Tina Duong

Lucile Packard Children's Hospital — United States

Medicine · Health Sciences

38h-index5.6kcitations210works3.62yr avg
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Research Topics

Neurogenetic and Muscular Disorders Research(119), Muscle Physiology and Disorders(80), RNA modifications and cancer(23), Congenital Anomalies and Fetal Surgery(21), Cerebral Palsy and Movement Disorders(18)

Publications204 total

Anti-competitive Agreement in the Franchise System in Vietnam under a Competitive Legal Perspective with Japan
The Asian Business Lawyer·2025
Anti-competitive Agreement in the Franchise System in Vietnam under a Competitive Legal Perspective with Japan
The Asian Business Lawyer·2025
Cerebrospinal fluid proteomic profiling reveals potential biomarkers and altered pathways in myotonic dystrophy type 1
Frontiers in Neuroscience·2025Open Access
Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patients.
Scientific Reports·2025· 1 citedOpen Access
Differences in swallowing efficacy of disease modifying treatment between infants receiving pre-symptomatic and symptomatic administration
Orphanet Journal of Rare Diseases·2025Open Access
Gene therapy for children with X-linked myotubular myopathy: a plain language summary of publication for the ASPIRO study
Therapeutic Advances in Rare Disease·2025Open Access
593PLongitudinal assessment of 4-year HFMSE changes in SMA II and III patients treated with nusinersen
Neuromuscular Disorders·2025
511PA real-world perspective on longitudinal quantitative muscle strength in treated adults with SMA
Neuromuscular Disorders·2025
224PDelayed exercise recovery ventilatory responses between individuals with neuromuscular disease
Neuromuscular Disorders·2025
215PVideo-based biomechanical analysis captures disease-specific movement signatures of myotonic dystrophy and facioscapulohumeral muscular dystrophy
Neuromuscular Disorders·2025
223PPrediction of VO2max and cardiopulmonary responses from ventilatory threshold VO2 in neuromuscular disease patients using machine learning
Neuromuscular Disorders·2025
141PA multicentre, prospective, longitudinal and observational natural history study for patients with nemaline myopathy in the UK with novel international collaboration
Neuromuscular Disorders·2025
Video-Based Biomechanical Analysis Captures Disease-Specific Movement Signatures of Different Neuromuscular Diseases
NEJM AI·2025· 6 citedOpen Access
Rehabilitation research in spinal muscular atrophy: a call to action
Journal of Neuromuscular Diseases·2025Open Access
Consensus recommendations and considerations for the delivery and monitoring of gene therapy in patients with Duchenne muscular dystrophy
Neuromuscular Disorders·2025· 3 cited
Optimizing MV CBCT Imaging Protocols Using NTCP and Secondary Cancer Risk: A Multi-Site Study in Breast, Pelvic, and Head & Neck Radiotherapy
arXiv (Cornell University)·2025Open Access
Correction: Serial casting for contractures in SMA: consensus derived guidelines for treatment
Frontiers in Neurology·2025· 2 citedOpen Access
Spinal Muscular Atrophy Functional Composite Score Revised (SMA-FCR) in Untreated and Nusinersen-Treated Patient Cohorts
Neurology·2025· 1 cited
Longitudinal Assessment of 4‐Year <scp>HFMSE</scp> Changes in <scp>SMA II</scp> and <scp>III</scp> Patients Treated With Nusinersen
European Journal of Neurology·2025· 4 citedOpen Access
Cardiopulmonary Recovery After Maximal Exercise in Individuals with Neuromuscular Disease and Limited Mobility
Journal of Clinical Medicine·2025Open Access
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Frequent Co-authors

John Day(26), Eugenio Mercuri(23), Francesco Muntoni(19), Richard S. Finkel(18), Basil T. Darras(17), Craig M. McDonald(16), Sally Dunaway Young(16), Erik Henricson(15), Jacqueline Montes(15), Amy Pasternak(14), Allan M. Glanzman(14), Giorgia Coratti(14), Maria Carmela Pera(14), Darryl C. De Vivo(14), Anna Mayhew(13), Avital Cnaan(12), Anne M. Connolly(12), Roberto De Sanctis(12), Marika Pane(12), Mariacristina Scoto(12)