-
1
-
-
77957180065
-
A peculiar form of peripheral neuropathy
-
Andrade C. A peculiar form of peripheral neuropathy. Brain 1952;75:408-427.
-
(1952)
Brain
, vol.75
, pp. 408-427
-
-
Andrade, C.1
-
2
-
-
33745342076
-
Contribuição para o estudo clínico e laboratorial da paramiloidose de Corino de Andrade
-
Ribeiro do Rosário M, Antunes L, Barros F. Contribuição para o estudo clínico e laboratorial da paramiloidose de Corino de Andrade. J Soc Cien Méd 1961;75:1-46.
-
(1961)
J Soc Cien Méd
, vol.75
, pp. 1-46
-
-
Ribeiro do Rosário, M.1
Antunes, L.2
Barros, F.3
-
3
-
-
33745385837
-
Études sur la paramyloïdose portugaise à forme polynévritique (type C. Andrade): I-Remarques sur le tableau clinique et résultats de quelques examens complémentaires
-
Antunes L, Ribeiro do Rosário M, Barros F, Silva P, Coelho B. Études sur la paramyloïdose portugaise à forme polynévritique (type C. Andrade): I-Remarques sur le tableau clinique et résultats de quelques examens complémentaires. Acta Neuropathol 1963;Suppl. 2:12-18.
-
(1963)
Acta Neuropathol
, vol.2
, Issue.SUPPL.
, pp. 12-18
-
-
Antunes, L.1
Ribeiro do Rosário, M.2
Barros, F.3
Silva, P.4
Coelho, B.5
-
4
-
-
0242466059
-
Clinique de la paramyloïdose du type portugais
-
Andrade C. Clinique de la paramyloïdose du type portugais. Acta Neuropathol 1963;Suppl.2:3-11.
-
(1963)
Acta Neuropathol
, vol.2
, Issue.SUPPL.
, pp. 3-11
-
-
Andrade, C.1
-
5
-
-
33745430016
-
La polyneuropathie amyloïde héréditaire
-
Klein D. La polyneuropathie amyloïde héréditaire. Acta Neuropathol 1963;Suppl. 2:49-53.
-
(1963)
Acta Neuropathol
, vol.2
, Issue.SUPPL.
, pp. 49-53
-
-
Klein, D.1
-
7
-
-
33745364850
-
Amiloidose primária com comprometimento meningo-radículo-neurítico
-
Julião OF, Mignone C. Amiloidose primária com comprometimento meningo-radículo-neurítico. Arq Neuro-psiq (S Paulo) 1955;13:1-12.
-
(1955)
Arq Neuro-psiq (S Paulo)
, vol.13
, pp. 1-12
-
-
Julião, O.F.1
Mignone, C.2
-
8
-
-
0042656145
-
Polineuropatia amiloidótica familiar
-
Mello AR. Polineuropatia amiloidótica familiar. J Bras Med 1959;1:161-218.
-
(1959)
J Bras Med
, vol.1
, pp. 161-218
-
-
Mello, A.R.1
-
9
-
-
0014300978
-
Polyneuritic amyloidosis in a Japanese family
-
Araki S, Mawatari S, Ohta M, Nakajima. A, Kuroiwa Y. Polyneuritic amyloidosis in a Japanese family. Arch Neurol 1968;18:593-602.
-
(1968)
Arch Neurol
, vol.18
, pp. 593-602
-
-
Araki, S.1
Mawatari, S.2
Ohta, M.3
Nakajima, A.4
Kuroiwa, Y.5
-
10
-
-
0018904859
-
Studies on Familial Amyloid Polyneuropathy in Ogawa Village, Japan
-
Kito S, Itoga E, Kamiya K, Kishida T, Yamamura Y. Studies on Familial Amyloid Polyneuropathy in Ogawa Village, Japan. Eur J Neurol 1980;19:141-151.
-
(1980)
Eur J Neurol
, vol.19
, pp. 141-151
-
-
Kito, S.1
Itoga, E.2
Kamiya, K.3
Kishida, T.4
Yamamura, Y.5
-
11
-
-
33745409726
-
Familial Amyloidotic Polyneuropathy in Japan - Review of recent studies in Kumamoto district
-
Araki S, Ikegawa S, Yi S, Ando Y, Murakami T, Miyazaki A, Nishiguchi S. Familial Amyloidotic Polyneuropathy in Japan - review of recent studies in Kumamoto district. Bol. Hosp. (HGSA, Porto) 1988; 3(9):29-41.
-
(1988)
Bol. Hosp. (HGSA, Porto)
, vol.3
, Issue.9
, pp. 29-41
-
-
Araki, S.1
Ikegawa, S.2
Yi, S.3
Ando, Y.4
Murakami, T.5
Miyazaki, A.6
Nishiguchi, S.7
-
12
-
-
0000262448
-
Atypical cases of familial amyloidotic polyneuropathy (FAP) type I in Japan
-
Costa PP, Freitas AF, Saraiva MJ, (eds). Familial Amyloidotic Polyneuropathy and other transthyretin related disorders
-
Araki S, Ikegawa S, Murakami T, et al. Atypical cases of familial amyloidotic polyneuropathy (FAP) type I in Japan. In: Costa PP, Freitas AF, Saraiva MJ, (eds). Familial Amyloidotic Polyneuropathy and other transthyretin related disorders. Porto: Arq. Med., 1990:267-270.
-
(1990)
Porto: Arq. Med.
, pp. 267-270
-
-
Araki, S.1
Ikegawa, S.2
Murakami, T.3
-
13
-
-
0014382710
-
Vitreous opacities in primary familial amyloidosis
-
Andersson R, Kassman T. Vitreous opacities in primary familial amyloidosis. Acta Opthal 1968;46:441-447.
-
(1968)
Acta Opthal
, vol.46
, pp. 441-447
-
-
Andersson, R.1
Kassman, T.2
-
14
-
-
84981368487
-
Hereditary Amyloidosis with Polyneuropathy
-
Andersson R. Hereditary Amyloidosis with Polyneuropathy. Acta Med Scand 1970;188:85-94.
-
(1970)
Acta Med Scand
, vol.188
, pp. 85-94
-
-
Andersson, R.1
-
15
-
-
0017183687
-
Familial Amyloidosis with Polyneuropathy: A Clinical Study Based on Patients Living in Northern Sweden
-
Andersson R. Familial Amyloidosis with Polyneuropathy: A Clinical Study Based on Patients Living in Northern Sweden. Acta Med Scand 1976;Suppl.590:1-64.
-
(1976)
Acta Med Scand
, vol.590
, Issue.SUPPL.
, pp. 1-64
-
-
Andersson, R.1
-
16
-
-
24844440154
-
FAP type I (Portuguese form) in the island of Mallorca (Spain)-study of five families
-
Munar-Quès M, Costa PP, Saraiva MJM. FAP type I (Portuguese form) in the island of Mallorca (Spain)-study of five families. Bol. Hosp. (HGSA, Porto) 1988;3(9):17-27.
-
(1988)
Bol. Hosp. (HGSA, Porto)
, vol.3
, Issue.9
, pp. 17-27
-
-
Munar-Quès, M.1
Costa, P.P.2
Saraiva, M.J.M.3
-
17
-
-
21244433163
-
Genetic epidemiology of familial amyloid polyneuropathy in the Balearic Islands (Spain)
-
Munar-Quès M, Saraiva MJ, Viader-Farre C, Zabay-Becerril J, Mullet-Ferrer J. Genetic epidemiology of familial amyloid polyneuropathy in the Balearic Islands (Spain). Amyloid 2005; 12(1):54-61.
-
(2005)
Amyloid
, vol.12
, Issue.1
, pp. 54-61
-
-
Munar-Quès, M.1
Saraiva, M.J.2
Viader-Farre, C.3
Zabay-Becerril, J.4
Mullet-Ferrer, J.5
-
18
-
-
32544460569
-
Hereditary amyloid neuropathy
-
Vinken PJ, Bruyn GW, (eds). Amsterdam and Oxford: North-Holland Publishing Company
-
Andrade C. Hereditary amyloid neuropathy. In: Vinken PJ, Bruyn GW, (eds). Handbook of Clinical Neurology. Amsterdam and Oxford: North-Holland Publishing Company, 1975:119-143.
-
(1975)
Handbook of Clinical Neurology
, pp. 119-143
-
-
Andrade, C.1
-
19
-
-
0002470418
-
Forty years of experience with type I amyloid neuropathy. Review of 483 cases
-
Glenner GG, Costa PP, Freitas AF, (eds). Amsterdam: Excerpta Medica
-
Coutinho P, Silva AM, Lima LJ. Forty years of experience with type I amyloid neuropathy. Review of 483 cases. In: Glenner GG, Costa PP, Freitas AF, (eds). Amyloid and amyloidosis. Amsterdam: Excerpta Medica, 1980:88-98.
-
(1980)
Amyloid and Amyloidosis
, pp. 88-98
-
-
Coutinho, P.1
Silva, A.M.2
Lima, L.J.3
-
20
-
-
0345245158
-
Clinical evaluation of late-onset cases in Type I (Andrade) Amyloid Neuropathy
-
Glenner GG, Costa PP, Freitas AF, (eds). Amsterdam: Excerpta Medica
-
Bastos Lima A, Martins da Silva A. Clinical evaluation of late-onset cases in Type I (Andrade) Amyloid Neuropathy. In: Glenner GG, Costa PP, Freitas AF, (eds). Amyloid and Amyloidosis. Amsterdam: Excerpta Medica, 1980:88-98.
-
(1980)
Amyloid and Amyloidosis
, pp. 88-98
-
-
Bastos Lima, A.1
Martins da Silva, A.2
-
21
-
-
0023254244
-
Onset in the Seventh Decade and Lack of Symptoms in Heterozygotes for the TTR Met30 Mutation in Hereditary Amyloid Neuropathy-TypeI (Portuguese, Andrade)
-
Sequeiros J, Saraiva MJM. Onset in the Seventh Decade and Lack of Symptoms in Heterozygotes for the TTR Met30 Mutation in Hereditary Amyloid Neuropathy-TypeI (Portuguese, Andrade). Am J Med Genet 1987;27:345-357.
-
(1987)
Am J Med Genet
, vol.27
, pp. 345-357
-
-
Sequeiros, J.1
Saraiva, M.J.M.2
-
22
-
-
4244132633
-
Sporadic, late-onset case of familial amyloid polyneuropathy type I (Andrade) - A Clinicopathological study
-
Yamamura Y, Kito S, Harada T, Katayama S, Shimoyama M, Takeshima T, Inai Y, Nakano T. Sporadic, late-onset case of familial amyloid polyneuropathy type I (Andrade) - a Clinicopathological study. "Amyloid and Amyloidosis 1990"; 1:698-701.
-
"Amyloid and Amyloidosis 1990"
, vol.1
, pp. 698-701
-
-
Yamamura, Y.1
Kito, S.2
Harada, T.3
Katayama, S.4
Shimoyama, M.5
Takeshima, T.6
Inai, Y.7
Nakano, T.8
-
23
-
-
0037046222
-
Familial transthyretin-type amyloid polyneuropathy in Japan
-
Ikeda S, Nakazato M, Ando Y. Familial transthyretin-type amyloid polyneuropathy in Japan. Neurol. 2002; 58:1001-1007.
-
(2002)
Neurol.
, vol.58
, pp. 1001-1007
-
-
Ikeda, S.1
Nakazato, M.2
Ando, Y.3
-
24
-
-
0010551538
-
Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy
-
Costa PP, Figueira A, Bravo F. Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy. Proc Natl Acad Sci USA 1978;75:4499-4503.
-
(1978)
Proc Natl Acad Sci USA
, vol.75
, pp. 4499-4503
-
-
Costa, P.P.1
Figueira, A.2
Bravo, F.3
-
25
-
-
0021266985
-
Amyloid Fibril Protein in Familial Amyloidotic Polyneuropathy, Portuguese Type - Definition of Molecular Abnormality in Transthyretin (Prealbumin)
-
Saraiva MJM, Costa PP, Birken S, Goodman DS. Amyloid Fibril Protein in Familial Amyloidotic Polyneuropathy, Portuguese Type - Definition of Molecular Abnormality in Transthyretin (Prealbumin). J Clin Invest 1984;74:104-109.
-
(1984)
J Clin Invest
, vol.74
, pp. 104-109
-
-
Saraiva, M.J.M.1
Costa, P.P.2
Birken, S.3
Goodman, D.S.4
-
26
-
-
0022338373
-
Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type
-
Saraiva MJM, Costa PP, Goodman DS. Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. J Clin Invest 1985;76:2171-2177.
-
(1985)
J Clin Invest
, vol.76
, pp. 2171-2177
-
-
Saraiva, M.J.M.1
Costa, P.P.2
Goodman, D.S.3
-
27
-
-
0020924805
-
Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy
-
Saraiva MJM, Costa PP, Birken S, Goodman DS. Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy. Trans Ass Am Phys 1983;96:261-270.
-
(1983)
Trans Ass Am Phys
, vol.96
, pp. 261-270
-
-
Saraiva, M.J.M.1
Costa, P.P.2
Birken, S.3
Goodman, D.S.4
-
28
-
-
0021012829
-
Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)
-
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.
-
(1983)
Biochem Biophys Res Commun
, vol.116
, pp. 880-888
-
-
Tawara, S.1
Nakazato, M.2
Kangawa, K.3
Matsuo, H.4
Araki, S.5
-
29
-
-
0023627362
-
Structurally abnormal transthyretin causing familial amyloidotic polyneuropathy in Sweden
-
Nakazato M, Steen L, Holmgren G, Matsukura S, Kangawa K, Matsuo H. Structurally abnormal transthyretin causing familial amyloidotic polyneuropathy in Sweden. Clin Chem Acta. 1987;167:341-342.
-
(1987)
Clin Chem Acta.
, vol.167
, pp. 341-342
-
-
Nakazato, M.1
Steen, L.2
Holmgren, G.3
Matsukura, S.4
Kangawa, K.5
Matsuo, H.6
-
30
-
-
0023856729
-
Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis
-
Holmgren G, Holmberg E, Lindstrom A, Lindtsrom E, Nordenson I, Sandgren O, Steen L, Svensson B, Lundgren E, Von Gabain A. Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis. Clin Genet 1988;33:176-180.
-
(1988)
Clin Genet
, vol.33
, pp. 176-180
-
-
Holmgren, G.1
Holmberg, E.2
Lindstrom, A.3
Lindtsrom, E.4
Nordenson, I.5
Sandgren, O.6
Steen, L.7
Svensson, B.8
Lundgren, E.9
Von Gabain, A.10
-
31
-
-
0009590411
-
The Majorcan focus of Familial Amyloidotic Polyneuropathy type I
-
Costa PP, Freitas AF, Saraiva MJ, (eds). Familial Amyloidotic Polyneuropathy and other Transthyretin related disorders
-
Munar-Quès M, Costa PP, Saraiva MJM. The Majorcan focus of Familial Amyloidotic Polyneuropathy type I. In: Costa PP, Freitas AF, Saraiva MJ, (eds). Familial Amyloidotic Polyneuropathy and other Transthyretin related disorders. Porto: Arq. Med., 1990:13-18.
-
(1990)
Porto: Arq. Med.
, pp. 13-18
-
-
Munar-Quès, M.1
Costa, P.P.2
Saraiva, M.J.M.3
-
32
-
-
0033432813
-
Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant
-
Palácios SA, Bittencourt P, Cancado E. Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant. Amyloid 1999;6:289-291.
-
(1999)
Amyloid
, vol.6
, pp. 289-291
-
-
Palácios, S.A.1
Bittencourt, P.2
Cancado, E.3
-
33
-
-
0023002761
-
Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy
-
Saraiva MJM, Costa PP, Goodman DS. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy. Neurol. 1986;36:1413-1417.
-
(1986)
Neurol.
, vol.36
, pp. 1413-1417
-
-
Saraiva, M.J.M.1
Costa, P.P.2
Goodman, D.S.3
-
34
-
-
13144292714
-
Genetic Study of Late-Onset in Hereditary Amyloid Neuropahty (HAN) - Type I (Portuguese, Andrade)
-
Isobe T, Araki A, Uchino F, Kito S, Tsubura E, (eds). New York. Plenum Press
-
Lobato L, Teixeira F, Sousa A, Sequeiros J. Genetic Study of Late-Onset in Hereditary Amyloid Neuropahty (HAN) - Type I (Portuguese, Andrade). In: Isobe T, Araki A, Uchino F, Kito S, Tsubura E, (eds). Amyloid and Amyloidosis. New York. Plenum Press, 1988:441-446.
-
(1988)
Amyloid and Amyloidosis
, pp. 441-446
-
-
Lobato, L.1
Teixeira, F.2
Sousa, A.3
Sequeiros, J.4
-
35
-
-
0343031137
-
Familial amyloidotic polyneuropathy: Screening of the population at risk in Portugal
-
Isobe T, Araki A, Uchino F, Kito S, Tsubura E, (eds). New York: Plenum Press
-
Costa PP, Saraiva MJM. Familial amyloidotic polyneuropathy: screening of the population at risk in Portugal. In: Isobe T, Araki A, Uchino F, Kito S, Tsubura E, (eds). Amyloid and Amyloidosis. New York: Plenum Press, 1988:425-428.
-
(1988)
Amyloid and Amyloidosis
, pp. 425-428
-
-
Costa, P.P.1
Saraiva, M.J.M.2
-
36
-
-
0028281999
-
A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected
-
Coelho T, Sousa A, Lourenço E, Ramalheira J. A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected. J Med Genet 1994;31:293-299.
-
(1994)
J Med Genet
, vol.31
, pp. 293-299
-
-
Coelho, T.1
Sousa, A.2
Lourenço, E.3
Ramalheira, J.4
-
37
-
-
26644444170
-
Início tardio na neuropatia amiloidótica hereditária - Tipo I (português, Andrade) - Variação familiar e modelos genéticos
-
Sousa A, Lobato L, Sequeiros J. Início tardio na neuropatia amiloidótica hereditária - tipo I (português, Andrade) - Variação familiar e modelos genéticos. Bol. Hosp. (HGSA,Porto) 1988;3:63-69.
-
(1988)
Bol. Hosp. (HGSA,Porto)
, vol.3
, pp. 63-69
-
-
Sousa, A.1
Lobato, L.2
Sequeiros, J.3
-
38
-
-
78651024089
-
The problem of anticipation in pedigrees of Dystrophia Myotonica
-
Penrose LS. The problem of anticipation in pedigrees of Dystrophia Myotonica. Ann Eugen 1948;14:125-132.
-
(1948)
Ann Eugen
, vol.14
, pp. 125-132
-
-
Penrose, L.S.1
-
39
-
-
0002184993
-
Anticipation of age-of-onset in fami-lial amy-loidotic polyneuropathy (Portu-guese type)
-
Natvig J et al. (eds): Kluwer Acade-mic Publishers, Dor-drecht, Nether-lands
-
Sousa A, Coelho T, Lobato L, Sequeiros J: Anticipation of age-of-onset in fami-lial amy-loidotic polyneuropathy (Portu-guese type). In: Natvig J et al. (eds): "Amyloid and Amyloi-d-o-sis 1990", pp. 694-697, Kluwer Acade-mic Publishers, Dor-drecht, Nether-lands, 1991.
-
(1991)
"Amyloid and Amyloi-d-o-sis 1990"
, pp. 694-697
-
-
Sousa, A.1
Coelho, T.2
Lobato, L.3
Sequeiros, J.4
-
40
-
-
0027241247
-
Familial amyloidotic polyneuropathy in Sweden: A pedigree analysis
-
Drugge U, Andersson R, Chizari F, Danielsson M, Holmgren G, Sandgren O, Sousa A. Familial amyloidotic polyneuropathy in Sweden: A pedigree analysis. J Med Genet 1993;30:388-392.
-
(1993)
J Med Genet
, vol.30
, pp. 388-392
-
-
Drugge, U.1
Andersson, R.2
Chizari, F.3
Danielsson, M.4
Holmgren, G.5
Sandgren, O.6
Sousa, A.7
-
41
-
-
0038530264
-
A variabilidade fenotípica da Polineuropatia Amloidótica Familiar: Um estudo de genética quantitativa em Portugal e na Suécia
-
Tese de doutoramento, ICBAS, UP
-
Sousa A, A variabilidade fenotípica da Polineuropatia Amloidótica Familiar: um estudo de genética quantitativa em Portugal e na Suécia. Tese de doutoramento, ICBAS, UP, 1995
-
(1995)
-
-
Sousa, A.1
-
42
-
-
16544368933
-
Anticipation of age-at-onset in Portuguese patients with familial amyloid polyneuropathy-type I (FAP-MET30)
-
Kyle R et al. (eds): Parthenon Publishers, New York and London
-
Sousa A, Coelho T, Lobato L, Sequeiros J: Anticipation of age-at-onset in Portuguese patients with familial amyloid polyneuropathy-type I (FAP-MET30). In: Kyle R et al. (eds): "Amyloid and Amyloidosis 1998", Parthenon Publishers, New York and London, pp. 209-211, 1999.
-
(1999)
"Amyloid and Amyloidosis 1998"
, pp. 209-211
-
-
Sousa, A.1
Coelho, T.2
Lobato, L.3
Sequeiros, J.4
-
43
-
-
0032788532
-
Genetic anticipation in Portuguese kindreds with familial amyloidotic poly-neuro-pathy is unlikely to be caused by triplet repeat expansions
-
Soares M, Buxbaum J, Sirugo G, Coelho T, Kastner D, Sousa A, Saraiva MJ. Genetic anticipation in Portuguese kindreds with familial amyloidotic poly-neuro-pathy is unlikely to be caused by triplet repeat expansions. Hum Genet 1999;104:480-485.
-
(1999)
Hum Genet
, vol.104
, pp. 480-485
-
-
Soares, M.1
Buxbaum, J.2
Sirugo, G.3
Coelho, T.4
Kastner, D.5
Sousa, A.6
Saraiva, M.J.7
-
44
-
-
0029562263
-
Genetic epidemiology of familial amy-loi-do-tic polyneuropathy (FAP) - Type I in Póvoa de Varzim/Vila do Conde (north of Por-tugal)
-
Sousa A, Coelho T, Barros J, Sequeiros J. Genetic epidemiology of familial amy-loi-do-tic polyneuropathy (FAP) - type I in Póvoa de Varzim/Vila do Conde (north of Por-tugal). Am J Med Genet 1995; 60:512-521.
-
(1995)
Am J Med Genet
, vol.60
, pp. 512-521
-
-
Sousa, A.1
Coelho, T.2
Barros, J.3
Sequeiros, J.4
-
45
-
-
33745346934
-
Genetic Epidemiology of familial amyloid polyneuropathy TTRMet30 in Portugal
-
Silva AM, Sousa A, Fonseca I, Coelho T: Genetic Epidemiology of familial amyloid polyneuropathy TTRMet30 in Portugal. Eur J Neurol, 2004; 11 (Suppl.2), p. 32.
-
(2004)
Eur J Neurol
, vol.11
, Issue.SUPPL. 2
, pp. 32
-
-
Silva, A.M.1
Sousa, A.2
Fonseca, I.3
Coelho, T.4
-
46
-
-
0027275791
-
Familial amyloidotic po-lyneuropathy in Sweden: Geographical distribution, age of onset and prevalence
-
Sousa A, Andersson R, Drugge U, Holmgren G, Sandgren O. Familial amyloidotic po-lyneuropathy in Sweden: geographical distribution, age of onset and prevalence. Hum Hered 1993; 43:288-294.
-
(1993)
Hum Hered
, vol.43
, pp. 288-294
-
-
Sousa, A.1
Andersson, R.2
Drugge, U.3
Holmgren, G.4
Sandgren, O.5
-
47
-
-
0026503781
-
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic sequences
-
Holmgren G, Bergström S, Drugge U, Lundgren E, Nording-Sikström C, Sandgren O, Sten L. Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic sequences. Clin Genet 1992;41:39-41.
-
(1992)
Clin Genet
, vol.41
, pp. 39-41
-
-
Holmgren, G.1
Bergström, S.2
Drugge, U.3
Lundgren, E.4
Nording-Sikström, C.5
Sandgren, O.6
Sten, L.7
-
48
-
-
0023823790
-
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy
-
Holmgren G, Haetnner E, Nordenson I, Sandgren O, Steen L, Lundgren E. Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy. Clin Genet 1988;34:333-338.
-
(1988)
Clin Genet
, vol.34
, pp. 333-338
-
-
Holmgren, G.1
Haetnner, E.2
Nordenson, I.3
Sandgren, O.4
Steen, L.5
Lundgren, E.6
-
49
-
-
0026411103
-
Vitreous involvement in familial amy-loi-dotic neuropathy: A genealogical and genetic study
-
Sandgren O, Drugge U, Holmgren G, Sousa A. Vitreous involvement in familial amy-loi-dotic neuropathy: a genealogical and genetic study. Clin Genet 1991; 40:452-460.
-
(1991)
Clin Genet
, vol.40
, pp. 452-460
-
-
Sandgren, O.1
Drugge, U.2
Holmgren, G.3
Sousa, A.4
|