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AJNR. American Journal of Neuroradiology|September 13, 2005
MR imaging and proton spectroscopy of neuronal injury in late-onset GM2 gangliosidosisMatilde Inglese, Annette O Nusbaum, Gregory M Pastores, et al.
Parkinsonism & Related Disorders|September 4, 2012
Parkinson's disease in patients and obligate carriers of Gaucher diseaseJoanna G Becker, Gregory M Pastores, Alessandro Di Rocco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2005
Late-onset Tay-Sachs disease: phenotypic characterization and genotypic correlations in 21 affected patientsOrit Neudorfer, Gregory M Pastores, Bai J Zeng, et al.
Journal of Child Neurology|March 21, 2008
Fidelity of gamma-glutamyl transferase (GGT) in differentiating skeletal muscle from liver damageXiomara Q Rosales, Mary-Lynn Chu, Christopher Shilling, et al.
Kidney International|January 12, 2002
Patients with Fabry disease on dialysis in the United StatesRavi Thadhani, Myles Wolf, Michael L West, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 23, 2013
A multicenter open-label treatment protocol (HGT-GCB-058) of velaglucerase alfa enzyme replacement therapy in patients with Gaucher disease type 1: safety and tolerabilityGregory M Pastores, Barry Rosenbloom, Neal Weinreb, et al.
Journal of Inherited Metabolic Disease|July 23, 2011
Gastrointestinal disturbances and their management in miglustat-treated patientsNadia Belmatoug, Alberto Burlina, Pilar Giraldo, et al.
Orphanet Journal of Rare Diseases|November 27, 2014
Agalsidase alfa in pediatric patients with Fabry disease: a 6.5-year open-label follow-up studyRaphael Schiffmann, Gregory M Pastores, Yeong-Hau H Lien, et al.
American Journal of Hematology|November 5, 2008
Life expectancy in Gaucher disease type 1Neal J Weinreb, Patrick Deegan, Katherine A Kacena, et al.
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