-
1
-
-
0019793034
-
Three forms of dominant amyloid neuropathy
-
Sack GM, Dumars KW, Gummerson KS, Law A, McKusick VA. Three forms of dominant amyloid neuropathy. Johns Hopkins Med J 1981;149:239-247.
-
(1981)
Johns Hopkins Med J
, vol.149
, pp. 239-247
-
-
Sack, G.M.1
Dumars, K.W.2
Gummerson, K.S.3
Law, A.4
McKusick, V.A.5
-
2
-
-
7244229899
-
Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twins
-
Holmgren G, Winkstrom L, Lundgren HE, Suhr OB. Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twins. J Intern Med 2004;256:453-456.
-
(2004)
J Intern Med
, vol.256
, pp. 453-456
-
-
Holmgren, G.1
Winkstrom, L.2
Lundgren, H.E.3
Suhr, O.B.4
-
3
-
-
0032803525
-
Two pairs of proven monozygotic twins discordant for familial amyloid neuropathy (FAP) TTR Met30
-
Munar-Qués M, Pedrosa JL, Coelho T, Gusmão L, Seruca R, Amorim A, Sequeiros J. Two pairs of proven monozygotic twins discordant for familial amyloid neuropathy (FAP) TTR Met30. J Med Genet 1999;36:629-632.
-
(1999)
J Med Genet
, vol.36
, pp. 629-632
-
-
Munar-Qués, M.1
Pedrosa, J.L.2
Coelho, T.3
Gusmão, L.4
Seruca, R.5
Amorim, A.6
Sequeiros, J.7
-
4
-
-
0034036638
-
Japanese monozygotic twins with familial amyloid polyneuropathy (FAP) (ATTR Val30Met)
-
Ando Y, Ohtsu Y, Terazaki H, Kibayashi K, Nakamura M, Ando E, Matsunaga N, Obayashi K, Uchino M, Ando M, Tsunenari S. Japanese monozygotic twins with familial amyloid polyneuropathy (FAP) (ATTR Val30Met). Amyloid 2000;7:133-136.
-
(2000)
Amyloid
, vol.7
, pp. 133-136
-
-
Ando, Y.1
Ohtsu, Y.2
Terazaki, H.3
Kibayashi, K.4
Nakamura, M.5
Ando, E.6
Matsunaga, N.7
Obayashi, K.8
Uchino, M.9
Ando, M.10
Tsunenari, S.11
-
5
-
-
14044275133
-
Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: Complexity in a single-gene disease
-
Soares ML, Coelho T, Sousa A, Batalov S, Conceição I, Sales-Luiz ML, Ritchie MD, Williams SM, Nievergelt CM, Schork NJ, Saraiva MJ, Buxbaum JN. Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease. Hum Mol Genet 2005;14:543-553.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 543-553
-
-
Soares, M.L.1
Coelho, T.2
Sousa, A.3
Batalov, S.4
Conceição, I.5
Sales-Luiz, M.L.6
Ritchie, M.D.7
Williams, S.M.8
Nievergelt, C.M.9
Schork, N.J.10
Saraiva, M.J.11
Buxbaum, J.N.12
-
6
-
-
1542543331
-
Genetic study of transthyretin amyloid neuropathies: Carrier risks among French and Portuguese families
-
Planté-Bordeneuve V, Carayol J, Ferreira A, Adams D, Clerget-Darpoux F, Misrahi M, Said G, Bonaïti-Pellié C. Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families. J Med Genet 2003;40:e120.
-
(2003)
J Med Genet
, vol.40
-
-
Planté-Bordeneuve, V.1
Carayol, J.2
Ferreira, A.3
Adams, D.4
Clerget-Darpoux, F.5
Misrahi, M.6
Said, G.7
Bonaïti-Pellié, C.8
-
7
-
-
0037046222
-
Familial transthyretin-type amyloid polyneuropathy in Japan: Clinical and genetic heterogeneity
-
Ikeda S, Nakazato M, Ando Y, Sobue G. Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity. Neurology 2002;58:1001-1007.
-
(2002)
Neurology
, vol.58
, pp. 1001-1007
-
-
Ikeda, S.1
Nakazato, M.2
Ando, Y.3
Sobue, G.4
-
8
-
-
45149083597
-
On the origin of the transthyretin Val30Met familial amyloid polyneuropathy
-
Zaros C, Genin E, Hellman U, Saporta MA, Languille L, Waddington-Cruz M, Suhr O, Misrahi M, Plante-Bordeneuve V. On the origin of the transthyretin Val30Met familial amyloid polyneuropathy. Ann Hum Genet 2008;72:478-484.
-
(2008)
Ann Hum Genet
, vol.72
, pp. 478-484
-
-
Zaros, C.1
Genin, E.2
Hellman, U.3
Saporta, M.A.4
Languille, L.5
Waddington-Cruz, M.6
Suhr, O.7
Misrahi, M.8
Plante-Bordeneuve, V.9
-
9
-
-
33845991494
-
Clinical variability in type I familial amyloid polyneuropathy (Val30Met): Comparison between late- and early-onset cases in Portugal
-
Conceição I, de Carvalho M. Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal. Muscle Nerve 2007;35:116-118.
-
(2007)
Muscle Nerve
, vol.35
, pp. 116-118
-
-
Conceição, I.1
de Carvalho, M.2
-
10
-
-
3242703067
-
Pathology of early- vs. late-onset TTR Met30 familial amyloid polyneuropathy
-
Koike H, Misu K, Sugiura M, Iijima M, Mori K, Yamamoto M, Hattori N, Mukai E, Ando Y, Ikeda S, Sobue G. Pathology of early- vs. late-onset TTR Met30 familial amyloid polyneuropathy. Neurology 2004;63:129-138.
-
(2004)
Neurology
, vol.63
, pp. 129-138
-
-
Koike, H.1
Misu, K.2
Sugiura, M.3
Iijima, M.4
Mori, K.5
Yamamoto, M.6
Hattori, N.7
Mukai, E.8
Ando, Y.9
Ikeda, S.10
Sobue, G.11
-
11
-
-
0242559064
-
Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan
-
Sobue G, Koike H, Misu K, Hattori N, Yamamoto M, Ikeda S, Ando Y, Nakazato M, Inukai A. Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan. Amyloid 2003;10 (Suppl 1): 32-38.
-
(2003)
Amyloid
, vol.10
, Issue.SUPPL. 1
, pp. 32-38
-
-
Sobue, G.1
Koike, H.2
Misu, K.3
Hattori, N.4
Yamamoto, M.5
Ikeda, S.6
Ando, Y.7
Nakazato, M.8
Inukai, A.9
-
12
-
-
0036846492
-
-
Koike H, Misu K, Ikeda S, Ando Y, Nakazato M, Ando E, Yamamoto M, Hattori N, Sobue G; for Study Group for Hereditary Neuropathy in Japan. Type I (Transthyretin Met30) familial amyloid polyneuropathy in Japan. Early- vs. late-onset form. Arch Neurol 2002;59:1771-1776.
-
Koike H, Misu K, Ikeda S, Ando Y, Nakazato M, Ando E, Yamamoto M, Hattori N, Sobue G; for Study Group for Hereditary Neuropathy in Japan. Type I (Transthyretin Met30) familial amyloid polyneuropathy in Japan. Early- vs. late-onset form. Arch Neurol 2002;59:1771-1776.
-
-
-
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