Lorne Clarke - Dissemin

Papers authored by Lorne Clarke

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2008 Lorne A. Clarke

Idursulfase for the treatment of mucopolysaccharidosis II

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François Feillet, Lorne Clarke

, Concetta Meli, Mark Lipson, Andrew A. Morris, Paul Harmatz, Diane R. Mould, Bruce Green, Alex Dorenbaum, Marcello Giovannini, Erik Foehr

Pharmacokinetics of Sapropterin in Patients with Phenylketonuria

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Lorne A. Clarke

The mucopolysaccharidoses: a success of molecular medicine

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2007 Graham B. Sinclair, Gareth Jevon, Karen E. Colobong, Derrick R. Randall, Francis Y. M. Choy, Lorne A. Clarke

Generation of a conditional knockout of murine glucocerebrosidase: Utility for the study of Gaucher disease

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L. A. Clarke

, J. E. Wraith, M. Beck, E. H. Kolodny, G. M. Pastores, J. Muenzer

A Phase III Extension Study of Aldurazyme®(Laronidase) in Mucopolysaccharidosis I

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Lorne A. Clarke

Mucopolysaccharidosis I

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Lorne A. Clarke

Mucopolysaccharidosis II (Hunter Syndrome)

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2006 Scot C. Leary, Andre Mattman, Timothy Wai, David C. Koehn, Lorne A. Clarke

, Suzanne Chan, Brenda Lomax, Patrice Eydoux, Hilary D. Vallance, Eric A. Shoubridge

A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathy

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Derrick R. Randall, Graham B. Sinclair, Karen E. Colobong, Elly Hetty, Lorne A. Clarke

Heparin cofactor II–thrombin complex in MPS I: A biomarker of MPS disease

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Elizabeth Braunlin, Shannon Mackey-Bojack, Angela Panoskaltsis-Mortari, James M. Berry, Ron T. McElmurry, Megan Riddle, Li-Yan Sun, Lorne A. Clarke

, Jakub Tolar

, Bruce R. Blazar

Cardiac Functional and Histopathologic Findings in Humans and Mice with Mucopolysaccharidosis Type I: Implications for Assessment of Therapeutic Interventions in Hurler Syndrome

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2005 Willa L. Downing, Jason D. Galpin, Sabine Clemens, Shauna M. Lauzon, A. Lacey Samuels, Mark S. Pidkowich, Lorne A. Clarke

, Allison R. Kermode

Synthesis of enzymatically active human α‐l‐iduronidase in Arabidopsis cgl (complex glycan‐deficient) seeds

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Brian P. Rempel, Lorne A. Clarke

, Stephen G. Withers

A homology model for human α-l-iduronidase: Insights into human disease

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C. Tyson, C. Harvard, R. Locker, J. M. Friedman, S. Langlois, M. E. S. Lewis, M. Van Allen, M. Somerville, L. Arbour, L. Clarke

, B. McGilivray, S. L. Yong, J. Siegel-Bartel, E. Rajcan-Separovic

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

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2004 James E. Wraith, Lorne A. Clarke

, Michael Beck, Edwin H. Kolodny, Gregory M. Pastores, Joseph Muenzer, David M. Rapoport, Kenneth I. Berger, Stuart J. Swiedler, Emil D. Kakkis, Tanja Braakman, Elenie Chadbourne, Karen Walton-Bowen, Gerald F. Cox

Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human α-L-iduronidase (laronidase)

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L. G. Sadleir, M. B. Connolly, D. Applegarth, G. Hendson, L. Clarke

, C. Rakshi, K. Farrell

Spasms in children with definite and probable mitochondrial disease*

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H. Vallance, T. Chaba, L. Clarke

, G. Taylor

Pseudo-lysosomal storage disease caused by EMLA cream

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Stavit A. Shalev, Lorne A. Clarke

, David Koehn, Sylvie Langlois, Elaine H. Zackai, Judith G. Hall, Donna M. Mcdonald McGinn

Long-term follow-up of three individuals with Kabuki syndrome

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2003 Neil Howell, Roelof-Jan Oostra, Piet A. Bolhuis, Liesbeth Spruijt, Lorne A. Clarke

, David A. Mackey, Gwen Preston, Corinna Herrnstadt

Sequence Analysis of the Mitochondrial Genomes from Dutch Pedigrees with Leber Hereditary Optic Neuropathy

Download from www.ncbi.nlm.nih.gov

Catharine E. Nieman, Alexander W. Wong, Shouming He, L. Clarke

, Lorne Clarke, John J. Hopwood, Stephen G. Withers

Family 39 a-L-iduronidases and b-D-xylosidases react through similar glycosyl-enzyme intermediates: Identification of the human iduronidase nucleophile

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2001 Peter M. Gillett, Richard A. Schreiber, Gareth P. Jevon, David M. Israel, Tom Warshawski, Hilary Vallance, Lorne A. Clarke

Mucopolysaccharidosis Type VII (Sly Syndrome) Presenting as Neonatal Cholestasis With Hepatosplenomegaly:

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Papers authored by Lorne Clarke