Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alessandra Tessa

Showing results (11-20 of 116) with videos related to

Pageof 12
Sort By:
International Journal of Molecular Sciences|October 16, 2024
Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of <i>HPDL</i>-Related Neurological DisordersMatteo Baggiani, Devid Damiani, Flavia Privitera, et al.
Molecular and Cellular Neurosciences|June 19, 2003
Human melanoma/NG2 chondroitin sulfate proteoglycan is expressed in the sarcolemma of postnatal human skeletal myofibers. Abnormal expression in merosin-negative and Duchenne muscular dystrophiesStefania Petrini, Alessandra Tessa, Rosalba Carrozzo, et al.
International Journal of Molecular Sciences|March 13, 2024
NOTCH1-Related Leukoencephalopathy: A Novel Variant and Literature ReviewStefania Della Vecchia, Alessandra Tessa, Rosa Pasquariello, et al.
Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 1, 2024
Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variabilityEttore Cioffi, Valeria Gioiosa, Alessandra Tessa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2011
Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive ParkinsonismArianna Guidubaldi, Carla Piano, Filippo M Santorelli, et al.
Neurogenetics|January 26, 2019
Clinical and molecular studies in two new cases of ARSACSIvana Ricca, Federica Morani, Giacomo Maria Bacci, et al.
Cerebellum (London, England)|October 7, 2011
Infantile childhood onset of spinocerebellar ataxia type 2Roberto Di Fabio, Filippo Santorelli, Enrico Bertini, et al.
Journal of the Neurological Sciences|March 22, 2017
SPG2 mimicking multiple sclerosis in a family identified using next generation sequencingAnna Rubegni, Carla Battisti, Alessandra Tessa, et al.
Neuromuscular Disorders : NMD|December 7, 2007
Heart transplantation in a child with LGMD2I presenting as isolated dilated cardiomyopathyAdele D'Amico, Stefania Petrini, Francesco Parisi, et al.
Pageof 12

Showing results (11-20 of 116) with videos related to

Sort By:
Pageof 12
International Journal of Molecular Sciences|October 16, 2024
Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of <i>HPDL</i>-Related Neurological DisordersMatteo Baggiani, Devid Damiani, Flavia Privitera, et al.
Molecular and Cellular Neurosciences|June 19, 2003
Human melanoma/NG2 chondroitin sulfate proteoglycan is expressed in the sarcolemma of postnatal human skeletal myofibers. Abnormal expression in merosin-negative and Duchenne muscular dystrophiesStefania Petrini, Alessandra Tessa, Rosalba Carrozzo, et al.
International Journal of Molecular Sciences|March 13, 2024
NOTCH1-Related Leukoencephalopathy: A Novel Variant and Literature ReviewStefania Della Vecchia, Alessandra Tessa, Rosa Pasquariello, et al.
Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 1, 2024
Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variabilityEttore Cioffi, Valeria Gioiosa, Alessandra Tessa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2011
Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive ParkinsonismArianna Guidubaldi, Carla Piano, Filippo M Santorelli, et al.
Neurogenetics|January 26, 2019
Clinical and molecular studies in two new cases of ARSACSIvana Ricca, Federica Morani, Giacomo Maria Bacci, et al.
Cerebellum (London, England)|October 7, 2011
Infantile childhood onset of spinocerebellar ataxia type 2Roberto Di Fabio, Filippo Santorelli, Enrico Bertini, et al.
Journal of the Neurological Sciences|March 22, 2017
SPG2 mimicking multiple sclerosis in a family identified using next generation sequencingAnna Rubegni, Carla Battisti, Alessandra Tessa, et al.
Neuromuscular Disorders : NMD|December 7, 2007
Heart transplantation in a child with LGMD2I presenting as isolated dilated cardiomyopathyAdele D'Amico, Stefania Petrini, Francesco Parisi, et al.
Pageof 12