Publications by authors named "Sefer Kumandas"

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Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome.
Seda Kanmaz, Sanem Yılmaz, Nihal Olgaç Dündar, Ayşe Aksoy, Mehmet Canpolat

J Child Neurol· November 2025

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Genotypic and Phenotypic Characterization of Axonal Charcot-Marie-Tooth Disease in Childhood: Identification of One Novel and Four Known Mutations.
Rojan İpek, Büşra Eser Çavdartepe, Sevcan Tuğ Bozdoğan, Erman Altunışık, Akçahan Akalın

Genes (Basel)· July 2025

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A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis.
Aslihan Kiraz, Murat Erdogan, Burhan Balta, Hakan Gumus, Mehmet Burak Mutlu, Sefer Kumandas

Neurogenetics· May 2025

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Neurological Complications in Children With Cancer: Experience From a Single Center in Türkiye.
Leyla Kara, Ekrem Unal, Huseyin Per, Sefer Kumandas, Mehmet Canpolat

J Clin Pract Res· March 2024

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Evaluating the brainstem in children with breath-holding spells.
Gul Demet Kaya Ozcora, Sefer Kumandas, Ayse Sagiroglu, Niyazi Acer, Selim Doganay

North Clin Istanb· November 2022

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Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study.
Sema Bozkaya-Yilmaz, Eda Karadag-Oncel, Nihal Olgac-Dundar, Pinar Gencpinar, Berrak Sarioglu, Sefer Kumandas

Eur J Pediatr· January 2022

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Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome.
Mehmet Canpolat, Gül Demet Kaya Özçora, Hakan Poyrazoğlu, Huseyin Per, Abdulhakim Çoşkun

Turk Arch Pediatr· November 2021

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The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
Atay Vural, Gülşah Şimşir, Şeyma Tekgül, Cemile Koçoğlu, Fulya Akçimen

Mov Disord· July 2021

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An analysis of 109 fetuses with prenatal diagnosis of complete agenesis of corpus callosum.
Ayşe Kaçar Bayram, Mehmet Serdar Kütük, Selim Doganay, Mahmut Tuncay Özgün, Hakan Gümüş

Neurol Sci· June 2020

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PEX10-related autosomal recessive cerebellar ataxia with hearing loss.
Gül Demet Kaya Özçora, Satoko Miyatake, Naomichi Matsumoto, Mehmet Canpolat, Murat Erdoğan

Acta Neurol Belg· April 2020

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Levels of Salivary Sialic Acid in Children with Autism Spectrum Disorder; Could It Be Related to Stereotypes and Hyperactivity?
Esra Demirci, Yunus Guler, Sevgi Ozmen, Mehmet Canpolat, Sefer Kumandas

Clin Psychopharmacol Neurosci· August 2019

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Pepper spray inhalation-induced acute polyneuropathy mimicking Guillain-Barre syndrome.
Gül Demet Kaya Özçora, Sevgi Çıraklı, Mehmet Canpolat, Selim Doğanay, Sefer Kumandaş

Turk Pediatri Ars· March 2019

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Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.
Alicia Guemez-Gamboa, Ahmet Okay Çağlayan, Valentina Stanley, Anne Gregor, Maha S Zaki, Sefer Kumandas

Ann Neurol· November 2018

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The use of rapamycin in patients with tuberous sclerosis complex: Long-term results.
Mehmet Canpolat, Hakan Gumus, Sefer Kumandas, Abdulhakim Coskun, Huseyin Per

Epilepsy Behav· November 2018

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Investigating the prevalence of febrile convulsion in Kayseri, Turkey: An assessment of the risk factors for recurrence of febrile convulsion and for development of epilepsy.
Mehmet Canpolat, Huseyin Per, Hakan Gumus, Ferhan Elmali, Sefer Kumandas

Seizure· February 2018

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Erratum: Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.
Mehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, Ruhan Dusunsel, Sefer Kumandas

Neuropediatrics· October 2017

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Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.
Mehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, Ruhan Dusunsel, Sefer Kumandas

Neuropediatrics· April 2017

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Glutaric Acidemia Type 1: A Case of Infantile Stroke.
Gül Demet Kaya Ozcora, Songul Gokay, Mehmet Canpolat, Fatih Kardaş, Mustafa Kendirci

JIMD Rep· April 2017

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Bone mineral density and bone metabolic markers' status in children with neurofibromatosis type 1.
Hatice Gamze Poyrazoğlu, Veysel Nijat Baş, Alev Arslan, Funda Bastug, Mehmet Canpolat, Sefer Kumandas

J Pediatr Endocrinol Metab· February 2017

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The Role of Diffusion-Weighted Imaging in the Evaluation of the Whole Brain in Isolated Unilateral Polymicrogyria.
Sureyya Burcu Görkem, Selim Doganay, Kazim Gumus, Ayse Bayram, Sefer Kumandas

J Child Neurol· December 2016

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Increased Serum Phthalates (MEHP, DEHP) and Bisphenol A Concentrations in Children With Autism Spectrum Disorder: The Role of Endocrine Disruptors in Autism Etiopathogenesis.
Fatih Kardas, Ayse Kacar Bayram, Esra Demirci, Leyla Akin, Sevgi Ozmen, Sefer Kumandas

J Child Neurol· April 2016

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Misdiagnosis of gastroesophageal reflux disease as epileptic seizures in children.
Ayşe Kaçar Bayram, Mehmet Canpolat, Neslihan Karacabey, Hakan Gumus, Sefer Kumandas

Brain Dev· March 2016

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Neurological features and management of Wilson disease in children: an evaluation of 12 cases.
Ayşe Kaçar Bayram, Hakan Gümüş, Duran Arslan, Güldemet Kaya Özçora, Sefer Kumandaş

Turk Pediatri Ars· March 2016

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Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome Induced by Levetiracetam in a Pediatric Patient.
Ayşe Kaçar Bayram, Mehmet Canpolat, Salih Levent Çınar, Fulya Tahan, Hakan Gumus

J Emerg Med· February 2016

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Clinical, Electrodiagnostic, and Genetic Features of Tangier Disease in an Adolescent Girl with Presentation of Peripheral Neuropathy.
Huseyin Per, Mehmet Canpolat, Ayşe Kaçar Bayram, Ege Ulgen, Burçin Baran, Sefer Kumandas

Neuropediatrics· December 2015

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