AbstractTo assess left ventricular diastolic filling in amyloid heart disease, 17 patients with familial amyloid polyneuropathy and 20 normal subjects were examined by radionuclide angiography. None of the patients showed clinical evidence of restrictive cardiomyopathy. All but two patients had normal left ventricular ejection fraction. Peak filling rate was significantly lower and time to peak filling rate was significantly greater in patients than in normal subjects (2.60 ± 0.52 versus 3.10 ± 0.44 EDV/s, p < 0.001, and 215 ± 53 versus 147 ± 18 ms, p < 0.001, respectively). The mean left ventricular filling volume during rapid diastolic filling and atrial systole in patients was 54.5 ± 19.5% and 44.2 ± 21.6% of the stroke volume, respectiv...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
One hundred thirty-two patients with biopsy-proven systemic amyloidosis underwent echocardiographic ...
BACKGROUND: Patients with AL amyloidosis often present with signs of congestive heart failure. AIM: ...
AbstractTo assess left ventricular diastolic filling in amyloid heart disease, 17 patients with fami...
Familial amyloidosis polyneuropathy (FAP) is an inherited disease caused by mutated transthyretin, w...
AbstractObjectives. This study attempted to assess myocardial sympathetic innervation using iodine-1...
AbstractSixty-four patients with primary systemic amyloidosis—53 with two-dimensional echocardiograp...
Indexes of left ventricular diastolic filling were measured by radionuclide ventriculography in 28 p...
AbstractTo assess right ventricular diastolic function in cardiac amyloidosis, pulsed wave Doppler u...
PubMedID: 16060129Objective. Cardiac deposition of AA amyloidosis may result in increasing left vent...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
SUMMARY To assess left ventnrcular (LV) diastolic filling at rest in patients with coronary artery d...
Aims: Multimodal imaging has allowed cardiac amyloidosis (CA) to be increasingly recognised as a tre...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
Background: Cardiac amyloidosis (CA), following a non-invasive diagnosis, constitutes an increasingl...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
One hundred thirty-two patients with biopsy-proven systemic amyloidosis underwent echocardiographic ...
BACKGROUND: Patients with AL amyloidosis often present with signs of congestive heart failure. AIM: ...
AbstractTo assess left ventricular diastolic filling in amyloid heart disease, 17 patients with fami...
Familial amyloidosis polyneuropathy (FAP) is an inherited disease caused by mutated transthyretin, w...
AbstractObjectives. This study attempted to assess myocardial sympathetic innervation using iodine-1...
AbstractSixty-four patients with primary systemic amyloidosis—53 with two-dimensional echocardiograp...
Indexes of left ventricular diastolic filling were measured by radionuclide ventriculography in 28 p...
AbstractTo assess right ventricular diastolic function in cardiac amyloidosis, pulsed wave Doppler u...
PubMedID: 16060129Objective. Cardiac deposition of AA amyloidosis may result in increasing left vent...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
SUMMARY To assess left ventnrcular (LV) diastolic filling at rest in patients with coronary artery d...
Aims: Multimodal imaging has allowed cardiac amyloidosis (CA) to be increasingly recognised as a tre...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
Background: Cardiac amyloidosis (CA), following a non-invasive diagnosis, constitutes an increasingl...
Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyl...
One hundred thirty-two patients with biopsy-proven systemic amyloidosis underwent echocardiographic ...
BACKGROUND: Patients with AL amyloidosis often present with signs of congestive heart failure. AIM: ...