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Çelebi, Hamide Betül Gerik
18  results:
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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/..
 
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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/..
 
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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..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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...
 
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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..
 
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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..
 
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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/..
 
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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/..
 
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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/..
 
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