Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective. (Q43598098)

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English	Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.	scientific article

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Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective (English)

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Claudio Rapezzi

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Giovanni Palladini

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Giampaolo Merlini

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Candida Cristina Quarta

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Massimiliano Lorenzini

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Francesco Cappelli

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Stefano Perlini

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Federico Perfetto

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Simone Longhi

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Fabrizio Salvi

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Francesco Grigioni

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Paola Rimessi

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Alessandra Ferlini

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Giorgio Arpesella

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Antonio Daniele Pinna

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28 June 2012

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European Heart Journal

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520-528

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6 February 2020

Transthyretin-related familial amyloidotic polyneuropathy

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21 January 2018

Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

1 reference

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21 January 2018

Hereditary transthyretin amyloidosis from a Scandinavian perspective.

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Phenotypic expression of familial amyloid polyneuropathy in Brazil.

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Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal.

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21 January 2018

Transthyretin-related amyloidoses and the heart: a clinical overview

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21 January 2018

Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans

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21 January 2018

Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant.

1 reference

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A Danish kindred with familial amyloid cardiomyopathy revisited: Identification of a mutant transthyretinmethionine111 variant in serum from patients and carriers

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21 January 2018

Amyloid heart disease

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Infiltrative cardiovascular diseases: cardiomyopathies that look alike

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Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004.

1 reference

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21 January 2018

Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy

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21 January 2018

Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types.

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21 January 2018

The molecular biology and clinical features of amyloid neuropathy

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ACC/AHA/ASE 2003 Guideline Update for the Clinical Application of Echocardiography: Summary Article: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (ACC/AHA/ASE Committee to Update the 1997

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21 January 2018

Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.

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Late occurrence of fatal aortitis: a complication of Aspergillus endocarditis following coronary artery bypass graft surgery.

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Prevalence of carpal tunnel syndrome in a general population

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Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant.

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21 January 2018

The biological and chemical basis for tissue-selective amyloid disease

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Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis

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21 January 2018

Why are some amyloidoses systemic? Does hepatic "chaperoning at a distance" prevent cardiac deposition in a transgenic model of human senile systemic (transthyretin) amyloidosis?

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21 January 2018

Gender-related risk of myocardial involvement in systemic amyloidosis.

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Pressure-volume relationships in patients with transthyretin (ATTR) cardiac amyloidosis secondary to V122I mutations and wild-type transthyretin: Transthyretin Cardiac Amyloid Study (TRACS).

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Orally administered diflunisal stabilizes transthyretin against dissociation required for amyloidogenesis

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

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