Treatment of AL amyloidosis with melphalan, prednisone, and colchicine.

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Published in Arthritis Rheum on May 01, 1986

Authors

M D Benson

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Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin. Proc Natl Acad Sci U S A (1984) 1.74

Autocrine induction of collagenase by serum amyloid A-like and beta 2-microglobulin-like proteins. Science (1989) 1.69

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C-reactive protein and the acute-phase response. J Lab Clin Med (1981) 1.67

Polymorphism of human plasma thyroxine binding prealbumin. Biochem Biophys Res Commun (1983) 1.60

Nomenclature of amyloid fibril proteins. Report from the meeting of the International Nomenclature Committee on Amyloidosis, August 8-9, 1998. Part 1. Amyloid (1999) 1.59

Serum amyloid A protein in amyloidosis, rheumatic, and enoplastic diseases. Arthritis Rheum (1979) 1.53

"A" protein of amyloidosis. Isolation of a cross-reacting component from serum by affinity chromatography. Arthritis Rheum (1975) 1.46

Kinetics of serum amyloid protein A in casein-induced murine amyloidosis. J Clin Invest (1977) 1.45

Lack of association of a restriction fragment length polymorphism for serum amyloid P gene with reactive amyloidosis. Arthritis Rheum (1989) 1.45

Synthesis and secretion of serum amyloid protein A (SAA) by hepatocytes in mice treated with casein. J Immunol (1980) 1.44

The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolution. J Biol Chem (1993) 1.42

Partial amino acid sequence homology between an heredofamilial amyloid protein and human plasma prealbumin. J Clin Invest (1981) 1.41

Amyloidosis of the shoulder in patients on chronic hemodialysis: sonographic findings. AJR Am J Roentgenol (1996) 1.41

Isolation and identification by sequence analysis of experimentally induced guinea pig amyloid fibrils. J Exp Med (1974) 1.39

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Murine amyloid protein AA in casein-induced experimental amyloidosis. Lab Invest (1977) 1.35

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid. Biochem Biophys Res Commun (1988) 1.35

Transthyretin: a review from a structural perspective. Cell Mol Life Sci (2001) 1.34

Localization of the human prealbumin gene to chromosome 18. Biochem Biophys Res Commun (1985) 1.32

Treatment of Wegener's granulomatosis with immunosuppressive agents. Description of renal ultrastructure. Arch Intern Med (1970) 1.29

Prealbumin and retinol binding protein serum concentrations in the Indiana type hereditary amyloidosis. Arthritis Rheum (1983) 1.23

Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss). J Clin Invest (1986) 1.23

Localization of the ankyrin-binding site on erythrocyte membrane protein, band 3. J Biol Chem (1989) 1.21

Suppression of in vitro antibody response by a serum factor (SAA) in experimentally induced amyloidosis. J Exp Med (1975) 1.21

Methylprednisolone pulse therapy for nonrenal lupus erythematosus. Ann Rheum Dis (1980) 1.14

Antigenic determinants in amyloid deposits. Nature (1970) 1.13

Generalized amyloid in a family of Swedish origin. A study of 426 family members in seven generations of a new kinship with neuropathy, nephropathy, and central nervous system involvement. Ann Intern Med (1977) 1.11

Nonexpression of the human serum amyloid A three (SAA3) gene. DNA Cell Biol (1991) 1.10

Familial and sporadic Alzheimer's disease: neuropathology cannot exclude a final common pathway. Neurology (1996) 1.10

In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosis. J Lipid Res (1992) 1.08

Fibrillar assemblage of variable segments of immunoglobulin light chains: an electron microscopic study. J Immunol (1973) 1.08

Effect of purified protein SAA on immune response in vitro: mechanisms of suppression. J Immunol (1979) 1.08

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A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis. Biochem Biophys Res Commun (1999) 1.08

DMSO and colchicine therapy in amyloid disease. Ann Rheum Dis (1984) 1.07

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations. Am J Pathol (2001) 1.07

A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy. J Med Genet (1992) 1.07

Neuropathy, M components, and amyloid. Lancet (1975) 1.07

DNA sequence evidence for polymorphic forms of human serum amyloid A (SAA). Biochem Genet (1986) 1.06

Antinuclear antibodies in systemic lupus erythematosus. Detection with horseradish-peroxidase-conjugated antibody. Ann Intern Med (1970) 1.05

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1. Am J Pathol (1999) 1.05

Tertiary structure of an amyloid immunoglobulin light chain protein: a proposed model for amyloid fibril formation. Proc Natl Acad Sci U S A (1995) 1.03

P-component of amyloid. Isolation from human serum by affinity chromatography. Arthritis Rheum (1976) 1.02

Cerebrovascular biomodelling: a technical note. Surg Neurol (1999) 1.01

Characterization of amyloid A protein in human secondary amyloidosis: the predominant deposition of serum amyloid A1. Biochim Biophys Acta (1995) 1.01

Serum amyloid protein levels in south american children with rheumatoid arthritis: a co-operative study. Ann Rheum Dis (1980) 1.01

Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE-122). J Lab Clin Med (1991) 1.00

Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloid. Arthritis Rheum (1987) 0.99

Adult survival with intrahepatic portal venous gas secondary to acute gastric dilatation, with a review of portal venous gas. Clin Radiol (1985) 0.99

Biophysical analysis of normal transthyretin: implications for fibril formation in senile systemic amyloidosis. Amyloid (2001) 0.99

Amino acid structures of multiple forms of amyloid-related serum protein SAA from a single individual. Biochemistry (1988) 0.98

SAA suppression of immune response in vitro: evidence for an effect on T cell-macrophage interaction. J Immunol (1982) 0.98

Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences. Clin Genet (1990) 0.98

Fibril formation from recombinant human serum amyloid A. Biochim Biophys Acta (1994) 0.97

Human serum amyloid A. Three hepatic mRNAs and the corresponding proteins in one person. J Clin Invest (1988) 0.97

Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis. J Clin Invest (1988) 0.97

Amyloid deposition in a renal transplant in familial Mediterranean fever. Ann Intern Med (1977) 0.97

Polymorphism in a kappa I primary (AL) amyloid protein (BAN). Mol Immunol (1986) 0.96

Identification of a novel substitution in the constant region of a gene coding for an amyloidogenic kappa1 light chain. Biochim Biophys Acta (1999) 0.94

In vitro degradation of serum amyloid A by cathepsin D and other acid proteases: possible protection against amyloid fibril formation. Scand J Immunol (1995) 0.93

Amino acid sequence of a kappa I primary (AL) amyloid protein (AND). Mol Immunol (1990) 0.93

Cerebellar calcification and lead. J Neurol Neurosurg Psychiatry (1985) 0.93

A cell culture system for the study of amyloid pathogenesis. Amyloid formation by peritoneal macrophages cultured with recombinant serum amyloid A. Am J Pathol (1999) 0.93

Tertiary structures of amyloidogenic and non-amyloidogenic transthyretin variants: new model for amyloid fibril formation. Amyloid (1998) 0.93

Organ-specific (localized) synthesis of Ig light chain amyloid. J Immunol (1999) 0.93

Thyroxine interactions with transthyretin: a comparison of 10 different naturally occurring human transthyretin variants. J Clin Endocrinol Metab (1993) 0.92

Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His. Neurology (2003) 0.92

A frame shift mutation in the fibrinogen A alpha chain gene in a kindred with renal amyloidosis. Blood (1996) 0.92

Amyloid fibril protein related to immunoglobulin lambda-chains. J Immunol (1975) 0.92

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Amino acid sequence of a lambda VI primary (AL) amyloid protein (WLT). Scand J Immunol (1985) 0.91

The Ile-84-->Ser amino acid substitution in transthyretin interferes with the interaction with plasma retinol-binding protein. J Biol Chem (1994) 0.91

Serum amyloid protein SAA, C-reactive protein and lysozyme in leprosy. Int J Lepr Other Mycobact Dis (1979) 0.91

Hereditary renal amyloidosis with a novel variant fibrinogen. J Clin Invest (1994) 0.91

SAA amyloid protein levels in amyloid-prone chronic inflammatory disorders. Lack of association with amyloid disease. J Rheumatol (1981) 0.91

Induction of beta-sheet structure in amyloidogenic peptides by neutralization of aspartate: a model for amyloid nucleation. J Mol Biol (1999) 0.90

Serum amyloid P-component levels in amyloidosis, connective tissue diseases, infection, and malignancy as compared to normal serum. J Lab Clin Med (1979) 0.90

Diffuse fasciitis and eosinophilia with symmetric polyarthritis. Ann Intern Med (1980) 0.89

Fractionation of primary amyloid fibrils. Characterization and chemical interaction of the subunits. Biochim Biophys Acta (1977) 0.89

Diagnosis of familial amyloidotic polyneuropathy in France. Clin Genet (1990) 0.89

A 25,000 molecular weight protein constituent of human amyloid fibrils related to amyloid protein AA. Arch Biochem Biophys (1975) 0.89

A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family. J Med Genet (1993) 0.88

Renal amyloidosis with a frame shift mutation in fibrinogen aalpha-chain gene producing a novel amyloid protein. Blood (1997) 0.88

Production and functional analysis of normal and variant recombinant human transthyretin proteins. J Biol Chem (1992) 0.88

Cardiac amyloidosis associated with the transthyretin Ile122 mutation in a Caucasian family. Amyloid (2001) 0.88

Erosive arthritis in hereditary amyloidosis. Arthritis Rheum (1983) 0.88

Biochemical characterization of a neuroserpin variant associated with hereditary dementia. Am J Pathol (2001) 0.87

Serum amyloid A in carcinoma of the lung. Cancer (1986) 0.87

Characterization of amyloid fibril beta-peptide in familial Alzheimer's disease with APP717 mutations. Biochem Biophys Res Commun (1993) 0.86

Differential plasma clearance of murine acute-phase serum amyloid A proteins SAA1 and SAA2. Biochem J (1997) 0.86

Antigenicity and cross-reactivity of denatured fibril proteins of primary, secondary, and myeloma associated amyloids. J Lab Clin Med (1975) 0.86