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List of works by Cengiz Yalcinkaya

A close look at EEG in subacute sclerosing panencephalitis

scientific article

A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?

scientific article published on 19 May 2012

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

scientific article published on 01 April 2010

A study on visual evoked responses in childhood epilepsy with occipital paroxysms

scientific article published on 01 June 2000

Alterations in cell-mediated immune response in subacute sclerosing panencephalitis

scientific article published on 11 October 2005

Anxiety and depression in children with epilepsy and their mothers

scientific article published in December 2004

Atypical MRI findings in Canavan disease: a patient with a mild course

scientific article

Beneficial Effects of Everolimus on Autism and Attention-Deficit/Hyperactivity Disorder Symptoms in a Group of Patients with Tuberous Sclerosis Complex.

scientific article published on 31 October 2016

Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study

scientific article

CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration

scientific article

Cerebrotendinous xanthomatosis: the effectiveness of high-dose piracetam for the treatment of cerebellar and sensorial ataxia.

scientific article published in December 2014

Challenges in diagnosing SSPE.

scientific article published on 15 October 2011

Clinical and neuroradiological approach to fucosidosis in a child with atypical presentation

scientific article

Clinical characteristics of 49 patients with psychogenic movement disorders in a tertiary clinic in Turkey

scientific article published in April 2009

Deficiency of alkaline ceramidase 3 with infancy-onset progressive leukoencephalopathy: a second case report

scientific article published on 20 August 2020

Delayed-onset dystonia associated with 3-oxothiolase deficiency

scientific article published in March 2001

Dysembryoplastic neuroepithelial tumors and gangliogliomas: clinical results of 52 patients

scientific article

Early diagnosed cerebrotendinous xanthomatosis patients: clinical, neuroradiological characteristics and therapy results of a single center from Turkey.

scientific article published on 22 October 2017

Elevated interleukin-12 and CXCL10 in subacute sclerosing panencephalitis

scientific article published on 13 October 2005

Epilepsy Surgery in Children with Lesional Partial Epilepsies

scientific article published on January 2015

Epilepsy in vacuolating megalencephalic leukoencephalopathy with subcortical cysts

scientific article published in September 2003

Familial Adult-onset Alexander Disease: Clinical and Neuroradiological Findings of Three Cases

scientific article published on June 2016

Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: relationship with hereditary fetal brain degeneration and fetal brain disruption sequence

scientific article published on July 2010

Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI)

scientific article published on 28 January 2010

Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia

scientific article published on 29 September 2009

High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease

scientific article

Hypomyelination and congenital cataract: broadening the clinical phenotype

scientific article

Ictal and interictal SPECT findings in childhood absence epilepsy

scientific article published on 01 June 2000

Identification of 3 Novel Patients with CLCN2-Related Leukoencephalopathy due to CLCN2 Mutations.

scientific article published on 26 July 2017

Inherited metabolic disorders in Turkish patients with autism spectrum disorders

scientific article published on 7 June 2015

MRI findings in pediatric neuro-Behçet's disease

scientific article published on 01 June 2004

MRI findings in succinic semialdehyde dehydrogenase deficiency

scientific article published on 01 February 2000

Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.

scientific article

Mucolipidosis type IV in a Turkish boy associated with a novel MCOLN1 mutation

scientific article

Neonatal nonketotic hyperglycinemia: diffusion-weighted magnetic resonance imaging and diagnostic clues

scientific article published on 24 December 2015

Neuroimaging findings of four patients with Sandhoff disease

scientific article published in August 1999

Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly

scientific article published on 15 April 2012

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population

scientific article published on 6 March 2008

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

scientific article published on 15 January 2010

Oxidative stress among L-2-hydroxyglutaric aciduria disease patients: evaluation of dynamic thiol/disulfide homeostasis

scientific article published on 29 November 2018

Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation

scientific article published on 29 July 2015

Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency

scientific article

Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome.

scientific article published on 29 January 2016

Progressive white-matter disease with primary cerebellar involvement: a separate entity?

scientific article published on 13 August 2002

Psychogenic movement disorders in two children

scientific article published on 01 November 2003

Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration

scientific article

Rhombencephalosynapsis: clinical findings and neuroimaging in 9 children.

scientific article published in August 2002

Seizures during treatment of Vitamin B12 deficiency

scientific article published on 5 December 2006

Siblings with cystic leukoencephalopathy and megalencephaly

scientific article published in October 2000

Two cases with progressive cystic leukoencephalopathy.

scientific article published in February 2009

Unilateral cerebellar and brain stem hypoplasia in a child with a postnatal diagnosis of dissecting aneurysm in basilar artery.

scientific article published on 6 August 2014

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