-
1
-
-
33750910096
-
Amyloidosis and neuropathy
-
Dyck PJ, Thomas PK, eds. 4th ed. Philadelphia: Elsevier Saunders
-
Kyle RA, Kelly JJ, Dyck PJ. Amyloidosis and neuropathy. In: Dyck PJ, Thomas PK, eds. Peripheral Neuropathy, 4th ed. Philadelphia: Elsevier Saunders; 2005:2427-2451.
-
(2005)
Peripheral Neuropathy
, pp. 2427-2451
-
-
Kyle, R.A.1
Kelly, J.J.2
Dyck, P.J.3
-
2
-
-
67149119593
-
Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens
-
Eriksson M, Schonland S, Yumlu S, et al. Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens. J Mol Diagn. 2009;11:257-262.
-
(2009)
J Mol Diagn
, vol.11
, pp. 257-262
-
-
Eriksson, M.1
Schonland, S.2
Yumlu, S.3
-
3
-
-
28244446220
-
Aspects on human amyloid forms and their fibril polypeptides
-
Westermark P. Aspects on human amyloid forms and their fibril polypeptides. FEBS J. 2005;272:5942-5949.
-
(2005)
FEBS J
, vol.272
, pp. 5942-5949
-
-
Westermark, P.1
-
4
-
-
0031266101
-
Diagnosis and treatment of amyloidosis
-
Hawkins PN. Diagnosis and treatment of amyloidosis. Ann Rheum Dis. 1997;56:631-633.
-
(1997)
Ann Rheum Dis
, vol.56
, pp. 631-633
-
-
Hawkins, P.N.1
-
5
-
-
33748474999
-
Amyloidosis
-
Kasper DL, Braunwald E, Fauci AS, et al, eds. 16th ed. New York: McGraw-Hill
-
Sipe JD, Cohen AS. Amyloidosis. In: Kasper DL, Braunwald E, Fauci AS, et al, eds. Harrison's Principles of Internal Medicine, 16th ed. New York: McGraw-Hill; 2005:2024-2029.
-
(2005)
Harrison's Principles of Internal Medicine
, pp. 2024-2029
-
-
Sipe, J.D.1
Cohen, A.S.2
-
6
-
-
0026519157
-
Incidence and natural history of primary systemic amyloidosis in Olmsted County Minnesota, 1950 through 1989
-
Kyle RA, Linos A, Beard CM, et al. Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989. Blood. 1992;79:1817-1822.
-
(1992)
Blood
, vol.79
, pp. 1817-1822
-
-
Kyle, R.A.1
Linos, A.2
Beard, C.M.3
-
7
-
-
0344172816
-
The degrees of plasma cell clonality and marrow infiltration adversely influence the prognosis of AL amyloidosis patients
-
Perfetti V, Colli Vignarelli M, Anesi E, et al. The degrees of plasma cell clonality and marrow infiltration adversely influence the prognosis of AL amyloidosis patients. Haematologica. 1999;84:218-221.
-
(1999)
Haematologica
, vol.84
, pp. 218-221
-
-
Perfetti, V.1
Colli Vignarelli, M.2
Anesi, E.3
-
8
-
-
60649083224
-
AL amyloidosis and progression to multiple myeloma with gain(1q)
-
Hoffman J, Jhanwar S, Comenzo RL. AL amyloidosis and progression to multiple myeloma with gain(1q). Br J Haematol. 2008;144:963-964.
-
(2008)
Br J Haematol
, vol.144
, pp. 963-964
-
-
Hoffman, J.1
Jhanwar, S.2
Comenzo, R.L.3
-
10
-
-
0026780774
-
Immunohistochemical characterization of amyloid proteins in sural nerves and clinical associations in amyloid neuropathy
-
Li K, Kyle RA, Dyck PJ. Immunohistochemical characterization of amyloid proteins in sural nerves and clinical associations in amyloid neuropathy. Am J Pathol. 1992;141:217-226.
-
(1992)
Am J Pathol
, vol.141
, pp. 217-226
-
-
Li, K.1
Kyle, R.A.2
Dyck, P.J.3
-
11
-
-
0032033026
-
Prognosis of patients with primary systemic amyloidosis who present with dominant neuropathy
-
Rajkumar SV, Gertz MA, Kyle RA. Prognosis of patients with primary systemic amyloidosis who present with dominant neuropathy. Am J Med. 1998; 104:232-237.
-
(1998)
Am J Med
, vol.104
, pp. 232-237
-
-
Rajkumar, S.V.1
Gertz, M.A.2
Kyle, R.A.3
-
12
-
-
0020564330
-
The electrodiagnostic findings in peripheral neuropathy associated with monoclonal gammopathy
-
Kelly JJ. The electrodiagnostic findings in peripheral neuropathy associated with monoclonal gammopathy. Muscle Nerve. 1983;6:504-509.
-
(1983)
Muscle Nerve
, vol.6
, pp. 504-509
-
-
Kelly, J.J.1
-
13
-
-
12144276283
-
Amyloid neuropathy: A retrospective study of 35 peripheral nerve biopsies
-
Vital C, Vital A, Bouillot-Eimer S, et al. Amyloid neuropathy: a retrospective study of 35 peripheral nerve biopsies. J Peripher Nerv Syst. 2004;9:232-241.
-
(2004)
J Peripher Nerv Syst
, vol.9
, pp. 232-241
-
-
Vital, C.1
Vital, A.2
Bouillot-Eimer, S.3
-
15
-
-
33750616035
-
Dangerous small B-cell clones
-
Merlini, G, Stone MJ. Dangerous small B-cell clones. Blood. 2006;108:2520-2530.
-
(2006)
Blood
, vol.108
, pp. 2520-2530
-
-
Merlini, G.1
Stone, M.J.2
-
16
-
-
0035879128
-
Eligibility for hematopoietic stem-cell transplantation for primary systemic amyloidosis is a favorable prognostic factor for survival
-
Dispenzieri A, Lacy MQ, Kyle RA, et al. Eligibility for hematopoietic stem-cell transplantation for primary systemic amyloidosis is a favorable prognostic factor for survival. J Clin Oncol. 2001;19:3350-3356.
-
(2001)
J Clin Oncol
, vol.19
, pp. 3350-3356
-
-
Dispenzieri, A.1
Lacy, M.Q.2
Kyle, R.A.3
-
17
-
-
34848818004
-
The molecular biology and clinical features of amyloid neuropathy
-
Benson MD, Kincaid JC. The molecular biology and clinical features of amyloid neuropathy. Muscle Nerve. 2007;36:411-423.
-
(2007)
Muscle Nerve
, vol.36
, pp. 411-423
-
-
Benson, M.D.1
Kincaid, J.C.2
-
18
-
-
77957180065
-
A peculiar form of peripheral neuropathy: Familiar atypical generalized amyloidosis with special involvement of the peripheral nerves
-
Andrade C. A peculiar form of peripheral neuropathy: familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain. 1952; 75:408-427.
-
(1952)
Brain
, vol.75
, pp. 408-427
-
-
Andrade, C.1
-
19
-
-
84981368487
-
Familial amyloidosis with polyneuropathy
-
Andersson R. Familial amyloidosis with polyneuropathy. Acta Med Scand. 1970;188:85-94.
-
(1970)
Acta Med Scand
, vol.188
, pp. 85-94
-
-
Andersson, R.1
-
20
-
-
0016913418
-
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 Suppl. 1976;590: 1-64.
-
(1976)
Acta Med Scand Suppl
, vol.590
, pp. 1-64
-
-
Andersson, R.1
-
21
-
-
0014300978
-
Polyneurotic amyloidosis in a Japanese family
-
Araki S, Mawatari S, Ohta M, et al. Polyneurotic 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
-
22
-
-
0019787701
-
Amyloid fibril protein in type i familial amyloidotic polyneuropathy in Japanese
-
Tawara S, Araki S, Toshimori K, et al. Amyloid fibril protein in type I familial amyloidotic polyneuropathy in Japanese. J Lab Clin Med. 1981;98:811-822.
-
(1981)
J Lab Clin Med
, vol.98
, pp. 811-822
-
-
Tawara, S.1
Araki, S.2
Toshimori, K.3
-
23
-
-
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
-
24
-
-
0035957104
-
Transthyretinassociated neuropathic amyloidosis: Pathogenesis and treatment
-
Hund E, Linke RP, Willig F, et al. Transthyretinassociated neuropathic amyloidosis: pathogenesis and treatment. Neurology. 2001;56:431-435.
-
(2001)
Neurology
, vol.56
, pp. 431-435
-
-
Hund, E.1
Linke, R.P.2
Willig, F.3
-
25
-
-
77949433680
-
Genotype-phenotype relationship in familial amyloid polyneuropathy
-
Nakazato M. Genotype-phenotype relationship in familial amyloid polyneuropathy. Neurol Med Chir (Tokyo). 1998;48:528-534.
-
(1998)
Neurol Med Chir (Tokyo)
, vol.48
, pp. 528-534
-
-
Nakazato, M.1
-
26
-
-
0032863087
-
Late-onset familial amyloid polyneuropathy type i (transthyretin Met30- associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features
-
Misu K, Hattori N, Nagamatsu M. Late-onset familial amyloid polyneuropathy type I (transthyretin Met30- associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features. Brain. 1999;122:1951-1962.
-
(1999)
Brain
, vol.122
, pp. 1951-1962
-
-
Misu, K.1
Hattori, N.2
Nagamatsu, M.3
-
27
-
-
0037046222
-
Familial transthyretin-type amyloid polyneuropathy in Japan: Clinical and genetic heterogeneity
-
Ikeda S, Nakazato M, Ando Y, et al. 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
-
28
-
-
0027275791
-
Familial amyloidotic polyneuropathy in Sweden: Geographical distribution, age of onset, and prevalence
-
Sousa A, Andersson R, Drugge U, et al. Familial amyloidotic polyneuropathy 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
-
29
-
-
0344074661
-
Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathy
-
Plante-Bordeneuve V, Lalu T, Misrahi M, et al. Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathy. Neurology. 1998;51:708-714.
-
(1998)
Neurology
, vol.51
, pp. 708-714
-
-
Plante-Bordeneuve, V.1
Lalu, T.2
Misrahi, M.3
-
30
-
-
0029562263
-
Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type i in Povoa do Varzim and Vila do Conde (North of Portugal)
-
Sousa A, Coelho T, Lobato L, et al. Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Povoa do Varzim and Vila do Conde (North of Portugal). Am J Med Genet. 1995;60: 512-521.
-
(1995)
Am J Med Genet
, vol.60
, pp. 512-521
-
-
Sousa, A.1
Coelho, T.2
Lobato, L.3
-
31
-
-
0023254244
-
Onset in the seventh decade and lack of symptoms in heterozygotes for the TTR met30 mutation in hereditary amyloid neuropathytype i (Portuguese, Andrade)
-
Sequeiros J, Saraiva MJ. Onset in the seventh decade and lack of symptoms in heterozygotes for the TTR met30 mutation in hereditary amyloid neuropathytype I (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.2
-
32
-
-
0023520915
-
Abnormal transthyretin in asymptomatic relatives in familial amyloidotic polyneuropathy
-
Nakazato M, Tanaka M, Yamamura Y, et al. Abnormal transthyretin in asymptomatic relatives in familial amyloidotic polyneuropathy. Arch Neurol. 1987;44: 1275-1278.
-
(1987)
Arch Neurol
, vol.44
, pp. 1275-1278
-
-
Nakazato, M.1
Tanaka, M.2
Yamamura, Y.3
-
33
-
-
0028281999
-
A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected
-
Coelho T, Sousa A, Lourenco E, et al. 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
Lourenco, E.3
-
34
-
-
0029095429
-
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy
-
Reilly MM, Adams D, Booth DR, et al. Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy. Brain. 1995;118: 849-856.
-
(1995)
Brain
, vol.118
, pp. 849-856
-
-
Reilly, M.M.1
Adams, D.2
Booth, D.R.3
-
35
-
-
0032803525
-
Two pairs of proven monozygotic twins discordant for familial amyloid polyneuropathy (FAP) TTR Met 30
-
Munar-Qués M, Pedrosa JL, Coelho T, et al. Two pairs of proven monozygotic twins discordant for familial amyloid polyneuropathy (FAP) TTR Met 30. 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
-
36
-
-
14044275133
-
Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: Complexity in a single-gene disease
-
Soares ML, Coelho T, Sousa A, et al. 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
-
37
-
-
12244256129
-
A case of vitreous amyloidosis without systemic symptoms in familial amyloidotic polyneuropathy
-
Kawaji T, Ando Y, Ando E, et al. A case of vitreous amyloidosis without systemic symptoms in familial amyloidotic polyneuropathy. Amyloid. 2004;11: 257-259.
-
(2004)
Amyloid
, vol.11
, pp. 257-259
-
-
Kawaji, T.1
Ando, Y.2
Ando, E.3
-
38
-
-
0032944025
-
Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis
-
Brett M, Persey MR, Reilly MM, et al. Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis. Brain. 1999;122: 183-190.
-
(1999)
Brain
, vol.122
, pp. 183-190
-
-
Brett, M.1
Persey, M.R.2
Reilly, M.M.3
-
39
-
-
0032886881
-
Oculoleptomeningeal amyloidosis associated with a new transthyretin variant Ser64
-
Uemichi T, Uitti RJ, Koeppen AH, et al. Oculoleptomeningeal amyloidosis associated with a new transthyretin variant Ser64. Arch Neurol. 1999;56: 1152-1155.
-
(1999)
Arch Neurol
, vol.56
, pp. 1152-1155
-
-
Uemichi, T.1
Uitti, R.J.2
Koeppen, A.H.3
-
40
-
-
0035838381
-
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu)
-
Ellie E, Camou F, Vital A, et al. Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu). Neurology. 2001;57: 135-137.
-
(2001)
Neurology
, vol.57
, pp. 135-137
-
-
Ellie, E.1
Camou, F.2
Vital, A.3
-
41
-
-
0037799503
-
Oculoleptomeningeal amyloidosis in a large kindred with a new transtryretin variant Tyr69His
-
Blevins G, Maccaulay R, Harder S, et al. Oculoleptomeningeal amyloidosis in a large kindred with a new transtryretin variant Tyr69His. Neurology. 2003;60: 1625-1630.
-
(2003)
Neurology
, vol.60
, pp. 1625-1630
-
-
Blevins, G.1
MacCaulay, R.2
Harder, S.3
-
42
-
-
0014444934
-
Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and pepticulcer
-
Van Allen MW, Frohlich JA, Davis JR. Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer. Neurology. 1969;19: 10-25.
-
(1969)
Neurology
, vol.19
, pp. 10-25
-
-
Van Allen, M.W.1
Frohlich, J.A.2
Davis, J.R.3
-
43
-
-
33748507136
-
Organ transplantation in hereditary apolipoprotein AI amyloidosis
-
Gillmore JD, Stangou AJ, Lachmann HJ, et al. Organ transplantation in hereditary apolipoprotein AI amyloidosis. Am J Transplant. 2006;6:2342-2347.
-
(2006)
Am J Transplant
, vol.6
, pp. 2342-2347
-
-
Gillmore, J.D.1
Stangou, A.J.2
Lachmann, H.J.3
-
44
-
-
0025006134
-
A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy
-
Nichols WC, Gregg RE, Brewer HB, et al. A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. Genomics. 1990;8: 318-323.
-
(1990)
Genomics
, vol.8
, pp. 318-323
-
-
Nichols, W.C.1
Gregg, R.E.2
Brewer, H.B.3
-
45
-
-
0025637651
-
Gelsolin variant (Asn- 187) in familial amyloidosis Finnish type
-
Ghiso J, Haltia M, Prelli F, et al. Gelsolin variant (Asn- 187) in familial amyloidosis, Finnish type. Biochem J. 1990;272:827-830.
-
(1990)
Biochem J
, vol.272
, pp. 827-830
-
-
Ghiso, J.1
Haltia, M.2
Prelli, F.3
-
46
-
-
0025647488
-
Mutation in gelsolin gene in Finnish hereditary amyloidosis
-
Levy E, Haltia M, Fernandez-Madrid I, et al. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med. 1990;172:1865-1867.
-
(1990)
J Exp Med
, vol.172
, pp. 1865-1867
-
-
Levy, E.1
Haltia, M.2
Fernandez-Madrid, I.3
-
47
-
-
0026936594
-
Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187
-
De La Chapelle A, Tolvanen R, Boysen G, et al. Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187. Nat Genet. 1992;2:157-160.
-
(1992)
Nat Genet
, vol.2
, pp. 157-160
-
-
De La Chapelle, A.1
Tolvanen, R.2
Boysen, G.3
-
48
-
-
0014640130
-
Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms
-
Meretoja J. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. Ann Clin Res. 1969;1:314-324.
-
(1969)
Ann Clin Res
, vol.1
, pp. 314-324
-
-
Meretoja, J.1
-
49
-
-
0015806355
-
Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy
-
Meretoja J. Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy. Clin Genet. 1973;4:173-185.
-
(1973)
Clin Genet
, vol.4
, pp. 173-185
-
-
Meretoja, J.1
-
50
-
-
0026495027
-
Familial amyloidosis of the Finnish type (FAF): A clinical study of 30 patients
-
Kiuru S. Familial amyloidosis of the Finnish type (FAF): a clinical study of 30 patients. Acta Neurol Scand. 1992;86:346-353.
-
(1992)
Acta Neurol Scand
, vol.86
, pp. 346-353
-
-
Kiuru, S.1
-
51
-
-
0018663987
-
Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy
-
Boysen G, Galassi G, Kamieniecka Z, et al. Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy. J Neurol Neurosurg Psychiatry. 1979;42:1020-1030.
-
(1979)
J Neurol Neurosurg Psychiatry
, vol.42
, pp. 1020-1030
-
-
Boysen, G.1
Galassi, G.2
Kamieniecka, Z.3
-
52
-
-
0022618523
-
Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy
-
Darras BT, Adelman LS, Mora JS, et al. Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy. Neurology. 1986;36:432-435.
-
(1986)
Neurology
, vol.36
, pp. 432-435
-
-
Darras, B.T.1
Adelman, L.S.2
Mora, J.S.3
-
53
-
-
0026410035
-
Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II
-
Gorevic PD, Munoz PC, Gorgone G, et al. Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II. N Engl J Med. 1991;325:1780-1785.
-
(1991)
N Engl J Med
, vol.325
, pp. 1780-1785
-
-
Gorevic, P.D.1
Munoz, P.C.2
Gorgone, G.3
-
54
-
-
0028018902
-
Familial amyloid polyneuropathy type IV (Finnish-type). A clinicopathological study
-
Makishita H, Yazaki M, Matsuda M, et al. Familial amyloid polyneuropathy type IV (Finnish-type). A clinicopathological study. Rinsho Shinkeigaku. 1994;34:431-437.
-
(1994)
Rinsho Shinkeigaku
, vol.34
, pp. 431-437
-
-
Makishita, H.1
Yazaki, M.2
Matsuda, M.3
-
55
-
-
0029890373
-
Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV
-
Akiya S, Nishio Y, Ibi K, et al. Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV. Ophthalmology. 1996;103: 1106-1110.
-
(1996)
Ophthalmology
, vol.103
, pp. 1106-1110
-
-
Akiya, S.1
Nishio, Y.2
Ibi, K.3
-
56
-
-
0032012657
-
Gelsolin-related familial amyloidosis, Finnish type (FAF) and its variants found worldwide. A review
-
Kiuru S. Gelsolin-related familial amyloidosis, Finnish type (FAF) and its variants found worldwide. A review. Amyloid. 1998;5:55-66.
-
(1998)
Amyloid
, vol.5
, pp. 55-66
-
-
Kiuru, S.1
-
57
-
-
0034057570
-
Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family
-
Stewart HS, Parveen R, Ridgway AE, et al. Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family. Br J Ophtalmol. 2000;84:390-394.
-
(2000)
Br J Ophtalmol
, vol.84
, pp. 390-394
-
-
Stewart, H.S.1
Parveen, R.2
Ridgway, A.E.3
-
58
-
-
0344443397
-
Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies
-
Conceiccao I, Sales-Luis ML, De Carvalho M, et al. Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studies. Muscle Nerve. 2003;28:715-721.
-
(2003)
Muscle Nerve
, vol.28
, pp. 715-721
-
-
Conceiccao, I.1
Sales-Luis, M.L.2
De Carvalho, M.3
-
59
-
-
33748942113
-
Familial systemic amyloidosis associated with bilateral sensorineural hearing loss and bilateral facial palsies
-
Hornigold R, Patel AV, Ward VMM, et al. Familial systemic amyloidosis associated with bilateral sensorineural hearing loss and bilateral facial palsies. J Laryngol Otol. 2006;120:778-780.
-
(2006)
J Laryngol Otol
, vol.120
, pp. 778-780
-
-
Hornigold, R.1
Patel, A.V.2
Ward, V.M.M.3
-
60
-
-
0028202117
-
Neuropathy in familial amyloidosis Finnish type (FAF): Electrophysiological studies
-
Kiuru S, Seppalainen A-M. Neuropathy in familial amyloidosis, Finnish type (FAF): electrophysiological studies. Muscle Nerve. 1994;17:299-304.
-
(1994)
Muscle Nerve
, vol.17
, pp. 299-304
-
-
Kiuru, S.1
Seppalainen, A.-M.2
-
61
-
-
33947627069
-
Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: A case report
-
Tanskanen M, Paetau A, Salonen O, et al. Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report. Amyloid. 2007;14:89-95.
-
(2007)
Amyloid
, vol.14
, pp. 89-95
-
-
Tanskanen, M.1
Paetau, A.2
Salonen, O.3
-
62
-
-
0027980608
-
Autonomic nervous system and cardiac involvement in familial amyloidosis, Finnish type (FAF)
-
Kiuru S, Matikainen E, Kupari M, et al. Autonomic nervous system and cardiac involvement in familial amyloidosis, Finnish type (FAF). J Neurol Sci. 1994; 126:40-48.
-
(1994)
J Neurol Sci
, vol.126
, pp. 40-48
-
-
Kiuru, S.1
Matikainen, E.2
Kupari, M.3
-
63
-
-
30344467836
-
Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p. Asp187Tyrmutation in the GSN gene
-
Chastan N, Baert-Desurmont S, Saugier-Veber P, et al. Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p. Asp187Tyrmutation in the GSN gene. Muscle Nerve. 2005;33:113-119.
-
(2005)
Muscle Nerve
, vol.33
, pp. 113-119
-
-
Chastan, N.1
Baert-Desurmont, S.2
Saugier-Veber, P.3
-
64
-
-
0033028206
-
Gelsolin-related spinal and cerebral amyloid angiopathy
-
Kiuru S, Salonen O, Haltia M. Gelsolin-related spinal and cerebral amyloid angiopathy. Ann Neurol. 1999; 45:305-311.
-
(1999)
Ann Neurol
, vol.45
, pp. 305-311
-
-
Kiuru, S.1
Salonen, O.2
Haltia, M.3
-
65
-
-
0017882460
-
Electroneurophysiological studies in familial amyloid polyneuropathy-Portuguese type
-
Sales Luis ML. Electroneurophysiological studies in familial amyloid polyneuropathy-Portuguese type. J Neurol Neurosurg Psychiatry. 1978;41:847-850.
-
(1978)
J Neurol Neurosurg Psychiatry
, vol.41
, pp. 847-850
-
-
Sales Luis, M.L.1
-
66
-
-
0014508556
-
Dissociated sensation in amyloidosis: Compound action potential, quantitative histologic and teased-fiber, and electron microscopic studies of sural nerve biopsies
-
Dyck PJ, Lambert EH. Dissociated sensation in amyloidosis: compound action potential, quantitative histologic and teased-fiber, and electron microscopic studies of sural nerve biopsies. Arch Neurol. 1969; 20:490-507.
-
(1969)
Arch Neurol
, vol.20
, pp. 490-507
-
-
Dyck, P.J.1
Lambert, E.H.2
-
68
-
-
60049096487
-
Ten-year followup of peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation
-
Shimojima Y, Morita H, Kobayashi S, et al. Ten-year followup of peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation. J Neurol. 2008;255:1220-1225.
-
(2008)
J Neurol
, vol.255
, pp. 1220-1225
-
-
Shimojima, Y.1
Morita, H.2
Kobayashi, S.3
-
69
-
-
0023091943
-
Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients
-
Ikeda S, Hanyu N, Hongo M, et al. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients. Brain. 1987;110:315-337.
-
(1987)
Brain
, vol.110
, pp. 315-337
-
-
Ikeda, S.1
Hanyu, N.2
Hongo, M.3
-
70
-
-
0025990675
-
Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)
-
Holmgren G, Steen L, Ekstedt J, et al. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30). Clin Genet. 1991;40:242-246.
-
(1991)
Clin Genet
, vol.40
, pp. 242-246
-
-
Holmgren, G.1
Steen, L.2
Ekstedt, J.3
-
72
-
-
0029159786
-
A case of familial amyloid polyneuropathy treated with partial liver transplantation using a graft from a living related donor
-
Matsunami H, Makuuchi M, Kawasaki S, et al. A case of familial amyloid polyneuropathy treated with partial liver transplantation using a graft from a living related donor. Transplantation. 1995;60:301-303.
-
(1995)
Transplantation
, vol.60
, pp. 301-303
-
-
Matsunami, H.1
Makuuchi, M.2
Kawasaki, S.3
-
73
-
-
0032724681
-
Outcome of liver transplantation for transthyretin amyloidosis: Follow-up of Japanese familial amyloidotic polyneuropathy patients
-
Tashima K, Ando Y, Terazaki H, et al. Outcome of liver transplantation for transthyretin amyloidosis: follow-up of Japanese familial amyloidotic polyneuropathy patients. J Neurol Sci. 1999 171:19-23.
-
(1999)
J Neurol Sci
, vol.171
, pp. 19-23
-
-
Tashima, K.1
Ando, Y.2
Terazaki, H.3
-
74
-
-
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;123:1495-1504.
-
(2000)
Brain
, vol.123
, pp. 1495-1504
-
-
Adams, D.1
Samuel, D.2
Goulon-Goeau, C.3
-
75
-
-
0035997532
-
Longterm quantitative evaluation of liver transplantation in familial amyloid polyneuropathy (Portuguese V30M)
-
De Carvalho M, Conceicao I, Bentes C, et al. Longterm quantitative evaluation of liver transplantation in familial amyloid polyneuropathy (Portuguese V30M). Amyloid. 2002;9:126-133.
-
(2002)
Amyloid
, vol.9
, pp. 126-133
-
-
De Carvalho, M.1
Conceicao, I.2
Bentes, C.3
-
76
-
-
0037367630
-
Peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation
-
Kobayashi S, Morita H, Asawa T, et al. Peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation. Amyloid. 2003;10:17-24.
-
(2003)
Amyloid
, vol.10
, pp. 17-24
-
-
Kobayashi, S.1
Morita, H.2
Asawa, T.3
-
77
-
-
0027232288
-
Synthesis and secretion of apolipoprotein A-I
-
Calandra S, Tarugi P. Synthesis and secretion of apolipoprotein A-I. Biochem Soc Trans. 1993;21:493.
-
(1993)
Biochem Soc Trans
, vol.21
, pp. 493
-
-
Calandra, S.1
Tarugi, P.2
-
78
-
-
0035870770
-
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apoliprotein AI Gly26Arg
-
Gillmore JD, Stangou AJ, Tennent GA, et al. Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apoliprotein AI Gly26Arg. Transplantation. 2001;71:986-992.
-
(2001)
Transplantation
, vol.71
, pp. 986-992
-
-
Gillmore, J.D.1
Stangou, A.J.2
Tennent, G.A.3
-
79
-
-
34547546793
-
Hereditary amyloidosis with progressive peripheral neuropathy associated with apolipoprotein AI Gly26Arg: Outcome of hepatorenal transplantation
-
Testro AG, Brennan SO, Macdonnell RAL, et al. Hereditary amyloidosis with progressive peripheral neuropathy associated with apolipoprotein AI Gly26Arg: outcome of hepatorenal transplantation. Liver Transpl. 2007;13:1028-1031.
-
(2007)
Liver Transpl
, vol.13
, pp. 1028-1031
-
-
Testro, A.G.1
Brennan, S.O.2
MacDonnell, R.A.L.3
-
80
-
-
0022312829
-
Peripheral neuropathies associated with monoclonal proteins: A clinical review
-
Kelly JJ. Peripheral neuropathies associated with monoclonal proteins: a clinical review. Muscle Nerve. 1985;8:138-150.
-
(1985)
Muscle Nerve
, vol.8
, pp. 138-150
-
-
Kelly, J.J.1
-
81
-
-
0027721944
-
Low diagnostic yield of sural nerve biopsy in patients with peripheral neuropathy and primary amyloidosis
-
Simmons Z, Blaivs M, Aguilera AJ, et al. Low diagnostic yield of sural nerve biopsy in patients with peripheral neuropathy and primary amyloidosis. J Neurol Sci. 1993;120:60-63.
-
(1993)
J Neurol Sci
, vol.120
, pp. 60-63
-
-
Simmons, Z.1
Blaivs, M.2
Aguilera, A.J.3
-
82
-
-
0020586058
-
Amyloid neuropathy in multiple myeloma and other plasma cell dyscrasias: A hypothesis of the pathogenesis of amyloid neuropathies
-
Verghese JP, Bradley WG, Nemni R, et al. Amyloid neuropathy in multiple myeloma and other plasma cell dyscrasias: a hypothesis of the pathogenesis of amyloid neuropathies. J Neurol Sci. 1983;59: 237-246.
-
(1983)
J Neurol Sci
, vol.59
, pp. 237-246
-
-
Verghese, J.P.1
Bradley, W.G.2
Nemni, R.3
-
83
-
-
0024605634
-
Peripheral nerve pathologic findings in familial amyloid polyneuropathy: A correlative study of proximal sciatic nerve and sural nerve lesions
-
Hanyu N, Ikeda S, Nakadai A, et al. Peripheral nerve pathologic findings in familial amyloid polyneuropathy: a correlative study of proximal sciatic nerve and sural nerve lesions. Ann Neurol. 1989;25:340-350.
-
(1989)
Ann Neurol
, vol.25
, pp. 340-350
-
-
Hanyu, N.1
Ikeda, S.2
Nakadai, A.3
-
84
-
-
0026029105
-
Unusual amyloid polyneuropathy with predominant lumbosacral nerve roots and plexus involvement
-
Antoine JC, Baril A, Guettier C, et al. Unusual amyloid polyneuropathy with predominant lumbosacral nerve roots and plexus involvement. Neurology. 1991;41:206-208.
-
(1991)
Neurology
, vol.41
, pp. 206-208
-
-
Antoine, J.C.1
Baril, A.2
Guettier, C.3
-
85
-
-
0017610906
-
Skeletal muscle pseudohypertrophy in primary amyloidosis
-
Whitaker JN, Hashimoto K, Quinones M. Skeletal muscle pseudohypertrophy in primary amyloidosis. Neurology. 1977;27:47-54.
-
(1977)
Neurology
, vol.27
, pp. 47-54
-
-
Whitaker, J.N.1
Hashimoto, K.2
Quinones, M.3
-
86
-
-
0020650193
-
Amyloid-associated muscle pseudohypertrophy and multiple myeloma in a man with hypernephroma
-
Elomaa I, Ekblom P, Somer T. Amyloid-associated muscle pseudohypertrophy and multiple myeloma in a man with hypernephroma. Acta Med Scand. 1983;214: 87-91.
-
(1983)
Acta Med Scand
, vol.214
, pp. 87-91
-
-
Elomaa, I.1
Ekblom, P.2
Somer, T.3
-
87
-
-
0023895292
-
Skeletal muscle amyloid deposition in AL- (Primary or myeloma-associated), AA- (Secondary), and prealbumin- Type amyloidosis
-
Yamada M, Tsukagoshi H, Hatakeyama S. Skeletal muscle amyloid deposition in AL- (primary or myeloma-associated), AA- (secondary), and prealbumin- type amyloidosis. J Neurol Sci. 1988;85:223-232.
-
(1988)
J Neurol Sci
, vol.85
, pp. 223-232
-
-
Yamada, M.1
Tsukagoshi, H.2
Hatakeyama, S.3
-
90
-
-
0022611471
-
Amyloid infiltration of the diaphragm as a cause of respiratory failure
-
Streeten EA, De La Monte SM, Kennedy TP. Amyloid infiltration of the diaphragm as a cause of respiratory failure. Chest. 1986;89:760-762.
-
(1986)
Chest
, vol.89
, pp. 760-762
-
-
Streeten, E.A.1
De La Monte, S.M.2
Kennedy, T.P.3
-
91
-
-
0023634459
-
Respiratory muscle weakness and ventilatory failure in AL amyloidosis with muscular pseudohypertrophy
-
Santiago RM, Scharnhorst D, Ratkin G, et al. Respiratory muscle weakness and ventilatory failure in AL amyloidosis with muscular pseudohypertrophy. Am J Med. 1987;83:175-178.
-
(1987)
Am J Med
, vol.83
, pp. 175-178
-
-
Santiago, R.M.1
Scharnhorst, D.2
Ratkin, G.3
|