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Items: 1 to 20 of 99

1.

Neuroarthropathy secondary to transthyretin amyloidosis (ATTR V30M).

Wilmes D, Wautier D, Jonckheere S, Cornu O, Yombi JC.

Acta Clin Belg. 2012 Sep-Oct;67(5):372-4.

PMID:
23189548
2.

Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M).

Lobato L.

J Nephrol. 2003 May-Jun;16(3):438-42. Review.

PMID:
12832749
3.

CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings.

Maia LF, Magalhães R, Freitas J, Taipa R, Pires MM, Osório H, Dias D, Pessegueiro H, Correia M, Coelho T.

J Neurol Neurosurg Psychiatry. 2015 Feb;86(2):159-67. doi: 10.1136/jnnp-2014-308107. Epub 2014 Aug 4.

PMID:
25091367
4.

Aging and transthyretin-related amyloidosis: pathologic examinations in pulmonary amyloidosis.

Ueda M, Ando Y, Haraoka K, Katsuragi S, Terasaki Y, Sugimoto M, Sun X, Uchino M.

Amyloid. 2006 Mar;13(1):24-30.

PMID:
16690497
5.

Effect of albumin on transthyretin and amyloidogenic transthyretin Val30Met disposition and tissue deposition in familial amyloidotic polyneuropathy.

Taguchi K, Jono H, Kugimiya-Taguchi T, Nagao S, Su Y, Yamasaki K, Mizuguchi M, Maruyama T, Ando Y, Otagiri M.

Life Sci. 2013 Dec 18;93(25-26):1017-22. doi: 10.1016/j.lfs.2013.10.031. Epub 2013 Nov 8.

PMID:
24211615
6.

Massive leptomeningeal amyloidosis associated with a Val30Met transthyretin gene.

Herrick MK, DeBruyne K, Horoupian DS, Skare J, Vanefsky MA, Ong T.

Neurology. 1996 Oct;47(4):988-92.

PMID:
8857732
7.

Familial amyloidotic polyneuropathy (ATTR Ser50Ile): the first autopsy case report.

Sakashita N, Ando Y, Obayashi K, Terazaki H, Yamashita T, Takei M, Kinjo M, Takahashi K.

Virchows Arch. 2000 Apr;436(4):345-50.

PMID:
10834537
8.

Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.

Koeppen AH, Wallace MR, Benson MD, Altland K.

Muscle Nerve. 1990 Nov;13(11):1065-75.

PMID:
2122246
9.

Risk of transmission of systemic transthyretin amyloidosis after domino liver transplantation.

Lladó L, Baliellas C, Casasnovas C, Ferrer I, Fabregat J, Ramos E, Castellote J, Torras J, Xiol X, Rafecas A.

Liver Transpl. 2010 Dec;16(12):1386-92. doi: 10.1002/lt.22174.

10.

Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy.

Yoshinaga T, Nakazato M, Ikeda S, Ohnishi A.

Neurology. 1992 Oct;42(10):2045-7.

PMID:
1407590
11.

Neuroarthropathy (Charcot joints) in familial amyloid polyneuropathy.

Pruzanski W, Baron M, Shupak R.

J Rheumatol. 1981 May-Jun;8(3):477-81.

PMID:
6270334
12.

Cardiac amyloidosis in African Americans: comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosis.

Connors LH, Prokaeva T, Lim A, Théberge R, Falk RH, Doros G, Berg A, Costello CE, O'Hara C, Seldin DC, Skinner M.

Am Heart J. 2009 Oct;158(4):607-14. doi: 10.1016/j.ahj.2009.08.006.

PMID:
19781421
13.

Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy.

Hattori T, Takei Y, Koyama J, Nakazato M, Ikeda S.

Amyloid. 2003 Dec;10(4):229-39.

PMID:
14986482
14.

A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.

Booth DR, Tan SY, Hawkins PN, Pepys MB, Frustaci A.

Circulation. 1995 Feb 15;91(4):962-7.

15.

Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent.

Jones LA, Skare JC, Cohen AS, Harding JA, Milunsky A, Skinner M.

Clin Genet. 1992 Feb;41(2):70-3.

PMID:
1544214
16.

Effect of nitric oxide in amyloid fibril formation on transthyretin-related amyloidosis.

Saito S, Ando Y, Nakamura M, Ueda M, Kim J, Ishima Y, Akaike T, Otagiri M.

Biochemistry. 2005 Aug 23;44(33):11122-9.

PMID:
16101296
17.
18.

Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis.

Ihse E, Ybo A, Suhr O, Lindqvist P, Backman C, Westermark P.

J Pathol. 2008 Oct;216(2):253-61. doi: 10.1002/path.2411.

PMID:
18729067
19.

Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy.

Ikeda S, Nakano T, Yanagisawa N, Nakazato M, Tsukagoshi H.

Eur Neurol. 1992;32(6):308-13.

PMID:
1490495
20.

High prevalence of ATTR amyloidosis in endomyocardial biopsy-proven cardiac amyloidosis patients.

Nakagawa M, Sekijima Y, Tojo K, Ikeda S.

Amyloid. 2013 Jun;20(2):138-40. doi: 10.3109/13506129.2013.790809. Epub 2013 May 2.

PMID:
23638696
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