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Author/Creator Moseley, Scott

1. Asfotase alfa for infants and young children with hypophosphatasia: 7 year outcomes of a single-arm, open-label, phase 2 extension trial. Issue 2 (February 2019)

Authors:
Whyte, Michael P; Simmons, Jill H; Moseley, Scott; Fujita, Kenji P; Bishop, Nicholas; Salman, Nada J; Taylor, John; Phillips, Dawn; McGinn, Mairead; McAlister, William H
Journal:
Lancet
Issue:
Volume 7:Issue 2(2019)
Page Start:
93
Record Type:
Journal Article
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2. P02 Development and validation of a Novel ICP-MS method to quantify different copper species in human plasma from patients with wilson disease. (20th September 2022)

Authors:
Ala, Aftab; Liang, Tao; Zhang, Haiting; Zhang, Linwen; Moseley, Scott; Guo, Ping; Chen, Meng; Hall, Tracey; Li, Ming; Swenson, Eugene; Pan, Wei-Jian; Meltzer, Brian; Pelto, Ryan; Ma, Mark
Journal:
Gut
Issue:
Volume 71(2022)Supplement 3
Page Start:
A32
Record Type:
Journal Article
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4. Validation of a Novel Scoring System for Changes in Skeletal Manifestations of Hypophosphatasia in Newborns, Infants, and Children: The Radiographic Global Impression of Change Scale. (14th February 2018)

Authors:
Whyte, Michael P; Fujita, Kenji P; Moseley, Scott; Thompson, David D; McAlister, William H
Journal:
Journal of bone and mineral research
Issue:
Volume 33:Number 5(2018)
Page Start:
868
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗