Foreword. Lysosomal storage diseases. Fabry disease - an overview. History of Fabry disease. Genetics of Fabry disease. Signs and symstoms of Fabry disease. Fabry disease in women and children. Diagnosis of Fabry disease. Treatment of Fabry disease. Importance of glycosylation in the development of enzyme replacement therapy. Clinical improvements following enzyme replacement therapy. References. Illustrated with black and color drawings, photographs and radiographs.
Estado: In very good condition | Illustrated softcover.
Editorial: Oxford PharmaGenesis | 2007
Páginas: 49
Medidas: 29'5x21'5 cms.
Fabry disease. Clinical manifestations, diagnosis ans therapy | Beck, Michael
SKU: F-2-4*
15,00 €Precio
