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Biagini, Philippe - - 2012
Hernandez-Rocha, Cristian - - 2012
- - 2012
Carroll, V. - - 2012
Bhengu, Louisa - - 2012
Background. Gaucher disease is an autosomal recessive lysosomal glycosphingolipid storage disorder resulting from a deficiency of lysosomal enzyme acid P-glucosidase (glucocerebrosidase). This partial enzyme deficiency results in accumulation of glycosphingolipid-laden macrophages (Gaucher cells) throughout the liver, spleen, bone marrow, skeleton, lungs and brain (only in types 2 and 3).
Green, R.J. - - 2012
Background. Allergic rhinitis (AR) is an important disease in South Africa. The South African Allergic Rhinitis Working Group (SAARWG) has published previous guidelines for AR diagnosis and management. Areas of concern have arisen that require additional information, including the management of AR in infancy, appropriate and inappropriate allergy testing, cost ...
Peer, Shazia - - 2012
Background. Concern exists about the quality of specialist training platforms at South African universities and teaching hospitals.
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