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Kumandas, Sefer
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1

Evaluation of immunization status in patients with cerebral..:

Bozkaya-Yilmaz, Sema ; Karadag-Oncel, Eda ; Olgac-Dundar, Nihal...
European Journal of Pediatrics.  181 (2021)  1 - p. 383-391 , 2021
Link: https://doi.org/10.1007/..
 
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2

An analysis of 109 fetuses with prenatal diagnosis of compl..:

Bayram, Ayşe Kaçar ; Kütük, Mehmet Serdar ; Doganay, Selim...
Neurological Sciences.  41 (2020)  6 - p. 1521-1529 , 2020
Link: https://doi.org/10.1007/..
 
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3

Levels of Salivary Sialic Acid in Children with Autism Spec..:

Demirci, Esra ; Guler, Yunus ; Ozmen, Sevgi..
Clinical Psychopharmacology and Neuroscience.  17 (2019)  3 - p. 415-422 , 2019
Link: https://doi.org/10.9758/..
 
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4

PEX10-related autosomal recessive cerebellar ataxia with he..:

Kaya Özçora, Gül Demet ; Miyatake, Satoko ; Matsumoto, Naomichi...
Acta Neurologica Belgica.  120 (2018)  2 - p. 429-432 , 2018
Link: https://doi.org/10.1007/..
 
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5

Loss of Protocadherin‐12Leads to Diencephalic‐Mesencephalic..:

Guemez‐Gamboa, Alicia ; Çağlayan, Ahmet Okay ; Stanley, Valentina...
Annals of Neurology.  84 (2018)  5 - p. 638-647 , 2018
Link: https://doi.org/10.1002/..
 
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6

The use of rapamycin in patients with tuberous sclerosis co..:

Canpolat, Mehmet ; Gumus, Hakan ; Kumandas, Sefer..
Epilepsy & Behavior.  88 (2018)  - p. 357-364 , 2018
Link: https://doi.org/10.1016/..
 
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7

Investigating the prevalence of febrile convulsion in Kayse..:

Canpolat, Mehmet ; Per, Huseyin ; Gumus, Hakan..
Seizure.  55 (2018)  - p. 36-47 , 2018
Link: https://doi.org/10.1016/..
 
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8

Analyzing autism spectrum disorder with structural and diff..:

Kumandas, Sefer ; Kaya Ozcora, Gul Demet ; Sagıroglu, Ayse...
European Journal of Paediatric Neurology.  21 (2017)  - p. e144 , 2017
Link: https://doi.org/10.1016/..
 
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9

Coenzyme Q10 deficiency; A treatable autosomal recessive ce..:

Kaya Ozcora, Gül Demet ; Basak, Nazlı ; Canpolat, Mehmet..
European Journal of Paediatric Neurology.  21 (2017)  - p. e136 , 2017
Link: https://doi.org/10.1016/..
 
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10

PEX10 mutation; Autosomal recessive cerebellar ataxia:

Canpolat, Mehmet ; Kaya Ozcora, Gül Demet ; Erdoğan, Murat..
European Journal of Paediatric Neurology.  21 (2017)  - p. e135 , 2017
Link: https://doi.org/10.1016/..
 
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11

Whole-exome sequence sometimes may be the only diagnostic m..:

Canpolat, Mehmet ; Ozcora, Gül Demet Kaya ; Kumandaş, Sefer
European Journal of Paediatric Neurology.  21 (2017)  - p. e105 , 2017
Link: https://doi.org/10.1016/..
 
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12

Evaluating brainstem in breath-holding spells:

Kaya Ozcora, Gül Demet ; Kumandaş, Sefer ; Sağıroğlu, Ayse...
European Journal of Paediatric Neurology.  21 (2017)  - p. e78 , 2017
Link: https://doi.org/10.1016/..
 
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13

Drug Reaction with Eosinophilia and Systemic Symptoms Syndr..:

Bayram, Ayşe Kaçar ; Canpolat, Mehmet ; Çınar, Salih Levent...
The Journal of Emergency Medicine.  50 (2016)  2 - p. e61-e66 , 2016
Link: https://doi.org/10.1016/..
 
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14

The Role of Diffusion-Weighted Imaging in the Evaluation of..:

Görkem, Sureyya Burcu ; Doganay, Selim ; Gumus, Kazim...
Journal of Child Neurology.  31 (2016)  14 - p. 1575-1578 , 2016
Link: https://doi.org/10.1177/..
 
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15

Misdiagnosis of gastroesophageal reflux disease as epilepti..:

Bayram, Ayşe Kaçar ; Canpolat, Mehmet ; Karacabey, Neslihan...
Brain and Development.  38 (2016)  3 - p. 274-279 , 2016
Link: https://doi.org/10.1016/..
 
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