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Cerebrovascular Diseases (Basel, Switzerland)
|
February 6, 2020
Isolated Insular Stroke: Clinical Presentation
Fabrizio Giammello, Domenico Cosenza, Carmela Casella, et al.
Annals of Neurology
|
September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia
Eleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.
Frontiers in Genetics
|
June 17, 2022
Case Report: Rare Homozygous <i>RNASEH1</i> Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
Arianna Manini, Leonardo Caporali, Megi Meneri, et al.
Neuromuscular Disorders : NMD
|
August 2, 2015
Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrum
Olimpia Musumeci, Andrea Thieme, Kristl G Claeys, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2010
Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength response
Sabrina Ravaglia, Anna Pichiecchio, Michela Ponzio, et al.
Autophagy
|
August 8, 2018
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis
Chiara Vantaggiato, Elena Panzeri, Marianna Castelli, et al.
Acta Neurologica Belgica
|
March 8, 2023
Paraneoplastic neurological syndromes of the central nervous system: a single institution 7-year case series
Fabrizio Giammello, Karol Galletta, Francesco Grillo, et al.
Neuromuscular Disorders : NMD
|
February 12, 2009
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in two
Benedikt Schoser, Saiju Jacob, David Hilton-Jones, et al.
Journal of Muscle Research and Cell Motility
|
March 30, 2006
Immunohistochemical analysis of human skeletal muscle AMP deaminase deficiency. Evidence of a correlation between the muscle HPRG content and the level of the residual AMP deaminase activity
Antonietta R M Sabbatini, Antonio Toscano, Mohammed Aguennouz, et al.
World Neurosurgery
|
June 1, 2024
Predictors of Good Functional Outcome in Patients with Tandem Occlusion After Revascularization Treatment: Single-Center Experience with 12-Month Follow-Up
Ludovica Ferraù, Fabrizio Giammello, Agostino Tessitore, et al.
Page
of 23
Search research articles
Search
Showing results (101-110 of 223) with videos related to
Sort By:
Page
of 23
Cerebrovascular Diseases (Basel, Switzerland)
|
February 6, 2020
Isolated Insular Stroke: Clinical Presentation
Fabrizio Giammello, Domenico Cosenza, Carmela Casella, et al.
Annals of Neurology
|
September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia
Eleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.
Frontiers in Genetics
|
June 17, 2022
Case Report: Rare Homozygous <i>RNASEH1</i> Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
Arianna Manini, Leonardo Caporali, Megi Meneri, et al.
Neuromuscular Disorders : NMD
|
August 2, 2015
Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrum
Olimpia Musumeci, Andrea Thieme, Kristl G Claeys, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2010
Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength response
Sabrina Ravaglia, Anna Pichiecchio, Michela Ponzio, et al.
Autophagy
|
August 8, 2018
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis
Chiara Vantaggiato, Elena Panzeri, Marianna Castelli, et al.
Acta Neurologica Belgica
|
March 8, 2023
Paraneoplastic neurological syndromes of the central nervous system: a single institution 7-year case series
Fabrizio Giammello, Karol Galletta, Francesco Grillo, et al.
Neuromuscular Disorders : NMD
|
February 12, 2009
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in two
Benedikt Schoser, Saiju Jacob, David Hilton-Jones, et al.
Journal of Muscle Research and Cell Motility
|
March 30, 2006
Immunohistochemical analysis of human skeletal muscle AMP deaminase deficiency. Evidence of a correlation between the muscle HPRG content and the level of the residual AMP deaminase activity
Antonietta R M Sabbatini, Antonio Toscano, Mohammed Aguennouz, et al.
World Neurosurgery
|
June 1, 2024
Predictors of Good Functional Outcome in Patients with Tandem Occlusion After Revascularization Treatment: Single-Center Experience with 12-Month Follow-Up
Ludovica Ferraù, Fabrizio Giammello, Agostino Tessitore, et al.
Page
of 23