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Neurology
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December 2, 2009
Autosomal recessive Bethlem myopathy
F Gualandi, A Urciuolo, E Martoni, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 21, 2018
A 5-center experience with intrathecal administration of nusinersen in SMA1 in Italy letter to the editor of european journal of pediatric neurology regarding the manuscript "single-center experience with intrathecal administration of nusinersen in children with spinal muscular atrophy type 1" written by pechmann and colleagues"
V A Sansone, M Pane, S Messina, et al.
Journal of Neurology
|
June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophy
A Prelle, G P Comi, C Rigoletto, et al.
Neurology
|
April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathies
M Sciacco, G Fagiolari, C Lamperti, et al.
Clinical Neuropathology
|
February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsy
P Bazzi, M Moggio, A Prelle, et al.
The Neuroradiology Journal
|
September 25, 2013
Cerebral amyloid angiopathy-related inflammation: an emerging disease
M Savoiardo, A Erbetta, J C Di Francesco, et al.
Neuromuscular Disorders : NMD
|
January 16, 2010
The Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): test development and reliability
A M Glanzman, E Mazzone, M Main, et al.
Organic & Biomolecular Chemistry
|
February 17, 2016
Reversible morphological changes of assembled supramolecular amphiphiles triggered by pH-modulated host-guest interactions
M A Olson, M S Messina, J R Thompson, et al.
Clinical Neuropathology
|
August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterization
A Prelle, M Sciacco, G P Comi, et al.
Muscle & Nerve
|
March 17, 2005
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
E Mercuri, S C Brown, P Nihoyannopoulos, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
Neurology
|
December 2, 2009
Autosomal recessive Bethlem myopathy
F Gualandi, A Urciuolo, E Martoni, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 21, 2018
A 5-center experience with intrathecal administration of nusinersen in SMA1 in Italy letter to the editor of european journal of pediatric neurology regarding the manuscript "single-center experience with intrathecal administration of nusinersen in children with spinal muscular atrophy type 1" written by pechmann and colleagues"
V A Sansone, M Pane, S Messina, et al.
Journal of Neurology
|
June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophy
A Prelle, G P Comi, C Rigoletto, et al.
Neurology
|
April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathies
M Sciacco, G Fagiolari, C Lamperti, et al.
Clinical Neuropathology
|
February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsy
P Bazzi, M Moggio, A Prelle, et al.
The Neuroradiology Journal
|
September 25, 2013
Cerebral amyloid angiopathy-related inflammation: an emerging disease
M Savoiardo, A Erbetta, J C Di Francesco, et al.
Neuromuscular Disorders : NMD
|
January 16, 2010
The Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): test development and reliability
A M Glanzman, E Mazzone, M Main, et al.
Organic & Biomolecular Chemistry
|
February 17, 2016
Reversible morphological changes of assembled supramolecular amphiphiles triggered by pH-modulated host-guest interactions
M A Olson, M S Messina, J R Thompson, et al.
Clinical Neuropathology
|
August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterization
A Prelle, M Sciacco, G P Comi, et al.
Muscle & Nerve
|
March 17, 2005
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
E Mercuri, S C Brown, P Nihoyannopoulos, et al.
Page
of 14