메뉴 건너뛰기




Volumn 81, Issue 2, 1996, Pages 105-109

Familial al-amyloidosis in three Italian siblings

Author keywords

AL amyloidosis; Familial amyloidosis; Monoclonal gammopathies; Waldenstrom's macroglobulinemia

Indexed keywords

ADULT; AGED; AMYLOID NEUROPATHY; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DNA DETERMINATION; FAMILIAL DISEASE; FEMALE; HUMAN; IMMUNOHISTOCHEMISTRY; KIDNEY AMYLOIDOSIS; MALE; MONOCLONAL IMMUNOGLOBULINEMIA; SJOEGREN SYNDROME; WALDENSTROEM MACROGLOBULINEMIA;

EID: 0030326547     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (24)
  • 2
    • 0025117402 scopus 로고
    • Amyloidosis: A final common pathway for protein deposition in tissues
    • Stone MJ, Amyloidosis: a final common pathway for protein deposition in tissues. Blood 1990; 75.531-45.
    • (1990) Blood , vol.75 , pp. 531-545
    • Stone, M.J.1
  • 4
    • 0027317623 scopus 로고
    • Homozygous familial amyloidosis, Finnish type: Demonstration of glomerular gelsolin-derived amyloid and non amyloid tubular gelsolin
    • Maury CP. Homozygous familial amyloidosis, Finnish type: demonstration of glomerular gelsolin-derived amyloid and non amyloid tubular gelsolin. Clin Nephrol 1993; 40:53-6.
    • (1993) Clin Nephrol , vol.40 , pp. 53-56
    • Maury, C.P.1
  • 5
    • 0027506498 scopus 로고
    • Human lysozyme gene mutation cause hereditary systemic amyloidosis
    • Pepys MB, Hawkins PN, Booth DR, et al. Human lysozyme gene mutation cause hereditary systemic amyloidosis. Nature 1993; 362:553-7.
    • (1993) Nature , vol.362 , pp. 553-557
    • Pepys, M.B.1    Hawkins, P.N.2    Booth, D.R.3
  • 6
    • 0027465319 scopus 로고
    • Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain
    • Benson ND, Liepmeks J, Uemichi T, Wheeler G, Correa R. Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. Nat Genet 1993; 3:252-4.
    • (1993) Nat Genet , vol.3 , pp. 252-254
    • Benson, N.D.1    Liepmeks, J.2    Uemichi, T.3    Wheeler, G.4    Correa, R.5
  • 7
    • 0028211154 scopus 로고
    • Hereditary renal amyloidosis with a novel variant fibrinogen
    • Uemichi T, Liepnieks JJ, Benson MD. Hereditary renal amyloidosis with a novel variant fibrinogen. J Clin Invest 1994; 93:731-6.
    • (1994) J Clin Invest , vol.93 , pp. 731-736
    • Uemichi, T.1    Liepnieks, J.J.2    Benson, M.D.3
  • 8
    • 0016263661 scopus 로고
    • Familial myeloma: Report of eight families and a study of serum proteins in their relatives
    • Maldonado JE, Kyle RA. Familial myeloma: report of eight families and a study of serum proteins in their relatives. Am J Med 1974; 57:875-84.
    • (1974) Am J Med , vol.57 , pp. 875-884
    • Maldonado, J.E.1    Kyle, R.A.2
  • 9
    • 0017718818 scopus 로고
    • Familial immunopathies: Report of nine families and survey of literature
    • Zawadzki ZA, Aizawa Y, Kraj MA, Harandin AR, Fisher B. Familial immunopathies: report of nine families and survey of literature. Cancer 1977; 40:2094-101.
    • (1977) Cancer , vol.40 , pp. 2094-2101
    • Zawadzki, Z.A.1    Aizawa, Y.2    Kraj, M.A.3    Harandin, A.R.4    Fisher, B.5
  • 14
    • 0025166995 scopus 로고
    • Amylose familiale de type AL et deficit en facteur X. Intérêt de la colchicine au long cours
    • Paris
    • De Wazieres B, Fest T, Humbert P, Vuitton D, Dufond IL. Amylose familiale de type AL et deficit en facteur X. Intérêt de la colchicine au long cours. Ann Med Interne (Paris) 1990; 141:388-90.
    • (1990) Ann Med Interne , vol.141 , pp. 388-390
    • De Wazieres, B.1    Fest, T.2    Humbert, P.3    Vuitton, D.4    Dufond, I.L.5
  • 15
    • 0028103850 scopus 로고
    • AL-Amyloidosis in monoclonal gammopathies
    • Miliani A, Bergesio F. AL-Amyloidosis in monoclonal gammopathies. Haematologica 1994; 79:364-6.
    • (1994) Haematologica , vol.79 , pp. 364-366
    • Miliani, A.1    Bergesio, F.2
  • 16
    • 5844252007 scopus 로고
    • TTR exon scanning by non-radioactive duplex SSCPs
    • Kisilevsky, R, Benson MD, Frangione B, Gauldie JR, Muckle T, Young ID, eds. New York:Parthenon Press
    • Torres MF, Almeida MR, Saraiva MJM, TTR exon scanning by non-radioactive duplex SSCPs. In: Kisilevsky, R, Benson MD, Frangione B, Gauldie JR, Muckle T, Young ID, eds. Amyloid and amyloidosis. New York:Parthenon Press, 1993:453-5.
    • (1993) Amyloid and Amyloidosis , pp. 453-455
    • Torres, M.F.1    Almeida, M.R.2    Saraiva, M.J.M.3
  • 18
    • 0014444934 scopus 로고
    • Inherited predisposition to generalized amyloidosis
    • Van Allen MV, Frohlich JA, Davis JR. Inherited predisposition to generalized amyloidosis. Neurology 1969; 19:10-25.
    • (1969) Neurology , vol.19 , pp. 10-25
    • Van Allen, M.V.1    Frohlich, J.A.2    Davis, J.R.3
  • 19
    • 0016913418 scopus 로고
    • Familial amyloidosis with polyneuropathy. A clinical study based on patients living in northern Sweden
    • Andersson R. Familial amyloidosis with polyneuropathy. A clinical study based on patients living in northern Sweden. Acta Med Scand 1976; (suppl. 590):1-64.
    • (1976) Acta Med Scand , Issue.590 SUPPL. , pp. 1-64
    • Andersson, R.1
  • 20
    • 0005130049 scopus 로고
    • Peripheral neuropathy associated with amyloidosis
    • Matthews, WB, ed. New York:Elsevier Science Publ.
    • Hersch MI, Mc Leod JC, Peripheral neuropathy associated with amyloidosis. In: Matthews, WB, ed. Handbook of clinical neurology, vol. 7, New York:Elsevier Science Publ., 1987:413-28.
    • (1987) Handbook of Clinical Neurology , vol.7 , pp. 413-428
    • Hersch, M.I.1    Mc Leod, J.C.2
  • 21
    • 0024232807 scopus 로고
    • Bilateral pleural effusions due to amyloidosis in a case of Waldenstrom's macroglobulinemia
    • Lindelman C, Biberfeld P, Christensson B, et al. Bilateral pleural effusions due to amyloidosis in a case of Waldenstrom's macroglobulinemia. Haematologica 1988; 73:407-9.
    • (1988) Haematologica , vol.73 , pp. 407-409
    • Lindelman, C.1    Biberfeld, P.2    Christensson, B.3
  • 22
  • 23
    • 0027492515 scopus 로고
    • Benign monoclonal gammopathy after 20 to 35 years of follow-up
    • Kyle RA. Benign monoclonal gammopathy after 20 to 35 years of follow-up. Mayo Clin Proc 1993; 68:26-36.
    • (1993) Mayo Clin Proc , vol.68 , pp. 26-36
    • Kyle, R.A.1
  • 24
    • 0020261545 scopus 로고
    • HLA antigens in amyloidosis associated with plasma cell dyscrasias (amyloid AL)
    • Rubinow A, Cohen AS. HLA antigens in amyloidosis associated with plasma cell dyscrasias (amyloid AL). J Rheumatol 1982; 9:942-3.
    • (1982) J Rheumatol , vol.9 , pp. 942-943
    • Rubinow, A.1    Cohen, A.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.