-
1
-
-
0034935464
-
Hereditary and acquired amyloid neuropathies
-
Adams D. Hereditary and acquired amyloid neuropathies. J Neurol 2001; 248: 647-657.
-
(2001)
J Neurol
, vol.248
, pp. 647-657
-
-
Adams, D.1
-
2
-
-
0002470418
-
Forty years of experience with type I amyloid polyneuropathy. Review of 483 cases
-
Glenner G, Pinho e Costa P, Falcao de Freitas A, eds. Amsterdam: Excerpta Medica
-
Coutinho P, Martins da Silva A, Lopes Lima J, et al. Forty years of experience with type I amyloid polyneuropathy. Review of 483 cases. In: Glenner G, Pinho e Costa P, Falcao de Freitas A, eds. Amyloid Ans Amyloidosis. Amsterdam: Excerpta Medica, 1980: 88-98.
-
(1980)
Amyloid Ans Amyloidosis
, pp. 88-98
-
-
Coutinho, P.1
Martins da Silva, A.2
Lopes Lima, J.3
-
3
-
-
0027312398
-
Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis
-
Holmgren G, Ericzon BG, Groth CG, et al. Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis. Lancet 1993; 341: 1113-1116.
-
(1993)
Lancet
, vol.341
, pp. 1113-1116
-
-
Holmgren, G.1
Ericzon, B.G.2
Groth, C.G.3
-
4
-
-
0033919415
-
The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation
-
Adams D, Samuel D, Goulon-Goeau C, et al. The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation. Brain 2000; 123(Pt 7): 1495-1504.
-
(2000)
Brain
, vol.123
, Issue.PART 7
, pp. 1495-1504
-
-
Adams, D.1
Samuel, D.2
Goulon-Goeau, C.3
-
5
-
-
35248817263
-
Liver transplantation for familial amyloidotic polyneuropathy (FAP): a single-center experience over 16 years
-
Yamamoto S, Wilczek HE, Nowak G, et al. Liver transplantation for familial amyloidotic polyneuropathy (FAP): a single-center experience over 16 years. Am J Transplant 2007; 7: 2597-2604.
-
(2007)
Am J Transplant
, vol.7
, pp. 2597-2604
-
-
Yamamoto, S.1
Wilczek, H.E.2
Nowak, G.3
-
6
-
-
84858248363
-
Long-term survival after liver transplantation in patients with familial amyloid polyneuropathy
-
Yamashita T, Ando Y, Okamoto S, et al. Long-term survival after liver transplantation in patients with familial amyloid polyneuropathy. Neurology 2012; 78: 637-643.
-
(2012)
Neurology
, vol.78
, pp. 637-643
-
-
Yamashita, T.1
Ando, Y.2
Okamoto, S.3
-
7
-
-
79959936896
-
Long-term data from the Familial Amyloidotic Polyneuropathy World Transplant Registry (FAPWTR)
-
Wilczek HE, Larsson M, Ericzon BG. Long-term data from the Familial Amyloidotic Polyneuropathy World Transplant Registry (FAPWTR). Amyloid 2011; 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
-
8
-
-
77955442857
-
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser
-
Yang NC, Lee MJ, Chao CC, et al. Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser. Neurology 2010; 75: 532-538.
-
(2010)
Neurology
, vol.75
, pp. 532-538
-
-
Yang, N.C.1
Lee, M.J.2
Chao, C.C.3
-
9
-
-
84880922624
-
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients
-
Luigetti M, Conte A, Del Grande A, et al. TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients. Neurol Sci 2012; 34: 1057-1063.
-
(2012)
Neurol Sci
, vol.34
, pp. 1057-1063
-
-
Luigetti, M.1
Conte, A.2
Del Grande, A.3
-
10
-
-
80054847815
-
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients
-
Cappellari M, Cavallaro T, Ferrarini M, et al. Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. J Peripher Nerv Syst 2011; 16: 119-129.
-
(2011)
J Peripher Nerv Syst
, vol.16
, pp. 119-129
-
-
Cappellari, M.1
Cavallaro, T.2
Ferrarini, M.3
-
11
-
-
84861428992
-
Regional difference and similarity of familial amyloidosis with polyneuropathy in France
-
Adams D, Lozeron P, Theaudin M, et al. Regional difference and similarity of familial amyloidosis with polyneuropathy in France. Amyloid 2012; 19(Suppl. 1): 61-64.
-
(2012)
Amyloid
, vol.19
, Issue.SUPPL. 1
, pp. 61-64
-
-
Adams, D.1
Lozeron, P.2
Theaudin, M.3
-
12
-
-
84861421529
-
The transthyretin amyloidoses: from delineating the molecular mechanism of aggregation linked to pathology to a regulatory-agency-approved drug
-
Johnson SM, Connelly S, Fearns C, Powers ET, Kelly JW. The transthyretin amyloidoses: from delineating the molecular mechanism of aggregation linked to pathology to a regulatory-agency-approved drug. J Mol Biol 2012; 421: 185-203.
-
(2012)
J Mol Biol
, vol.421
, pp. 185-203
-
-
Johnson, S.M.1
Connelly, S.2
Fearns, C.3
Powers, E.T.4
Kelly, J.W.5
-
13
-
-
84862222705
-
Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial
-
Coelho T, Maia LF, Martins da Silva A, et al. Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial. Neurology 2012; 79: 785-792.
-
(2012)
Neurology
, vol.79
, pp. 785-792
-
-
Coelho, T.1
Maia, L.F.2
Martins da Silva, A.3
-
14
-
-
0032981905
-
NIS-LL: the primary measurement scale for clinical trial endpoints in diabetic peripheral neuropathy
-
Bril V. NIS-LL: the primary measurement scale for clinical trial endpoints in diabetic peripheral neuropathy. Eur Neurol 1999; 41(Suppl. 1): 8-13.
-
(1999)
Eur Neurol
, vol.41
, Issue.SUPPL. 1
, pp. 8-13
-
-
Bril, V.1
-
15
-
-
0021016478
-
Familial amyloidosis with polyneuropathy. A long-term follow-up of 21 patients with special reference to gastrointestinal symptoms
-
Steen L, Ek B. Familial amyloidosis with polyneuropathy. A long-term follow-up of 21 patients with special reference to gastrointestinal symptoms. Acta Med Scand 1983; 214: 387-397.
-
(1983)
Acta Med Scand
, vol.214
, pp. 387-397
-
-
Steen, L.1
Ek, B.2
-
16
-
-
37749050387
-
A brief compound test for assessment of autonomic and sensory-motor dysfunction in familial amyloid polyneuropathy
-
Denier C, Ducot B, Husson H, et al. A brief compound test for assessment of autonomic and sensory-motor dysfunction in familial amyloid polyneuropathy. J Neurol 2007; 254: 1684-1688.
-
(2007)
J Neurol
, vol.254
, pp. 1684-1688
-
-
Denier, C.1
Ducot, B.2
Husson, H.3
-
17
-
-
0018888594
-
Evaluation of patients with advanced cancer using the Karnofsky performance status
-
Yates JW, Chalmer B, McKegney FP. Evaluation of patients with advanced cancer using the Karnofsky performance status. Cancer 1980; 45: 2220-2224.
-
(1980)
Cancer
, vol.45
, pp. 2220-2224
-
-
Yates, J.W.1
Chalmer, B.2
McKegney, F.P.3
-
18
-
-
0029904204
-
Consensus statement on the definition of orthostatic hypotension, pure autonomic failure, and multiple system atrophy. The Consensus Committee of the American Autonomic Society and the American Academy of Neurology
-
Consensus statement on the definition of orthostatic hypotension, pure autonomic failure, and multiple system atrophy. The Consensus Committee of the American Autonomic Society and the American Academy of Neurology. Neurology 1996;46:1470.
-
(1996)
Neurology
, vol.46
, pp. 1470
-
-
-
19
-
-
0029112095
-
Diabetic polyneuropathy in controlled clinical trials: Consensus Report of the Peripheral Nerve Society
-
Diabetic polyneuropathy in controlled clinical trials: Consensus Report of the Peripheral Nerve Society. Ann Neurol 1995;38:478-482.
-
(1995)
Ann Neurol
, vol.38
, pp. 478-482
-
-
-
20
-
-
62949147825
-
European Medicines Agency
-
(accessed 25/06/2013)
-
European Medicines Agency. http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Public_assessment_report/human/002294/WC500117838.pdf. (accessed 25/06/2013)
-
-
-
-
21
-
-
84855598855
-
Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas
-
Koike H, Tanaka F, Hashimoto R, et al. Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas. J Neurol Neurosurg Psychiatry 2012; 83: 152-158.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. 152-158
-
-
Koike, H.1
Tanaka, F.2
Hashimoto, R.3
-
22
-
-
77956208060
-
A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operation
-
Shirota Y, Iwata A, Ishiura H, et al. A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operation. Intern Med 2010; 49: 1627-1631.
-
(2010)
Intern Med
, vol.49
, pp. 1627-1631
-
-
Shirota, Y.1
Iwata, A.2
Ishiura, H.3
-
24
-
-
84861451481
-
Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy
-
Ackermann EJ, Guo S, Booten S, et al. Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy. Amyloid 2012; 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
-
25
-
-
84874450641
-
Interim clinical update for ALN-TTR01, a novel RNAI therapeutic for the treatment of transthyretin amyloidosis
-
Coelho T, Suhr O, Adams D, et al. Interim clinical update for ALN-TTR01, a novel RNAI therapeutic for the treatment of transthyretin amyloidosis. J Peripher Nerv Syst 2011; 16: S25.
-
(2011)
J Peripher Nerv Syst
, vol.16
-
-
Coelho, T.1
Suhr, O.2
Adams, D.3
-
26
-
-
84861423778
-
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study
-
Obici L, Cortese A, Lozza A, et al. Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study. Amyloid 2012; 19(Suppl. 1): 34-36.
-
(2012)
Amyloid
, vol.19
, Issue.SUPPL. 1
, pp. 34-36
-
-
Obici, L.1
Cortese, A.2
Lozza, A.3
|