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Journal of Neurology
|
July 14, 2021
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network
V Montano, D Orsucci, V Carelli, et al.
Journal of Neurology
|
July 11, 2025
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa
T Mongini, G Gadaleta, P Alonge, et al.
Neuropathology and Applied Neurobiology
|
June 3, 2017
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD)
M Ripolone, R Violano, D Ronchi, et al.
Journal of Neurology
|
November 15, 2011
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years
C Angelini, C Semplicini, S Ravaglia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 19, 2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population
O Musumeci, G la Marca, M Spada, et al.
Journal of Neurology
|
August 18, 2022
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort
V Montano, P Lopriore, F Gruosso, et al.
Journal of Neurology
|
July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian Network
D Orsucci, C Angelini, E Bertini, et al.
Orphanet Journal of Rare Diseases
|
July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients
C Fiorillo, G Astrea, M Savarese, et al.
Brain : a Journal of Neurology
|
February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Journal of Neurology
|
July 14, 2021
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network
V Montano, D Orsucci, V Carelli, et al.
Journal of Neurology
|
July 11, 2025
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa
T Mongini, G Gadaleta, P Alonge, et al.
Neuropathology and Applied Neurobiology
|
June 3, 2017
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD)
M Ripolone, R Violano, D Ronchi, et al.
Journal of Neurology
|
November 15, 2011
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years
C Angelini, C Semplicini, S Ravaglia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 19, 2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population
O Musumeci, G la Marca, M Spada, et al.
Journal of Neurology
|
August 18, 2022
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort
V Montano, P Lopriore, F Gruosso, et al.
Journal of Neurology
|
July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian Network
D Orsucci, C Angelini, E Bertini, et al.
Orphanet Journal of Rare Diseases
|
July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients
C Fiorillo, G Astrea, M Savarese, et al.
Brain : a Journal of Neurology
|
February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Page
of 4