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Ceylan, Ahmet Cevdet
136  results:
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1

Evaluation of the Patients with the Diagnosis of Pontocereb..:

Cavusoglu, Dilek ; Ozturk, Gulten ; Turkdogan, Dilsad...
The Cerebellum.  , 2024
Link: https://doi.org/10.1007/..
 
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2

Validation of SMA screening kits with SMN1 gene analysis in..:

Gülşen, Murat ; Ceylan, Ahmet Cevdet ; Bahsi, Taha..
Clinica Chimica Acta.  555 (2024)  - p. 117793 , 2024
Link: https://doi.org/10.1016/..
 
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3

Evaluation of clinical, laboratory, and molecular genetic f..:

Yılmaz, Begüm ; Ceylan, Ahmet Cevdet ; Gündüz, Mehmet...
European Journal of Pediatrics.  , 2023
Link: https://doi.org/10.1007/..
 
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4

Impact of Inflammation-Related Genes on COVID-19: Prospecti..:

Ceylan, Ahmet Cevdet ; Çavdarlı, Büşranur ; Ceylan, Gülay Güleç...
The Tohoku Journal of Experimental Medicine.  261 (2023)  3 - p. 179-185 , 2023
Link: https://doi.org/10.1620/..
 
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5

Prevalence of DDC genotypes in patients with aromatic L-ami..:

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
Molecular Genetics and Metabolism.  139 (2023)  3 - p. 107624 , 2023
Link: https://doi.org/10.1016/..
 
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6

Corrigendum to: Prevalence of DDC genotypes in patients wit..:

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
Molecular Genetics and Metabolism.  139 (2023)  4 - p. 107647 , 2023
Link: https://doi.org/10.1016/..
 
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7

Homozygous SLC20A2 mutations cause congenital CMV infection..:

Ceylan, Ahmet Cevdet ; Kireker Köylü, Oya ; Özyürek, Hamit...
Acta Neurologica Belgica.  123 (2022)  5 - p. 1757-1761 , 2022
Link: https://doi.org/10.1007/..
 
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8

Investigation of sub‐chromosomal changes in males with idio..:

Çitli, Şenol ; Ceylan, Ahmet Cevdet ; Erdemir, Fikret
Andrologia.  54 (2022)  9 - p. , 2022
Link: https://doi.org/10.1111/..
 
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9

High diagnostic yield of targeted next‐generation sequencin..:

Çavdarlı, Büşranur ; Köken, Özlem Yayici ; Satılmış, Saide Betül Arslan...
Annals of Human Genetics.  87 (2022)  3 - p. 104-114 , 2022
Link: https://doi.org/10.1111/..
 
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10

A novel missense mutation in the UBE2A gene causes intellec..:

Arslan Satılmış, Saide Betül ; Kurt, Emin Emre ; Akçay, Ebru Perim..
The Journal of Gene Medicine.  23 (2021)  2 - p. , 2021
Link: https://doi.org/10.1002/..
 
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11

Genetic and phenotypic features of patients with childhood ..:

Arslan, Elif Acar ; Öncel, İbrahim ; Ceylan, Ahmet Cevdet..
Brain and Development.  42 (2020)  1 - p. 6-18 , 2020
Link: https://doi.org/10.1016/..
 
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12

Autosomal recessive spinocerebellar ataxia 18 caused by hom..:

Ceylan, Ahmet Cevdet ; Acar Arslan, Elif ; Erdem, Haktan Bağış...
Acta Neurologica Belgica.  121 (2020)  6 - p. 1457-1462 , 2020
Link: https://doi.org/10.1007/..
 
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13

SMN1 gene copy number analysis for spinal muscular atrophy ..:

Ceylan, Ahmet Cevdet ; Erdem, Haktan Bağış ; Şahin, İbrahim.
Neurological Sciences.  41 (2020)  9 - p. 2575-2584 , 2020
Link: https://doi.org/10.1007/..
 
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14

A special association between Charcot-Marie-Tooth type 1A d..:

Doğan, Yahya ; Gül, Şule ; Ceylan, Ahmet Cevdet.
Multiple Sclerosis and Related Disorders.  35 (2019)  - p. 83-85 , 2019
Link: https://doi.org/10.1016/..
 
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15

First cardiac manifestation of hypotonia-cystinuria syndrom:

Kılıç, Mustafa ; Ceylan, Ahmet Cevdet ; Örün, Utku Arman.
Metabolic Brain Disease.  33 (2018)  4 - p. 1375-1379 , 2018
Link: https://doi.org/10.1007/..
 
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