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Alessandra Tessa

Showing results (61-70 of 116) with videos related to

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Cerebellum (London, England)|September 4, 2024
Pseudodominance in RFC1-Spectrum DisorderGrazia Maria Igea Falcone, Alessandra Tessa, Ignazio Giuseppe Arena, et al.
Molecular Medicine (Cambridge, Mass.)|November 13, 2002
Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathyGabriele Siciliano, Fabio Monzani, Maria Laura Manca, et al.
Journal of Neurology|March 3, 2005
The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathyValentina Scarano, Pietro Mancini, Chiara Criscuolo, et al.
Multiple Sclerosis and Related Disorders|June 23, 2020
A new paraplegin mutation in a patient with primary progressive multiple sclerosisAngelo Bellinvia, Luisa Pastò, Claudia Niccolai, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 2, 2024
Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating PolyradiculoneuropathyIsabella Di Sarno, Stefano Tozza, Filippo Maria Santorelli, et al.
Journal of Neurology|June 5, 2016
A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findingsAlexandros A Polymeris, Alessandra Tessa, Katherine Anagnostopoulou, et al.
Journal of Neurology|February 26, 2016
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 familyLuca Leonardi, Lucia Ziccardi, Christian Marcotulli, et al.
Genes|November 27, 2024
Small Complex Rearrangement in <i>HINT1</i>-Related Axonal NeuropathyAlessandra Tessa, Mariapaola Schifino, Eliana Salvo, et al.
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
Brain Sciences|March 6, 2021
Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center ExperienceVittorio Riso, Salvatore Rossi, Tommaso F Nicoletti, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
Cerebellum (London, England)|September 4, 2024
Pseudodominance in RFC1-Spectrum DisorderGrazia Maria Igea Falcone, Alessandra Tessa, Ignazio Giuseppe Arena, et al.
Molecular Medicine (Cambridge, Mass.)|November 13, 2002
Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathyGabriele Siciliano, Fabio Monzani, Maria Laura Manca, et al.
Journal of Neurology|March 3, 2005
The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathyValentina Scarano, Pietro Mancini, Chiara Criscuolo, et al.
Multiple Sclerosis and Related Disorders|June 23, 2020
A new paraplegin mutation in a patient with primary progressive multiple sclerosisAngelo Bellinvia, Luisa Pastò, Claudia Niccolai, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 2, 2024
Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating PolyradiculoneuropathyIsabella Di Sarno, Stefano Tozza, Filippo Maria Santorelli, et al.
Journal of Neurology|June 5, 2016
A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findingsAlexandros A Polymeris, Alessandra Tessa, Katherine Anagnostopoulou, et al.
Journal of Neurology|February 26, 2016
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 familyLuca Leonardi, Lucia Ziccardi, Christian Marcotulli, et al.
Genes|November 27, 2024
Small Complex Rearrangement in <i>HINT1</i>-Related Axonal NeuropathyAlessandra Tessa, Mariapaola Schifino, Eliana Salvo, et al.
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
Brain Sciences|March 6, 2021
Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center ExperienceVittorio Riso, Salvatore Rossi, Tommaso F Nicoletti, et al.
Pageof 12