SCOPUS 정보 검색 플랫폼

Lancet

Volumn 357, Issue 9250, 2001, Pages 138-140

Anderson-Fabry's disease: α-galactosidase deficiency

(3) Peters, F P J a Vermeulen, A b Kho, T L b

a Sittard Geleen Heerlen (Netherlands)

b MAASTRICHT UNIVERSITY MEDICAL CENTER (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GALACTOSIDASE; ANALGESIC AGENT; CARBAMAZEPINE; GLYCOPHOSPHOLIPID; GLYCOSPHINGOLIPID; PHENYTOIN;

ADULT; ARTICLE; BONE MARROW TRANSPLANTATION; CASE REPORT; CORNEA DYSTROPHY; ENZYME REPLACEMENT; FABRY DISEASE; FEMALE; GENE THERAPY; HUMAN; LIPID STORAGE; LYSOSOME STORAGE DISEASE; PAIN; PARESTHESIA; POLARIZATION MICROSCOPY; PRIORITY JOURNAL; SKIN BIOPSY; TELANGIECTASIA;

EID: 0035852488 PISSN: 01406736 EISSN: None Source Type: Journal
DOI: 10.1016/S0140-6736(00)03554-6 Document Type: Review

Times cited : (50)

References (5)

1
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2
- 0030725023
- Fabry' disease: A multidisciplinary disorder
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- Peters, F.P.J.¹ Sommer, A.² Vermuelen, A.³

3
- 0033543108
- Circulating α-galactosidase A derived from transduced bone marrow cells: Relevance for corrective gene transfer for Fabry disease
- (1999) Hum Gen Therap , vol.10 , pp. 1931-1939
- Takena, T.¹ Qin, G.² Brady, R.O.³

4
- 0033018496
- Accelerated transport and maturation lysocomal α-galactosidase A in Fabry lymphoblasts by enzyme inhibitor
- (1999) Nat Med , vol.5 , pp. 112-115
- Fan, J.Q.¹ Satoshi, I.² Asano, N.³

5
- 0000889058
- α-galactosidase A deficiency: Fabry disease
- Scriver CR, Beaudet AL, Sly WS, Velle D, eds. The metabolic and molecular bases of inherited disease, 6th ed. New York: McGraw-Hill
- (1996) , pp. 2741-2784
- Desnick, R.J.¹ Ioannou, Y.A.² Eng, C.M.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.