PubMed (cited) for id: 176300

Year	Number of Results
1948	1
1952	1
1956	2
1958	1
1959	1
1962	2
1964	3
1965	1
1966	1
1967	3
1968	1
1969	2
1970	1
1973	1
1974	2
1975	1
1977	1
1978	1
1979	1
1980	2
1981	7
1982	3
1983	9
1984	9
1985	12
1986	16
1987	9
1988	7
1989	7
1990	11
1991	13
1992	26
1993	12
1994	9
1995	4
1996	8
1997	6
1998	6
1999	6
2000	3
2001	7
2002	4
2003	5
2004	4
2005	3
2007	1
2008	2
2009	2
2010	1
2015	1
2017	1
2024	0

1

Transthyretin V122I (pV142I)* cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans.

Buxbaum JN, Ruberg FL. Buxbaum JN, et al. Genet Med. 2017 Jul;19(7):733-742. doi: 10.1038/gim.2016.200. Epub 2017 Jan 19. Genet Med. 2017. PMID: 28102864 Free PMC article. Review.

2

The amyloidogenic V122I transthyretin variant in elderly black Americans.

Quarta CC, Buxbaum JN, Shah AM, Falk RH, Claggett B, Kitzman DW, Mosley TH, Butler KR, Boerwinkle E, Solomon SD. Quarta CC, et al. N Engl J Med. 2015 Jan 1;372(1):21-9. doi: 10.1056/NEJMoa1404852. N Engl J Med. 2015. PMID: 25551524 Free PMC article.

3

Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.

Yang NC, Lee MJ, Chao CC, Chuang YT, Lin WM, Chang MF, Hsieh PC, Kan HW, Lin YH, Yang CC, Chiu MJ, Liou HH, Hsieh ST. Yang NC, et al. Neurology. 2010 Aug 10;75(6):532-8. doi: 10.1212/WNL.0b013e3181ec7fda. Neurology. 2010. PMID: 20697105

4

Transthyretin: the servant of many masters.

Buxbaum JN, Reixach N. Buxbaum JN, et al. Cell Mol Life Sci. 2009 Oct;66(19):3095-101. doi: 10.1007/s00018-009-0109-0. Epub 2009 Jul 31. Cell Mol Life Sci. 2009. PMID: 19644733 Free PMC article. Review.

5

Highly selective leptomeningeal amyloidosis with transthyretin variant Ala25Thr.

Hagiwara K, Ochi H, Suzuki S, Shimizu Y, Tokuda T, Murai H, Shigeto H, Ohyagi Y, Iwata M, Iwaki T, Kira JI. Hagiwara K, et al. Neurology. 2009 Apr 14;72(15):1358-60. doi: 10.1212/WNL.0b013e3181a0fe74. Neurology. 2009. PMID: 19365058 No abstract available.

6

The problem of anticipation in pedigrees of dystrophia myotonica.

PENROSE LS. PENROSE LS. Ann Eugen. 1948 Apr;14(2):125-32. doi: 10.1111/j.1469-1809.1947.tb02384.x. Ann Eugen. 1948. PMID: 18863976 No abstract available.

7

On the origin of the transthyretin Val30Met familial amyloid polyneuropathy.

Zaros C, Genin E, Hellman U, Saporta MA, Languille L, Wadington-Cruz M, Suhr O, Misrahi M, Planté-Bordeneuve V. Zaros C, et al. Ann Hum Genet. 2008 Jul;72(Pt 4):478-84. doi: 10.1111/j.1469-1809.2008.00439.x. Epub 2008 May 5. Ann Hum Genet. 2008. PMID: 18460047

8

Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression.

Liu YT, Lee YC, Yang CC, Chen ML, Lin KP. Liu YT, et al. J Neurol Sci. 2008 Apr 15;267(1-2):91-9. doi: 10.1016/j.jns.2007.10.011. Epub 2007 Nov 26. J Neurol Sci. 2008. PMID: 18022643

9

Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.

Holmgren G, Hellman U, Lundgren HE, Sandgren O, Suhr OB. Holmgren G, et al. J Med Genet. 2005 Dec;42(12):953-6. doi: 10.1136/jmg.2005.033720. Epub 2005 Jun 1. J Med Genet. 2005. PMID: 15930086 Free PMC article.

10

The biological and chemical basis for tissue-selective amyloid disease.

Sekijima Y, Wiseman RL, Matteson J, Hammarström P, Miller SR, Sawkar AR, Balch WE, Kelly JW. Sekijima Y, et al. Cell. 2005 Apr 8;121(1):73-85. doi: 10.1016/j.cell.2005.01.018. Cell. 2005. PMID: 15820680 Free article.

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