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Neuromuscular Disorders : NMD
|
January 22, 2004
Pilot trial of phenylbutyrate in spinal muscular atrophy
Eugenio Mercuri, Enrico Bertini, Sonia Messina, et al.
Neuromuscular Disorders : NMD
|
November 27, 2004
Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations
Heinz Jungbluth, Mark R Davis, Clemens Müller, et al.
Neuromuscular Disorders : NMD
|
April 20, 2020
Screening for early symptoms of respiratory involvement in myotonic dystrophy type 1 using the Respicheck questionnaire
Elisa De Mattia, Andrea Lizio, Elisa Falcier, et al.
Neuromuscular Disorders : NMD
|
December 4, 2019
A critical review of patient and parent caregiver oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in spinal muscular atrophy
Sonia Messina, Anna Lia Frongia, Laura Antonaci, et al.
Annals of Neurology
|
March 13, 2010
Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine
Eugenio Mercuri, Emma Clements, Amaka Offiah, et al.
Neuromuscular Disorders : NMD
|
June 27, 2008
Daily salbutamol in young patients with SMA type II
Marika Pane, Susanna Staccioli, Sonia Messina, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 26, 2020
Which are the factors influencing NIV adaptation and tolerance in ALS patients?
Massimo Russo, Carmen Bonanno, Claudia Profazio, et al.
European Journal of Human Genetics : EJHG
|
July 16, 2009
SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR
Francesco Danilo Tiziano, Anna Maria Pinto, Stefania Fiori, et al.
Neurology
|
August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational study
Eugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.
Brain Sciences
|
January 20, 2021
A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy
Gian Luca Vita, Maria Sframeli, Norma Licata, et al.
Page
of 17
Search research articles
Search
Showing results (41-50 of 162) with videos related to
Sort By:
Page
of 17
Neuromuscular Disorders : NMD
|
January 22, 2004
Pilot trial of phenylbutyrate in spinal muscular atrophy
Eugenio Mercuri, Enrico Bertini, Sonia Messina, et al.
Neuromuscular Disorders : NMD
|
November 27, 2004
Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations
Heinz Jungbluth, Mark R Davis, Clemens Müller, et al.
Neuromuscular Disorders : NMD
|
April 20, 2020
Screening for early symptoms of respiratory involvement in myotonic dystrophy type 1 using the Respicheck questionnaire
Elisa De Mattia, Andrea Lizio, Elisa Falcier, et al.
Neuromuscular Disorders : NMD
|
December 4, 2019
A critical review of patient and parent caregiver oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in spinal muscular atrophy
Sonia Messina, Anna Lia Frongia, Laura Antonaci, et al.
Annals of Neurology
|
March 13, 2010
Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine
Eugenio Mercuri, Emma Clements, Amaka Offiah, et al.
Neuromuscular Disorders : NMD
|
June 27, 2008
Daily salbutamol in young patients with SMA type II
Marika Pane, Susanna Staccioli, Sonia Messina, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 26, 2020
Which are the factors influencing NIV adaptation and tolerance in ALS patients?
Massimo Russo, Carmen Bonanno, Claudia Profazio, et al.
European Journal of Human Genetics : EJHG
|
July 16, 2009
SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR
Francesco Danilo Tiziano, Anna Maria Pinto, Stefania Fiori, et al.
Neurology
|
August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational study
Eugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.
Brain Sciences
|
January 20, 2021
A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy
Gian Luca Vita, Maria Sframeli, Norma Licata, et al.
Page
of 17