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Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Sleep Medicine
|
February 21, 2017
Sleep disorders in spinal muscular atrophy
Maria C Pera, Domenico M Romeo, Alessandra Graziano, et al.
Neuromuscular Disorders : NMD
|
March 28, 2021
The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure
Valeria A Sansone, Alice Pirola, Andrea Lizio, et al.
Children (Basel, Switzerland)
|
May 16, 2023
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study
Claudia Brogna, Marika Pane, Giorgia Coratti, et al.
Plos One
|
October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
Andrea Barp, Luca Bello, Luisa Politano, et al.
Annals of Neurology
|
June 23, 2019
Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world data
Marika Pane, Giorgia Coratti, Valeria A Sansone, et al.
Journal of Medical Genetics
|
December 30, 2018
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol
Francesco Danilo Tiziano, Rosa Lomastro, Emanuela Abiusi, et al.
European Journal of Pediatrics
|
January 20, 2022
Body mass index in type 2 spinal muscular atrophy: a longitudinal study
Gloria Ferrantini, Giorgia Coratti, Roberta Onesimo, et al.
The Journal of Pediatrics
|
February 10, 2020
Respiratory Needs in Patients with Type 1 Spinal Muscular Atrophy Treated with Nusinersen
Valeria A Sansone, Alice Pirola, Emilio Albamonte, et al.
European Journal of Human Genetics : EJHG
|
October 18, 2012
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study
Francesco D Tiziano, Rosa Lomastro, Lorena Di Pietro, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 162) with videos related to
Sort By:
Page
of 17
Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Sleep Medicine
|
February 21, 2017
Sleep disorders in spinal muscular atrophy
Maria C Pera, Domenico M Romeo, Alessandra Graziano, et al.
Neuromuscular Disorders : NMD
|
March 28, 2021
The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure
Valeria A Sansone, Alice Pirola, Andrea Lizio, et al.
Children (Basel, Switzerland)
|
May 16, 2023
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study
Claudia Brogna, Marika Pane, Giorgia Coratti, et al.
Plos One
|
October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
Andrea Barp, Luca Bello, Luisa Politano, et al.
Annals of Neurology
|
June 23, 2019
Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world data
Marika Pane, Giorgia Coratti, Valeria A Sansone, et al.
Journal of Medical Genetics
|
December 30, 2018
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol
Francesco Danilo Tiziano, Rosa Lomastro, Emanuela Abiusi, et al.
European Journal of Pediatrics
|
January 20, 2022
Body mass index in type 2 spinal muscular atrophy: a longitudinal study
Gloria Ferrantini, Giorgia Coratti, Roberta Onesimo, et al.
The Journal of Pediatrics
|
February 10, 2020
Respiratory Needs in Patients with Type 1 Spinal Muscular Atrophy Treated with Nusinersen
Valeria A Sansone, Alice Pirola, Emilio Albamonte, et al.
European Journal of Human Genetics : EJHG
|
October 18, 2012
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study
Francesco D Tiziano, Rosa Lomastro, Lorena Di Pietro, et al.
Page
of 17