Muscular Atrophy, Spinal
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Subject Areas on Research
- Acute vincristine neurotoxicity in the presence of hereditary motor and sensory neuropathy type I.
- An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.
- Anesthesia for cesarean section in a patient with spinal muscular atrophy.
- Distinguishing clinical and electrodiagnostic features of X-linked bulbospinal neuronopathy.
- Genome engineering: a new approach to gene therapy for neuromuscular disorders.
- Impact of Movement Disorders on Management of Spinal Deformity in the Elderly.
- Impact of growth friendly interventions on spine and pulmonary outcomes of patients with spinal muscular atrophy.
- Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.
- Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.
- Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.
- Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.
- Spinal Muscular Atrophy: Inheritance, Screening, and Counseling for the Obstetric Provider.
- Spinal muscular atrophy care in the COVID-19 pandemic era.
- Successful Combination of Neuraxial and Regional Anesthesia in a Child With Advanced Spinal Muscular Atrophy Type 1 Receiving Maintenance Nusinersen Therapy: A Case Report.
- The importance of managing the patient and not the gene: expanded phenotype of GLE1-associated arthrogryposis.
- Tracheal intubation without muscle relaxants for caesarean section in patients with spinal muscular atrophy.