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Kumandaş, Sefer
70
results:
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1
CLP1 associated pontocerebellar hypoplasia:
Ozcora, Gul
;
Aktas, Dilek
;
Kumandas, Sefer
Annals of Medical Research. 28 (2021) 3 - p. 614 , 2021
Link:
https://doi.org/10.5455/..
?
2
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/..
?
3
A Rare Cause of Spasticity and Microcephaly: Argininemia:
Soylu Üstkoyuncu, Pembe
;
Kendirci, Mustafa
;
Gökay, Songül
...
Turkish Journal Of Neurology. 26 (2020) 3 - p. 250-252 , 2020
Link:
https://doi.org/10.4274/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
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/..
?
8
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/..
?
9
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/..
?
10
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/..
?
11
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/..
?
12
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/..
?
13
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/..
?
14
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/..
?
15
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/..
1-15