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Author/Creator Reimschisel, Tyler

2. Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant. Issue 3 (1st February 2018)

Authors:
Pomerantz, Daniel J.; Ferdinandusse, Sacha; Cogan, Joy; Cooper, David N.; Reimschisel, Tyler; Robertson, Amy; Bican, Anna; McGregor, Tracy; Gauthier, Jackie; Millington, David S.; Andrae, Jaime L. W.; Tschannen, Michael R.; Helbling, Daniel C.; Demos, Wendy M.; Denis, Simone; Wanders, Ronald J. A...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 3(2018)
Page Start:
692
Record Type:
Journal Article
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3. Estimating the probability of IQ impairment from blood phenylalanine for phenylketonuria patients: a hierarchical meta‐analysis. Issue 5 (30th November 2012)

Authors:
Fonnesbeck, Christopher J.; McPheeters, Melissa L.; Krishnaswami, Shanthi; Lindegren, Mary Louise; Reimschisel, Tyler
Journal:
Journal of inherited metabolic disease
Issue:
Volume 36:Issue 5(2013)
Page Start:
757
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗