HV Vinters - Stroke, 1987 - Am Heart Assoc Historical Perspective The clinicopathologic entity of cerebral congophilic or
amyloid angiopathy (CAA) has been recognized since die early part of this
century, though it has at- tained the 'limelight' over the past decade ... Cited by 543 - Related articles - All 5 versions
- ►ahajournals.org [PDF] HV Vinters, JJ Gilbert - Stroke, 1983 - Am Heart Assoc SUMMARY Ten histologic sections were sampled from similar cortical regions in
each of 84 autopsy brains removed from patients aged 60 to 97 years. The
sections were stained by the Congo-red method and examined under polarized ... Cited by 207 - Related articles - All 4 versions
- ►nih.gov [PDF] MR Wallace, FE Dwulet, PM Conneally, MD … - Journal of Clinical Investigation, 1986 - pubmedcentral.nih.gov Familial amyloidotic polyneuropathy (FAP) is an autosomal dominant late-onset
disorder characterized by the extracellular deposition of amyloid fibrils. In
all cases studied these fibrils have been found to be composed of plasma ... Cited by 92 - Related articles - All 6 versions
- ►oxfordjournals.org K Misu, N Hattori, M Nagamatsu, S Ikeda, Y … - Brain, 1999 - Oxford Univ Press Clinicopathological and genetic features were assessed on 35 Japanese families
affected by late-onset familial amyloid polyneuropathy type I (transthyretin
Met30-associated familial amyloid polyneuropathy, FAP TTR Met30) whose ... Cited by 57 - Related articles - BL Direct - All 6 versions
- ►nih.gov [PDF] MD Benson - Journal of Clinical Investigation, 1981 - pubmedcentral.nih.gov ABSTR A C T Amyloid fibril protein has been iso- lated from the tissues of a
patient of Swedish ancestry with autosomal dominant heredofamilial amyloidosis.
After solubilization in guanidine HCl, a significant amount of the protein ... Cited by 43 - Related articles - All 5 versions
G Holmgren, E Holmberg, A Lindstrom, E … - Clin Genet, 1988 - interscience.wiley.com Genomic DNA from 17 Swedish patients with familial amyloidotic polyneuropathy
(FAP), and 50 healthy controls were tested with a cDNA transthyretin probe. In
seven of the patients, FAP was not reported in either of their parents. All ... Cited by 39 - Related articles - All 3 versions
M Brett, MR Persey, MM Reilly, T Revesz, … - Brain, 1999 - Oxford Univ Press We report a middle-aged woman with a novel transthyretin (TTR) variant,
Leu12Pro. She had extensive amyloid deposition in the leptomeninges and liver as
well as the involvement of the heart and peripheral nervous system which ... Cited by 37 - Related articles - BL Direct - All 8 versions
M Mascalchi, F Salvi, MG Pirini, A D'Errico, A … - Neurology, 1999 - AAN Enterprises From Sezione di Radiodiagnostica (Drs. Mascalchi and Villari), Dipartimento di
Fisiopatologia, Clinica Università di Firenze; Divisione di Neurologia Ospedale
Bellaria (Drs. Salvi, Plasmati, and Tassinari), Università di Bologna; ... Cited by 38 - Related articles - BL Direct - All 6 versions
MD Benson, MR Wallace, E Tejada, H … - Arthritis Care & Research - interscience.wiley.com A family with hereditary amyloidosis characterized by peripheral neuropathy and
cardiomyopathy is described. Lack of eye involvement sets their disease apart
from the Indiana/Swiss familial amyloidotic polyneuropathy type II. The ... Cited by 38 - Related articles - All 3 versions
MD Benson, JC Kincaid - Muscle and Nerve, 2007 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 34 - Related articles - BL Direct - All 3 versions
