John W. Day, Ph.D.

Affiliations: 
2013 Anthropology Harvard University, Cambridge, MA, United States 
Area:
Arab Studies
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"John Day"

Parents

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Steve Caton grad student 2013 Harvard
 (In the City, Out of Place: Dispossession and the Economics of Belonging in Southeastern Turkey.)

Collaborators

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Alex Chia Yu Chang collaborator 2014- Stanford (Chemistry Tree)
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Publications

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Coratti G, Lucibello S, Pera MC, et al. (2020) Gain and loss of abilities in type II SMA: A 12-month natural history study. Neuromuscular Disorders : Nmd
Finkel RS, Day JW, De Vivo DC, et al. (2020) RESTORE: A Prospective Multinational Registry of Patients with Genetically Confirmed Spinal Muscular Atrophy - Rationale and Study Design. Journal of Neuromuscular Diseases
Tao F, Beecham GW, Rebelo AP, et al. (2019) Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Journal of Neuromuscular Diseases
Tao F, Beecham GW, Rebelo AP, et al. (2019) Variation in SIPA1L2 is Correlated with Phenotype Modification in CMT Type 1A. Annals of Neurology
Pera MC, Coratti G, Mazzone ES, et al. (2019) Revised Upper Limb Module for Spinal Muscular Atrophy: 12 month changes. Muscle & Nerve
Shell R, Day J, Chiriboga C, et al. (2019) S61 Onasemnogene abeparvovec gene-replacement therapy (GRT) for spinal muscular atrophy type 1 (SMA1): preliminary pulmonary and ventilatory findings from the phase 3 study (STR1VE) Thorax. 74
Day JW, Chiriboga CA, Crawford TO, et al. (2019) 066 Avxs-101 gene-replacement therapy (GRT) for spinal muscular atrophy type 1 (SMA1): pivotal phase 3 study (STR1VE) update Journal of Neurology, Neurosurgery & Psychiatry. 90: A22.1-A22
Day JW, Chiriboga CA, Crawford TO, et al. (2019) 250 AVXS-101 phase 3 study in spinal muscular atrophy type 1 Journal of Neurology, Neurosurgery, and Psychiatry. 90
Ramsey D, Scoto M, Mayhew A, et al. (2019) P.220The revised Hammersmith scale (RHS) for spinal muscular atrophy: longitudinal trajectories in a large international cohort of patients with type 2 and 3 SMA Neuromuscular Disorders. 29
Wang ET, Treacy D, Eichinger K, et al. (2018) Transcriptome alterations in myotonic dystrophy skeletal muscle and heart. Human Molecular Genetics
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