Joe T.R. Clarke

Natural course of Fabry disease: changing pattern of causes of death in FOS – Fabry Outcome Survey

Atul Mehta, Joe T.R. Clarke, Roberto Giugliani et al. · Journal of Medical Genetics · 2009 · 302 citations · Full text

Gaucher disease type 1: Revised recommendations on evaluations and monitoring for adult patients

Neal J. Weinreb, Mario Carlos Aggio, Hans C. Andersson et al. · Seminars in Hematology · 2004 · 169 citations

Adult Patients, Clinical Epidemiology, Diagnosis +2

The conversion of phenylalanine to tyrosine in man. Direct measurement by continuous intravenous tracer infusions of L-[ring-2H5]phenylalanine and L-[1-13C]tyrosine in the postabsorptive state

Joe T.R. Clarke, Dennis M. Bier · Metabolism · 1982 · 137 citations

Therapeutic Drug Monitoring, Biochemistry, Medicine +8

Mutation analysis ofPEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype

Nancy Braverman, Li Chen, Paul Lin et al. · Human Mutation · 2002 · 132 citations

Efficient analysis of urinary glycosaminoglycans by LC-MS/MS in mucopolysaccharidoses type I, II and VI

Christiane Auray‐Blais, Patrick Bhérer, René Gagnon et al. · Molecular Genetics and Metabolism · 2010 · 107 citations

Glycoproteomics, Urology, Urinary Glycosaminoglycans +6