Fazeli, W
136  Ergebnisse:
Personensuche X
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1

Clinical and genetic spectrum of SCN2A-associated episodic ..:

Schwarz, N. ; Bast, T. ; Gaily, E....
European Journal of Paediatric Neurology.  23 (2019)  3 - p. 438-447 , 2019
 
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2

FV 20 Dominant mutation causes familial episodic ataxia and..:

Fazeli, W.
Clinical Neurophysiology.  130 (2019)  8 - p. e131-e132 , 2019
 
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3

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

D'Onofrio, G ; Accogli, A ; Severino, M...
https://discovery.ucl.ac.uk/id/eprint/10170801/1/s00439-023-02552-2.pdf.  , 2023
 
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4

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

Johannesen, KM ; Iqbal, S ; Guazzi, M...
https://discovery.ucl.ac.uk/id/eprint/10143074/2/McTague_GABRB3%20mapping%20manuscript%20revision%20clean.pdf.  , 2022
 
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6

RHOBTB2 mutations expand the phenotypic spectrum of alterna..:

Zagaglia, S ; Steel, D ; Krithika, S...
https://discovery.ucl.ac.uk/id/eprint/10124148/4/Sisodiya_RHOBTB2%20for%20Neurology%20revisions_March21.pdf.  , 2021
 
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Clinical and genetic spectrum of SCN2A-associated episodic ..:

Schwarz, N ; Bast, T ; Gaily, E...
Schwarz , N , Bast , T , Gaily , E , Golla , G , Gorman , K M , Griffiths , L R , Hahn , A , Hukin , J , King , M , Korff , C , Miranda , M J , Møller , R S , Neubauer , B , Smith , R A , Smol , T , Striano , P , Stroud , B , Vaccarezza , M , Kluger , G , Lerche , H & Fazeli , W 2019 , ' Clinical and genetic spectrum of SCN2A-associated episodic ataxia ' , European Journal of Paediatric Neurology , vol. 23 , no. 3 , pp. 438-447 . https://doi.org/10.1016/j.ejpn.2019.03.001.  , 2019
 
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11

Contributors:

, In: Metabolic Syndrome,
 
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12

List of contributors:

, In: Nutritional Management of Renal Disease,
 
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15

List of Contributors:

, In: Principles of Gender-Specific Medicine,
 
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