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Sedat IŞIKAY
109
results:
Search for persons
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Format
Online (109)
Mediatypes
Articles (Online) (34)
OpenAccess-fulltext (75)
Languages
english (100)
Sorted by: Relevance
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?
1
Botulinum toxin type A for the treatment of limb myokymia: ..:
Isikay, Sedat
Annals of Indian Academy of Neurology. 25 (2022) 5 - p. 928 , 2022
Link:
https://doi.org/10.4103/..
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2
Developmental genomics of limb malformations: Allelic serie..:
Duan, Ruizhi
;
Hijazi, Hadia
;
Gulec, Elif Yilmaz
...
Human Genetics and Genomics Advances. 3 (2022) 4 - p. 100132 , 2022
Link:
https://doi.org/10.1016/..
?
3
Eating-induced electroclinical and electrographical seizure..:
Yılmaz, Kutluhan
;
Işıkay, Sedat
Acta Neurologica Belgica. 122 (2021) 6 - p. 1607-1609 , 2021
Link:
https://doi.org/10.1007/..
?
4
Late diagnosis of pyridoxine-dependent epilepsy in two adol..:
Işıkay, Sedat
Annals of Indian Academy of Neurology. 24 (2021) 5 - p. 770 , 2021
Link:
https://doi.org/10.4103/..
?
5
Childhood pineal glioblastoma: Case report:
Atalay, Tugay
;
Isikay, Sedat
;
Guzel, Ebru
..
Journal of Pediatric Neurosciences. 16 (2021) 4 - p. 338 , 2021
Link:
https://doi.org/10.4103/..
?
6
High prevalence of multilocus pathogenic variation in neuro..:
Mitani, Tadahiro
;
Isikay, Sedat
;
Gezdirici, Alper
...
The American Journal of Human Genetics. 108 (2021) 10 - p. 1981-2005 , 2021
Link:
https://doi.org/10.1016/..
?
7
Multiple cerebral hemorrhages during the course of Guillain..:
ISIKAY, Sedat
;
SIRIKCI, Akif
Journal of Pediatric Neurosciences. 15 (2020) 2 - p. 105 , 2020
Link:
https://doi.org/10.4103/..
?
8
Hereditary chin trembling:
Isikay, Sedat
Journal of Pediatric Neurosciences. 15 (2020) 1 - p. 66 , 2020
Link:
https://doi.org/10.4103/..
?
9
Biallelic GRM7 variants cause epilepsy, microcephaly, and c..:
Marafi, Dana
;
Mitani, Tadahiro
;
Isikay, Sedat
...
Annals of Clinical and Translational Neurology. 7 (2020) 5 - p. 610-627 , 2020
Link:
https://doi.org/10.1002/..
?
10
Spontaneous Pneumocephalus Secondary to Positive Ventilatio..:
Işıkay, Sedat
The Indian Journal of Pediatrics. 86 (2019) 4 - p. 390-391 , 2019
Link:
https://doi.org/10.1007/..
?
11
Biallelic VARS variants cause developmental encephalopathy ..:
Siekierska, Aleksandra
;
Stamberger, Hannah
;
Deconinck, Tine
...
Nature Communications. 10 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
12
Congenital muscular dystrophy due to novel compound heteroz..:
Isikay, Sedat
;
Şirikçi, Akif
Journal of Pediatric Neurosciences. 13 (2018) 4 - p. 462 , 2018
Link:
https://doi.org/10.4103/..
?
13
Unusual hair findings in a child with cardiofaciocutaneous ..:
Işikay, Sedat
;
Karaer, Kadri
International Journal of Dermatology. 58 (2018) 3 - p. 354-356 , 2018
Link:
https://doi.org/10.1111/..
?
14
RANBP2 Mutation in Clinically Undiagnosed Acute Necrotizing..:
Işıkay, Sedat
;
Şahin, Yavuz
The Indian Journal of Pediatrics. 85 (2018) 9 - p. 820-821 , 2018
Link:
https://doi.org/10.1007/..
?
15
Phenotypic expansion illuminates multilocus pathogenic vari..:
Karaca, Ender
;
Posey, Jennifer E.
;
Coban Akdemir, Zeynep
...
Genetics in Medicine. 20 (2018) 12 - p. 1528-1537 , 2018
Link:
https://doi.org/10.1038/..
1-15