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Çelebi, Hamide Betül Gerik
18
results:
Search for persons
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Format
Online (18)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (8)
Languages
english (16)
Sorted by: Relevance
Sorted by: Year
?
1
Molecular analyses of ADAMTS-1, -4, -5, and IL-17 a cytokin..:
Buran, Tahir
;
Batır, Muhammet Burak
;
Çam, Fethi Sırrı
...
BMC Gastroenterology. 23 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
2
CLINICAL AND GENETIC CHARACTERISTICS OF PATIENTS WITH UNEXP..:
Çelebi, Hamide Betül Gerik
;
Aydın, Hilal
;
Bolat, Hilmi
.
IBRO Neuroscience Reports. 15 (2023) - p. S537 , 2023
Link:
https://doi.org/10.1016/..
?
3
A retrospective cohort study investigating the etiology of ..:
Şahin, Ahmet Hikmet
;
Angin, Güngör
;
Gerik Çelebi, Hamide Betül
..
Journal of Surgery and Medicine. 7 (2023) 7 - p. 421-424 , 2023
Link:
https://doi.org/10.28982..
?
4
Coinheritance of novel mutations in NAGLU causing mucopolys..:
Gun Bilgic, Dilek
;
Gerik Celebi, Hamide Betul
;
Aydin Gumus, Aydeniz
...
Journal of Clinical Neuroscience. 82 (2020) - p. 214-218 , 2020
Link:
https://doi.org/10.1016/..
?
5
A new clinical entity in T704M mutation in periodic paralys..:
Gun Bilgic, Dilek
;
Aydin Gumus, Aydeniz
;
Gerik Celebi, Hamide Betul
...
Journal of Clinical Neuroscience. 78 (2020) - p. 203-206 , 2020
Link:
https://doi.org/10.1016/..
?
6
A novel frameshift mutation in two siblings with merosin-de..:
Ayça, Senem
;
Gerik Çelebi, Hamide Betül
;
Polat, Muzaffer
.
European Journal of Paediatric Neurology. 21 (2017) - p. e228-e229 , 2017
Link:
https://doi.org/10.1016/..
?
7
Van Der Knaap disease; A case having a defined mutation and..:
Gerik Çelebi, Hamide Betül
European Journal of Paediatric Neurology. 21 (2017) - p. e129-e130 , 2017
Link:
https://doi.org/10.1016/..
?
8
A case of pyridoxine dependent epilepsy admitted with statu..:
Ayça, Senem
;
Gerik Çelebi, Hamide Betül
;
Çam, Sırrı
.
European Journal of Paediatric Neurology. 21 (2017) - p. e191-e192 , 2017
Link:
https://doi.org/10.1016/..
?
9
A novel de nova missense LMNA mutation in a Turkish patient..:
Gerik Çelebi, Hamide Betül
;
Ayça, Senem
;
Polat, Muzaffer
.
European Journal of Paediatric Neurology. 21 (2017) - p. e227 , 2017
Link:
https://doi.org/10.1016/..
?
10
Molecular analyses of ADAMTS-1, -4, -5, and IL-17 a cytokin..:
Buran, Tahir
;
Batır, Muhammet Burak
;
Çam, Fethi Sırrı
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552413/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
11
Gelişim geriliği/entellektüel yetersizliği olan çocuklarda ..:
Bolat, Hilmi
;
Çelebi, Hamide Betül Gerik
;
Bolat, Gül Ünsel
...
Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi. , 2022
Link:
https://hdl.handle.net/2..
?
12
The role of next generation sequencing in diagnosis of pati..:
Bolat, Hilmi
;
Çelebi, Hamide Betül Gerik
10.12996/gmj.2022.87. , 2022
Link:
https://hdl.handle.net/2..
?
13
A novel CACNA1A mutation in a neonate with severe encephalo..:
Ozdil, Mine
;
Eroglu, Arzu
;
Gerik-Celebi, Hamide Betul
Acta Neurologica Belgica. 124 (2023) 2 - p. 705-708 , 2023
Link:
https://doi.org/10.1007/..
?
14
Molecular analyses of ADAMTS-1, -4, -5, and IL-17 a cytokin..:
Tahir Buran
;
Muhammet Burak Batır
;
Fethi Sırrı Çam
...
https://doi.org/10.1186/s12876-023-02985-z. , 2023
Link:
https://doi.org/10.1186/..
?
15
CLINICAL AND GENETIC CHARACTERISTICS OF PATIENTS WITH UNEXP..:
Hamide Betül Gerik Çelebi
;
Hilal Aydın
;
Hilmi Bolat
.
http://www.sciencedirect.com/science/article/pii/S266724212301120X. , 2023
Link:
https://doi.org/10.1016/..
1-15