Publications by authors named "Faruk Incecik"

97Publications

Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population.

Authors:
Faruk Incecik Ozlem M Herguner Neslihan O Mungan

J Pediatr Neurosci 2020 Apr-Jun;15(2):86-89. Epub 2020 Jun 27.

Department of Pediatric Metabolism and Nutrition, Faculty of Medicine, Cukurova University, Adana, Turkey.

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June 2020

Effect of Levetiracetam Usage on Serum Creatine Phosphokinase Concentration in Patients with Epilepsy.

Authors:
Faruk Incecik Ozlem M Herguner Seyda Besen

J Pediatr Neurosci 2020 Apr-Jun;15(2):81-85. Epub 2020 Jun 27.

Division of Child Neurology, Department of Pediatrics, Cukurova University Faculty of Medicine, Adana, Turkey.

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June 2020

Dysarthria, Ataxia, and Dystonia Associated with Gene Mutation: A Case Report of a Turkish Child.

Authors:
Duygu G Ozcanyuz Faruk Incecik Ozlem M Herguner Neslihan O Mungan Sevcan T Bozdogan

Ann Indian Acad Neurol 2020 May-Jun;23(3):399-401. Epub 2020 Jun 10.

Department of Medical Genetics, Cukurova University Faculty of Medicine, Adana, Turkey.

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June 2020

Coexistence of Type 1 Diabetes Mellitus and Periventricular Heterotopia in a Child: A Case Report.

Authors:
Faruk Incecik Fatih Gürbüz

J Pediatr Neurosci 2020 Jan-Mar;15(1):67-68. Epub 2020 Mar 18.

Department of Pediatric Endocrinology, Faculty of Medicine, Cukurova University, Adana, Turkey.

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March 2020

Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients.

Authors:
Gülen Gül Mert Neslihan Özcan Özlem Hergüner Şakir Altunbaşak Faruk Incecik Atıl Bişgin Serdar Ceylaner

Acta Neurol Belg 2019 Nov 26. Epub 2019 Nov 26.

Intergen Genetic Laboratory, Ankara, Turkey.

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November 2019

Early-onset progressive encephalopathy associated with NAXE gene variants: a case report of a Turkish child.

Authors:
Faruk Incecık Serdar Ceylaner

Acta Neurol Belg 2020 Jun 22;120(3):733-735. Epub 2019 Nov 22.

InterGen Genetic Research Centre, Ankara, Turkey.

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June 2020

A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia.

Authors:
Rabia Miray Kisla Ekinci Sibel Balcı Atil Bisgin Ilgen Sasmaz Goksel Leblebisatan Faruk Incecik Mustafa Yilmaz

Pediatr Hematol Oncol 2019 Sep 14;36(6):376-381. Epub 2019 Sep 14.

Department of Pediatric Rheumatology, Cukurova University Faculty of Medicine , Adana , Turkey.

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September 2019

Dynamic thiol/disulphide homeostasis in children with neurofibromatosis type 1 and tuberous sclerosis.

Authors:
Faruk Incecik Gamze Avcıoğlu Özcan Erel Salim Neşelioğlu Seyda Besen Sakir Altunbaşak

Acta Neurol Belg 2019 Sep 28;119(3):419-422. Epub 2019 Feb 28.

Department of Pediatric Neurology, Cukurova University Faculty of Medicine, Adana, Turkey.

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September 2019

D-bifunctional Protein Deficiency: A Case Report of a Turkish Child.

Authors:
Faruk Incecik Neslihan O Mungan

Ann Indian Acad Neurol 2019 Jan-Mar;22(1):119-121

Department of Pediatric Metabolism, Cukurova University Faculty of Medicine, Adana, Turkey.

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January 2019

Factors affecting epilepsy prognosis in patients with tuberous sclerosis.

Authors:
Gülen Gül Mert Şakir Altunbaşak Özlem Hergüner Faruk İncecik Hilal Cansever Övetti Neslihan Özcan Duygu Kuşçu İlker Ünal

Childs Nerv Syst 2019 03 23;35(3):463-468. Epub 2019 Jan 23.

Department of Biostatistics, Cukurova University, Adana, Turkey.

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March 2019

Dynamic thiol/disulphide homeostasis in children with Duchenne muscular dystrophy.

Authors:
Faruk Incecik Gamze Avcıoğlu Özcan Erel Salim Neşelioğlu Ozlem M Hergüner

Acta Neurol Belg 2019 Jun 3;119(2):215-218. Epub 2019 Jan 3.

Department of Pediatric Neurology, Cukurova University Faculty of Medicine, Toros mah. 78186 sok., Yeşilpark Evleri, Kat: 7, No: 13, Adana, Turkey.

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June 2019

Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features.

Authors:
Faruk Incecik Seyda Besen Sevcan Tug Bozdogan

Ann Indian Acad Neurol 2018 Oct-Dec;21(4):335-339

Department of Medical Genetics, Faculty of Medicine, Cukurova University, Adana, Turkey.

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December 2018

Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child.

Authors:
Faruk Incecik Ozlem M Hergüner Atil Bisgin

J Pediatr Neurosci 2018 Jul-Sep;13(3):355-357

Department of Pediatrics, Medical Genetics, Cukurova University Faculty of Medicine, Adana, Turkey.

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October 2018

MEDNIK syndrome with a frame shift causing mutation in AP1S1 gene and literature review of the clinical features.

Authors:
Faruk Incecik Atil Bisgin Mustafa Yılmaz

Metab Brain Dis 2018 12 23;33(6):2065-2068. Epub 2018 Sep 23.

Department of Pediatric Immunology, Cukurova University Faculty of Medicine, Adana, Turkey.

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December 2018

Late-Onset Leigh Syndrome due to Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia.

Authors:
Faruk Incecik Ozlem M Herguner Seyda Besen Sevcan T Bozdoğan Neslihan O Mungan

J Pediatr Neurosci 2018 Apr-Jun;13(2):205-207

Division of Pediatric Metabolism, Faculty of Medicine, Cukurova University, Adana, Turkey.

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August 2018

Methotrexate-induced pseudotumor cerebri in a patient with juvenile idiopathic arthritis.

Authors:
Faruk Incecik Duygu G Ozcanyuz Mustafa Yılmaz

Acta Neurol Belg 2019 Mar 6;119(1):141-142. Epub 2018 Aug 6.

Division of Pediatric Neurology, Cukurova University Faculty of Medicine, Toros mah. 78186 sok., Yeşilpark Evleri, Kat: 7, no: 13, Adana, Turkey.

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March 2019

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration.

Authors:
Ashleigh E Schaffer Martin W Breuss Ahmet Okay Caglayan Nouriya Al-Sanaa Hind Y Al-Abdulwahed Hande Kaymakçalan Cahide Yılmaz Maha S Zaki Rasim O Rosti Brett Copeland Seung Tae Baek Damir Musaev Eric C Scott Tawfeg Ben-Omran Ariana Kariminejad Hulya Kayserili Faezeh Mojahedi Majdi Kara Na Cai Jennifer L Silhavy Seham Elsharif Elif Fenercioglu Bruce A Barshop Bulent Kara Rengang Wang Valentina Stanley Kiely N James Rahul Nachnani Aneesha Kalur Hisham Megahed Faruk Incecik Sumita Danda Yasemin Alanay Eissa Faqeih Gia Melikishvili Lobna Mansour Ian Miller Biayna Sukhudyan Jamel Chelly William B Dobyns Kaya Bilguvar Rami Abou Jamra Murat Gunel Joseph G Gleeson

Nat Genet 2018 08 16;50(8):1093-1101. Epub 2018 Jul 16.

Department of Neuroscience, Rady Children's Institute for Genomic Medicine, Howard Hughes Medical Institute, University of California, San Diego, San Diego, CA, USA.

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August 2018

Neuro-ichthyotic Syndromes: A Case Series.

Authors:
Faruk Incecık Ozlem M Herguner Mehmet N Ozbek Serdal Gungor Mustafa Yılmaz Wiliam B Rizzo Gülen G Mert

J Pediatr Neurosci 2018 Jan-Mar;13(1):34-38

Department of Pediatric Neurology, Faculty of Medicine, Cukurova University, Adana, Turkey.

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June 2018

Spinocerebellar Ataxia-21 in a Turkish Child.

Authors:
Faruk Incecik Ozlem M Herguner Patrick Willems Neslihan O Mungan

Ann Indian Acad Neurol 2018 Jan-Mar;21(1):68-70

Department of Pediatric Neurology, Medical Faculty, Cukurova University, Adana, Turkey.

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May 2018

Unusual side effects due to clobazam: a case report with edema of the extremities.

Authors:
Faruk Incecik Duygu Güner Ozcanyüz

Acta Neurol Belg 2018 Sep 10;118(3):521-522. Epub 2018 Mar 10.

Division of Pediatric Neurology, Department of Pediatrics, Cukurova University Faculty of Medicine, Toros mah., Barış Manço Bul. 78178 sok., Yeşilpark evleri, kat: 7, no: 13, Çukurova, Adana, Turkey.

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September 2018