Publications by authors named "Mine Caliskan"

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A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy.
Zehra Yavas Abali, Ezgi Gokpinar Ili, Firdevs Bas, Melis Ulak Ozkan, Çagrı Gulec, Mine Caliskan

Horm Res Paediatr· April 2024

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Functional Bandaging in Children with Idiopathic Toe-Walking.
Deniz Tuncer, N Ekin Akalan, M Mine Caliskan, Yener Temelli, Pakize Yigit

J Am Podiatr Med Assoc· November 2023

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Genetic and clinical evaluation of congenital myasthenic syndromes with long-term follow-up: experience of a tertiary center in Turkey.
Edibe Pembegul Yildiz, Mehmet Akif Kilic, Emek Uyur Yalcin, Fulya Kurekci, Ridvan Avci

Acta Neurol Belg· October 2023

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Shear Wave Elastography in Patients with Spinal Muscular Atrophy Types 2 and 3.
Burçin Nazlı Karacabey, Zuhal Bayramoğlu, Orhan Coşkun, Zeynep Nur Akyol Sarı, Melis Ulak Özkan

Neuropediatrics· August 2023

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Late onset Aicardi-Goutières syndrome case report: a rare white matter disease mimicking as pseudo-enzyme deficiency.
Melis Ulak Ozkan, Selahattin Katar, Edibe Pembegul Yildiz, Nur Aydinli, Mine Caliskan

Acta Neurol Belg· February 2022

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Clinically isolated syndrome and multiple sclerosis in children: a single center study.
Gonca Bektaş, Melis Ulak Özkan, Edibe Pembegül Yıldız, Tuğçe Aksu Uzunhan, Serra Sencer

Turk J Pediatr· August 2021

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Evaluation of eating behaviors in childhood epilepsy with centrotemporal spikes: Case-control study.
Orhan Coskun, Osman Kipoglu, Burcin Nazli Karacabey, Mehmet Akif Kilic, Derya Simsek Ceran, Mine Caliskan

Epilepsy Behav· July 2021

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Voice Analysis to Differentiate the Dopaminergic Response in People With Parkinson's Disease.
Anubhav Jain, Kian Abedinpour, Ozgur Polat, Mine Melodi Çalışkan, Afsaneh Asaei

Front Hum Neurosci· May 2021

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Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey.
Olcay Ünver, Dilşad Türkdoğan, Serhat Güler, Osman Kipoğlu, Mesut Güngör

Eur J Paediatr Neurol· January 2021

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Ambulation, lesion level, and health-related quality of life in children with myelomeningocele.
Ebru Şeker Abanoz, Meral Özmen, Mine Çalışkan, Gülbin Gökçay, Nur Aydınlı

Childs Nerv Syst· March 2020

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Evaluation of the prognostic factors in school age children who experienced neonatal seizures.
Edibe Pembegul Yıldız, Burak Tatlı, Melis Ulak Ozkan, Emine Erarslan, Nur Aydınlı

Epilepsy Behav· January 2020

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Epileptic spasm and other forms of epilepsy in presumed perinatal arterial ischemic stroke in Turkey after more than 10 years follow-up: A single centre study.
Gonca Bektaş, Osman Kipoğlu, Edibe Pembegül Yıldız, Nur Aydınlı, Mine Çalışkan

Brain Dev· September 2019

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Autism spectrum disorder and attention-deficit/hyperactivity disorder-related symptoms in benign childhood epilepsy with centrotemporal spikes: A prospective case-control study.
Gonca Bektaş, Uğur Tekin, Edibe Pembegül Yıldız, Nur Aydınlı, Mine Çalışkan

Epilepsy Behav· June 2019

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Short-term neurological outcomes in ischemic and hemorrhagic pediatric stroke.
Tuğçe Aksu Uzunhan, Nur Aydinli, Mine Çalişkan, Burak Tatli, Meral Özmen

Pediatr Int· February 2019

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Efficacy of rufinamide in childhood refractory epilepsy.
Edibe Pembegül Yıldız, Zeynep Hızlı, Gonca Bektaş, Melis Ulak-Özkan, Burak Tatlı

Turk J Pediatr· February 2019

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Efficacy of Stiripentol and the Clinical Outcome in Dravet Syndrome.
Edibe Pembegul Yıldız, Melis Ulak Ozkan, Tugce Aksu Uzunhan, Gonca Bektaş, Burak Tatlı

J Child Neurol· January 2019

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Hereditary spastic paraplegia type 35 caused by a novel FA2H mutation.
Gonca Bektaş, Gözde Yeşil, Edibe Pembegül Yıldız, Nur Aydınlı, Mine Çalışkan

Turk J Pediatr· December 2018

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Variant Guillain-Barré syndrome in a patient with Hodgkin lymphoma: AMSAN.
Işık Odaman Al, Başak Koç, Cengiz Bayram, Ezgi Uysalol Paslı, Edibe Pembegül Yıldız

Turk Pediatri Ars· December 2018

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Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up.
Gonca Bektaş, Gözde Yeşil, Melis Ulak Özkan, Edibe Pembegül Yıldız, Tuğçe Aksu Uzunhan

Clin Neurol Neurosurg· August 2018

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Predictive factors of drug-resistant epilepsy in children presenting under 2 years of age: experience of a tertiary center in Turkey.
Edibe Pembegul Yildiz, Dilek Gunes, Gonca Bektas, Tugce Aksu Uzunhan, Burak Tatli, Mine Caliskan

Acta Neurol Belg· March 2018

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Spinal muscular atrophy with progressive myoclonic epilepsy linked to mutations in ASAH1.
Edibe Pembegül Yildiz, Gözde Yesil, Gonca Bektas, Mine Caliskan, Burak Tatlı

Clin Neurol Neurosurg· January 2018

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Lacosamide treatment of childhood refractory focal epilepsy: the first reported side effect in paediatric patients.
Edibe Pembegul Yildiz, Melis Ulak Ozkan, Gonca Bektas, Tuğçe Aksu Uzunhan, Nur Aydinli, Mine Caliskan

Childs Nerv Syst· November 2017

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A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.
Edibe Pembegul Yildiz, Gozde Yesil, Melis Ulak Ozkan, Gonca Bektas, Mine Caliskan

Seizure· October 2017

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The influence of levetiracetam on psychosocial and behavioral functioning in children: A case-control and follow-up study.
Gonca Bektaş, Uğur Tekin, Melis Ulak Özkan, Edibe Pembegül Yıldız, Mine Çalışkan

Epilepsy Behav· July 2017

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Psychosocial and behavioral functioning and their relationship to seizure timing in children with benign epilepsy with centrotemporal spikes.
Gonca Bektaş, Uğur Tekin, Edibe Pembegül Yıldız, Tuğçe Aksu Uzunhan, Burak Tatlı

Brain Dev· June 2017

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