Publications by authors named "Gul Serdaroglu"

Claim this Profile
T
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Extreme delta brush activity: Could it be a marker for early diagnosis and prognosis of anti- NMDA (N-methyl-D-aspartate) encephalitis?
Hande Gazeteci Tekin, Sarenur Gökben, Gül Serdaroğlu

Turk Pediatri Ars· March 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prevalence and severity of malnutrition in pediatric neurology outpatients with respect to underlying diagnosis and comorbid nutrition and feeding related problems.
Hande Tekin, Hasan Tekgül, Sanem Yılmaz, Dilek Arslangiray, Hediye Reyhan

Turk J Pediatr· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PRUNE1: a disease-causing gene for secondary microcephaly.
Mert Karakaya, Sanem Yilmaz, Markus Storbeck, Irmgard Hoelker, Raoul Heller, Gül Serdaroglu

Brain· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights.
Uluç Yiş, Kerstin Becker, Semra Hız Kurul, Gökhan Uyanik, Erhan Bayram

J Child Neurol· July 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency.
Sanem Yilmaz, Mine Serin, Ebru Canda, Cenk Eraslan, Hande Tekin, Gul Serdaroglu

Metab Brain Dis· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy.
Sarenur Gokben, Huseyin Onay, Sanem Yilmaz, Tahir Atik, Gul Serdaroglu

Acta Neurol Belg· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evaluation of ten prognostic factors affecting the outcome of West syndrome.
Sanem Yilmaz, Hasan Tekgul, Gul Serdaroglu, Ayfer Akcay, Sarenur Gokben

Acta Neurol Belg· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis.
Sanem Yilmaz, Tuncer Turhan, Serdar Ceylaner, Sarenur Gökben, Hasan Tekgul, Gul Serdaroglu

Childs Nerv Syst· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene.
Sarenur Gökben, Gül Serdaroğlu, Sanem Yılmaz, Thierry Bienvenu, Serdar Ceylaner

Turk J Pediatr· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Different Neurologic Aspects of Nutritional B12 Deficiency in Infancy.
Sanem Yilmaz, Gul Serdaroglu, Hasan Tekgul, Sarenur Gokben

J Child Neurol· April 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder.
Sanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, Cenk Eraslan, Grazia M S Mancini

Brain Dev· January 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Ictal urinary urge: localization and lateralization value in a pediatric case.
Sanem Yilmaz, Sarenur Gokben, Tuncer Turhan, Gul Serdaroglu, Hasan Tekgul

Childs Nerv Syst· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Seizures due to high dose camphor ingestion.
Hande Gazeteci Tekin, Sarenur Gökben, Gül Serdaroğlu

Turk Pediatri Ars· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Histopathological and genetic features of patients with limb girdle muscular dystrophy type 2C.
Gülden Dınız, Filiz Hazan, Hülya Tosun Yildirim, Aycan Unalp, Muzaffer Polat

Turk Patoloji Derg· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Electrophysiologic assessment of spasticity in children using H-reflex.
Hasan Tekgül, Muzaffer Polat, Ayşe Tosun, Gül Serdaroğlu, Sarenur Gökben

Turk J Pediatr· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan gene.
Gulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, Gul Serdaroglu, Filiz Hazan

Case Rep Genet· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical characteristics and outcome of children with electrical status epilepticus during slow wave sleep.
Sanem Yilmaz, Gul Serdaroglu, Ayfer Akcay, Sarenur Gokben

J Pediatr Neurosci· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Early-onset acquired myasthenia gravis secondary to anti-muscle-specific kinase autoantibodies.
Sanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, Ayfer Akcay

J Child Neurol· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Changing views of cerebral palsy over 35 years: the experience of a center.
Ayşe Tosun, Sarenur Gökben, Gül Serdaroğlu, Muzaffer Polat, Hasan Tekgül

Turk J Pediatr· July 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Neurocognitive evaluation in children with occipital lobe epilepsy.
Muzaffer Polat, Sarenur Gokben, Ayse Tosun, Gul Serdaroglu, Hasan Tekgul

Seizure· May 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Use of buspirone and fluoxetine for breathing problems in Rett syndrome.
Sarenur Gökben, Ulkü Akyol Ardıç, Gül Serdaroğlu

Pediatr Neurol· March 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Paroxysmal dystonia as a rare initial manifestation of multiple sclerosis.
Sanem Yilmaz, Gul Serdaroglu, Sarenur Gokben, Hasan Tekgul

J Child Neurol· December 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A case of neurobrucellosis presenting with isolated intracranial hypertension.
Sanem Yilmaz, Gul Serdaroglu, Sarenur Gokben, Hasan Tekgul

J Child Neurol· October 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation.
Marianne Rohrbach, Anthony Vandersteen, Uluç Yiş, Gul Serdaroglu, Esra Ataman

Orphanet J Rare Dis· June 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis