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Page 1
Showing results for gaucher s
Search for Gatcher S instead (2 results)
Niemann-Pick's and Gaucher's diseases.
Stern G. Stern G. Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S143-6. doi: 10.1016/S1353-8020(13)70034-8. Parkinsonism Relat Disord. 2014. PMID: 24262167 Review.
A short account is presented of the evolution of knowledge concerning Niemann-Pick's and Gaucher's diseases, two autosomal recessive genetic disturbances of lysosomal storage function. ...
A short account is presented of the evolution of knowledge concerning Niemann-Pick's and Gaucher's diseases, two autosomal rec …
Gaucher's Disease. Pathological features.
Pastores GM. Pastores GM. Baillieres Clin Haematol. 1997 Dec;10(4):739-49. doi: 10.1016/s0950-3536(97)80037-6. Baillieres Clin Haematol. 1997. PMID: 9497861 Review.
Gaucher's disease is the most common lysosomal storage disease. The pathological features are a consequence of the progressive accumulation of glucosylceramide within mononuclear phagocytes. ...The general clinico-pathological features of Gaucher's dis …
Gaucher's disease is the most common lysosomal storage disease. The pathological features are a consequence of the progressive …
Gaucher's disease.
Bohra V, Nair V. Bohra V, et al. Indian J Endocrinol Metab. 2011 Jul;15(3):182-6. doi: 10.4103/2230-8210.83402. Indian J Endocrinol Metab. 2011. PMID: 21897894 Free PMC article.
Gaucher's disease (GD) is the most common amongst the various disorders classified under the lysosomal storage disorders. ...
Gaucher's disease (GD) is the most common amongst the various disorders classified under the lysosomal storage disorders. ...
Gaucher's disease: a review.
Morales LE. Morales LE. Ann Pharmacother. 1996 Apr;30(4):381-8. doi: 10.1177/106002809603000411. Ann Pharmacother. 1996. PMID: 8729893 Review.
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 English-language literature perta …
OBJECTIVE: To review the epidemiology, pathophysiology, clinical features, diagnosis, and treatment of Gaucher's disease, focu …
Gaucher's disease in pregnancy.
Rosnes JS, Sharkey MF, Veille JC, Mueller-Heubach E. Rosnes JS, et al. Obstet Gynecol Surv. 1996 Sep;51(9):549-58. doi: 10.1097/00006254-199609000-00022. Obstet Gynecol Surv. 1996. PMID: 8873155 Review.
Similarly, the genetic variability of Gaucher's disease is diverse, and in some aspects affects phenotypic expression. Type 1 Gaucher's disease, however, usually present with less severe symptoms, at more advanced age, and is particularly amenable to e …
Similarly, the genetic variability of Gaucher's disease is diverse, and in some aspects affects phenotypic expression. Type 1 …
Gaucher's disease and cancer: a sphingolipid perspective.
Barth BM, Shanmugavelandy SS, Tacelosky DM, Kester M, Morad SA, Cabot MC. Barth BM, et al. Crit Rev Oncog. 2013;18(3):221-34. doi: 10.1615/critrevoncog.2013005814. Crit Rev Oncog. 2013. PMID: 23510065 Free PMC article. Review.
Some suggest that the effects of Gaucher's disease may be linked to cancer, while others implicate the therapies used to treat Gaucher's disease. ...This review should reveal that it is most practical to associate elevated glucosylceramide, which accom …
Some suggest that the effects of Gaucher's disease may be linked to cancer, while others implicate the therapies used to treat …
Gaucher's disease: past, present and future.
Brady RO. Brady RO. Baillieres Clin Haematol. 1997 Dec;10(4):621-34. doi: 10.1016/s0950-3536(97)80031-5. Baillieres Clin Haematol. 1997. PMID: 9497855 Review.
A patient with what is now known as Gaucher's disease was first described by P.C.E. Gaucher in 1882. Fifty years later, Aghion reported that patients with this condition accumulated a sphingoglycolipid called glucocerebroside. ...Evidence was presented in 199 …
A patient with what is now known as Gaucher's disease was first described by P.C.E. Gaucher in 1882. Fifty years later, …
Gaucher's disease and pregnancy.
Fasouliotis SJ, Ezra Y, Schenker JG. Fasouliotis SJ, et al. Am J Perinatol. 1998 May;15(5):311-8. doi: 10.1055/s-2007-993950. Am J Perinatol. 1998. PMID: 9643638 Review.
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. ...Pregnancy concurrent with Gaucher's disease has seve …
Gaucher's disease is an autosomal recessive lysosomal storage disease, resulting from a deficiency of the enzyme glucocerebros …
Gaucher's disease: molecular, genetic and enzymological aspects.
Grabowski GA, Horowitz M. Grabowski GA, et al. Baillieres Clin Haematol. 1997 Dec;10(4):635-56. doi: 10.1016/s0950-3536(97)80032-7. Baillieres Clin Haematol. 1997. PMID: 9497856 Review.
The molecular, genetic and enzymological abnormalities in Gaucher's disease have been delineated during the past decade. Although our understanding of the primary predisposition to the Gaucher's disease phenotypes has improved, the relationships remain …
The molecular, genetic and enzymological abnormalities in Gaucher's disease have been delineated during the past decade. Altho …
Gaucher's disease: clinical features and natural history.
Cox TM, Schofield JP. Cox TM, et al. Baillieres Clin Haematol. 1997 Dec;10(4):657-89. doi: 10.1016/s0950-3536(97)80033-9. Baillieres Clin Haematol. 1997. PMID: 9497857 Review.
Gaucher's disease is an inherited disorder characterized by pathological storage of glycolipid in mononuclear phagocytes: it is a multi-system disease associated with striking variation in its clinical manifestations, severity and course. ...Here we describe the cli …
Gaucher's disease is an inherited disorder characterized by pathological storage of glycolipid in mononuclear phagocytes: it i …
8,505 results