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Related to Fabry's disease: Pompe disease
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Fukuhara N, Suzuki M, Fujita N, Tsubaki T Fabry's disease on the mechanism of the peripheral nerve involvement.
Fabry's disease is one of the genetic disorders grouped together as lysosomal storage disease.
A female heterozygous patient with Fabry's disease with renal accumulation of trihexosyl ceramide detected with a monoclonal antibody.
Psychosis in a patient with Fabry's disease and treatment with aripiprazole.
Fabry's disease is a fat-storage disorder, which impairs circulation, leading to kidney failure, heart attacks and strokes.
Fabry's disease is caused by an insufficiency of the lysosomal enzyme [alpha]-galactosidase A.
Key Words: conduction defects, Fabry's disease, first-degree atrio-ventricular block, restrictive physiology, right bundle branch block
The rare, fatal genetic condition in this instance is Fabry's disease.
GlobalData, the industry analysis specialist, has released its new report, Fabry's Disease Therapeutics - Pipeline Assessment and Market Forecasts to 2018.
1973) Renal pathologic lesions and functional alterations in a man with Fabry's disease.
Safety and efficacy of recombinant human alphagalactosidase A-replacement therapy in Fabry's disease.