Search research articles
Contact Us
Filters
Showing results (601-610 of 638) with videos related to
Page
of 64
Sort By:
Plos Currents
|
February 3, 2015
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys
Marika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Brain Communications
|
July 9, 2021
International retrospective natural history study of <i>LMNA</i>-related congenital muscular dystrophy
Rabah Ben Yaou, Pomi Yun, Ivana Dabaj, et al.
Plos One
|
January 15, 2014
6 Minute walk test in Duchenne MD patients with different mutations: 12 month changes
Marika Pane, Elena S Mazzone, Maria Pia Sormani, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 16, 2023
Emergencies cards for neuromuscular disorders 1<sup>st</sup> Consensus Meeting from UILDM - Italian Muscular Dystrophy Association Workshop report
Fabrizio Racca, Valeria A Sansone, Federica Ricci, et al.
Neuromuscular Disorders : NMD
|
December 29, 2023
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study
Giorgia Coratti, Marika Pane, Claudia Brogna, et al.
Clinical Epigenetics
|
October 23, 2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
Claudia Strafella, Domenica Megalizzi, Giulia Trastulli, et al.
Frontiers in Genetics
|
March 21, 2020
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study
Marcella Neri, Rachele Rossi, Cecilia Trabanelli, et al.
European Journal of Heart Failure
|
May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy
Maria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.
Neurology
|
June 10, 2016
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients
Marco Savarese, Giuseppina Di Fruscio, Annalaura Torella, et al.
Brain : a Journal of Neurology
|
November 5, 2024
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity
Domenico Gorgoglione, Daniele Sabbatini, Pietro Riguzzi, et al.
Page
of 64
Search research articles
Search
Showing results (601-610 of 638) with videos related to
Sort By:
Page
of 64
Plos Currents
|
February 3, 2015
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys
Marika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Brain Communications
|
July 9, 2021
International retrospective natural history study of <i>LMNA</i>-related congenital muscular dystrophy
Rabah Ben Yaou, Pomi Yun, Ivana Dabaj, et al.
Plos One
|
January 15, 2014
6 Minute walk test in Duchenne MD patients with different mutations: 12 month changes
Marika Pane, Elena S Mazzone, Maria Pia Sormani, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 16, 2023
Emergencies cards for neuromuscular disorders 1<sup>st</sup> Consensus Meeting from UILDM - Italian Muscular Dystrophy Association Workshop report
Fabrizio Racca, Valeria A Sansone, Federica Ricci, et al.
Neuromuscular Disorders : NMD
|
December 29, 2023
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study
Giorgia Coratti, Marika Pane, Claudia Brogna, et al.
Clinical Epigenetics
|
October 23, 2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
Claudia Strafella, Domenica Megalizzi, Giulia Trastulli, et al.
Frontiers in Genetics
|
March 21, 2020
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study
Marcella Neri, Rachele Rossi, Cecilia Trabanelli, et al.
European Journal of Heart Failure
|
May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy
Maria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.
Neurology
|
June 10, 2016
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients
Marco Savarese, Giuseppina Di Fruscio, Annalaura Torella, et al.
Brain : a Journal of Neurology
|
November 5, 2024
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity
Domenico Gorgoglione, Daniele Sabbatini, Pietro Riguzzi, et al.
Page
of 64