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Publications by M. Pane
Salbutamol Increases Survival Motor Neuron (SMN) Transcript Levels in Leucocytes of Spinal Muscular Atrophy (SMA) Patients: Relevance for Clinical Trial Design
Journal of Medical Genetics
Genetics
The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): Test Development and Reliability
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Related publications
Muscle-Specific SMN Reduction Reveals Motor Neuron–independent Disease in Spinal Muscular Atrophy Models
Journal of Clinical Investigation
Medicine
The Need for SMN-Independent Treatments of Spinal Muscular Atrophy (SMA) to Complement SMN-Enhancing Drugs
Frontiers in Neurology
Neurology
SMN Blood Levels in a Porcine Model of Spinal Muscular Atrophy
Journal of Neuromuscular Diseases
Neurology
Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy
Neural Plasticity
Neurology
Dysregulation of Synaptogenesis Genes Antecedes Motor Neuron Pathology in Spinal Muscular Atrophy
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Role for SMN Exon 7 Splicing in the Selective Vulnerability of Motor Neurons in Spinal Muscular Atrophy
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
Cost of Illness of Spinal Muscular Atrophy (SMA) in Italy
Global and Regional Health Technology Assessment
Health Policy
ADrosophila Melanogastermodel of Spinal Muscular Atrophy Reveals a Function for SMN in Striated Muscle
Journal of Cell Biology
Medicine
Cell Biology