Argentinian patients of European ancestry with familial amyloid polyneuropathy

References

• Andrade C. A peculiar form of peripheral neuropathy. Familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain 1952; 75: 408–427
   PubMed Web of Science ®Google Scholar
• Costa P P, Figueira A S, Bravo F R. Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy. Proc Natl Acad Sci USA 1978; 75: 4499–4503
   PubMed Web of Science ®Google Scholar
• Tawara S, Nakazato M, Kangawa K, Matsuo H, Araki S. Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type). Biochem Biophys Res Commun 1983; 116: 880–888
   PubMed Web of Science ®Google Scholar
• Saraiva M JM, Birken S, Costa P P, Goodman D S. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin). J Clin Invest 1984; 1A: 104–119
   Google Scholar
• Dwulet F E, Benson M D. Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin. Proc Natl Acad Sci USA 1984; 81: 694–698
   PubMed Web of Science ®Google Scholar
• Ikeda S, Nakano T, Yanagisawa N, Nakazato M, Tsukagoshi H. Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy. Eur Neurol 1992; 32: 308–313
   PubMed Web of Science ®Google Scholar
• Nakazato M, Ikeda S, Shiomi K, Matsukura S, Yoshida K, Shimizu H, Atsumi T, Kangawa K, Matsuo H. Identification of a novel transthyretin variant (Val 30 Leu) associated with familial amyloidotic polyneuropathy. FEBSLett 1992; 306: 206–208
   PubMed Web of Science ®Google Scholar
• Erbsloh F. Eine seltene Form der chronisch fortschreitenden Polyneuritis (familiare Paramyloidose). Mat Med Nordmark 1961; 13: 157–165
   Google Scholar
• Juliao O F, Queiroz L S, de Faria J, Lopes. Portuguese type of familial amyloid polyneuropathy. Anatomo-clinical study of a Brazilian family. Eur Neurol 1974; 11: 180–195
   PubMed Web of Science ®Google Scholar
• Benson M D. Inherited amyloidosis. J Med Genet 1991; 28: 73–78
   PubMedGoogle Scholar
• Curcio F I, Scornik J S, Ale J S, Curcio H F. Enfermedad de Corino Andrade. Estudio clinico-patologico. Prensa Med Argent 1970; 57: 1611–1615
   Google Scholar
• Ikeda S, Hanyu N, Hongo M, Yoshioka J, Oguchi H, Yanagisawa N, Kobayashi T, Tsukagoshi H, Ito N, Yokota T. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients. Brain 1987; 315–337
   PubMed Web of Science ®Google Scholar
• Holt I J, Harding A E, Middleton L, Chrysostomou G, Said G, King R HM, Thomas P K. Molecular genetics of amyloid neuropathy in Europe. Lancet 1989; ii: 524–526
   Google Scholar
• Munar-Ques M, Costa P P, Saraiva M JM, Munar-Bernat C. Asymptomatic carriers in the Majorcan focus of FAP I. 2nd International Symposium on Familial Amyloidotic Polyneuropathy and Other Transthyretin Related Disorders, Skelleftea, June, 1–31992, 72
   Google Scholar
• Saraiva M JM, Sherman W, Goodman D S. Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin. J Lab Clin Med 1986; 108: 17–22
   Google Scholar
• Kincaid J C, Wallace M R, Benson M D. Late-onset familial amyloid polyneuropathy in an American family of English origin. Neurology 1989; 39: 861–863
   PubMed Web of Science ®Google Scholar
• Nakazato M, Steen L, Holmgren G, Kurihara T, Matsukura S, Kangawa K, Matsuo H. Structurally abnormal transthyretin causing familial amyloidotic polyneuropathy in Sweden. Clin Chim Acta 1987; 167: 341–342
   PubMed Web of Science ®Google Scholar
• Ferlini A, Romeo G, Tassinari C A, Saraiva M JM, Costa P P, Salvi F. Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studies. Adv Neurol 1988; 48: 201–208
   Google Scholar
• Skare J, Yazici H, Erken E, Dede H, Cohen A, Milunsky A, Skinner M. Homozygosity for the met 30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy. Hum Genet 1990; 86: 89–90
   PubMed Web of Science ®Google Scholar
• Miyazato M, Nakazato M, Yamamura Y, Kangawa K, Matsuo H, Matsukura S. Variant transthyretin in familial amyloidotic polyneuropathy (FAP). Amyloid and Amyloidosis 1990, J B Natvig, O Forre, G Husby, A Husebekk, B Skogen, K Sletten, P Westermark. Kluwer, Dordrecht, Boston, London 1991; 618–621
   Google Scholar
• Skinner M, Skare J, Simms R W, Libbey C A, Cohen A S. Familial amyloidosis at the Boston University Amyloid Research Center. 2nd International Symposium on Familial Amyloidotic Polyneuropathy and Other Transthyretin Related Disorders, Skelleftea, June, 1–31992, 24
   Google Scholar
• Bhatia K, Reilly M, Adams D, Davis M B, Hawkes C H, Thomas P K, Said G, Harding A E. Transthyretin gene mutations in British and French patients with amyloid neuropathy. J Neurol Neumsurg Psychiatry 1993; 56: 694–697
   PubMedGoogle Scholar
• Jones L A, Keller U, Skare J, Heim S, Skinner M. Familial amyloidotic polyneuropathy (FAP) in a family of Southeast Asian descent. Presented at the VII International Symposium on Amyloidosis, Kingston, July, 11–151993, 122
   Google Scholar
• Yoshioka K, Furuya H, Sasaki H, Saraiva M JM, Costa P P, Sakaki Y. Haplotype analysis of familial amyloidotic polyneuropathy. Hum Genet 1989; 82: 9–13
   PubMed Web of Science ®Google Scholar
• Reilly M M, King R HM. Familial amyloid polyneuropathy. Brain Pathology 1993; 3: 165–176
   PubMed Web of Science ®Google Scholar