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Vamshi K. Rao
Vamshi K. Rao
Ann and Robert H. Lurie Children's Hospital of Chicago/ Northwestern University Feinberg School of
Verified email at luriechildrens.org
Title
Cited by
Cited by
Year
Safety, tolerability, and efficacy of viltolarsen in boys with Duchenne muscular dystrophy amenable to exon 53 skipping: a phase 2 randomized clinical trial
PR Clemens, VK Rao, AM Connolly, AD Harper, JK Mah, EC Smith, ...
JAMA neurology 77 (8), 982-991, 2020
2042020
Comparative proteomes of the proliferating C2C12 myoblasts and fully differentiated myotubes reveal the complexity of the skeletal muscle differentiation program
NS Tannu, VK Rao, RM Chaudhary, F Giorgianni, AE Saeed, Y Gao, ...
Molecular & Cellular Proteomics 3 (11), 1065-1082, 2004
1142004
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy
S Byrne, L Jansen, JM U-King-Im, A Siddiqui, HGW Lidov, I Bodi, L Smith, ...
Brain 139 (3), 765-781, 2016
1102016
Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late
SM Hammond, RG Gogliotti, V Rao, A Beauvais, R Kothary, CJ DiDonato
PloS one 5 (12), e15887, 2010
842010
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID‐19 pandemic
A Veerapandiyan, KR Wagner, S Apkon, CM McDonald, KD Mathews, ...
Muscle & nerve 62 (1), 41-45, 2020
732020
Gene therapy for spinal muscular atrophy: an emerging treatment option for a devastating disease
VK Rao, D Kapp, M Schroth
Journal of managed care & specialty pharmacy 24 (12-a Suppl), S3-S16, 2018
712018
Paraffin-wax-coated plates as matrix-assisted laser desorption/ionization sample support for high-throughput identification of proteins by peptide mass fingerprinting
NS Tannu, J Wu, VK Rao, HS Gadgil, MJ Pabst, IC Gerling, R Raghow
Analytical biochemistry 327 (2), 222-232, 2004
672004
Combination molecular therapies for type 1 spinal muscular atrophy
Y Harada, VK Rao, K Arya, NL Kuntz, CJ DiDonato, ...
Muscle & nerve 62 (4), 550-554, 2020
632020
Spinal muscular atrophy care in the COVID‐19 pandemic era
A Veerapandiyan, AM Connolly, RS Finkel, K Arya, KD Mathews, ...
Muscle & nerve 62 (1), 46-49, 2020
482020
Long-term functional efficacy and safety of viltolarsen in patients with Duchenne muscular dystrophy
PR Clemens, VK Rao, AM Connolly, AD Harper, JK Mah, CM McDonald, ...
Journal of neuromuscular diseases 9 (4), 493-501, 2022
342022
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy
JM Kwon, K Arya, N Kuntz, HC Phan, C Sieburg, KJ Swoboda, ...
Annals of clinical and translational neurology 9 (6), 810-818, 2022
202022
Efficacy and safety of viltolarsen in boys with Duchenne muscular dystrophy: results from the phase 2, open-label, 4-year extension study
PR Clemens, VK Rao, AM Connolly, AD Harper, JK Mah, CM McDonald, ...
Journal of neuromuscular diseases, 1-9, 2023
182023
PIGQ glycosylphosphatidylinositol‐anchored protein deficiency: characterizing the phenotype
LJ Starr, JW Spranger, VK Rao, R Lutz, AT Yetman
American Journal of Medical Genetics Part A 179 (7), 1270-1275, 2019
162019
Symptomatic cerebral vasospasm following resection of a medulloblastoma in a child
VK Rao, A Haridas, TT Nguyen, R Lulla, MS Wainwright, JL Goldstein
Neurocritical care 18, 84-88, 2013
132013
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 …
PR Clemens, VK Rao, AM Connolly, AD Harper, JK Mah, EC Smith
102020
Investigators CINRGDNHS (2020) Safety, tolerability, and efficacy of viltolarsen in boys with duchenne muscular dystrophy amenable to exon 53 skipping: a phase 2 randomized …
PR Clemens, VK Rao, AM Connolly, AD Harper, JK Mah, EC Smith, ...
doi. org/10.1001/jaman eurol, 2020
82020
Spinal muscular atrophy diagnosed by newborn screening
M Lopez-Chacon, AN Buehner, VK Rao
Pediatric Neurology Briefs 33, 5, 2019
72019
Friedreich’s ataxia: clinical presentation of a compound heterozygote child with a rare nonsense mutation and comparison with previously published cases
VK Rao, CJ DiDonato, PD Larsen
Case Reports in Neurological Medicine 2018, 2018
62018
Transforaminal intrathecal access for injection of nusinersen in adult and pediatric patients with spinal muscular atrophy
T Shokuhfar, RN Abdalla, MC Hurley, P Nazari, SA Ansari, S Ajroud-Driss, ...
Journal of Pediatric Neurology 18 (02), 088-094, 2020
52020
P. 337Dystrophin restoration by exon 53 skipping in patients with Duchenne muscular dystrophy after viltolarsen treatment: phase 2 study update
P Clemens, V Rao, A Connolly, C Zaidman, A Harper, J Mah, ...
Neuromuscular Disorders 29, S165-S166, 2019
52019
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