Suchergebnisse - "Gerik-Celebi, Hamide Betul"

PubPharm (6)

1

A novel CACNA1A mutation in a neonate with severe encephalopathy at birth

enthalten in: Acta neurologica Belgica | 2024

von Ozdil, M. | Eroglu, A. | Gerik-Celebi, H.

2

Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders

enthalten in: Molecular syndromology | 2024

von Gerik-Celebi, H. | Unsel-Bolat, G. | Bolat, H.

3

A novel CACNA1A mutation in a neonate with severe encephalopathy at birth

enthalten in: Acta neurologica Belgica | 2023

von Ozdil, M. | Eroglu, A. | Gerik-Celebi, H.

4

Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy

enthalten in: Molecular syndromology | 2023

von Gerik-Celebi, H. | Aydin, H. | Bolat, H. | +1

5

Coinheritance of novel mutations in NAGLU causing mucopolysaccharidosis type IIIB and in DDHD2 causing spastic paraplegia54 in a Turkish family

enthalten in: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia | 2020

von Gun Bilgic, D. | Gerik Celebi, H. | Aydin Gumus, A. | +8

6

A new clinical entity in T704M mutation in periodic paralysis

enthalten in: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia | 2020

von Gun Bilgic, D. | Aydin Gumus, A. | Gerik Celebi, H. | +3

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