Publications by authors named "Serhat Guler"

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Spastic cerebral palsy and quality of life in children aged 6-12 years: exploring key associated factors.
Lütfiye Koru, Serhat Güler, Sema Saltık

Turk J Pediatr· September 2025

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A Novel Intragenic Duplication of CREBBP in Rubinstein-Taybi Syndrome: A Case Report Expanding the Genotype-Phenotype Spectrum.
Enes Dursun, Eyyup Uctepe, Serhat Guler, Hanifenur Mancilar, Ahmet Yesilyurt

Mol Syndromol· August 2025

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Effects of motor imagery adding to physiotherapy and rehabilitation program in children with Duchenne Muscular Dystrophy: does it make a difference?
Gülsena Utku Umut, Arzu Razak Özdi̇nçler, Fitnat Uluğ, Serhat Güler, Sema Saltık

Eur J Paediatr Neurol· July 2025

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Exploring the Correlations Between Language Impairments, Central Auditory Processing Disorder, Neuropsychiatric Functions, and Seizure Timing in Children With Self-Limited Epilepsy With Centrotemporal Spikes.
Oğuzhan Tin, Sema Saltık, Halide Çetin Kara, Zehra Koyuncu, Kevser Sak

J Child Neurol· May 2025

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Respiratory functions, respiratory muscle strength and fatigue in patients with pediatric-onset multiple sclerosis: a comparative cross-sectional study.
Pelin Vural, Buket Akinci, Serhat Guler, Sema Saltik, Yonca Zenginler Yazgan

Acta Neurol Belg· February 2025

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Children With Type I Interferonopathy: Commonalities and Diversities in a Large Patient Cohort.
Fatih Haslak, Huseyin Kilic, Sezgin Sahin, Busra Hotaman, Nur Memnune Cebi, Serhat Guler

J Rheumatol· December 2024

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Long-Term Disease Course of Pontocerebellar Hypoplasia Type 10.
Serhat Guler, Ayca Dilruba Aslanger, Turkan Uygur Sahin, Alpay Alkan, Cengiz Yalcinkaya

Pediatr Neurol· September 2024

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Exploring the Influence of Concurrent Nutritional Therapy on Children with Spinal Muscular Atrophy Receiving Nusinersen Treatment.
Eymen Pinar, Bilal Berke Ayvaz, Erkan Akkus, Ipek Ulkersoy, Tugce Damla Dilek, Serhat Guler

Children (Basel)· July 2024

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The effects of online exercise training on physical functions and quality of life in patients with pediatric-onset multiple sclerosis.
Pelin Vural, Yonca Zenginler Yazgan, Ela Tarakci, Serhat Guler, Sema Saltik

Mult Scler Relat Disord· June 2023

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Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals.
Ken Saida, Reza Maroofian, Toru Sengoku, Tadahiro Mitani, Alistair T Pagnamenta, Serhat Guler

Genet Med· January 2023

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Six-Minute Walk Performance and Related Factors in Pediatric-Onset Multiple Sclerosis.
Yonca Zenginler Yazgan, Pelin Vural, Recep Ormen, Buket Akinci, Ela Tarakci, Serhat Guler

J Child Neurol· April 2022

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The effects of nusinersen treatment on respiratory status of children with spinal muscular atrophy.
Evrim Hepkaya, Ayşe Ayzıt Kılınç Sakallı, İpek Ülkersoy, Azer Kılıç Başkan, Hüseyin Arslan

Pediatr Int· January 2022

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The impact of SARS-CoV2 on the anxiety levels of subjects and on the anxiety and depression levels of their parents.
Tugce Damla Dilek, Zehra Boybay, Nursena Kologlu, Oguzhan Tin, Serhat Güler

Mult Scler Relat Disord· January 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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Expanding Clinical Phenotype of TRAPPC12-Related Childhood Encephalopathy: Two Cases and Review of Literature.
Ayca Dilruba Aslanger, Emine Demiral, Seyma Sonmez-Sahin, Serhat Guler, Beyza Goncu

Neuropediatrics· December 2020

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Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report.
Hasan Önal, Atilla Ersen, Hakan Gemici, Erdal Adal, Serhat Güler

J Clin Res Pediatr Endocrinol· November 2018

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Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?
Serhat Güler, Gözde Yeşil, Hasan Önal

Balkan Med J· December 2017

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Rare vascular pathology sinus pericranii; becomes symptomatic with pseudotumor cerebri.
Serhat Güler, Burak Tatlı

Turk J Pediatr· September 2017

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Non epileptic paroxysmal events in childhood.
Burak Tatlı, Serhat Güler

Turk Pediatri Ars· June 2017

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Onychomadesis: A rare adverse effect in early-period valproic acid therapy.
Serhat Güler, İlhan Işık, Akın İşcan

Turk Pediatri Ars· June 2017

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Mixture models reveal multiple positional bias types in RNA-Seq data and lead to accurate transcript concentration estimates.
Andreas Tuerk, Gregor Wiktorin, Serhat Güler

PLoS Comput Biol· May 2017

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Relationship between the corpus callosum and neurocognitive disabilities in children with NF-1: diffusion tensor imaging features.
Sinem Aydin, Serpil Kurtcan, Alpay Alkan, Serhat Guler, Mekiya Filiz

Clin Imaging· January 2017

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The impact of epilepsy on preschool children and their families.
Müberra Tanriverdi, Fatma Karantay Mutluay, Devrim Tarakçi, Serhat Güler, Akin Iscan

Epilepsy Behav· September 2016

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Corrigendum: Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.
Cas Simons, Lachlan D Rash, Joanna Crawford, Linlin Ma, Ben Cristofori-Armstrong, Serhat Guler

Nat Genet· March 2015

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Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.
Cas Simons, Lachlan D Rash, Joanna Crawford, Linlin Ma, Ben Cristofori-Armstrong, Serhat Guler

Nat Genet· January 2015

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