SCOPUS 정보 검색 플랫폼

Revista de Nefrologia, Dialisis y Trasplante

Volumn 27, Issue 3, 2007, Pages 99-102

Nephrological manifestations of patients with Fabry disease in Argentina;Manifestaciones nefrológicas de pacientes con Enfermedad de Fabry en Argentina

(3) Marcelo Neumann, Pablo a Martínez, Pablo b Rozenfeld, Paula c

a HOSPITAL ITALIANO DE BUENOS AIRES (Argentina)

b Hospital Interzonal de Bahía Blanca (Argentina)

c UNIVERSIDAD NACIONAL DE LA PLATA (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOLIPID;

ARGENTINA; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE ASSOCIATION; FABRY DISEASE; FEMALE; HEMODIALYSIS; HUMAN; KIDNEY FAILURE; MALE; PROTEINURIA;

EID: 36348975206 PISSN: 03263428 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (2)

References (10)

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- Enzymatic defect in Fabry disease
- Brady RO, Gal AE, Bradley RM et al. Enzymatic defect in Fabry disease. N Engl J Med 1967: 276: 1163-1167.
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- Brady, R.O.¹ Gal, A.E.² Bradley, R.M.³

2
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- Dehout F, Schwarting A, Beck M, et al. Effects of enzyme replacement therapy with agalsidase alfa on glomerular filtration rate in patients with Fabry disease: preliminary data. Acta Paediatr Suppl. 2003; 92:14-5; discussion 5.
- Dehout F, Schwarting A, Beck M, et al. Effects of enzyme replacement therapy with agalsidase alfa on glomerular filtration rate in patients with Fabry disease: preliminary data. Acta Paediatr Suppl. 2003; 92:14-5; discussion 5.

3
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- Fabry disease. Alpha galactosidase deficiency
- Kint JA. Fabry disease. Alpha galactosidase deficiency. Science 1970: 167: 1268-1269.
- (1970) Science , vol.167 , pp. 1268-1269
- Kint, J.A.¹

4
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- Prevalence of lysosomal storage disorders
- Meikle PJ, Hopwood JJ, Clague AE et al. Prevalence of lysosomal storage disorders. JAMA 1999: 281: 249-254.
- (1999) JAMA , vol.281 , pp. 249-254
- Meikle, P.J.¹ Hopwood, J.J.² Clague, A.E.³

5
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- Pediatric Fabry disease
- Ries M, Gupta S, Moore D et al. Pediatric Fabry disease. Pediatrics 2005: 115: e344-e355.
- (2005) Pediatrics , vol.115
- Ries, M.¹ Gupta, S.² Moore, D.³

6
- 0034766525
- Anderson-Fabry disease: Clinical manifestations and impact of disease in a cohort of 98 hemizygous males
- MacDermot KD, Holmes A, Miners AH. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. J Med Genet 2001: 38: 750-760.
- (2001) J Med Genet , vol.38 , pp. 750-760
- MacDermot, K.D.¹ Holmes, A.² Miners, A.H.³

7
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- Enzyme replacement therapy in Fabry disease: A randomized controlled trial
- Schiffmann R, Kopp JB, Austin HA 3rd et al. Enzyme replacement therapy in Fabry disease: a randomized controlled trial. JAMA 2001; 285: 2743-9.
- (2001) JAMA , vol.285 , pp. 2743-2749
- Schiffmann, R.¹ Kopp, J.B.² Austin 3rd, H.A.³

8
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- Patients with Fabry disease on dialysis in the United States
- Thadhani R, Wolf M, West ML, et al: Patients with Fabry disease on dialysis in the United States. Kidney Int 61:249-255, 2002.
- (2002) Kidney Int , vol.61 , pp. 249-255
- Thadhani, R.¹ Wolf, M.² West, M.L.³

9
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- Tsakiris D, Simpson HK, Jones EH, et al: Report onmanagement of renal failure in Europe, XXVI, 1995. Rarediseases in renal replacement therapy in the ERA-EDTA.
- Report onmanagement of renal failure in Europe
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10
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- Registry
- suppl 7
- Registry. Nephrol Dial Transplant 11:S4-S20, 1996 (suppl 7).
- (1996) Nephrol Dial Transplant , vol.11

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.