Familial amyloidotic neuropathy
André, C.; Novis, S.A.
Neurology 38(3): 510
1988
ISSN/ISBN: 0028-3878 PMID: 3347366 Document Number: 307091
Document emailed within 1 workday
Related Documents
Sakaki, Y.; Sasaki, H. 1985: DNA diagnosis of familial amyloidotic polyneuropathy Rinsho Byori. Japanese Journal of Clinical Pathology 33 Spec no 65: 134-139Buades Reinés, J.; Dolz, C. 1995: Familial amyloidotic polyneuropathy and liver transplantation Gastroenterologia y Hepatologia 18(9): 480-482
Ando, Y.; Tanaka, Y.; Yamashita, T.; Tashima, K.; Sakashita, N.; Nakamura, M.; Uchino, M.; Ando, M. 1995: Familial amyloidotic polyneuropathy (FAP) type i and the therapies Rinsho Shinkeigaku 35(12): 1430-1432
Maeda, S.; Mita, S.; Araki, S.; Shimada, K. 1986: Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy Molecular Biology and Medicine 3(4): 329-338
Yi, S.; Takahashi, K.; Araki, S.; Yamamura, K. 1995: Transgenic mouse model of familial amyloidotic polyneuropathy type I: its production, biological features, and usefulness Laboratory Animal Science 45(2): 173-175
Viana, J.d.S.; Bento, C.; Vieira, H.; Neves, S.; Seco, C.; Elvas, L.; Coelho, L.; Ferrão, J.; Tomé, L.; Perdigoto, R.; Craveiro, A.L.; Providência, L.A.; Furtado, A.L. 1999: Haemodynamics during liver transplantation in familial amyloidotic polyneuropathy: study of the intraoperative cardiocirculatory data of 50 patients Revista Portuguesa de Cardiologia: Orgao Oficial da Sociedade Portuguesa de Cardiologia 18(7-8): 689-697
Suzuki, Y.; Suzuki, T.; Ikeda, S. 1991: Enzyme-linked immunosorbent assay of transthyretin devised for semimicro plasma diagnosis of familial amyloidotic polyneuropathy Journal of Laboratory and Clinical Medicine 118(2): 194-199
Olofsson, B.O.; Backman, C.; Boman, K. 1988: Familial amyloidotic polyneuropathy in northern Sweden. A cross-sectional and longitudinal study of cardiac function with echocardiography Arctic Medical Research 47 Suppl. 1: 423-425
Fonseca, C.; Ceia, F.; Nogueira, J.S.; Alves, M.; Carvalho, M.; Luís, M.d.L.; Luís, A.S. 1991: Myocardiopathy caused by Portuguese-type familial amyloidotic polyneuropathy. Sequential morphologic and functional study of 60 patients Revista Portuguesa de Cardiologia: Orgao Oficial da Sociedade Portuguesa de Cardiologia 10(12): 909-916
Diaz, J.; Acosta, F.; Tovar, I.; Cañizares, F.; Moreno, J.; Contreras, R.F.; Bueno, F.S.; Robles, R.; Martinez, P.; Parrilla, P. 1995: Sympathetic nervous system response to surgical stress in patients with familial amyloidotic polyneuropathy undergoing orthotopic liver transplantation Transplantation Proceedings 27(4): 2295
Yamamoto, T.; Matsunaga, K.; Ohnishi, A.; Nakazato, M.; Murai, Y. 1996: A late onset familial amyloidotic polyneuropathy (FAP) with a novel variant transthyretin characterized by a basic-for-acidic amino acid substitution (Glu61-->Lys) Rinsho Shinkeigaku 36(9): 1065-1068
Vahar-Matiar, H.; Petzold, J.; Müller, J. 1975: Familial recurring polytopic neuropathy Der Nervenarzt 46(1): 31-37
Lobzin, V.S.; Tsatskina, N.D. 1988: Hereditary familial forms of neuropathy of the facial nerve Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 88(11): 7-10
Pou Serradell, A.; De Paiva, V.J.; Alameda, F.; Lloreta, J.; Blasco, R.; Piqueras, A. 1992: Familial recurrent paralysis of the brachial plexus. Tomaculous neuropathy Revue Neurologique (Paris) 148(2): 123-128
Partsch, H. 1970: Hereditary sensory neuropathy (Denny-Brown) (Familial acroosteolysis) Wiener Klinische Wochenschrift 82(8): 129-136
Lance, J.W.; Burke, D.J.; Pollard, J. 1978: Pseudomyotonia and tetany in a familial neuropathy resembling Charcot-Marie-Tooth disease Transactions of the American Neurological Association 103: 22-26
Carrizosa, J.; Lin, K.Y.; Myerson, R.M. 1973: Gastrointestinal neuropathy in familial amyloidosis. Report of a case with severe diarrhea without steatorrhea or malabsorption American Journal of Gastroenterology 59(6): 541-546
Julien, J.; Vallat, J.M.; Vital, C.; Coiffu, B.; Legendre, P.; Vallat, M. 1975: Familial amyloid neuropathy of Corino Andrade. Ultrastructural study of the peripheral nerve in 2 patients Revue Neurologique (Paris) 131(4): 229-241
Cavallari, V.; Di Pasquale, M.R.; Scuderi, D. 1981: Hereditary neuropathy with a tendency to compression paralysis. Electrophysiological, morphometric and ultrastructural study of 2 familial cases Acta Neurologica 3(1): 187-196
Minauchi, Y.; Kohka, M.; Igata, A.; Ohkatsu, Y. 1982: A familial case with hereditary pressure-sensitive neuropathy, with "tomacula"--the first case in Japan Rinsho Shinkeigaku 22(10): 918-925