Similar articles for PMID: 8579098

Year	Number of Results
1992	4
1993	1
1994	3
1995	1
1996	8
1997	2
1998	2
1999	4
2000	4
2001	3
2003	2
2004	1
2006	3
2007	4
2008	3
2011	1
2012	1
2013	1
2014	3
2015	1
2017	1
2018	1
2022	2
2024	0

1

Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G).

Vidal R, Garzuly F, Budka H, Lalowski M, Linke RP, Brittig F, Frangione B, Wisniewski T. Vidal R, et al. Am J Pathol. 1996 Feb;148(2):361-6. Am J Pathol. 1996. PMID: 8579098 Free PMC article.

2

Coexistence of transthyretin- and Aβ-type cerebral amyloid angiopathy in a patient with hereditary transthyretin V30M amyloidosis.

Sakai K, Asakawa M, Takahashi R, Ishida C, Nakamura R, Hamaguchi T, Ono K, Iwasa K, Yamada M. Sakai K, et al. J Neurol Sci. 2017 Oct 15;381:144-146. doi: 10.1016/j.jns.2017.08.3240. Epub 2017 Aug 31. J Neurol Sci. 2017. PMID: 28991667 No abstract available.

3

Characterization of a transthyretin-related amyloid fibril protein from cerebral amyloid angiopathy in type I familial amyloid polyneuropathy.

Kametani F, Ikeda S, Yanagisawa N, Ishi T, Hanyu N. Kametani F, et al. J Neurol Sci. 1992 Apr;108(2):178-83. doi: 10.1016/0022-510x(92)90048-p. J Neurol Sci. 1992. PMID: 1517749

4

Leptomeningeal amyloid and variant transthyretins.

Benson MD. Benson MD. Am J Pathol. 1996 Feb;148(2):351-4. Am J Pathol. 1996. PMID: 8579096 Free PMC article. Review. No abstract available.

5

Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His.

Blevins G, Macaulay R, Harder S, Fladeland D, Yamashita T, Yazaki M, Hamidi Asl K, Benson MD, Donat JR. Blevins G, et al. Neurology. 2003 May 27;60(10):1625-30. doi: 10.1212/01.wnl.0000065901.18353.ab. Neurology. 2003. PMID: 12771253

6

Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly).

Garzuly F, Vidal R, Wisniewski T, Brittig F, Budka H. Garzuly F, et al. Neurology. 1996 Dec;47(6):1562-7. doi: 10.1212/wnl.47.6.1562. Neurology. 1996. PMID: 8960746

7

Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid.

Azevedo EP, Pereira HM, Garratt RC, Kelly JW, Foguel D, Palhano FL. Azevedo EP, et al. Biochemistry. 2011 Dec 27;50(51):11070-83. doi: 10.1021/bi201365r. Epub 2011 Nov 30. Biochemistry. 2011. PMID: 22091638

8

Transthyretin amyloidosis: a new mutation associated with dementia.

Petersen RB, Goren H, Cohen M, Richardson SL, Tresser N, Lynn A, Gali M, Estes M, Gambetti P. Petersen RB, et al. Ann Neurol. 1997 Mar;41(3):307-13. doi: 10.1002/ana.410410305. Ann Neurol. 1997. PMID: 9066351

9

A stop-codon mutation in the BRI gene associated with familial British dementia.

Vidal R, Frangione B, Rostagno A, Mead S, Révész T, Plant G, Ghiso J. Vidal R, et al. Nature. 1999 Jun 24;399(6738):776-81. doi: 10.1038/21637. Nature. 1999. PMID: 10391242

10

A case of transthyretin-related cerebral amyloid angiopathy. The other side of hereditary transthyretin amyloidosis.

Lemarchant B, Lebouvier T, Delbeuck X, Gibier JB, Tard C. Lemarchant B, et al. Acta Neurol Belg. 2022 Apr;122(2):571-573. doi: 10.1007/s13760-021-01854-4. Epub 2022 Jan 18. Acta Neurol Belg. 2022. PMID: 35040071

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