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Galati Rando, Rosanna
8  Ergebnisse:
Personensuche X
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1

A de novo ARIH2 gene mutation was detected in a patient wit..:

Vinci, Mirella ; Treccarichi, Simone ; Galati Rando, Rosanna...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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2

STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to De..:

Vinci, Mirella ; Costanza, Carola ; Galati Rando, Rosanna...
International Journal of Molecular Sciences.  24 (2023)  22 - p. 16436 , 2023
Link: https://doi.org/10.3390/..
 
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3

Role of COMT V158M Polymorphism in the Development of Dysto..:

Nicotera, Antonio Gennaro ; Di Rosa, Gabriella ; Turriziani, Laura...
Brain Sciences.  11 (2021)  10 - p. 1293 , 2021
Link: https://doi.org/10.3390/..
 
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4

Poly (ADP-ribose) polymerase-1 (PARP-1) −410C/T polymorphis..:

Salluzzo, Maria Grazia ; Cosentino, Filomena I. ; Romano, Carmelo...
Journal of the Neurological Sciences.  363 (2016)  - p. 95-96 , 2016
Link: https://doi.org/10.1016/..
 
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5

STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to De..:

Vinci, Mirella ; Costanza, Carola ; Galati Rando, Rosanna...
info:eu-repo/semantics/altIdentifier/pmid/38003627.  , 2023
Link: https://hdl.handle.net/1..
 
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6

Killer-specific secretory (Ksp37) gene expression in subjec..:

Salemi, Michele ; Barone, Concetta ; Morale, Maria Concetta...
Neurological Sciences.  37 (2016)  5 - p. 793-795 , 2016
Link: https://doi.org/10.1007/..
 
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7

Role of COMT V158M Polymorphism in the Development of Dysto..:

Antonio Gennaro Nicotera ; Gabriella Di Rosa ; Laura Turriziani...
https://www.mdpi.com/2076-3425/11/10/1293.  , 2021
Link: https://doi.org/10.3390/..
 
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8

Role of COMT V158M Polymorphism in the Development of Dysto..:

Antonio Gennaro Nicotera ; Gabriella Di Rosa ; Laura Turriziani...
Molecular and Cellular Neuroscience.  , 2021
Link: https://doi.org/10.3390/..
 
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