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Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: The Transthyretin Amyloidosis Cardiac Study (TRACS)

The American heart journal, 2012-08, Vol.164 (2), p.222-228.e1

2012

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Cardiac amyloidosis in African Americans: Comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosis

The American heart journal, 2009-10, Vol.158 (4), p.607-614

2009

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Diagnostic and Prognostic Utility of Cardiovascular Magnetic Resonance Imaging in Light-Chain Cardiac Amyloidosis

The American journal of cardiology, 2009-02, Vol.103 (4), p.544-549

2009

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Light-Chain Amyloidosis With Echocardiographic Features of Hypertrophic Cardiomyopathy

The American journal of cardiology, 2008-03, Vol.101 (5), p.674-676

2008

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186. Early Life Origins of Risky Sexual Behavior in Adolescence

Journal of adolescent health, 2011, Vol.48 (2), p.S114-S115

2011

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Thermodynamic Stability of a κI Immunoglobulin Light Chain: Relevance to Multiple Myeloma

Biophysical journal, 2005-06, Vol.88 (6), p.4232-4242

2005

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Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene

Kidney international, 2001-11, Vol.60 (5), p.1658-1665

2001

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A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy

Amyloid, 2004-03, Vol.11 (1), p.61-66

2004

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Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities

Amyloid, 2002, Vol.9 (4), p.263-267

2002

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Amyloidosis

Kelley's Textbook of Rheumatology, 2013, p.1889-1897

Ninth Edition, 2013

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Haplotype analysis of common transthyretin mutations

Human genetics, 1995-09, Vol.96 (3), p.350-354

1995

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A new transthyretin variant (His 69) associated with vitreous amyloid in an FAP family

Amyloid, 1994, Vol.1 (1), p.17-22

1994

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Haplotype analysis of His 58, Ala 60 and Tyr 77 types of familial amyloidotic polyneuropathy

Amyloid, 1994, Vol.1 (2), p.75-79

1994

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Isolation and identification by sequence analysis of experimentally induced guinea pig amyloid fibrils

The Journal of experimental medicine, 1974-09, Vol.140 (3), p.871-876

1974

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Uncertain value of urinary sediments in the diagnosis of amyloidosis

The New England journal of medicine, 1977-10, Vol.297 (15), p.821-823

1977

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A 25,000 molecular weight protein constituent of human amyloid fibrils related to amyloid protein AA

Archives of biochemistry and biophysics, 1975-01, Vol.171 (1), p.197-205

1975

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Amino terminal sequence of amyloid P-component isolated from serum

The Journal of laboratory and clinical medicine, 1978-07, Vol.92 (1), p.78

1978

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Fractionation of Primary Amyloid Fibrils Characterization and Chemical Interaction of the Subunits

Biochimica et biophysica acta, 1977-01, Vol.491 (1), p.167-176

1977

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Lack of association of a restriction fragment length polymorphism for serum amyloid P gene with reactive amyloidosis

Arthritis and rheumatism, 1989-10, Vol.32 (10), p.1325-1327

1989

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“A” protein of amyloidosis isolation of a cross‐reacting component from serum by affinity chromatography

Arthritis and rheumatism, 1975-07, Vol.18 (4), p.315-322

1975

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P‐component of amyloid. Isolation from human serum by affinity chromatography

Arthritis and rheumatism, 1976-07, Vol.19 (4), p.749-754

1976

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Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: The Transthyretin Amyloidosis Cardiac Study (TRACS)

Cardiac amyloidosis in African Americans: Comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosis

Diagnostic and Prognostic Utility of Cardiovascular Magnetic Resonance Imaging in Light-Chain Cardiac Amyloidosis

Light-Chain Amyloidosis With Echocardiographic Features of Hypertrophic Cardiomyopathy

186. Early Life Origins of Risky Sexual Behavior in Adolescence

Thermodynamic Stability of a κI Immunoglobulin Light Chain: Relevance to Multiple Myeloma

Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene

A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy

Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities

Amyloidosis

Haplotype analysis of common transthyretin mutations

A new transthyretin variant (His 69) associated with vitreous amyloid in an FAP family

Haplotype analysis of His 58, Ala 60 and Tyr 77 types of familial amyloidotic polyneuropathy

Isolation and identification by sequence analysis of experimentally induced guinea pig amyloid fibrils

Uncertain value of urinary sediments in the diagnosis of amyloidosis

A 25,000 molecular weight protein constituent of human amyloid fibrils related to amyloid protein AA

Amino terminal sequence of amyloid P-component isolated from serum

Fractionation of Primary Amyloid Fibrils Characterization and Chemical Interaction of the Subunits

Lack of association of a restriction fragment length polymorphism for serum amyloid P gene with reactive amyloidosis

“A” protein of amyloidosis isolation of a cross‐reacting component from serum by affinity chromatography

P‐component of amyloid. Isolation from human serum by affinity chromatography

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