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Minerva Pediatrica
|
April 4, 2007
Noninvasive ventilation with positive airway pressure in paediatric intensive care
G Ottonello, G Villa, L Doglio, 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.
Neurology
|
May 24, 2006
Expanding the clinical spectrum of POMT1 phenotype
A D'Amico, A Tessa, C Bruno, et al.
European Journal of Neurology
|
March 23, 2016
Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2
C Fiorillo, F Moro, G Brisca, et al.
Neurology
|
January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)
C Bruno, E Bertini, A Federico, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 10, 2000
Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype
F Galbiati, D Volonte, J B Chu, et al.
Clinical Genetics
|
February 20, 2018
Expanding the histopathological spectrum of CFL2-related myopathies
F Fattori, C Fiorillo, C Rodolico, et al.
Journal of the Neurological Sciences
|
February 19, 2019
Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability
D Tolomeo, A Rubegni, M Severino, et al.
European Journal of Neurology
|
October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen
V A Sansone, G Coratti, M C Pera, et al.
Neuromuscular Disorders : NMD
|
January 5, 2000
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy
C Wallgren-Pettersson, K Pelin, P Hilpelä, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Minerva Pediatrica
|
April 4, 2007
Noninvasive ventilation with positive airway pressure in paediatric intensive care
G Ottonello, G Villa, L Doglio, 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.
Neurology
|
May 24, 2006
Expanding the clinical spectrum of POMT1 phenotype
A D'Amico, A Tessa, C Bruno, et al.
European Journal of Neurology
|
March 23, 2016
Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2
C Fiorillo, F Moro, G Brisca, et al.
Neurology
|
January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)
C Bruno, E Bertini, A Federico, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 10, 2000
Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype
F Galbiati, D Volonte, J B Chu, et al.
Clinical Genetics
|
February 20, 2018
Expanding the histopathological spectrum of CFL2-related myopathies
F Fattori, C Fiorillo, C Rodolico, et al.
Journal of the Neurological Sciences
|
February 19, 2019
Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability
D Tolomeo, A Rubegni, M Severino, et al.
European Journal of Neurology
|
October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen
V A Sansone, G Coratti, M C Pera, et al.
Neuromuscular Disorders : NMD
|
January 5, 2000
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy
C Wallgren-Pettersson, K Pelin, P Hilpelä, et al.
Page
of 5