Background:Familial amyloidotic polyneuropathy (FAP) is a rare disease diagnosed in Brazil and worldwide. The frequency of cardiovascular involvement in Brazilian FAP patients is unknown.Objective:Detect the frequency of cardiovascular involvement and correlate the cardiovascular findings with the modified polyneuropathy disability (PND) score.Methods:In a national reference center, 51 patients were evaluated with clinical examination, electrocardiography (ECG), echocardiography (ECHO), and 24-hour Holter. Patients were classified according to the modified PND score and divided into groups: PND 0, PND I, PND II, and PND > II (which included PND IIIa, IIIb, and IV). We chose the classification tree as the statistical method to analyze the as...
The aim of this study is to assess the prevalence of cardiac involvement in hereditary transthyretin...
A 32-year-old man with family history of amyloidosis was admitted to the hospital because of orthost...
To report the clinical, pathologic and molecular genetic features of a Chinese family with familial ...
Background:Familial amyloidotic polyneuropathy (FAP) is a rare disease diagnosed in Brazil and world...
Summary: A systematic investigation was performed in patients with familial amyloidotic poly-neuropa...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant disease due to the mutati...
SummaryBackgroundCardiac amyloidosis due to familial amyloid polyneuropathy (FAP) includes restricti...
Familial amyloidosis polyneuropathy (FAP) is an inherited disease caused by mutated transthyretin, w...
Familial amyloidosis with polyneuropathy (FAP) was first reported from Portugal in 1952, but since t...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant inherited disease. FAP ca...
© 2016 European Society of Cardiology. All rights reserved.Background: Rhythm disturbances and condu...
BACKGROUND: Cardiac complications are common in familial amyloidotic polyneuropathy (FAP), in which ...
International audienceBACKGROUND: Familial amyloid polyneuropathy (FAP) mainly targets the periphera...
Sixteen (16) patients with Familial Amyloidotic Polyneuropathy-Portuguese Type (FAP) were evaluated ...
The aim of this study is to assess the prevalence of cardiac involvement in hereditary transthyretin...
A 32-year-old man with family history of amyloidosis was admitted to the hospital because of orthost...
To report the clinical, pathologic and molecular genetic features of a Chinese family with familial ...
Background:Familial amyloidotic polyneuropathy (FAP) is a rare disease diagnosed in Brazil and world...
Summary: A systematic investigation was performed in patients with familial amyloidotic poly-neuropa...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant disease due to the mutati...
SummaryBackgroundCardiac amyloidosis due to familial amyloid polyneuropathy (FAP) includes restricti...
Familial amyloidosis polyneuropathy (FAP) is an inherited disease caused by mutated transthyretin, w...
Familial amyloidosis with polyneuropathy (FAP) was first reported from Portugal in 1952, but since t...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant inherited disease. FAP ca...
© 2016 European Society of Cardiology. All rights reserved.Background: Rhythm disturbances and condu...
BACKGROUND: Cardiac complications are common in familial amyloidotic polyneuropathy (FAP), in which ...
International audienceBACKGROUND: Familial amyloid polyneuropathy (FAP) mainly targets the periphera...
Sixteen (16) patients with Familial Amyloidotic Polyneuropathy-Portuguese Type (FAP) were evaluated ...
The aim of this study is to assess the prevalence of cardiac involvement in hereditary transthyretin...
A 32-year-old man with family history of amyloidosis was admitted to the hospital because of orthost...
To report the clinical, pathologic and molecular genetic features of a Chinese family with familial ...