Cengiz Yalcinkaya

Summary

Affiliation: Istanbul University
Country: Turkey

Publications

  1. doi request reprint A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?
    Cengiz Yalcinkaya
    Istanbul University, Cerrahpasa Medical Faculty, Department of Neurology, Division of Child Neurology, Istanbul, Turkey
    Neuropediatrics 43:159-61. 2012
  2. ncbi request reprint Epilepsy in vacuolating megalencephalic leukoencephalopathy with subcortical cysts
    Cengiz Yalcinkaya
    Division of Child Neurology, Department of Neurology, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey
    Seizure 12:388-96. 2003
  3. doi request reprint A close look at EEG in subacute sclerosing panencephalitis
    Nurhak Demir
    Department of Neurology, Dokuz Eylül Faculty of Medicine, Dokuz Eylul Univercity, Inciralti, Izmir, Turkey
    J Clin Neurophysiol 30:348-56. 2013
  4. ncbi request reprint Alterations in cell-mediated immune response in subacute sclerosing panencephalitis
    Sibel P Yentür
    Department of Physiology, Istanbul Medical Faculty, Istanbul University, Turkey
    J Neuroimmunol 170:179-85. 2005
  5. doi request reprint Challenges in diagnosing SSPE
    Ozdem Erturk
    Department of Neurology, Cerrahpasa Faculty of Medicine, Istanbul University, 34098 Fatih, Istanbul, Turkey
    Childs Nerv Syst 27:2041-4. 2011
  6. doi request reprint Mucolipidosis type IV in a Turkish boy associated with a novel MCOLN1 mutation
    Beyhan Tuysuz
    Istanbul University, Cerrahpasa Medical Faculty, Department of Pediatric Genetics, Istanbul, Turkey
    Brain Dev 31:702-5. 2009
  7. ncbi request reprint Elevated interleukin-12 and CXCL10 in subacute sclerosing panencephalitis
    Guher Saruhan-Direskeneli
    Department of Physiology, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey
    Cytokine 32:104-10. 2005
  8. doi request reprint Epilepsy Surgery in Children with Lesional Partial Epilepsies
    Ozdem Erturk
    Istanbul University, Cerrahpasa School of Medicine, Department of Neurology, Istanbul, Turkey
    Turk Neurosurg 25:900-4. 2015
  9. doi request reprint Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features
    Beyhan Tuysuz
    Department of Pediatric Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey
    Am J Med Genet A 164:1677-85. 2014
  10. ncbi request reprint Beneficial Effects of Everolimus on Autism and Attention-Deficit/Hyperactivity Disorder Symptoms in a Group of Patients with Tuberous Sclerosis Complex
    Ayse Kilincaslan
    1 Department of Child and Adolescent Psychiatry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
    J Child Adolesc Psychopharmacol . 2016

Collaborators

Detail Information

Publications17

  1. doi request reprint A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?
    Cengiz Yalcinkaya
    Istanbul University, Cerrahpasa Medical Faculty, Department of Neurology, Division of Child Neurology, Istanbul, Turkey
    Neuropediatrics 43:159-61. 2012
    ..It is an open question whether this is an association by chance or a feature of PMLD not previously noted...
  2. ncbi request reprint Epilepsy in vacuolating megalencephalic leukoencephalopathy with subcortical cysts
    Cengiz Yalcinkaya
    Division of Child Neurology, Department of Neurology, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey
    Seizure 12:388-96. 2003
    ..The elucidation of the underlying molecular defect may explain the unusual pathogenetic relation between this leukoencephalopathy and the associated seizures...
  3. doi request reprint A close look at EEG in subacute sclerosing panencephalitis
    Nurhak Demir
    Department of Neurology, Dokuz Eylül Faculty of Medicine, Dokuz Eylul Univercity, Inciralti, Izmir, Turkey
    J Clin Neurophysiol 30:348-56. 2013
    ..To define atypical clinical and EEG features of patients with subacute sclerosing panencephalitis that may require an overview of differential diagnosis...
  4. ncbi request reprint Alterations in cell-mediated immune response in subacute sclerosing panencephalitis
    Sibel P Yentür
    Department of Physiology, Istanbul Medical Faculty, Istanbul University, Turkey
    J Neuroimmunol 170:179-85. 2005
    ..The recall responses were lower in SSPE as reported in measles before...
  5. doi request reprint Challenges in diagnosing SSPE
    Ozdem Erturk
    Department of Neurology, Cerrahpasa Faculty of Medicine, Istanbul University, 34098 Fatih, Istanbul, Turkey
    Childs Nerv Syst 27:2041-4. 2011
    ..In this report, we summarize the clinical features of patients with SSPE who have uncommon presentations or features of the disease or coexisting medical conditions which may lead to diagnostic difficulties...
  6. doi request reprint Mucolipidosis type IV in a Turkish boy associated with a novel MCOLN1 mutation
    Beyhan Tuysuz
    Istanbul University, Cerrahpasa Medical Faculty, Department of Pediatric Genetics, Istanbul, Turkey
    Brain Dev 31:702-5. 2009
    ..Serine 456 is conserved in mucolipin proteins throughout evolution, therefore the mutation is considered as causative for the severe phenotype of this patient...
  7. ncbi request reprint Elevated interleukin-12 and CXCL10 in subacute sclerosing panencephalitis
    Guher Saruhan-Direskeneli
    Department of Physiology, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey
    Cytokine 32:104-10. 2005
    ..These results demonstrate that immune response against MV in SSPE may be impaired, although some T cell/Th1 inducing stimulations are present...
  8. doi request reprint Epilepsy Surgery in Children with Lesional Partial Epilepsies
    Ozdem Erturk
    Istanbul University, Cerrahpasa School of Medicine, Department of Neurology, Istanbul, Turkey
    Turk Neurosurg 25:900-4. 2015
    ..Surgery for epilepsy is a significant treatment alternative with favorable outcomes in the pediatric age group. In this study we present the surgical outcomes of pediatric population referred to our center...
  9. doi request reprint Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features
    Beyhan Tuysuz
    Department of Pediatric Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey
    Am J Med Genet A 164:1677-85. 2014
    ....
  10. ncbi request reprint Beneficial Effects of Everolimus on Autism and Attention-Deficit/Hyperactivity Disorder Symptoms in a Group of Patients with Tuberous Sclerosis Complex
    Ayse Kilincaslan
    1 Department of Child and Adolescent Psychiatry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
    J Child Adolesc Psychopharmacol . 2016
    ..The aim of the present study is to describe the effects of everolimus on emotional and behavioral symptoms and refractory epilepsy in a group of patients with TSC...
  11. doi request reprint Unilateral cerebellar and brain stem hypoplasia in a child with a postnatal diagnosis of dissecting aneurysm in basilar artery
    Sinem Akkas-Yazici
    Division of Pediatric Neurology, Department of Neurology, Cerrahpasa School of Medicine, Istanbul University, Istanbul, Turkey
    Neuropediatrics 45:392-5. 2014
    ..The pathogenetic mechanisms for cerebellar disruption are certainly multifactorial in origin, although ischemic arterial etiologies were often undervalued. ..
  12. pmc Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation
    Beyhan Tuysuz
    Department of Pediatric Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, 34098, Turkey
    JIMD Rep 26:7-12. 2016
    ..320G>A; p.Trp107X in SRD5A3. Epilepsy and glaucoma have been reported only once in the 19 described SRD5A3-congenital glycosylation defect patients, and corneal clouding not at all. ..
  13. doi request reprint Multiple small hyperintense lesions in the subcortical white matter on cranial MR images in two Turkish brothers with cold-induced sweating syndrome caused by a novel missense mutation in the CRLF1 gene
    Beyhan Tuysuz
    Department of Pediatric Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey
    Brain Dev 35:596-601. 2013
    ..However, multiple small hyperintense lesions in subcortical white matter on T2 weighted and fluid attenuation inversion recovery (FLAIR) images may support the clinical diagnosis of CISS...
  14. doi request reprint Unilateral cerebellar hypoplasia with different clinical features
    Gulcin Benbir
    Cerrahpasa Medical Faculty, Department of Neurology, Division of Pediatric Neurology, Istanbul University, Turkey
    Cerebellum 10:49-60. 2011
    ....
  15. doi request reprint Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population
    Beyhan Tuysuz
    Department of Pediatrics, Division of Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey
    Neurogenetics 9:119-25. 2008
    ..This report broadens the spectrum of mutations in NTRK1 that cause HSAN IV and demonstrates a founder mutation in the Turkish population...
  16. doi request reprint Clinical characteristics of 49 patients with psychogenic movement disorders in a tertiary clinic in Turkey
    Sibel Ertan
    Department of Neurology, Cerrahpasa Faculty of Medicine, Istanbul University, Istanbul, Turkey
    Mov Disord 24:759-62. 2009
    ..Although our data was obtained from a different culture, our results showed that hospital-based frequency and phenomenological features between our PMD group and previously reported ones are similar...
  17. ncbi request reprint Anxiety and depression in children with epilepsy and their mothers
    Orhan Baki
    Department of Neurology, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey
    Epilepsy Behav 5:958-64. 2004
    ..In this cross-sectional study we aimed to examine the association between epilepsy in childhood and adolescence, and anxiety and depression in these patients and their mothers...