E-LIB Suche - Ergebnisse für: Candayan, Ayşe

1

Genotypic And Phenotypic Features of Patients with GJB1 Mut..:

Parman, Fatma Yesim ; Cakar, Arman ; Candayan, Ayse..
Neurology. 100 (2023) 17_supplement_2 - p. , 2023

Link: https://doi.org/10.1212/..

2

Phenotypic and Genetic Heterogeneity of Adult Patients with..:

Perić, Stojan ; Marković, Vladana ; Candayan, Ayşe...
Cells. 11 (2022) 18 - p. 2804 , 2022

Link: https://doi.org/10.3390/..

3

Central Nervous System Involvement in HINT1 Neuropathy: An ..:

Çakar, Arman ; Acarlı, Ayşe Nur Özdağ ; Candayan, Ayse...
Neurology. 98 (2022) 18_supplement - p. , 2022

Link: https://doi.org/10.1212/..

4

Phenotypical spectrum ofSACSvariants: Neuromuscular perspec..:

Çakar, Arman ; İnci, Meltem ; Özdağ Acarlı, Ayşe Nur...
Acta Neurologica Scandinavica. 145 (2022) 5 - p. 619-626 , 2022

Link: https://doi.org/10.1111/..

5

Single Center Experience of SORD Neuropathy in Turkey (P1-1..:

Çakar, Arman ; Candayan, Ayse ; Durmus, Hacer..
Neurology. 98 (2022) 18_supplement - p. , 2022

Link: https://doi.org/10.1212/..

6

Cerebellar ataxia, neuropathy and vestibular areflexia synd..:

Çakar, Arman ; Şahin, Erdi ; Tezel, Seden...
Acta Neurologica Belgica. 122 (2021) 4 - p. 939-945 , 2021

Link: https://doi.org/10.1007/..

7

Autosomal Recessive Charcot-Marie-Tooth Disease in Turkey (..:

Parman, Yesim ; Cakar, Arman ; Candayan, Ayse...
Neurology. 92 (2019) 15_supplement - p. , 2019

Link: https://doi.org/10.1212/..

8

The first biallelic missense mutation in the FXN gene in a ..:

Candayan, Ayşe ; Yunisova, Gulshan ; Çakar, Arman...
neurogenetics. 21 (2019) 1 - p. 73-78 , 2019

Link: https://doi.org/10.1007/..

9

Clinical and Genetic Features in X-Linked Charcot-Marie-Too..:

Parman, Yesim ; Durmus, Hacer ; Candayan, Ayse...
Neurology. 90 (2018) 15_supplement - p. , 2018

Link: https://doi.org/10.1212/..

10

Evaluation techniques:

, In: Nanobiomaterials Science, Development and Evaluation,

Yesilkir-Baydar, Serap ; Oztel, Olga N. ; Cakir-Koc, Rabia. - p. 211-232 , 2017

Link: https://doi.org/10.1016/..

11

MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild..:

Ylikallio, Emil ; Woldegebriel, Rosa ; Tumiati, Manuela...
Brain. 140 (2017) 8 - p. 2093-2103 , 2017

Link: https://doi.org/10.1093/..

12

List of Contributors:

, In: Nanobiomaterials Science, Development and Evaluation,

Aavani, Farzaneh ; Ahadian, Samad ; Altuntaş, Ebru... - p. ix-xi , 2017

Link: https://doi.org/10.1016/..

13

CHARCOT-MARIE-TOOTH DISEASE IN TURKEY: CLINICAL AND GENETIC..:

Akcay, Halil Ibrahim ; Durmus, Hacer ; Deymeer, Feza...
Neurology. 88 (2017) 16_supplement - p. , 2017

Link: https://doi.org/10.1212/..

14

Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropa..:

Candayan, Ayşe ; Parman, Yeşim ; Battaloğlu, Esra
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941236/. , 2022

Link: http://www.ncbi.nlm.nih...

15

Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropa..:

Candayan, Ayse ; Parman, Yesim ; Battaloglu, Esra
https://aperta.ulakbim.gov.tr/record/255499. , 2022

Link: https://aperta.ulakbim.g..