D Haratz, N Manny, I Raz - Journal of Molecular Medicine, 1990 - Springer Gaucher's disease is an autosomal recessive dis- order characterized by a deficiency of
glucocere- brosidase resulting in an accumulation of glucocer- ebroside in the reticuloendothelial
system. The main manifestations of the disease are hepato- splenomegaly, bone lesions, ... Cited by 8 - Related articles - All 2 versions
TJ Lester, GA Grabowski, J Goldblatt, IZ Leiderman, … - The American journal of …, 1984 - Elsevier A 35-year-old Ashkenazi woman with Gaucher's disease was evaluated for persistent
thrombocytopenia. The diagnosis of Gaucher's disease was made by bone marrow aspiration
and confirmed by the determination of glucocerebrosidase levels in leukocytes and ... Cited by 8 - Related articles - All 4 versions
- ►bmj.com [PDF] DR Jones, J Hoffman, R Downie, M … - Postgraduate medical …, 1991 - pubmedcentral.nih.gov Adult or type I Gaucher's' disease is characterized by hepatic and splenic accumulation of
glucocere- broside, an intermediate product of membrane lipid metabolism. Bone involvement
is frequent but only rarely are other organs affected; cerebral involvement is not a major ... Cited by 6 - Related articles - All 6 versions
[CITATION] Disorders involving the monocytemacrophage system-The 'storage disease'
JB Alavi, J Hansell - Seminars in nuclear medicine, 1984 - Elsevier Radiolabeling techniques for white cells, platelets, and erythrocytes are reviewed. The early
studies using diisopropylfluoro- 32 P contributed to an understanding of the production and circulation
of the blood elements, and 51 Cr proved useful in localizing sites of cell migration or ... Cited by 2 - Related articles - All 5 versions
OW Press, H Fingert, IT Lott, CR … - Archives of Internal …, 1983 - archinte.highwire.org TVTannosidosis is a rare, autosomal-recessive, lysosomal- -L'-*- storage disease caused by
deficiency of the enzyme a-mannosidase. Diffuse accumulation of mannose-rich oligosaccharides
in leukocytes, neurons, liver, and spleen results in the characteristic clinical features of ... Cited by 1 - Related articles - All 3 versions
LB Kahn - S. Afr. Med. J, 1974 - 196.33.159.102 Cases included in this study were those diagnosed from 1935 to 1973 in the Department of
Path~logy at the University of Cape Town Medical School (Groote Schuur and Red Cross
Hospitals). There were 12 such patients, in 2 of whom detailed clinical information was ... Cited by 1 - Related articles - View as HTML - All 2 versions
N Suvajdžić-Vuković D - Bilten za hematologiju, 2004 - CEON/ CEES Gošeova bolest je najčešća glikolipidna tezauroza koja se nasleđuje autozomno recesivno au
osnovi bolesti je mutacija gena koji kodira enzim glukocerebrozidazu. U odsustvu enzima dolazi
do nagomilavanja glukocerobrozida u makrofazima jetre, slezine, kostne srži a ređe ... Related articles - Cached