Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52.

Autor: D'Amore, Angelica^1,2,3 (AUTHOR), Tessa, Alessandra¹ (AUTHOR), Naef, Valentina¹ (AUTHOR), Bassi, Maria Teresa⁴ (AUTHOR), Citterio, Andrea⁴ (AUTHOR), Romaniello, Romina⁵ (AUTHOR), Fichi, Gianluca¹ (AUTHOR), Galatolo, Daniele¹ (AUTHOR), Mero, Serena¹ (AUTHOR), Battini, Roberta⁶ (AUTHOR), Bertocci, Giulia¹ (AUTHOR), Baldacci, Jacopo¹ (AUTHOR), Sicca, Federico^1,6 (AUTHOR), Gemignani, Federica² (AUTHOR), Ricca, Ivana¹ (AUTHOR), Rubegni, Anna¹ (AUTHOR), Hirst, Jennifer⁷ (AUTHOR), Marchese, Maria¹ (AUTHOR), Sahin, Mustafa³ (AUTHOR), Ebrahimi‐Fakhari, Darius³ (AUTHOR)

Publikováno v: Annals of Clinical & Translational Neurology. Apr2020, Vol. 7 Issue 4, p584-589. 6p.

SPG8 mutations in Italian families: clinical data and literature review.

Autor: Ginanneschi, Federica¹ (AUTHOR) ginanneschi@unisi.it, D'Amore, Angelica^2,3 (AUTHOR), Barghigiani, Melissa² (AUTHOR), Tessa, Alessandra² (AUTHOR), Rossi, Alessandro¹ (AUTHOR), Santorelli, Filippo Maria² (AUTHOR)

Publikováno v: Neurological Sciences. Mar2020, Vol. 41 Issue 3, p699-703. 5p. 1 Diagram, 1 Chart.

Editorial: In vitro and in vivo models for neurodevelopmental disorders.

Autor: D'Amore, Angelica, Marchese, Maria, Afshar-Saber, Wardiya, Hameed, Mustafa Q.

Publikováno v: Frontiers in Neuroscience; 2023, p1-3, 3p

Next Generation Molecular Studies of Hereditary Spastic Paraplegias in Men and Zebrafish

Autor: D'Amore, Angelica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1820::96611bfa736313e1bc2bc345a0e421f5
http://hdl.handle.net/11365/1105261

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