Publications by authors named "Meral Topcu"

89Publications

International consensus classification of hippocampal sclerosis and etiologic diversity in children with temporal lobectomy.

Epilepsy Behav 2020 Aug 31;112:107380. Epub 2020 Aug 31.

Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.yebeh.2020.107380DOI Listing
August 2020

Long-term effects of vagus nerve stimulation in refractory pediatric epilepsy: A single-center experience.

Epilepsy Behav 2020 Sep 27;110:107147. Epub 2020 Jun 27.

Hacettepe University Faculty of Medicine, Department of Pediatric Neurology; currently retired from Hacettepe University, Department of Pediatric Neurology.

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http://dx.doi.org/10.1016/j.yebeh.2020.107147DOI Listing
September 2020

Genetic and phenotypic features of patients with childhood ataxias diagnosed by next-generation sequencing gene panel.

Brain Dev 2020 Jan 4;42(1):6-18. Epub 2019 Sep 4.

Hacettepe University, School of Medicine, Department of Child Neurology, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.braindev.2019.08.004DOI Listing
January 2020

Prenatal enzymatic diagnosis of lysosomal storage diseases using cultured amniotic cells, uncultured chorionic villus samples, and fetal blood cells: Hacettepe experience.

Prenat Diagn 2019 11 22;39(12):1080-1085. Epub 2019 Aug 22.

Division of Perinatology, Department of Obstetrics and Gynecology, Hacettepe University, Ankara, Turkey.

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http://dx.doi.org/10.1002/pd.5547DOI Listing
November 2019

The experience of allogeneic hematopoietic stem cell transplantation in a patient with X-linked adrenoleukodystrophy.

Transfus Apher Sci 2020 Feb 22;59(1):102583. Epub 2019 Jul 22.

Hacettepe Universty, Faculty of Medicine, Department of Hematology, Turkey.

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http://dx.doi.org/10.1016/j.transci.2019.06.019DOI Listing
February 2020

Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defect.

J Inherit Metab Dis 2019 03 30;42(2):381-388. Epub 2019 Jan 30.

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

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http://dx.doi.org/10.1002/jimd.12016DOI Listing
March 2019

Mystery Case: Pontine tegmental cap dysplasia in a neonate.

Neurology 2018 11;91(22):e2100-e2101

From the Departments of Pediatric Neurology (N.B., M.T., H.T.) and Pediatric Genetics (P.O.S.-K.), Hacettepe University Ihsan Dogramaci Children's Hospital; and Department of Radiology (S.P.), Hacettepe University Hospitals, Ankara, Turkey.

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http://dx.doi.org/10.1212/WNL.0000000000006578DOI Listing
November 2018

Neurologic Involvement in Primary Immunodeficiency Disorders.

J Child Neurol 2018 04 8;33(5):320-328. Epub 2018 Feb 8.

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

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http://dx.doi.org/10.1177/0883073817754176DOI Listing
April 2018

Niemann-Pick disease type C in the newborn period: a single-center experience.

Eur J Pediatr 2017 Dec 27;176(12):1669-1676. Epub 2017 Sep 27.

Department of Pediatric Gastroenterology, Hacettepe University Children's Hospital, Sihhiye, 06100, Ankara, Turkey.

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http://dx.doi.org/10.1007/s00431-017-3020-yDOI Listing
December 2017

Childhood hereditary ataxias: experience from a tertiary referral university hospital in Turkey.

Acta Neurol Belg 2017 Dec 29;117(4):857-865. Epub 2017 Apr 29.

Department of Pediatric Neurology, Hacettepe University School of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1007/s13760-017-0786-7DOI Listing
December 2017

Evaluation of central nervous system in patients with glycogen storage disease type 1a.

Turk J Pediatr 2016 ;58(1):12-18

Divisions of Pediatric Gastroenterology and Hepatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.24953/turkjped.2016.01.002DOI Listing
May 2017

Otorhinolaryngological, audiovestibular and swallowing manifestations of patients with Niemann-Pick disease Type C.

Int J Pediatr Otorhinolaryngol 2016 Jan 23;80:1-4. Epub 2015 Nov 23.

Hacettepe University School of Medicine, Department of Physical Therapy and Rehabilitation, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.ijporl.2015.11.009DOI Listing
January 2016

The seizure semiology consistent with frontal lobe symptomatogenic zone in children.

Turk J Pediatr 2016 ;58(6):583-591

Division of Pediatric Neurology, Deparment of Pediatrics, Istanbul Medipol University, Istanbul, Turkey.

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http://dx.doi.org/10.24953/turkjped.2016.06.003DOI Listing
January 2016

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

Vertigo in childhood: a retrospective series of 100 children.

Eur J Paediatr Neurol 2015 Mar 18;19(2):226-32. Epub 2014 Dec 18.

Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2014.12.009DOI Listing
March 2015

Somatic mutations in cerebral cortical malformations.

N Engl J Med 2014 Aug;371(8):733-43

From the Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Howard Hughes Medical Institute (S.S.J., A.-T.N.L., A.M.D., B.J.B., X.Z., R.S.H., J.N.P., A.R., S.S., B.K.M., T.W.Y., C.A.W.), and the Departments of Laboratory Medicine (J.W., Y.S., B.L.W.) and Neurology (M.S., A.P.), Boston Children's Hospital, the Departments of Pediatrics (S.S.J., A.-T.N.L., A.M.D., B.J.B., X.Z., R.S.H., J.N.P., A.R., S.S., B.K.M., T.W.Y., C.A.W.), Neurology (S.S.J., A.-T.N.L., A.M.D., B.J.B., X.Z., R.S.H., J.N.P., A.R., S.S., B.K.M., T.W.Y., C.A.W., M.S., A.P.), and Pathology (Y.S., B.L.W.), Harvard Medical School, the Department of Neurology, Beth Israel Deaconess Medical Center (B.S.C.), and the Department of Neurology, Massachusetts General Hospital (T.W.Y.) - all in Boston; the Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore (S.S.J.); the Department of Genome Sciences, University of Washington, Seattle (M.K., M.B., D.A.N., J.S.); the Department of Laboratory Medicine, Shanghai Children's Medical Center, Shanghai (J.W., Y.S.); the Division of Neurology, Department of Pediatrics, Hacettepe University School of Medicine, Sihhiye, Ankara, Turkey (M.T.); the Neurogenetics Unit, Montreal Neurological Hospital and Institute, Department of Neurology and Neurosurgery (D.A., E.A.) and Department of Human Genetics (E.A.), McGill University, Montreal; the Department of Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, Brussels (B.D.); the Pediatric Neurology Unit and Laboratories, Children's Hospital A. Meyer-University of Florence, Florence, Italy (E.P., R.G.); the Department of Medicine, University of Melbourne, Austin Health, Heidelberg (I.E.S., S.F.B.), Department of Paediatrics, Royal Children's Hospital, University of Melbourne, and the Florey Institute of Neuroscience and Mental Health, Melbourne (I.E.S.), and the Department of Neurology, Royal Children's Hospital, Murdoch Children'

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http://dx.doi.org/10.1056/NEJMoa1314432DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274952PMC
August 2014

Successful treatment of cataplexy in patients with early-infantile Niemann-Pick disease type C: use of tricyclic antidepressants.

Eur J Paediatr Neurol 2014 Nov 6;18(6):811-5. Epub 2014 Aug 6.

Pediatric Neurology, Hacettepe University Children's Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.ejpn.2014.07.009DOI Listing
November 2014

Electrical status epilepticus during sleep: a study of 22 patients.

Brain Dev 2015 Feb 9;37(2):250-64. Epub 2014 May 9.

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

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http://dx.doi.org/10.1016/j.braindev.2014.04.007DOI Listing
February 2015

Usefulness of long-term video-EEG monitoring in children at a tertiary care center.

Turk J Pediatr 2013 Nov-Dec;55(6):591-7

Royal College of Surgeons in Ireland, Dublin, Ireland, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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August 2014

Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning.

Science 2014 Feb;343(6172):764-8

Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Broad Institute of MIT and Harvard, and Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.1126/science.1244392DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480613PMC
February 2014

Etiological yield of SNP microarrays in idiopathic intellectual disability.

Eur J Paediatr Neurol 2014 May 25;18(3):327-37. Epub 2014 Jan 25.

Hacettepe University, Department of Pediatric Genetics, Ankara, Turkey; Hacettepe University, Department of Medical Genetics, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.ejpn.2014.01.004DOI Listing
May 2014

Health-related quality of life in adolescents with psychogenic nonepileptic seizures.

Epilepsy Behav 2013 Dec 11;29(3):516-20. Epub 2013 Oct 11.

Department of Child and Adolescent Psychiatry, Hacettepe University Faculty of Medicine, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.yebeh.2013.09.015DOI Listing
December 2013

Treatment of a severe conversion disorder in a 10-year-old boy: a case study and overview.

Turk J Pediatr 2012 Jul-Aug;54(4):413-8

Department of Child and Adolescent Psychiatry, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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August 2013

Developmental abnormalities and mental retardation: diagnostic strategy.

Handb Clin Neurol 2013 ;111:211-7

Child Neurology Section, Department of Pediatrics, Hacettepe University, Ankara, Turkey. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-52891-9.00021-XDOI Listing
April 2014

Childhood disabilities: reappraisal in the high-tech era.

Authors:
Meral Topçu

Dev Med Child Neurol 2012 Jun;54(6):483

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http://dx.doi.org/10.1111/j.1469-8749.2012.04311.xDOI Listing
June 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

Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosis.

Clin Biochem 2012 May 3;45(7-8):571-4. Epub 2012 Jan 3.

Department of Medical Biochemistry, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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https://linkinghub.elsevier.com/retrieve/pii/S00099120110278
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http://dx.doi.org/10.1016/j.clinbiochem.2011.12.019DOI Listing
May 2012

Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote man.

Clin Biochem 2011 Jul 4;44(10-11):809-12. Epub 2011 May 4.

Hacettepe University, Faculty of Medicine, Department of Medical Biochemistry, 06100, Ankara, Turkey.

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http://linkinghub.elsevier.com/retrieve/pii/S000991201100327
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http://dx.doi.org/10.1016/j.clinbiochem.2011.04.022DOI Listing
July 2011

Novel mutations of the MLC1 gene in Turkish patients.

Eur J Med Genet 2011 May-Jun;54(3):281-3. Epub 2010 Dec 9.

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

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http://dx.doi.org/10.1016/j.ejmg.2010.11.014DOI Listing
September 2011

Mutations in PNKP cause microcephaly, seizures and defects in DNA repair.

Nat Genet 2010 Mar 31;42(3):245-9. Epub 2010 Jan 31.

[1] Howard Hughes Medical Institute, Department of Neurology, Beth Israel Deaconess Medical Center and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts, USA. [2] These authors contributed equally to the work.

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http://dx.doi.org/10.1038/ng.526DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2835984PMC
March 2010

Structural abnormalities of the brain other than molar tooth sign in Joubert syndrome-related disorders.

Diagn Interv Radiol 2010 Mar 27;16(1):3-6. Epub 2010 Jan 27.

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

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http://dx.doi.org/10.4261/1305-3825.DIR.2673-09.1DOI Listing
March 2010

Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.

Brain 2009 Mar 5;132(Pt 3):810-9. Epub 2009 Feb 5.

Folkhälsan Institute of Genetics, Department of Medical Genetics and Neuroscience Center, University of Helsinki, Finland.

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http://dx.doi.org/10.1093/brain/awn366DOI Listing
March 2009

Lamotrigine in children with refractory epilepsy.

Turk J Pediatr 2008 Sep-Oct;50(5):426-31

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

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January 2009

Surgery for epilepsy in children with dysembryoplastic neuroepithelial tumor: clinical spectrum, seizure outcome, neuroradiology, and pathology.

Childs Nerv Syst 2009 Apr 5;25(4):485-91. Epub 2008 Dec 5.

Department of Neurosurgery, Hacettepe University School of Medicine, 06100, Ankara, Turkey.

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http://link.springer.com/10.1007/s00381-008-0762-x
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http://dx.doi.org/10.1007/s00381-008-0762-xDOI Listing
April 2009

Osteoid osteoma in a 16-year-old boy presenting with atrophy of the left thigh: diagnostic difficulties.

Turk J Pediatr 2008 Jul-Aug;50(4):373-6

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

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December 2008

Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy.

Neurol Res 2009 Feb 3;31(1):60-6. Epub 2008 Sep 3.

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

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http://dx.doi.org/10.1179/016164108X323762DOI Listing
February 2009

Recurrent pseudotumoral hemicerebellitis: neuroimaging findings.

Pediatr Radiol 2008 Apr 8;38(4):462-6. Epub 2008 Jan 8.

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

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http://dx.doi.org/10.1007/s00247-007-0725-5DOI Listing
April 2008

Malformations of cortical development and epilepsy: evaluation of 101 cases (part II).

Turk J Pediatr 2007 Apr-Jun;49(2):131-40

Department of Pediatrics, Inönü University, Faculty of Medicine, Malatya, Turkey.

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November 2007

Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I).

Turk J Pediatr 2007 Apr-Jun;49(2):120-30

Department of Pediatrics, Inönü University Faculty of Medicine, Malatya, Turkey.

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http://www.diclemedj.org/upload/sayi/33/Dicle%20Med%20J-0220
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November 2007

Impact of recent seizures on cerebral blood flow in patients with sturge-weber syndrome: study of 2 cases.

J Child Neurol 2007 May;22(5):617-20

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

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http://dx.doi.org/10.1177/0883073807302597DOI Listing
May 2007

The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter.

Am J Hum Genet 2007 Jul 14;81(1):136-46. Epub 2007 May 14.

Folkhälsan Institute of Genetics, Biomedicum Helsinki, P.O. Box 63 (Haartmaninkatu 8), 00014 University of Helsinki, Helsinki, Finland.

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http://dx.doi.org/10.1086/518902DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950917PMC
July 2007

Neurologic outcome in patients with MRI pattern of damage typical for neonatal hypoglycemia.

Brain Dev 2007 Jun 8;29(5):285-92. Epub 2006 Dec 8.

Department of Pediatrics, Section of Pediatric Neurology, Hacettepe University Medical Faculty, Ihsan Doğramaci Children's Hospital, Sihhiye 06100, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.braindev.2006.09.011DOI Listing
June 2007

Vigabatrin in pediatric patients with refractory epilepsy.

Turk J Pediatr 2006 Jan-Mar;48(1):25-30

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

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April 2006

Outcome and long term follow-up after corpus callosotomy in childhood onset intractable epilepsy.

Childs Nerv Syst 2006 Oct 14;22(10):1322-7. Epub 2006 Mar 14.

Division of Pediatrics, Section of Pediatric Neurology, Hacettepe University Medical Faculty, Ihsan Doğramaci Children's Hospital, 06100, Sihhiye, Ankara, Turkey.

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http://dx.doi.org/10.1007/s00381-006-0045-3DOI Listing
October 2006

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.

Ann Neurol 2005 Nov;58(5):680-7

Division of Newborn Medicine, Department of Medicine, Children's Hospital Boston and Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.1002/ana.20616DOI Listing
November 2005

Streptococcus oralis as a risk factor for middle cerebral artery thrombosis.

J Child Neurol 2005 Jul;20(7):611-3

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

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http://dx.doi.org/10.1177/08830738050200071401DOI Listing
July 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

Benign familial infantile convulsions: phenotypic variability in a family.

J Child Neurol 2005 Jun;20(6):535-8

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

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http://dx.doi.org/10.1177/08830738050200061401DOI 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

Surgical management of temporal lobe tumor-related epilepsy in children.

J Neurosurg 2005 Apr;102(3 Suppl):280-7

Departments of Neurosurgery and Pediatric Neurology, Hacettepe University Medical School, Ankara, Turkey.

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http://dx.doi.org/10.3171/ped.2005.102.3.0280DOI Listing
April 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

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Nat Genet 2004 Sep 22;36(9):1008-13. Epub 2004 Aug 22.

Division of Neurogenetics and Howard Hughes Medical Institute, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, NRB 266, 77 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA.

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http://dx.doi.org/10.1038/ng1419DOI Listing
September 2004

Sphingolipidoses in Turkey.

Brain Dev 2004 Sep;26(6):363-6

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

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http://dx.doi.org/10.1016/j.braindev.2003.09.006DOI Listing
September 2004

The prognosis and survival of childhood acute lymphoblastic leukemia with central nervous system relapse.

Pediatr Hematol Oncol 2004 Apr-May;21(3):279-89

Hacettepe University, Faculty of Medicine, Department of Pediatrics, Pediatric Hematology and Neurology Unit, 06100 Ankara, Turkey.

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http://www.tandfonline.com/doi/full/10.1080/0888001049027709
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http://dx.doi.org/10.1080/08880010490277097DOI Listing
October 2004

Infantile convulsions and paroxysmal choreoathetosis in a consanguineous family.

Pediatr Neurol 2004 May;30(5):349-53

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

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http://dx.doi.org/10.1016/j.pediatrneurol.2003.11.003DOI Listing
May 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

Benign neonatal sleep myoclonus mimicking status epilepticus.

J Child Neurol 2004 Jan;19(1):62-3

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

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http://dx.doi.org/10.1177/08830738040190010708DOI Listing
January 2004

Clinical, electrophysiological and neuropsychological findings of twenty-two children with mesial temporal sclerosis.

Turk J Pediatr 2003 Jul-Sep;45(3):221-30

Department of Child Neurology, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey.

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February 2004

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Nat Genet 2004 Jan 30;36(1):69-76. Epub 2003 Nov 30.

Division of Neurogenetics and Howard Hughes Medical Institute, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, USA.

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http://dx.doi.org/10.1038/ng1276DOI Listing
January 2004

Stroke owing to noncompaction of myocardium.

J Child Neurol 2003 Jun;18(6):437-9

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

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http://jcn.sagepub.com/content/18/6/437.full.pdf
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http://dx.doi.org/10.1177/08830738030180061501DOI Listing
June 2003

Biochemical and molecular characterization of mutant hexosaminidase A in a Turkish family.

Pediatr Int 2003 Feb;45(1):16-22

Departments of Biochemistry, Hacettepe University Faculty of Medicine, 06100 Ankara, Turkey.

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http://dx.doi.org/10.1046/j.1442-200x.2003.01669.xDOI Listing
February 2003

Hydrotherapy for Rett syndrome.

J Rehabil Med 2003 Jan;35(1):44-5

School of Physical Therapy and Rehabilitation, Hacettepe University, TR-06100 Samanpazari, Ankara, Turkey.

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http://dx.doi.org/10.1080/16501970306107DOI Listing
January 2003

Willingness to participate in clinical treatment research among older African Americans and Whites.

Gerontologist 2003 Feb;43(1):62-72

University of Medicine and Dentistry of New Jersey, Newark 07107, USA.

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http://dx.doi.org/10.1093/geront/43.1.62DOI Listing
February 2003

Gender prevalence in childhood multiple sclerosis and myasthenia gravis.

J Child Neurol 2002 May;17(5):390-2

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

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http://dx.doi.org/10.1177/088307380201700516DOI Listing
May 2002

Evoked potentials in children with Wilson's disease.

Brain Dev 2002 Aug;24(5):276-80

Department of Pediatric Neurology, Hacettepe University Hospitals, Ankara, Turkey.

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http://dx.doi.org/10.1016/s0387-7604(02)00055-4DOI Listing
August 2002

Medulloblastoma in a child with the metabolic disease L-2-hydroxyglutaric aciduria.

Pediatr Neurosurg 2002 Jul;37(1):22-6

Department of Neurosurgery, Pediatric Neurology Unit, Hacettepe University School of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1159/000065097DOI Listing
July 2002

Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.

Eur J Hum Genet 2002 Jan;10(1):77-81

Department of Pediatric Neurology, Hacettepe University School of Medicine, Sihhiye, Ankara 0600, Turkey.

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http://dx.doi.org/10.1038/sj.ejhg.5200745DOI Listing
January 2002

The effect of hand splints on stereotypic hand behavior in Rett's syndrome.

Turk J Pediatr 2002 Jan-Mar;44(1):25-9

School of Physical Therapy and Rehabilitation, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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March 2002