Profil bibliographique

Stacy Dixon

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

19Publications signalées

289Citations signalées

3Affiliations récentes

Institutions déclarées

University of Colorado System University of Colorado Anschutz University of Colorado Denver

Domaines associés

Neurogenetic and Muscular Disorders ResearchMuscle Physiology and DisordersAmyloidosis: Diagnosis, Treatment, OutcomesInflammatory Myopathies and DermatomyositisAlzheimer's disease research and treatments

Publications récentes

2026 articleOpenAlex

Evaluating Functional Changes and Outcome Measure Responsiveness in Limb Girdle Muscular Dystrophy: A 12-month Analysis of the 10-meter Run Time, NSAD, and PUL (S7.002)

Roshni Patel, Lindsay Alfano, Tahseen Mozaffar, Katherine Mathews et autres

0 citationsNeurology

2026 articleOpenAlex

Phase II/III Study of Ulviprubart in Inclusion Body Myositis: Study Design, Patient Characteristics, and Topline Results (S7.007)

Namita Goyal, Pedro M Machado, Dana P. Ascherman, Olivier Benveniste et autres

0 citationsNeurology

Accès ouvert 2026 articleOpenAlex

Natural history of limb girdle muscular dystrophy R1 (LGMDR1): a GRASP consortium study

Stephanie Hunn, Andrew R. Findlay, Lindsay N. Alfano, Aileen Jones et autres

0 citationsNeuromuscular Disorders

Accès ouvert 2026 conference-paperOpenAlex

Phase 2/3 study of an investigational anti-inflammatory biologic therapy in inclusion body myositis

Namita Goyal, Pedro Machado, Dana Ascherman, Olivier Benveniste et autres

0 citationsGhent University Academic Bibliography (Ghent University)

Accès ouvert 2025 articleOpenAlex

Clinical Trial Readiness in Limb Girdle Muscular Dystrophy R1 (LGMDR1): A GRASP Consortium Study

Stephanie Hunn, Lindsay N. Alfano, Aileen Jones, Amanda Butler et autres

3 citationsAnnals of Clinical and Translational Neurology

2025 articleOpenAlex

Motor Outcomes to Validate Evaluations in Facioscapulohumeral Muscular Dystrophy (MOVE FSHD): Interim Baseline Data and Potential Predictors for FSHD (S16.005)

Michaela Walker, Channa Hewamadduma, Russell J. Butterfield, John Day et autres

0 citationsNeurology

Accès ouvert 2025 articleOpenAlex

Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy

David Adams, Jonas Wixner, Michael Polydefkis, John L. Berk et autres

35 citationsJAMA Neurology

Accès ouvert 2024 articleOpenAlex

Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study

Amy Doody, Lindsay N. Alfano, Jordi Díaz‐Manera, Linda Lowes et autres

6 citationsBMC Neurology

Accès ouvert 2023 articleOpenAlex

Practical Guidance for the Use of Patisiran in the Management of Polyneuropathy in Hereditary Transthyretin-Mediated Amyloidosis

Stacy Dixon, Xuan Kang, Dianna Quan

10 citationsTherapeutics and Clinical Risk Management

2023 articleOpenAlex

Advance Care Planning Among Patients With Amyotrophic Lateral Sclerosis: Patient Perspectives on Goals of Care Conversations

Joel Phillips, Stacy Dixon, Tracy Koehler, Benzi M. Kluger

9 citationsAmerican Journal of Hospice and Palliative Medicine®

Accès ouvert 2021 articleOpenAlex

Treatment preference among patients with spinal muscular atrophy (SMA): a discrete choice experiment

Alisha Monnette, Er Chen, Dongzhe Hong, Alessandra N. Bazzano et autres

38 citationsOrphanet Journal of Rare Diseases

Accès ouvert 2020 preprintOpenAlex

Treatment Preference among Patients with Spinal Muscular Atrophy (SMA): A Discrete Choice Experiment

Alisha Monnette, Er Chen, Dongzhe Hong, Alessandra N. Bazzano et autres

2 citationsResearch Square

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