Vamshi K Rao

6PUBLICATIONS
12CO-AUTHORS
Gene and molecular therapyNeurology and neuromuscular diseasesRehabilitationGene expression (incl. microarray and other genome-wide approaches)Pharmaceutical delivery technologies
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Publications (6)

|Aug 07, 2026
Access to novel therapies for Duchenne muscular dystrophy-Insights from expert treating physicians.

|Aug 07, 2026
Muscle channelopathies: A review.

|Nov 24, 2023
Predicting outcomes for spinal muscular atrophy: When the diagnosis no longer means what it used to mean.

Erin E Toaz, Nisha M Pinto, Vamshi K Rao

|Sep 04, 2023
Expansion of the phenotypic spectrum associated with pathogenic missense variation in DHX16.

Andy Drackley, Lenika De Simone, Nancy Kuntz

|May 14, 2022
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy.

Jennifer M Kwon, Kapil Arya, Nancy Kuntz

|Aug 31, 2018
Friedreich's Ataxia: Clinical Presentation of a Compound Heterozygote Child with a Rare Nonsense Mutation and Comparison with Previously Published Cases.

Vamshi K Rao, Christine J DiDonato, Paul D Larsen

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Frequent Collaborators

2 joint publications

Aravindhan Veerapandiyan

1 joint publications

Jennifer M Kwon

1 joint publications

Andy Drackley

1 joint publications

Lenika De Simone