Volume 10, supplement issue 1, December 2015
First European Congress on Hereditary ATTR amyloidosis
116 articles in this issue
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TTR-FAP: a single-center experience in Sicily, an Italian endemic area
Authors (first, second and last of 8)
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Unravelling the epidemiology of late-onset and asymptomatic carriers of FAP ATTR V30M in a Portuguese population
Authors (first, second and last of 6)
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The hidden story behind gender differences in familial amyloid polyneuropathy (FAP) ATTRV30M
Authors (first, second and last of 8)
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Clinical, epidemiological, genetic, and electrophysiological characteristics of transthyretin familial amyloid polyneuropathies in Israel
Authors (first, second and last of 4)
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The phenotypical expression of an European inherited TTR amyloidosis in Brazil
Authors (first, second and last of 5)
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DISCOVERY: a study examining the prevalence of transthyretin mutations in subjects suspected of having cardiac amyloidosis
Authors (first, second and last of 8)
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Analysis of disease progression in patients with transthyretin cardiac amyloidosis
Authors (first, second and last of 8)
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Vasculopathy in transthyretin Val30Met familial amyloid polyneuropathy
Authors (first, second and last of 7)
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Misdiagnoses of transthyretin amyloidosis: a clinical and electrodiagnostic study
Authors (first, second and last of 7)
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Quantitative MR-neurographic parameters can determine and specify nerve injury in amyloid related polyneuropathy
Authors (first, second and last of 8)
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Positron Emission Tomography (PET) utilizing Pittsburgh compound B (PIB) detects amyloid heart deposits in hereditary transthyretin amyloidosis (ATTR).
Authors (first, second and last of 8)
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DPD Scintigraphy for diagnosis of amyloidosis in 1191 patients– a single centre experience
Authors (first, second and last of 8)
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Multi-modality imaging in cardiac ATTR amyloidosis: agreement between echocardiography, MRI and DPD-scintigraphy
Authors (first, second and last of 8)
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ATTR Amyloidosis: development of cardiac symptoms during 6 years of follow up in different ATTR-variants
Authors (first, second and last of 6)
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Ocular manifestations of transthyretin-related familial amyloid polyneuropathy
Authors (first, second and last of 8)
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Phase 2 open-label extention (OLE) study of patisiran, an investigational siRNA agent for familial amyloidotic polyneuropathy (FAP)
Authors (first, second and last of 8)
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Diflunisal therapy for cardiac ATTR amyloidosis: a longitudinal, prospective, single centre study
Authors (first, second and last of 8)
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Diflunisal in late-onset FAP patients with moderate to severe neuropathy
Authors (first, second and last of 7)
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Familial Amyloid Polyneuropathy treatment with Tafamidis – evaluation of one- and two-year treatment in Porto, Portugal
Authors (first, second and last of 8)