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Alessandra Tessa

Showing results (51-60 of 116) with videos related to

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Metabolites|February 25, 2022
2-Year-Old and 3-Year-Old Italian ALS Patients with Novel <i>ALS2</i> Mutations: Identification of Key Metabolites in Their Serum and PlasmaMukesh Gautam, Renata Del Carratore, Benjamin Helmold, et al.
Biochemical and Biophysical Research Communications|February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathyVittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
Cephalalgia : an International Journal of Headache|March 15, 2011
A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutationLucio Santoro, Fiore Manganelli, Maria Roberta Fortunato, et al.
Pediatric Neurology|March 24, 2009
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutationsAlessandro Simonati, Alessandra Tessa, Bernardo Dalla Bernardina, et al.
International Journal of Molecular Sciences|February 25, 2023
Converging Role for REEP1/SPG31 in Oxidative StressValentina Naef, Maria C Meschini, Alessandra Tessa, et al.
Annals of Clinical and Translational Neurology|April 3, 2020
Expanding the clinical and genetic heterogeneity of SPAX5Claudia Dosi, Daniele Galatolo, Anna Rubegni, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 27, 2017
Leigh-like neuroimaging features associated with new biallelic mutations in OPA1Anna Rubegni, Tiziana Pisano, Giacomo Bacci, et al.
Neurogenetics|February 9, 2024
Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literatureEttore Cioffi, Gianluca Coppola, Olimpia Musumeci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 29, 2020
Spinocerebellar ataxia type 48: last but not leastGiovanna De Michele, Daniele Galatolo, Melissa Barghigiani, et al.
European Journal of Neurology|February 23, 2023
New cellular imaging-based method to distinguish the SPG4 subtype of hereditary spastic paraplegiaFrancesca Sardina, Davide Valente, Gaia Fattorini, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
Metabolites|February 25, 2022
2-Year-Old and 3-Year-Old Italian ALS Patients with Novel <i>ALS2</i> Mutations: Identification of Key Metabolites in Their Serum and PlasmaMukesh Gautam, Renata Del Carratore, Benjamin Helmold, et al.
Biochemical and Biophysical Research Communications|February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathyVittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
Cephalalgia : an International Journal of Headache|March 15, 2011
A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutationLucio Santoro, Fiore Manganelli, Maria Roberta Fortunato, et al.
Pediatric Neurology|March 24, 2009
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutationsAlessandro Simonati, Alessandra Tessa, Bernardo Dalla Bernardina, et al.
International Journal of Molecular Sciences|February 25, 2023
Converging Role for REEP1/SPG31 in Oxidative StressValentina Naef, Maria C Meschini, Alessandra Tessa, et al.
Annals of Clinical and Translational Neurology|April 3, 2020
Expanding the clinical and genetic heterogeneity of SPAX5Claudia Dosi, Daniele Galatolo, Anna Rubegni, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 27, 2017
Leigh-like neuroimaging features associated with new biallelic mutations in OPA1Anna Rubegni, Tiziana Pisano, Giacomo Bacci, et al.
Neurogenetics|February 9, 2024
Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literatureEttore Cioffi, Gianluca Coppola, Olimpia Musumeci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 29, 2020
Spinocerebellar ataxia type 48: last but not leastGiovanna De Michele, Daniele Galatolo, Melissa Barghigiani, et al.
European Journal of Neurology|February 23, 2023
New cellular imaging-based method to distinguish the SPG4 subtype of hereditary spastic paraplegiaFrancesca Sardina, Davide Valente, Gaia Fattorini, et al.
Pageof 12