Results 161 to 170 of about 10,573,620 (195)

Thrombocytopenia in Gaucher's Disease

Annals of Internal Medicine, 1971
Abstract A 63-year-old man with Gaucher's disease presented with bleeding secondary to thrombocytopenia.
D, Green, H A, Battifora, R T, Smith, E C, Rossi   +3 more
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Gaucher’s Disease

New England Journal of Medicine, 2022
Ludovic Suner, François Delhommeau
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Myopathy in Gaucher disease

Journal of Inherited Metabolic Disease, 2008
SummaryGaucher disease is a recessively inherited lysosomal storage disorder, caused by deficiency of glucocerebrosidase activity. Affected individuals usually present with hepatosplenomegaly, anaemia, thrombocytopenia, and skeletal diseases. A wide range of neurological manifestations have also been recognized in Gaucher patients including acute ...
Li-Kai, Tsai, Yin-Hsiu, Chien, Chih-Chao, Yang, Wuh-Liang, Hwu   +3 more
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Gaucher's Disease: A Review

Annals of Pharmacotherapy, 1996
OBJECTIVE: To review the epidemiology, pathophysiology, clinical features, diagnosis, and treatment of Gaucher's disease, focusing on the role of enzyme replacement therapy. DATA SOURCES: a MEDLINE search (from 1984 to July 1995) of ...
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Gaucher's Disease and Pregnancy

American Journal of Perinatology, 1998
Gaucher's disease is an autosomal recessive lysosomal storage disease, resulting from a deficiency of the enzyme glucocerebrosidase, which is required for the lysosomal degradation of glycolipids. The clinical manifestations of the disease show a large heterogeneity, including hepatosplenomegaly, "bone crisis" and fracture, anemia, thrombocytopenia and,
S J, Fasouliotis, Y, Ezra, J G, Schenker
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Gaucher's Disease in Pregnancy

Obstetrical & Gynecological Survey, 1996
Gaucher's disease is an autosomal recessive lysosomal storage disease, resulting from a deficiency of the enzyme glucocerebrosidase, important for the physiologic recycling of cell membrane lipids. The clinical symptoms and disease presentations of Gaucher's disease are heterogeneous, including hepatosplenomegaly, bone "crisis" and fracture, anemia ...
J S, Rosnes, M F, Sharkey, J C, Veille, E, Mueller-Heubach   +3 more
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Gaucher's disease and pregnancy

European Journal of Obstetrics & Gynecology and Reproductive Biology, 1996
A 24-year-old primigravid woman with adult type Gaucher's disease was admitted at 28 weeks of pregnancy. She was asthenic and the abdomen was markedly protuberant due to hepatosplenomegaly. A conservative approach with close monitorization of both mother and baby was planned.
A, Ayhan, Z S, Tuncer, H, Simşek
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SPLENECTOMY IN GAUCHER'S DISEASE

Archives of Surgery, 1929
The literature on Gaucher's disease, by reason of its comparative paucity, has been kept well abreast of the time. It seems unnecessary to record a review of it. At the Mayo Clinic, in 530 cases in which splenectomy was performed during the period of seventeen years, 1913 to 1929, inclusive, Gaucher's disease was encountered four times.
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Neuropathic Gaucher disease

Wiener Medizinische Wochenschrift, 2010
Gaucher disease (GD) has been conventionally demarcated into clinical variants, based on the presence or absence of primary central nervous system (CNS) involvement. In cases with primary CNS involvement (types 2 and 3 GD), distinctions have been made on the basis of severity and rate of disease progression.
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Phenotype, diagnosis, and treatment of Gaucher's disease.

The Lancet, 2008
G. Grabowski
semanticscholar   +1 more source