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Author Details

Faruk Incecik
Cukurova University Faculty of Medicine
2004
106
13
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37969881A Retrospective Cohort Study of Traumatic Brain Injury in Children: A Single-Institution Experience and Determinants of Neurologic Outcome.J Crit Care Med (Targu Mures)2023
37480521Posttraumatic epilepsy in critically ill children with traumatic brain injury.Childs Nerv Syst2023
36532829Peripheral facial nerve palsy in children: clinical manifestations, treatment and prognosis.Egypt J Neurol Psychiatr Neurosurg2022
31773638Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients.Acta Neurol Belg2021
33838667Evaluation of the relationship between NIRS (near-infrared spectroscopy) and optic nerve sheath diameter measurement in children with increased intracranial pressure: a pilot study.Ital J Pediatr2021
33578440The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS.Neuropediatrics2021
35110065Evaluation of Pediatric Brain Death and Organ Donation: 10-Year Experience in a Pediatric Intensive Care Unit in Turkey.Turk Arch Pediatr2021
32435315Coexistence of Type 1 Diabetes Mellitus and Periventricular Heterotopia in a Child: A Case Report.J Pediatr Neurosci2020
33623291Acetazolamide-Induced Agranulocytosis in a Patient with Pseudotumor Cerebri.Ann Indian Acad Neurol2020
33623276Different Clinical Manifestations of Three Prime Repair Exonuclease 1 Mutation: A Case Series.Ann Indian Acad Neurol2020
33688131Mitochondrial Membrane Protein-Associated Neurodegeneration: A Case Series of Six Children.Ann Indian Acad Neurol2020
31758406Early-onset progressive encephalopathy associated with NAXE gene variants: a case report of a Turkish child.Acta Neurol Belg2020
33042236Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population.J Pediatr Neurosci2020
33042235Effect of Levetiracetam Usage on Serum Creatine Phosphokinase Concentration in Patients with Epilepsy.J Pediatr Neurosci2020
32606554Dysarthria, Ataxia, and Dystonia Associated with <i>COX20 (FAM36A)</i> Gene Mutation: A Case Report of a Turkish Child.Ann Indian Acad Neurol2020
30692775D-bifunctional Protein Deficiency: A Case Report of a Turkish Child.Ann Indian Acad Neurol2019
30083940Methotrexate-induced pseudotumor cerebri in a patient with juvenile idiopathic arthritis.Acta Neurol Belg2019
31522599A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia.Pediatr Hematol Oncol2019
30820867Dynamic thiol/disulphide homeostasis in children with neurofibromatosis type 1 and tuberous sclerosis.Acta Neurol Belg2019
30607902Dynamic thiol/disulphide homeostasis in children with Duchenne muscular dystrophy.Acta Neurol Belg2019
30673834Factors affecting epilepsy prognosis in patients with tuberous sclerosis.Childs Nerv Syst2019
29349679Autoimmune encephalitis associated with glutamic acid decarboxylase antibodies: a case series.Acta Neurol Belg2018
30244301MEDNIK syndrome with a frame shift causing mutation in AP1S1 gene and literature review of the clinical features.Metab Brain Dis2018
30013181Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration.Nat Genet2018
30090137Late-Onset Leigh Syndrome due to <i>NDUFV1</i> Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia.J Pediatr Neurosci2018
29899769Neuro-ichthyotic Syndromes: A Case Series.J Pediatr Neurosci2018
30271475Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child.J Pediatr Neurosci2018
30532373Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features.Ann Indian Acad Neurol2018
29524094Unusual side effects due to clobazam: a case report with edema of the extremities.Acta Neurol Belg2018
29720801Spinocerebellar Ataxia-21 in a Turkish Child.Ann Indian Acad Neurol2018
27418363Finger drop sign in a child with acute motor and sensory axonal neuropathy form of Guillain-Barré syndrome.Acta Neurol Belg2017
28140735Risk factors affecting prognosis in infantile spasm.Int J Neurosci2017
28032298Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency.Acta Neurol Belg2017
27011634Intravenous levetiracetam in critically ill children.Ann Indian Acad Neurol2016
28163531Alternating Hemiplegia of Childhood in a Child Misdiagnosed as Intractable Epilepsy.J Neurosci Rural Pract2016
26399431Acute rhabdomyolysis associated with levetiracetam therapy in a child.Acta Neurol Belg2016
27841212Limbic encephalitis associated with anti-leucine-rich glioma-inactivated-1 protein antibodies in a child.Neurol India2016
27857812Mitochondrial membrane protein-associated neurodegeneration in a Turkish patient.J Pediatr Neurosci2016
27195040Guillain-Barré syndrome with hyperreflexia and bilateral papillitis in a child.J Pediatr Neurosci2016
27188289Tyrosinemia type 1 and irreversible neurologic crisis after one month discontinuation of nitisone.Metab Brain Dis2016
24657010Prognostic significance of failure of the initial antiepileptic drug in children with benign childhood epilepsy with centrotemporal spikes.Brain Dev2015
26425029Electroconvulsive therapy for refractory status epilepticus in a child: A case report.Ann Indian Acad Neurol2015
27411423A Presentation of Lyme Disease: Pseudotumor Cerebri.Turk J Pediatr2015
27186704Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literature.Turk J Pediatr2015
26717333Neurofibromatosis type 1 and cardiac manifestations.Turk Kardiyol Dern Ars2015
26962340Merosin-negative congenital muscular dystrophy: Report of five cases.J Pediatr Neurosci2015
26713033Urinary and fecal incontinence during levetiracetam therapy.Ann Indian Acad Neurol2015
26905117Fatal glioblastoma multiforme in a child with neurofibromatosis type 1.Indian J Cancer2015
26148632Acute myeloid leukemia in a child with segmental neurofibromatosis.J Cancer Res Ther2015
26167008First-drug treatment failures in 42 Turkish children with idiopathic childhood occipital epilepsies.J Neurosci Rural Pract2015
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Collaborators

Joseph G Gleeson
University of California
Co-authored papers 3
Maha S Zaki
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 2
Eric Scott
Rady Children's Institute for Genomic Medicine, University of California
Co-authored papers 2
Brett Copeland
University of California
Co-authored papers 2
Rasim O Rosti
University of Virginia
Co-authored papers 2
William B Dobyns
University of Minnesota
Co-authored papers 2
Jennifer L Silhavy
University of California
Co-authored papers 2
Susanne Roosing
Radboud University Medical Center
Co-authored papers 1
Franco Stanzial
Genetic Counseling Service - Regional Hospital of Bolzano
Co-authored papers 1
Faezeh Mojahedi
Blood Borne Infections Research Center, Academic Center for Education
Co-authored papers 1
Francesco Emma
Ospedale Pediatrico Bambino Gesu IRCCS
Co-authored papers 1
Joanne M Drautz
University of New Mexico
Co-authored papers 1
Elide Miccinilli
Fondazione IRCCS Casa Sollievo della Sofferenza
Co-authored papers 1
Pedro Aza-Blanc
Sanford-Burnham-Prebys Medical Discovery Institute
Co-authored papers 1
Stefano D'Arrigo
Fondazione IRCCS Istituto Neurologico Carlo Besta
Co-authored papers 1
Eugen Boltshauser
Children's University Hospital
Co-authored papers 1
Brian D Dynlacht
New York University Cancer Institute, New York University School of Medicine
Co-authored papers 1
Bruce A Barshop
University of California San Diego
Co-authored papers 1
Rose-Mary Boustany
American University of Beirut Medical Center
Co-authored papers 1
Petter Str??mme
University of Oslo
Co-authored papers 1
Colin A Johnson
University of Leeds Leeds Institute of Medical Research at St James's
Co-authored papers 1
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 1
Ariana Kariminejad
Clinical Genetics Deaprtment
Co-authored papers 1
Ji Eun Lee
Soonchunhyang University College of Medicine, Bucheon Hospital
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H??lya Kayserili
Istanbul University
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Maja Steinlin
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Release 1.2