International audienceOBJECTIVES This study sought to compare techniques evaluating cardiac dysautonomia and predicting the risk of death of patients with hereditary transthyretin amyloidosis (mATTR) after liver transplantation (LT). BACKGROUND mATTR is a multisystemic disease involving mainly the heart and the peripheral nervous system. LT is the reference treatment, and pre-operative detection of high-risk patients is critical. Cardiovascular dysautonomia is commonly encountered in ATTR and may affect patient outcome, although it is not known yet which technique should be used in the field to evaluate it. METHODS In a series of 215 consecutive mATTR patients who underwent LT, cardiac dysautonomia was assessed by a dedicated clinical score...
Transthyretin cardiac amyloidosis is a restrictive cardiomyopathy ((ATTR-CM), caused by an extracell...
Over the last decade, new medical treatment modalities have emerged based on increased insights into...
OBJECTIVES: The aims of the study were to explore the ability of native myocardial T1 mapping by car...
International audienceOBJECTIVES This study sought to compare techniques evaluating cardiac dysauton...
Background. Although orthotopic liver transplantation (OLT) and combined heart and liver transplanta...
From First European Congress on Hereditary ATTR amyloidosisParis, France. 2-3 November 2015Internati...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...
Background Hereditary transthyretin amyloid (ATTRm) amyloidosis is a systemic disease mainly affecti...
none10noBackground and Objective. Although combined heart and liver transplantation (CHLT) is an ac...
Background: Hereditary transthyretin amyloidosis (ATTR) is a lethal disease in which misfolded trans...
ObjectivesWe sought to evaluate noninvasive parameters by electrocardiography, echocardiography, tec...
BACKGROUND: Nuclear imaging modalities using 123Iodine-metaiodobenzylguanidine (123I-MIBG) and bone ...
International audienceWe report the case of a 62-year-old man hospitalized in May 2015 for symptomat...
: Transthyretin cardiac amyloidosis (ATTR-CA) is a systemic disorder resulting from the extracellula...
Abstract Aims Transthyretin amyloid cardiomyopathy (ATTR‐CM) is a progressive, fatal disorder that r...
Transthyretin cardiac amyloidosis is a restrictive cardiomyopathy ((ATTR-CM), caused by an extracell...
Over the last decade, new medical treatment modalities have emerged based on increased insights into...
OBJECTIVES: The aims of the study were to explore the ability of native myocardial T1 mapping by car...
International audienceOBJECTIVES This study sought to compare techniques evaluating cardiac dysauton...
Background. Although orthotopic liver transplantation (OLT) and combined heart and liver transplanta...
From First European Congress on Hereditary ATTR amyloidosisParis, France. 2-3 November 2015Internati...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...
Background Hereditary transthyretin amyloid (ATTRm) amyloidosis is a systemic disease mainly affecti...
none10noBackground and Objective. Although combined heart and liver transplantation (CHLT) is an ac...
Background: Hereditary transthyretin amyloidosis (ATTR) is a lethal disease in which misfolded trans...
ObjectivesWe sought to evaluate noninvasive parameters by electrocardiography, echocardiography, tec...
BACKGROUND: Nuclear imaging modalities using 123Iodine-metaiodobenzylguanidine (123I-MIBG) and bone ...
International audienceWe report the case of a 62-year-old man hospitalized in May 2015 for symptomat...
: Transthyretin cardiac amyloidosis (ATTR-CA) is a systemic disorder resulting from the extracellula...
Abstract Aims Transthyretin amyloid cardiomyopathy (ATTR‐CM) is a progressive, fatal disorder that r...
Transthyretin cardiac amyloidosis is a restrictive cardiomyopathy ((ATTR-CM), caused by an extracell...
Over the last decade, new medical treatment modalities have emerged based on increased insights into...
OBJECTIVES: The aims of the study were to explore the ability of native myocardial T1 mapping by car...