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The Importance of Correct Phenotyping in Gaucher Disease
Christopher M. Harris
SensoriMotor Laboratory Centre for Theoretical and Computational Neuroscience, University of Plymouth, UK
Pauline Campbell
SensoriMotor Laboratory Centre for Theoretical and Computational Neuroscience, University of Plymouth, UK
Key Words: Gaucher disease phenotyping
References
- Perretti A., Parenti G., Balbi P., et al. Study of multimodal evoked potentials in patients with type I Gaucher disease. J Child Neurol. 2005;20:124-128.[Abstract/Free Full Text]
- Campbell PE, Harris CM, Vellodi A. Deterioration of the auditory brainstem response in children with type 3 Gaucher disease. Neurology. 2004;63:385-387.[Abstract/Free Full Text]
- Campbell PE, Harris CM, Sirimanna T., Vellodi A. A model of neuronopathic Gaucher disease. J Inherited Metab Dis. 2003; 26:629-639.[CrossRef][Medline]
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- Bamiou D., Campbell P., Liasis A., et al. Audiometric abnormalities in children with Gaucher disease type 3. Neuropediatrics. 2001;32:136-141.[CrossRef][Web of Science][Medline]
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- Vellodi A., Bembi B., de Villemeur TB, et al. Management of neuronopathic Gaucher disease: a European consensus. J Inherited Metab Dis. 2001;24:319-327.[CrossRef][Medline]
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- Futerman AH, Sussman JL, Horowitz M., et al. New directions in the treatment of Gaucher disease. Trends Pharmacol Sci. 2004;25:147-151.[CrossRef][Medline]
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- Harris CM, Taylor DS, Vellodi A. Ocular motor abnormalities in Gaucher disease. Neuropediatrics. 1999;30:289-293.[Medline]
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- Cassidy L., Taylor D., Harris CM Abnormal supranuclear eye movements in the child: a practical guide to examination and interpretation. Survey Ophthalmol. 2000;44:479-506.[CrossRef][Web of Science][Medline]
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Journal of Child Neurology, Vol. 22, No. 8,
1056-1057 (2007)
DOI: 10.1177/0883073807305783

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