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Author Details
Full Name
Vamshi K Rao
Affiliation
Lurie Children's Hospital of Chicago
ORCID
Career Start Year
2010
Papers
23
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36872785
Longitudinal Assessment of Timed Function Tests in Ambulatory Individuals with SMA Treated with Nusinersen.
J Neuromuscul Dis
2023
38009078
A Virtual Reality Exergame: Clinician-Guided Breathing and Relaxation for Children with Muscular Dystrophy.
2023 IEEE Conf Virtual Real 3D User Interfaces Abstr Workshops
2023
37651972
Measuring the Efficacy of Thymectomy for Pediatric Myasthenia Gravis Across Tertiary Children's Hospitals.
Pediatr Neurol
2023
37005891
Efficacy and Safety of Viltolarsen in Boys With Duchenne Muscular Dystrophy: Results From the Phase 2, Open-Label, 4-Year Extension Study.
J Neuromuscul Dis
2023
35362613
Palliative care in Duchenne muscular dystrophy: Goals of care discussions and beyond.
Muscle Nerve
2022
35634851
Long-Term Functional Efficacy and Safety of Viltolarsen in Patients with Duchenne Muscular Dystrophy.
J Neuromuscul Dis
2022
35567422
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy.
Ann Clin Transl Neurol
2022
33361607
Parent Project Muscular Dystrophy Females with Dystrophinopathy Conference, Orlando, Florida June 26 - June 27, 2019.
J Neuromuscul Dis
2021
32453377
Safety, Tolerability, and Efficacy of Viltolarsen in Boys With Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A Phase 2 Randomized Clinical Trial.
JAMA Neurol
2020
32710634
Combination molecular therapies for type 1 spinal muscular atrophy.
Muscle Nerve
2020
32329921
Spinal muscular atrophy care in the COVID-19 pandemic era.
Muscle Nerve
2020
32329920
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic.
Muscle Nerve
2020
32174747
Utility of Repetitive Nerve Stimulation in Myopathies.
Pediatr Neurol Briefs
2020
31148362
PIGQ glycosylphosphatidylinositol-anchored protein deficiency: Characterizing the phenotype.
Am J Med Genet A
2019
31929716
Spinal Muscular Atrophy Diagnosed by Newborn Screening.
Pediatr Neurol Briefs
2019
30582825
Gene Therapy for Spinal Muscular Atrophy: An Emerging Treatment Option for a Devastating Disease.
J Manag Care Spec Pharm
2018
30159187
Friedreich's Ataxia: Clinical Presentation of a Compound Heterozygote Child with a Rare Nonsense Mutation and Comparison with Previously Published Cases.
Case Rep Neurol Med
2018
26917586
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy.
Brain
2016
27397628
Guidelines for Corticosteroid use in Treatment of DMD.
Pediatr Neurol Briefs
2016
26933528
Delay in Diagnosis of Duchenne Muscular Dystrophy.
Pediatr Neurol Briefs
2015
26933604
Orofacial EMG in Congenital Multiple Cranial Neuropathies.
Pediatr Neurol Briefs
2015
22911499
Symptomatic cerebral vasospasm following resection of a medulloblastoma in a child.
Neurocrit Care
2013
21249120
Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late.
PLoS One
2010
1 - 23 of 23
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Hart G W Lidov
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1
David K Manchester
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Anthony C Chin
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1
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1
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