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Molecular Genetics and Metabolism Reports|June 23, 2016
Atypical presentation of mucopolysaccharidosis type IVAEric T Rush
Orphanet Journal of Rare Diseases|July 18, 2018
Childhood hypophosphatasia: to treat or not to treatEric T Rush
Seminars in Pediatric Neurology|May 4, 2010
Identification of an X-linked deletion syndrome through comparative genomic hybridization microarrayEric T Rush, G Bradley Schaefer
AACE Clinical Case Reports|January 23, 2020
PHOSPHATURIC MESENCHYMAL HEEL TUMOR PRESENTING WITH TUMOR-INDUCED OSTEOMALACIATarandeep Kaur, Eric T Rush, Rajib K Bhattacharya
American Journal of Medical Genetics. Part A|August 18, 2017
Dolichol kinase deficiency (DOLK-CDG): Two new cases and expansion of phenotypeEric T Rush, Craig V Baker, William B Rizzo
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 17, 2017
A retrospective review of initial bisphosphonate infusion in an inpatient vs. outpatient setting for bisphosphonate naïve patientsRose M Kreikemeier, Heather Gosnell, Lisa M Halbur, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
Evaluation and comparison of safety, convenience and cost of administering intravenous pamidronate infusions to children in the home and ambulatory care settingsEric T Rush, Kristi DeHaai, Rose M Kreikemeier, et al.
Molecular Genetics and Metabolism|April 5, 2021
Investigation of ALPL variant states and clinical outcomes: An analysis of adults and adolescents with hypophosphatasia treated with asfotase alfaPriya S Kishnani, Guillermo Del Angel, Shanggen Zhou, et al.
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