-
1
-
-
77957180065
-
A peculiar form of peripheral neuropathy; Familiar atypical generalized amyloidosis with special involvement of the peripheral nerves
-
1:STN:280:DyaG3s%2Fgt1Cjsw%3D%3D 12978172 10.1093/brain/75.3.408
-
Andrade C (1952) A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain 75:408-427
-
(1952)
Brain
, vol.75
, pp. 408-427
-
-
Andrade, C.1
-
2
-
-
81255211674
-
Familial amyloid polyneuropathy
-
1:CAS:528:DC%2BC3MXhsV2gsbrP 22094129 10.1016/S1474-4422(11)70246-0
-
Plante-Bordeneuve V, Said G (2011) Familial amyloid polyneuropathy. Lancet Neurol 10(12):1086-1097
-
(2011)
Lancet Neurol
, vol.10
, Issue.12
, pp. 1086-1097
-
-
Plante-Bordeneuve, V.1
Said, G.2
-
3
-
-
84873979913
-
Guideline of transthyretin-related hereditary amyloidosis for clinicians
-
Ando Y, Coelho T, Berk JL, Cruz MW, Ericzon BG, Ikeda S, Lewis WD, Obici L, Planté-Bordeneuve V, Rapezzi C, Said G, Salvi F (2013) Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet J Rare Dis 20(8-31):1-18
-
(2013)
Orphanet J Rare Dis
, vol.20
, Issue.8-31
, pp. 1-18
-
-
Ando, Y.C.1
-
4
-
-
34848818004
-
The molecular biology and clinical features of amyloid neuropathy
-
1:CAS:528:DC%2BD2sXht1emu7nO 17554795 10.1002/mus.20821
-
Benson MD, Kincaid JC (2007) The molecular biology and clinical features of amyloid neuropathy. Muscle Nerve 36:411-423
-
(2007)
Muscle Nerve
, vol.36
, pp. 411-423
-
-
Benson, M.D.1
Kincaid, J.C.2
-
5
-
-
84862234023
-
Tafamidis, a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade
-
1:CAS:528:DC%2BC38XptlWjtb4%3D 3386102 22645360 10.1073/pnas.1121005109
-
Bulawa CE, Connelly S, Devit M et al (2012) Tafamidis, a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade. Proc Natl Acad Sci USA 109(24):9629-9634
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, Issue.24
, pp. 9629-9634
-
-
Bulawa, C.E.1
Connelly, S.2
Devit, M.3
-
6
-
-
84874259441
-
Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: An Italian perspective
-
1:CAS:528:DC%2BC3sXivFaqtLs%3D 22745357 10.1093/eurheartj/ehs123
-
Rapezzi C, Quarta CC, Obici L et al (2013) Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective. Eur Heart J 34(7):520-528
-
(2013)
Eur Heart J
, vol.34
, Issue.7
, pp. 520-528
-
-
Rapezzi, C.1
Quarta, C.C.2
Obici, L.3
-
7
-
-
0242559073
-
Familial amyloid polyneuropathy: Mechanisms leading to nerve degeneration
-
14640035
-
Said G (2003) Familial amyloid polyneuropathy: mechanisms leading to nerve degeneration. Amyloid 10(Suppl 1):7-12
-
(2003)
Amyloid
, vol.10
, Issue.SUPPL. 1
, pp. 7-12
-
-
Said, G.1
-
8
-
-
84878892253
-
Neurophysiological markers of small fibre neuropathy in TTR-FAP mutation carriers
-
23306657 10.1007/s00415-012-6816-8
-
Lefaucheur JP, Ng Wing Tin S, Kerschen P et al (2013) Neurophysiological markers of small fibre neuropathy in TTR-FAP mutation carriers. J Neurol 260:1497-1503
-
(2013)
J Neurol
, vol.260
, pp. 1497-1503
-
-
Lefaucheur, J.P.1
Ng Wing Tin, S.2
Kerschen, P.3
-
9
-
-
84892512585
-
Neurophysiological techniques to detect early small-fiber dysfunction in transthyretin amyloid polyneuropathy
-
Conceição I, Costa J, Castro J, de Carvalho M (2014) Neurophysiological techniques to detect early small-fiber dysfunction in transthyretin amyloid polyneuropathy. Muscle Nerve 49(2):181-186
-
(2014)
Muscle Nerve
, vol.49
, Issue.2
, pp. 181-186
-
-
Conceição, I.C.1
-
10
-
-
0002470418
-
Forty years of experience with type i amyloid neuropathy. Review of 483 cases
-
Glenner GG, Pinho e Costa P, Falcao de Freitas A (eds) Amsterdam
-
Coutinho P, Martins da Silva A, Lopes Lima J, Resende Barbosa A (1980) Forty years of experience with type I amyloid neuropathy. Review of 483 cases. In: Glenner GG, Pinho e Costa P, Falcao de Freitas A (eds) Amyloid and amyloidosis. Excerpta Medica, Amsterdam pp 88-98
-
(1980)
Amyloid and Amyloidosis. Excerpta Medica
, pp. 88-98
-
-
Coutinho, P.1
Martins Da Silva, A.2
Lopes Lima, J.3
Resende Barbosa, A.4
-
11
-
-
0037046222
-
Familial transthyretin-type amyloid polyneuropathy in Japan: Clinical and genetic heterogeneity
-
1:CAS:528:DC%2BD38XjtlCiurY%3D 11940682 10.1212/WNL.58.7.1001
-
Ikeda S, Nakazato M, Ando Y et al (2002) Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity. Neurology 58:1001-1007
-
(2002)
Neurology
, vol.58
, pp. 1001-1007
-
-
Ikeda, S.1
Nakazato, M.2
Ando, Y.3
-
12
-
-
34547883905
-
Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP)
-
17698792 10.1212/01.wnl.0000267338.45673.f4
-
Planté-Bordeneuve V, Ferreira A, Lalu T et al (2007) Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP). Neurology 69:693-698
-
(2007)
Neurology
, vol.69
, pp. 693-698
-
-
Planté-Bordeneuve, V.1
Ferreira, A.2
Lalu, T.3
-
13
-
-
70849089760
-
The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy
-
1:CAS:528:DC%2BD1MXht1WitrnL 19626479 10.1080/13506120903094074
-
Koike H, Morozumi S, Kawagashira Y et al (2009) The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy. Amyloid 16:142-148
-
(2009)
Amyloid
, vol.16
, pp. 142-148
-
-
Koike, H.1
Morozumi, S.2
Kawagashira, Y.3
-
14
-
-
0242391993
-
Clinical and pathological findings of non-Val30Met TTR type familial amyloid polyneuropathy in Japan
-
1:CAS:528:DC%2BD3sXpvFShu7o%3D 14640041
-
Ikeda S, Takei Y, Tokuda T, Nakazato M, Ando Y (2003) Clinical and pathological findings of non-Val30Met TTR type familial amyloid polyneuropathy in Japan. Amyloid 10(Suppl 1):39-47
-
(2003)
Amyloid
, vol.10
, Issue.SUPPL. 1
, pp. 39-47
-
-
Ikeda, S.1
Takei, Y.2
Tokuda, T.3
Nakazato, M.4
Ando, Y.5
-
15
-
-
73049097522
-
Amyloid heart disease
-
20109604 10.1016/j.pcad.2009.11.007
-
Falk RH, Dubrey SW (2010) Amyloid heart disease. Prog Cardiovasc Dis 52:347-361
-
(2010)
Prog Cardiovasc Dis
, vol.52
, pp. 347-361
-
-
Falk, R.H.1
Dubrey, S.W.2
-
16
-
-
39049117075
-
Gender-related risk of myocardial involvement in systemic amyloidosis
-
1:CAS:528:DC%2BD1cXhslWnsbw%3D 18266120 10.1080/13506120701815373
-
Rapezzi C, Riva L, Quarta CC et al (2008) Gender-related risk of myocardial involvement in systemic amyloidosis. Amyloid 15(1):40-48
-
(2008)
Amyloid
, vol.15
, Issue.1
, pp. 40-48
-
-
Rapezzi, C.1
Riva, L.2
Quarta, C.C.3
-
17
-
-
0031028712
-
Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans
-
1:STN:280:DyaK2s7mtV2htg%3D%3D 9017939 10.1056/NEJM199702133360703
-
Jacobson DR, Pastore RD, Yaghoubian R et al (1997) Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans. N Engl J Med 336(7):466-473
-
(1997)
N Engl J Med
, vol.336
, Issue.7
, pp. 466-473
-
-
Jacobson, D.R.1
Pastore, R.D.2
Yaghoubian, R.3
-
18
-
-
54249138124
-
Heterogeneity of penetrance in hereditary transthyretin amyloid neuropathy in the Swedish population
-
1:CAS:528:DC%2BD1cXht1KntLvN 2738945 18925456 10.1080/13506120802193720
-
Hellman U, Alarcon F, Lundgren HE et al (2008) Heterogeneity of penetrance in hereditary transthyretin amyloid neuropathy in the Swedish population. Amyloid 15(3):181-186
-
(2008)
Amyloid
, vol.15
, Issue.3
, pp. 181-186
-
-
Hellman, U.1
Alarcon, F.2
Lundgren, H.E.3
-
19
-
-
84896709791
-
Overcoming artifact: Anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M
-
24046394 10.1136/jnnp-2013-305383
-
Lemos C, Coelho T, Alves-Ferreira M et al (2014) Overcoming artifact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M. J Neurol Neurosurg Psychiatry 85:326-330
-
(2014)
J Neurol Neurosurg Psychiatry
, vol.85
, pp. 326-330
-
-
Lemos, C.1
Coelho, T.2
Alves-Ferreira, M.3
-
20
-
-
84873028718
-
Liver transplantation and transthyretin amyloidosis
-
1:CAS:528:DC%2BC3sXhsFeltr0%3D 23169427 10.1002/mus.23521
-
Benson M (2013) Liver transplantation and transthyretin amyloidosis. Muscle Nerve 47:157-162
-
(2013)
Muscle Nerve
, vol.47
, pp. 157-162
-
-
Benson, M.1
-
21
-
-
79959936896
-
Long term data from the Familial Amyloidotic Polyneuropathy World Transplant Registry (FAPWTR)
-
10.3109/13506129.2011.574354072
-
Wilczek HE, Larsson M, Ericzon BG (2011) Long term data from the Familial Amyloidotic Polyneuropathy World Transplant Registry (FAPWTR). Amyloid 18(Suppl. 1):188-190
-
(2011)
Amyloid
, vol.18
, Issue.SUPPL.. 1
, pp. 188-190
-
-
Wilczek, H.E.1
Larsson, M.2
Ericzon, B.G.3
-
22
-
-
84858248363
-
Long term survival after liver transplantation in patients with familial amyloid polyneuropathy
-
1:CAS:528:DC%2BC38XjtV2mtrk%3D 22345221 10.1212/WNL.0b013e318248df18
-
Yamashita T, Ando Y, Okamoto S, Misumi Y et al (2012) Long term survival after liver transplantation in patients with familial amyloid polyneuropathy. Neurology 78:637-643
-
(2012)
Neurology
, vol.78
, pp. 637-643
-
-
Yamashita, T.1
Ando, Y.2
Okamoto, S.3
Misumi, Y.4
-
23
-
-
79951681211
-
Variation in amount of wildtype transthyretin in different fibril and tissue types in ATTR amyloidosis
-
1:CAS:528:DC%2BC3MXntVCrtw%3D%3D 10.1007/s00109-010-0695-1
-
Ihse E, Suhr OB, Hellman U, Westermark P (2011) Variation in amount of wildtype transthyretin in different fibril and tissue types in ATTR amyloidosis. J Mol Med (Berl) 89:171-180
-
(2011)
J Mol Med (Berl)
, vol.89
, pp. 171-180
-
-
Ihse, E.1
Suhr, O.B.2
Hellman, U.3
Westermark, P.4
-
24
-
-
78149300882
-
Acquired amyloid polyneuropathy in a Portuguese patient after domino liver transplantation
-
20928908 10.1002/mus.21806
-
Conceição I, Evangelista T, Castro J et al (2010) Acquired amyloid polyneuropathy in a Portuguese patient after domino liver transplantation. Muscle Nerve 42:836-839
-
(2010)
Muscle Nerve
, vol.42
, pp. 836-839
-
-
Conceição, I.1
Evangelista, T.2
Castro, J.3
-
25
-
-
84889238225
-
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy
-
1:CAS:528:DC%2BC3sXhtl2jurfI 3825212 23974642 10.1007/s00415-013-7051-7
-
Coelho T, Maia LF, da Silva AM et al (2013) Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy. J Neurol 260:2802-2814
-
(2013)
J Neurol
, vol.260
, pp. 2802-2814
-
-
Coelho, T.1
Maia, L.F.2
Da Silva, A.M.3
-
26
-
-
84890954073
-
Repurposing diflunisal for familial amyloid polyneuropathy: A randomized clinical trial
-
Diflunisal Trial Consortium et al. 1:CAS:528:DC%2BC2cXitFejur8%3D 24368466
-
Berk JL, Suhr OB, Obici L, Diflunisal Trial Consortium et al (2013) Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. JAMA 310:2658-2667
-
(2013)
JAMA
, vol.310
, pp. 2658-2667
-
-
Berk, J.L.1
Suhr, O.B.2
Obici, L.3
-
27
-
-
84883118140
-
Safety and efficacy of RNAi therapy for transthyretin amyloidosis
-
1:CAS:528:DC%2BC3sXhtlyis7fK 23984729 10.1056/NEJMoa1208760
-
Coelho T, Adams D, Silva A et al (2013) Safety and efficacy of RNAi therapy for transthyretin amyloidosis. N Engl J Med 369:819-829
-
(2013)
N Engl J Med
, vol.369
, pp. 819-829
-
-
Coelho, T.1
Adams, D.2
Silva, A.3
-
28
-
-
84861451481
-
Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy
-
1:CAS:528:DC%2BC38XnsF2rt70%3D 22494066 10.3109/13506129.2012.673140
-
Ackermann EJ, Guo S, Booten S et al (2012) Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy. Amyloid 19(Suppl 1):43-44
-
(2012)
Amyloid
, vol.19
, Issue.SUPPL. 1
, pp. 43-44
-
-
Ackermann, E.J.1
Guo, S.2
Booten, S.3
-
29
-
-
0038375018
-
4′-iodo-4′-Deoxydoxorubicin and tetracyclines disrupt transthyretin amyloid fibrils in vitro producing noncytotoxic species: Screening for TTR fibrils disrupters
-
1:CAS:528:DC%2BD3sXjsFClsbk%3D 12724338 10.1096/fj.02-0764com
-
Cardoso I, Merlini G, Saraiva MJ et al (2003) 4′-iodo-4′- Deoxydoxorubicin and tetracyclines disrupt transthyretin amyloid fibrils in vitro producing noncytotoxic species: screening for TTR fibrils disrupters. FASEB J 17(8):803-809
-
(2003)
FASEB J
, vol.17
, Issue.8
, pp. 803-809
-
-
Cardoso, I.1
Merlini, G.2
Saraiva, M.J.3
-
30
-
-
84861423778
-
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: A phase II study
-
1:CAS:528:DC%2BC38XnsF2rtL8%3D 22551192 10.3109/13506129.2012.678508
-
Obici L, Cortese A, Lozza A et al (2012) Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study. Amyloid 19(Suppl 1):34-36
-
(2012)
Amyloid
, vol.19
, Issue.SUPPL. 1
, pp. 34-36
-
-
Obici, L.1
Cortese, A.2
Lozza, A.3
-
31
-
-
78149282151
-
Antibodies to human serum amyloid P component eliminate visceral amyloid deposits
-
1:CAS:528:DC%2BC3cXhtlWmu7jJ 2975378 20962779 10.1038/nature09494
-
Bodin K, Ellmerich S, Kahan MC et al (2010) Antibodies to human serum amyloid P component eliminate visceral amyloid deposits. Nature 468(7320):93-97
-
(2010)
Nature
, vol.468
, Issue.7320
, pp. 93-97
-
-
Bodin, K.1
Ellmerich, S.2
Kahan, M.C.3
-
32
-
-
84871378837
-
The Transthyretin Amyloidosis Outcomes Survey (THAOS) registry: Design and methodology
-
23193943 10.1185/03007995.2012.754349
-
Planté-Bordeneuve V, Suhr OB, Maurer MS et al (2013) The Transthyretin Amyloidosis Outcomes Survey (THAOS) registry: design and methodology. Curr Med Res Opin 29:77-84
-
(2013)
Curr Med Res Opin
, vol.29
, pp. 77-84
-
-
Planté-Bordeneuve, V.1
Suhr, O.B.2
Maurer, M.S.3
|