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Fazeli, Walid
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1

Whole-Exome sequencing identifies GYS2 biallelic variants i..:

Ilyas, Muhammad ; Holzwarth, Dorothea ; Ishaq, Rafaqat...
Seizure: European Journal of Epilepsy.  116 (2024)  - p. 74-80 , 2024
Link: https://doi.org/10.1016/..
 
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2

Genetic diagnostics in epilepsies: recommendations of the C..:

Boßelmann, Christian ; Borggräfe, Ingo ; Fazeli, Walid...
Clinical Epileptology.  36 (2023)  3 - p. 224-237 , 2023
Link: https://doi.org/10.1007/..
 
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3

De Novo Variants in RAB11B Cause Various Degrees of Global ..:

Ahmad, Natalie ; Fazeli, Walid ; Schließke, Sophia...
Pediatric Neurology.  148 (2023)  - p. 164-171 , 2023
Link: https://doi.org/10.1016/..
 
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4

Genotype–phenotype correlation in contactin-associated prot..:

D'Onofrio, Gianluca ; Accogli, Andrea ; Severino, Mariasavina...
Human Genetics.  142 (2023)  7 - p. 909-925 , 2023
Link: https://doi.org/10.1007/..
 
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5

The phenotypic spectrum of PCDH12 associated disorders - Fi..:

Fazeli, Walid ; Bamborschke, Daniel ; Moawia, Abubakar...
European Journal of Paediatric Neurology.  36 (2022)  - p. 7-13 , 2022
Link: https://doi.org/10.1016/..
 
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6

MR imaging in children with transverse myelitis and acquire..:

El Naggar, Ines ; Cleaveland, Robert ; Wendel, Eva-Maria...
Multiple Sclerosis and Related Disorders.  67 (2022)  - p. 104068 , 2022
Link: https://doi.org/10.1016/..
 
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7

Aseptic Meningitis, Mucocutaneous Lesions and Arthritis aft..:

Bogs, Thomas ; Saleh, Nadia ; Yavuz, Suleyman Tolga...
Vaccines.  10 (2022)  2 - p. 325 , 2022
Link: https://doi.org/10.3390/..
 
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8

Structural mapping of GABRB3 variants reveals genotype–phen..:

Johannesen, Katrine M. ; Iqbal, Sumaiya ; Guazzi, Milena...
Genetics in Medicine.  24 (2022)  3 - p. 681-693 , 2022
Link: https://doi.org/10.1016/..
 
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9

RHOBTB2Mutations Expand the Phenotypic Spectrum of Alternat..:

Zagaglia, Sara ; Steel, Dora ; Krithika, S....
Neurology.  96 (2021)  11 - p. , 2021
Link: https://doi.org/10.1212/..
 
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10

Innovative Therapien inder Neuropädiatrie:

Friese, Johannes ; Fazeli, Walid ; Kirschner, Janbernd
Pädiatrie.  33 (2021)  S2 - p. 32-37 , 2021
Link: https://doi.org/10.1007/..
 
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11

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neur..:

Döring, Jan Henje ; Saffari, Afshin ; Bast, Thomas...
Biomedicines.  8 (2020)  11 - p. 456 , 2020
Link: https://doi.org/10.3390/..
 
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12

De novo BK channel variant causes epilepsy by affecting vol..:

Li, Xia ; Poschmann, Sibylle ; Chen, Qiuyun...
European Journal of Human Genetics.  26 (2018)  2 - p. 220-229 , 2018
Link: https://doi.org/10.1038/..
 
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13

A TUBB6 mutation is associated with autosomal dominant non-..:

Fazeli, Walid ; Herkenrath, Peter ; Stiller, Barbara...
Human Molecular Genetics.  26 (2017)  20 - p. 4055-4066 , 2017
Link: https://doi.org/10.1093/..
 
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14

Early-life exposure to caffeine affects the construction an..:

Fazeli, Walid ; Zappettini, Stefania ; Marguet, Stephan Lawrence...
Experimental Neurology.  295 (2017)  - p. 88-103 , 2017
Link: https://doi.org/10.1016/..
 
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15

Mendeliome sequencing enables differential diagnosis and tr..:

Fazeli, Walid ; Karakaya, Mert ; Herkenrath, Peter...
Molecular and Cellular Pediatrics.  3 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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