Doç. Dr. Özdem Ertürk Çetin

Challenges in diagnosing SSPE

Child's Nervous System, 2011

DOI 10.1007/s00381-011-1603-x PMID 22002104 11 atıf (Europe PMC) Kaynak: ORCID

Hypomyelination and Congenital Cataract Broadening the Clinical Phenotype

Archives of Neurology, 2011

DOI 10.1001/archneurol.2011.201 PMID 21911699 24 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting Dystrophin

American Journal of Medical Genetics Part A, 2010

DOI 10.1002/ajmg.a.33312 PMID 20358624 8 atıf (Europe PMC) Kaynak: OpenAlex

Four Novel SCN1A Mutations in Turkish Patients With Severe Myoclonic Epilepsy of Infancy (SMEI)

Journal of Child Neurology, 2010

DOI 10.1177/0883073809357241 PMID 20110217 4 atıf (Europe PMC) Kaynak: OpenAlex

Adult-Onset Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Normal Lactate: Case Report

Turk Noroloji Dergisi / Turkish Journal of Neurology, 2010

Kaynak: ORCID

Efficacy of Nebivolol and Amitriptyline in the Prophylaxis of Cyclic Vomiting Syndrome A Case Report

Neurologist, 2010

DOI 10.1097/nrl.0b013e3181b120a6 PMID 20827121 7 atıf (Europe PMC) Kaynak: ORCID

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy

Neurogenetics, 2010

DOI 10.1007/s10048-009-0232-y PMID 20082205 21 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

Apraxia in Parkinson’s disease and multiple system atrophy

European Journal of Neurology, 2009

DOI 10.1111/j.1468-1331.2009.02905.x PMID 20050896 13 atıf (Europe PMC) Kaynak: OpenAlex

Assessment of praxis function in patients with multiple system atrophy

Movement Disorders, 2009

Kaynak: ORCID

THE ROLE OF PET IN MRI NEGATIVE EPILEPSIES

Epilepsia, 2009

Kaynak: ORCID