Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyloidosis. Clusters of patients have been reported predominantly from Portugal, Japan and Sweden. The present study examines the involvement of the heart in individuals with the Swedish variety of FAP. During long-term ECG recording in 16 patients, a high frequency of disturbances of sinus node function and atrioventricular conduction were observed. Long-term ECG may help considerably in the evaluation of symptoms attributable to disturbances of heart rhythm in FAP. A retrospective survey of 20 patients with FAP treated with a pacemaker showed that the indication for pacing was advanced atrioventricular block (12 cases), dysfunction of the sinu...
none6noAmyloid heart disease is one of the most frequent types of cardiomyopathy with restrictive pa...
BACKGROUND: Cardiac complications are common in familial amyloidotic polyneuropathy (FAP), in which ...
AbstractTo assess left ventricular diastolic filling in amyloid heart disease, 17 patients with fami...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
Summary: A systematic investigation was performed in patients with familial amyloidotic poly-neuropa...
Familial amyloidosis with polyneuropathy (FAP) was first reported from Portugal in 1952, but since t...
Background:Familial amyloidotic polyneuropathy (FAP) is a rare disease diagnosed in Brazil and world...
Familial amyloidosis polyneuropathy (FAP) is an inherited disease caused by mutated transthyretin, w...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant disease due to the mutati...
To determine the prevalence of cardiac arrhythmias in patients with systemic amyloidosis 24 hour ele...
AbstractObjectives. This study attempted to assess myocardial sympathetic innervation using iodine-1...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant inherited disease. FAP ca...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...
SummaryBackgroundCardiac amyloidosis due to familial amyloid polyneuropathy (FAP) includes restricti...
A 32-year-old man with family history of amyloidosis was admitted to the hospital because of orthost...
none6noAmyloid heart disease is one of the most frequent types of cardiomyopathy with restrictive pa...
BACKGROUND: Cardiac complications are common in familial amyloidotic polyneuropathy (FAP), in which ...
AbstractTo assess left ventricular diastolic filling in amyloid heart disease, 17 patients with fami...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
Summary: A systematic investigation was performed in patients with familial amyloidotic poly-neuropa...
Familial amyloidosis with polyneuropathy (FAP) was first reported from Portugal in 1952, but since t...
Background:Familial amyloidotic polyneuropathy (FAP) is a rare disease diagnosed in Brazil and world...
Familial amyloidosis polyneuropathy (FAP) is an inherited disease caused by mutated transthyretin, w...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant disease due to the mutati...
To determine the prevalence of cardiac arrhythmias in patients with systemic amyloidosis 24 hour ele...
AbstractObjectives. This study attempted to assess myocardial sympathetic innervation using iodine-1...
IntroductionFamilial amyloid polyneuropathy (FAP) is an autosomic dominant inherited disease. FAP ca...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...
SummaryBackgroundCardiac amyloidosis due to familial amyloid polyneuropathy (FAP) includes restricti...
A 32-year-old man with family history of amyloidosis was admitted to the hospital because of orthost...
none6noAmyloid heart disease is one of the most frequent types of cardiomyopathy with restrictive pa...
BACKGROUND: Cardiac complications are common in familial amyloidotic polyneuropathy (FAP), in which ...
AbstractTo assess left ventricular diastolic filling in amyloid heart disease, 17 patients with fami...