008 Nov-Dec;50(6):572-6

Unit of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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March 2009

Prevalence of cystinuria among elementary schoolchildren in Eskisehir, Turkey.

Scand J Urol Nephrol 2009 ;43(2):138-41

Department of Pediatrics, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.

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http://dx.doi.org/10.1080/00365590802625060DOI Listing
May 2009

The effect of passive smoking and breast feeding on serum antioxidant vitamin (A, C, E) levels in infants.

Acta Paediatr 2009 Mar 29;98(3):531-6. Epub 2008 Oct 29.

Department of Pediatrics, Keciören Training and Research Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1111/j.1651-2227.2008.01084.xDOI Listing
March 2009

Vitamin D receptor gene polymorphisms in Turkish children with vitamin D deficient rickets.

Turk J Pediatr 2008 Jan-Feb;50(1):30-3

Departments of Medical Biology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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May 2008

Pearson syndrome associated with hemophagocytic syndrome in a child.

Turk J Haematol 2008 Mar;25(1):54-5

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March 2008

Neonatal non-ketotic hyperglycinemia: report of five cases.

Pediatr Int 2008 Feb;50(1):121-3

Department of Neonatology, Dr Sami Ulus Children's Hospital, Ankara, Turkey.

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http://doi.wiley.com/10.1111/j.1442-200X.2007.02513.x
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http://dx.doi.org/10.1111/j.1442-200X.2007.02513.xDOI Listing
February 2008

Lymphocytic vacuolization in sialic acid storage disease.

Am J Hematol 2008 Oct;83(10):821

Division of Pediatric Hematology, Faculty of Medicine, Hacettepe University, Sihhiye, Ankara, Turkey.

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http://dx.doi.org/10.1002/ajh.21097DOI Listing
October 2008

Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents.

Pediatr Hematol Oncol 2007 Sep;24(6):453-5

Department of Pediatric Hematology, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1080/08880010701451293DOI Listing
September 2007

Serum zinc levels in children with acute gastroenteritis.

Pediatr Int 2007 Jun;49(3):314-7

Division of Child Neurology, Department of Pediatrics, Hacettepe University Facutly of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1111/j.1442-200X.2007.02371.xDOI Listing
June 2007

Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient.

Turk J Pediatr 2007 Jan-Mar;49(1):75-6

Unit of Nutrition and Metabolism, Department of Pediatrics, Hacettepe University, Faculty of Medicine, Ankara, Turkey.

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May 2007

Assessment of tetrahydrobiopterin responsiveness in Turkish hyperphenylalaninemic patients.

Turk J Pediatr 2007 Jan-Mar;49(1):1-6

Nutrition and Metabolism Unit, Department of Pediatrics, Hacettepe University, Faculty of Medicine, Ankara, Turkey.

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May 2007

The relationship between serum selenium levels and frequent wheeze in children.

Turk J Pediatr 2006 Oct-Dec;48(4):308-12

Unit of Pediatric Allergy and Asthma, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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April 2007

A newborn with VLCAD deficiency. Clinical, biochemical, and histopathological findings.

Eur J Pediatr 2007 Oct 6;166(10):1077-80. Epub 2007 Jan 6.

Faculty of Medicine, Department of Pediatrics, Neonatology Unit, University of Kirikkale, Kirikkale, Turkey.

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http://dx.doi.org/10.1007/s00431-006-0350-6DOI Listing
October 2007

Plasma free carnitine levels in 0-12-month-old infants in relation to feeding styles.

Int J Vitam Nutr Res 2006 May;76(3):117-23

Kirikkale University Faculty of Medicine, Department of Pediatrics, Turkey.

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http://dx.doi.org/10.1024/0300-9831.76.3.117DOI Listing
May 2006

Haematological findings in children with inborn errors of metabolism.

J Inherit Metab Dis 2006 Oct 12;29(5):607-11. Epub 2006 Aug 12.

Pediatric Hematology Unit, Hacettepe University School of Medicine, Ankara, Turkey,

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http://link.springer.com/10.1007/s10545-006-0379-8
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http://dx.doi.org/10.1007/s10545-006-0379-8DOI Listing
October 2006

Fanconi-Bickel syndrome in three Turkish patients with different homozygous mutations.

Turk J Pediatr 2005 Apr-Jun;47(2):167-9

Section of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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September 2005

Neurophysiologic features in glutaric aciduria type I.

Turk J Pediatr 2005 Apr-Jun;47(2):153-8

Section of Pediatric Neurology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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September 2005

Repetitive EEG recordings are necessary for the diagnosis of early myoclonic encephalopathy.

Neurol India 2005 Jun;53(2):235-7

Department of Pediatric, Pediatric Neurology Unit, Hacettepe University Faculty of Medicine, Turkey.

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http://dx.doi.org/10.4103/0028-3886.16423DOI Listing
June 2005

Two cases of glycine encephalopathy accompanied by pes equinovarus.

J Child Neurol 2005 Jun;20(6):533-5

Department of Neonatology, Sami Ulus Children's Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1177/08830738050200061301DOI Listing
June 2005

L-2-hydroxyglutaric aciduria: a report of 29 patients.

Turk J Pediatr 2005 Jan-Mar;47(1):1-7

Section of Neurology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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June 2005

The molecular basis of familial hypercholesterolaemia in Turkish patients.

Atherosclerosis 2005 May;180(1):63-71

Centre for Cardiovascular Genetics, British Heart Foundation Laboratories, Rayne Building, Royal Free and University College London Medical School, London WC1E 6JJ, UK.

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http://dx.doi.org/10.1016/j.atherosclerosis.2004.12.042DOI Listing
May 2005

Molybdenum cofactor deficiency presenting with severe metabolic acidosis and intracranial hemorrhage.

J Child Neurol 2005 Feb;20(2):155-7

Department of Pediatrics, Hacettepe University School of Medicine, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1177/08830738050200021501DOI Listing
February 2005

Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletion.

J Child Neurol 2005 Jan;20(1):83-4

Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1177/08830738050200011304DOI Listing
January 2005

Plasma carnitine levels in preterm infants with respiratory distress syndrome.

Pediatr Int 2005 Feb;47(1):49-52

University of Hacettepe, Ihsan Dogramaci Children's Hospital, Neonatology Unit, Ankara, Turkey.

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http://dx.doi.org/10.1111/j.1442-200x.2005.01998.xDOI Listing
February 2005

L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1.

Hum Mol Genet 2004 Nov 22;13(22):2803-11. Epub 2004 Sep 22.

Department of Pediatrics, Child Neurology, Hacettepe University Medical Faculty, Ankara, Turkey.

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http://dx.doi.org/10.1093/hmg/ddh300DOI Listing
November 2004

A boy with spastic paraparesis and dyspnea.

J Child Neurol 2004 May;19(5):397-8

Department of Pediatrics, Section of Nutrition and Metabolism, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1177/088307380401900517DOI Listing
May 2004

Refeeding problems in a severe anorexia nervosa case.

Int J Adolesc Med Health 2004 Jan-Mar;16(1):65-9

Department of Pediatrics, Adolescent Unit, Metabolism and Nutrition Unit, Department of Child and Adolescent Psychiatry, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1515/ijamh.2004.16.1.65DOI Listing
August 2004

Serum selenium levels in acute gastroenteritis of possible viral origin.

J Trop Pediatr 2004 04;50(2):78-81

Hacettepe University, Ihsan Doğramaci Children's Hospital, Department of Pediatric Neurology, Ankara, Turkey.

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http://dx.doi.org/10.1093/tropej/50.2.78DOI Listing
April 2004

Effect of topiramate on enlargement of head in Canavan disease: a new option for treatment of megalencephaly.

Turk J Pediatr 2004 Jan-Mar;46(1):67-71

Section of Neurology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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June 2004

Is vitamin D hypothesis for schizophrenia valid? Independent segregation of psychosis in a family with vitamin-D-dependent rickets type IIA.

Prog Neuropsychopharmacol Biol Psychiatry 2004 Mar;28(2):255-66

Department of Psychiatry, Faculty of Medicine, Hacettepe University, 06100 Sihhiye, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.pnpbp.2003.10.002DOI Listing
March 2004

Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children.

Pediatr Nephrol 2003 Dec 30;18(12):1255-9. Epub 2003 Oct 30.

Unit of Pediatric Nephrology, Hacettepe University, Ankara, Turkey,

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http://dx.doi.org/10.1007/s00467-003-1264-4DOI Listing
December 2003

Immune function in children with classical phenylketonuria and tetrahydrobiopterin deficiencies.

Indian Pediatr 2003 Sep;40(9):822-33

Nutrition and Metabolism Unit, Department of Pediatrics, Hacettepe University Faculty of Medicine, Sihhiye, Ankara 06100, Turkey. ktevfik@ hotmail.com

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September 2003

Factors playing a role in the development of decreased bone mineral density in juvenile chronic arthritis.

Rheumatol Int 2003 May 12;23(3):127-9. Epub 2003 Mar 12.

Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Hacettepe University, 06100 Sihhiye, Ankara, Turkey.

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http://dx.doi.org/10.1007/s00296-002-0265-0DOI Listing
May 2003