MD BENSON, AS COHEN - Annals of Internal Medicine, 1977 - Am Coll Physicians We report a new kinship with systemic amyloid presenting as peripheral
neuropathy in the fourth and fifth decades of life. A progressive sensory and
motor loss starting in the lower extremities occurs from this disease, and ... Cited by 52 - Related articles - All 2 versions
R Andersson - Acta Med Scand, 1970 - interscience.wiley.com Abstract. An account, mainly clinical, is given of 18 cases of hereditary
amyloidosis with polyneuropathy. Common to all cases were progressive peripheral
sensory-motor nervous disturbances starting in the legs. Gastrointestinal ... Cited by 89 - Related articles - All 2 versions
SHUI IKEDA, N HANYU, M HONGO, J … - Brain, 1987 - Oxford Univ Press A clinicopathological study was made on 65 patients from a small area of Nagano
Prefecture, Japan, with hereditary generalized amyloidosis with polyneuropathy
to clarify the clinical variety of the disease. Forty-five patients from ... Cited by 79 - Related articles - All 7 versions
Y Takaoka, F Tashiro, S Yi, S Maeda, K … - Transgenic research, 1997 - Springer 1Institute of Molecular Embryology and Genetics, 2Department of Pathology,
Kumamoto University School of Medicine, Kumamoto 862, Japan (Fax 81-96-373-5321)
, 3Department of Biochemistry, Yamanashi Medical College, Yamanashi, ... Cited by 15 - Related articles - BL Direct - All 5 versions
FE Dwulet, MD Benson - Biochemical and biophysical research communications, 1983 - ncbi.nlm.nih.gov Amyloid fibrils from an individual with heredofamilial amyloidosis were found to
be composed of plasma prealbumin. To study this protein a three step procedure
to isolate prealbumin from plasma was developed. It entailed ion exchange ... Cited by 102 - Related articles
M NAKAZATO, K SHIOMI, M MIYAZATO, S … - Internal Medicine, 1992 - Journal@rchive We studied 107 cases and 64 carriers of type I familial amyloidotic
polyneuropathy (FAP) residing in 16 districts in Japan. The age of onset of
illness ranged from 20 to 71 years old, with a mean of 40.1 ± 12.8 years ... Cited by 14 - Related articles - All 3 versions
PÅ Hofer, R Andersson - Acta Pathologica, Microbiologica et Immunologica …, 1981 - interscience.wiley.com The pathology of primary familial amyloidosis with polyneuropathy is described
on the basis of post-mortem examination of six cases from Northern Sweden.
Clinically the disease is characterized by progressive sensory and motor ... Cited by 41 - Related articles - All 4 versions
GEN SOBUE, N NAKAO, KEN MURAKAMI, T … - Brain, 1990 - Oxford Univ Press The neuropathological changes were examined in 2 cases of type I familial
amyloid polyneuropathy (FAP), confirmed by a genetic study with human
transthyretin (prealbumin) cDNA. These cases were from different foci of ... Cited by 29 - Related articles - All 5 versions
S WAKASUGI, T INOMOTO, S YI, M NAITO, … - Proceedings of the Japan Academy. Ser. B: Physical …, 1987 - Journal@rchive Amyloidosis comprises a heterogenous group of diseases of diverse etiology
characterized by the extracellular deposition of a number of fibrillar proteins
which may be distinguished from each other biochemically and ... Cited by 18 - Related articles
Y Sakaki, K Yoshioka, H Tanahashi, H Furuya … - Molecular biology & medicine, 1989 - ncbi.nlm.nih.gov 1: Mol Biol Med. 1989 Apr;6(2):161-8. Human transthyretin (prealbumin) gene
and molecular genetics of familial amyloidotic polyneuropathy. ... Cited by 18 - Related articles
