D GREEN, HA BATTIFORA, ROYT SMITH, … - Annals of Internal …, 1971 - Am Coll Physicians A 63-year-old man with Gaucher's disease presented with bleeding secondary to
thrombocytopenia. Bone marrow examination showed many typical Gaucher cells and adequate
numbers of megakaryocytes. A 51 Cr platelet survival study indicated a markedly ... Cited by 9 - 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
WAL Heaton, P Jacobs - S Afr Med J, 1974 - 196.33.159.102 Because of the lack of one of the iso-enzymes of beta glucosidase,' the phagocytic cells of the
reticulo-endothelial system are unable to metabolise glucocerebroside, so that this and other
lipids accumulate in the cells. The bone marrow, liver, and particularly the spleen, ... Cited by 2 - Related articles - View as HTML - All 2 versions
FW Davis, A Genecin, EW Smith - Bulletin of the Johns Hopkins …, 1949 - ncbi.nlm.nih.gov 1: Bull Johns Hopkins Hosp. 1949 Feb;84(2):176-9. Gaucher's disease with thrombocytopenia,
an instance of selective hypersplenism. DAVIS FW, GENECIN A, SMITH EW. Mesh Terms: Blood
Platelets*; Hypersplenism*. PMID: 18109352 [PubMed - indexed for MEDLINE].
Cited by 6 - Related articles
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
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
