Fabry Disease: New Insights for the Healthcare Professional: 2011 Edition: ScholarlyPaper

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ScholarlyEditions, Jan 9, 2012 - Medical - 27 pages

Fabry Disease: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Sphingolipidoses in a compact format.

The editors have built Fabry Disease: New Insights for the Healthcare Professional: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Sphingolipidoses in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Fabry Disease: New Insights for the Healthcare Professional: 2011 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility.


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Vasculopathy in patients with Fabry disease current controversies and research directions
Study of urinary proteomes in AndersonFabry disease
Fabry disease mimicking hypertrophic cardiomyopathy genetic screening needed for establishing the diagnosis in women
Frequency of unrecognized Fabry disease among young EuropeanAmerican and AfricanAmerican men with first ischemic stroke
Cardiac magnetic resonance imaging in patients with Fabrys disease
Newborn screening for Fabry disease in Taiwan reveals a high incidence of the lateronset GLA mutation c936+919GA IVS4+919GA
Recent studies by V Mirceva and coauthors add new data to Fabry disease findings
Does geographical location influence the phenotype of Fabry disease in women in Europe?
New mutation in female patient with renal variant of Fabry disease and HIV
Neurological Manifestation of Fabry disease A Case Report
Plasma globotriaosylsphingosine diagnostic value and relation to clinical manifestations of Fabry disease
Screening for Fabry disease in highrisk populations a systematic review
Fabry disease in patients with migraine with aura
Frequency of Fabry disease in male and female haemodialysis patients in Spain
Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns

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