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Teuta Domi

Showing results (11-20 of 38) with videos related to

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Journal of Neurology|November 21, 2025
The genetic architecture of primary lateral sclerosis in a cohort of Italian patientsParide Schito, Teuta Domi, Tommaso Russo, et al.
Neurology|March 17, 2023
Clinical Features and Biomarkers to Differentiate Primary and Amyotrophic Lateral Sclerosis in Patients With an Upper Motor Neuron SyndromeParide Schito, Tommaso Russo, Teuta Domi, et al.
Frontiers in Neurology|August 1, 2022
Profiling morphologic MRI features of motor neuron disease caused by <i>TARDBP</i> mutationsEdoardo Gioele Spinelli, Alma Ghirelli, Nilo Riva, et al.
Plos One|February 25, 2012
Urokinase plasminogen receptor and the fibrinolytic complex play a role in nerve repair after nerve crush in mice, and in human neuropathiesCristina Rivellini, Giorgia Dina, Emanuela Porrello, et al.
Development (Cambridge, England)|February 24, 2012
Vimentin regulates peripheral nerve myelinationDaniela Triolo, Giorgia Dina, Carla Taveggia, et al.
Skeletal Muscle|September 9, 2015
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1ATeuta Domi, Emanuela Porrello, Daniele Velardo, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 23, 2019
Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72Yuri Matteo Falzone, Marta Radaelli, Federica Agosta, et al.
European Journal of Neurology|June 23, 2026
Tolerability, Safety and Effectiveness of Sigh Introduction During Non-Invasive Mechanical Ventilation Cycles in Patients With Amyotrophic Lateral SclerosisNilo Riva, Paride Schito, Tommaso Russo, et al.
Frontiers in Nutrition|July 6, 2026
Perspective and quality of life in amyotrophic lateral sclerosis patients undergoing percutaneous endoscopic gastrostomyNilo Riva, Enrica Finotto, Paride Schito, et al.
Frontiers in Neuroscience|June 29, 2023
A novel <i>GRN</i> mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Journal of Neurology|November 21, 2025
The genetic architecture of primary lateral sclerosis in a cohort of Italian patientsParide Schito, Teuta Domi, Tommaso Russo, et al.
Neurology|March 17, 2023
Clinical Features and Biomarkers to Differentiate Primary and Amyotrophic Lateral Sclerosis in Patients With an Upper Motor Neuron SyndromeParide Schito, Tommaso Russo, Teuta Domi, et al.
Frontiers in Neurology|August 1, 2022
Profiling morphologic MRI features of motor neuron disease caused by <i>TARDBP</i> mutationsEdoardo Gioele Spinelli, Alma Ghirelli, Nilo Riva, et al.
Plos One|February 25, 2012
Urokinase plasminogen receptor and the fibrinolytic complex play a role in nerve repair after nerve crush in mice, and in human neuropathiesCristina Rivellini, Giorgia Dina, Emanuela Porrello, et al.
Development (Cambridge, England)|February 24, 2012
Vimentin regulates peripheral nerve myelinationDaniela Triolo, Giorgia Dina, Carla Taveggia, et al.
Skeletal Muscle|September 9, 2015
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1ATeuta Domi, Emanuela Porrello, Daniele Velardo, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 23, 2019
Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72Yuri Matteo Falzone, Marta Radaelli, Federica Agosta, et al.
European Journal of Neurology|June 23, 2026
Tolerability, Safety and Effectiveness of Sigh Introduction During Non-Invasive Mechanical Ventilation Cycles in Patients With Amyotrophic Lateral SclerosisNilo Riva, Paride Schito, Tommaso Russo, et al.
Frontiers in Nutrition|July 6, 2026
Perspective and quality of life in amyotrophic lateral sclerosis patients undergoing percutaneous endoscopic gastrostomyNilo Riva, Enrica Finotto, Paride Schito, et al.
Frontiers in Neuroscience|June 29, 2023
A novel <i>GRN</i> mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
Pageof 4