Publications by authors named "Sinan Comu"

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Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review.
Adnan Deniz, Sinan Çomu, Mesut Güngör, Yonca Anık, Bülent Kara

J Pediatr Genet· June 2024

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Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder.
Arman Çakar, Meltem İnci, Ayşe Nur Özdağ Acarlı, Sinan Çomu, Ayşe Candayan

Acta Neurol Scand· May 2022

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NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy.
Ahmet Okay Caglayan, Sinan Comu, Jacob F Baranoski, Yesim Parman, Hande Kaymakçalan

Eur J Med Genet· January 2015

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Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features.
Beyhan Tüysüz, Kaya Bilguvar, Naci Koçer, Cengiz Yalçınkaya, Okay Çağlayan

Am J Med Genet A· July 2014

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An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures.
Ozlem Yalçin, Betül Baykan, Kadriye Ağan, Zuhal Yapici, Destina Yalçin, Sinan Comu

Epilepsia· May 2011

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Etiologies of seizures in young children admitted to an inner city hospital in a developing country.
Feyzullah Cetinkaya, Ece Sennaroglu, Sinan Comu

Pediatr Emerg Care· November 2008

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Epilepsy in vacuolating megalencephalic leukoencephalopathy with subcortical cysts.
Cengiz Yalçinkaya, Adnan Yüksel, Sinan Comu, Gülhatun Kiliç, Ozlem Cokar

Seizure· September 2003

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