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Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 24, 2012
Endothelial ultrastructural alterations of intramuscular capillaries in infantile mitochondrial cytopathies: "mitochondrial angiopathy"Harvey B Sarnat, Laura Flores-Sarnat, Robin Casey, et al.
JIMD Reports|February 23, 2013
In vivo bone architecture in pompe disease using high-resolution peripheral computed tomographyAneal Khan, Zachary Weinstein, David A Hanley, et al.
BMC Medical Genetics|January 18, 2006
Peroxisomal proliferator activated receptor-gamma deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3)Gordon A Francis, Gang Li, Robin Casey, et al.
Journal of Inherited Metabolic Disease|July 7, 2011
Longitudinal observations of serum heparin cofactor II-thrombin complex in treated Mucopolysaccharidosis I and II patientsLorne Andrew Clarke, Harmony Hemmelgarn, Karen Colobong, et al.
The Journal of Physical Chemistry. B|July 21, 2006
Hydrophobic distal pocket affects NO-heme geminate recombination dynamics in dehaloperoxidase and H64V myoglobinStefan Franzen, Audrius Jasaitis, Jennifer Belyea, et al.
Frontiers in Dementia|June 18, 2026
National and international models of involving people with lived experience in dementia policy, advocacy and researchEllen Snowball, Robin Casey, Karen Myers Barnett, et al.
The Journal of Pediatrics|August 1, 2009
Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation updateAnke K Bergmann, Inderneel Sahai, Jill F Falcone, et al.
Neuromuscular Disorders : NMD|January 26, 2015
Safety and efficacy of alternative alglucosidase alfa regimens in Pompe diseaseLaura E Case, Carl Bjartmar, Claire Morgan, et al.
Molecular Genetics and Metabolism|May 31, 2008
Heparin cofactor II-thrombin complex: a biomarker of MPS diseaseDerrick R Randall, Karen E Colobong, Harmony Hemmelgarn, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
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