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Current Opinion in Neurology
|
October 1, 1994
Idiopathic inflammatory myopathies: inclusion-body myositis, polymyositis, and dermatomyositis
V Askanas, W K Engel, M Mirabella
Chemical Science
|
January 6, 2023
Influence of the solvent in the self-assembly and binding properties of [1 + 1] tetra-imine bis-calix[4]pyrrole cages
Chiara F M Mirabella, Gemma Aragay, Pablo Ballester
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
November 24, 2011
Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle
A Broccolini, T Gidaro, R Morosetti, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
August 17, 2011
Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration
R Morosetti, C Gliubizzi, A Broccolini, et al.
Annals of Neurology
|
March 1, 1996
Use of anti-neurofilament antibody to identify paired-helical filaments in inclusion-body myositis
V Askanas, R B Alvarez, M Mirabella, et al.
JACS Au
|
February 28, 2025
Acceleration and Selectivity of 1,3-Dipolar Cycloaddition Reactions Included in a Polar [4 + 2] Octa-imine Bis-calix[4]pyrrole Cage
Yifan Li, Chiara F M Mirabella, Gemma Aragay, et al.
Neurology
|
September 20, 2000
Apoptotic features accompany acute quadriplegic myopathy
S Di Giovanni, M Mirabella, A D'Amico, et al.
Brain : a Journal of Neurology
|
December 28, 1999
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanism
M Mirabella, S Di Giovanni, G Silvestri, et al.
Acta Neurologica Belgica
|
January 1, 2009
ANCA-related vasculitic neuropathy mimicking motor neuron disease
M Luigetti, G Tasca, M Mirabella, et al.
Journal of Neuropathology and Experimental Neurology
|
July 1, 1996
Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies
M Mirabella, R B Alvarez, M Bilak, et al.
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of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Current Opinion in Neurology
|
October 1, 1994
Idiopathic inflammatory myopathies: inclusion-body myositis, polymyositis, and dermatomyositis
V Askanas, W K Engel, M Mirabella
Chemical Science
|
January 6, 2023
Influence of the solvent in the self-assembly and binding properties of [1 + 1] tetra-imine bis-calix[4]pyrrole cages
Chiara F M Mirabella, Gemma Aragay, Pablo Ballester
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
November 24, 2011
Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle
A Broccolini, T Gidaro, R Morosetti, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
August 17, 2011
Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration
R Morosetti, C Gliubizzi, A Broccolini, et al.
Annals of Neurology
|
March 1, 1996
Use of anti-neurofilament antibody to identify paired-helical filaments in inclusion-body myositis
V Askanas, R B Alvarez, M Mirabella, et al.
JACS Au
|
February 28, 2025
Acceleration and Selectivity of 1,3-Dipolar Cycloaddition Reactions Included in a Polar [4 + 2] Octa-imine Bis-calix[4]pyrrole Cage
Yifan Li, Chiara F M Mirabella, Gemma Aragay, et al.
Neurology
|
September 20, 2000
Apoptotic features accompany acute quadriplegic myopathy
S Di Giovanni, M Mirabella, A D'Amico, et al.
Brain : a Journal of Neurology
|
December 28, 1999
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanism
M Mirabella, S Di Giovanni, G Silvestri, et al.
Acta Neurologica Belgica
|
January 1, 2009
ANCA-related vasculitic neuropathy mimicking motor neuron disease
M Luigetti, G Tasca, M Mirabella, et al.
Journal of Neuropathology and Experimental Neurology
|
July 1, 1996
Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies
M Mirabella, R B Alvarez, M Bilak, et al.
Page
of 5