Similar articles for PMID: 1322359

Year	Number of Results
1986	1
1989	1
1990	7
1991	9
1992	11
1993	8
1994	5
1995	4
1996	2
1997	2
1998	2
1999	5
2000	3
2001	4
2002	2
2003	3
2004	3
2006	2
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2010	2
2011	3
2012	3
2013	2
2014	2
2015	1
2016	4
2017	3
2018	4
2019	2
2020	2
2021	3
2022	1
2024	0

1

Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family.

de la Chapelle A, Kere J, Sack GH Jr, Tolvanen R, Maury CP. de la Chapelle A, et al. Genomics. 1992 Jul;13(3):898-901. doi: 10.1016/0888-7543(92)90182-r. Genomics. 1992. PMID: 1322359

2

Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.

Hiltunen T, Kiuru S, Hongell V, Heliö T, Palo J, Peltonen L. Hiltunen T, et al. Am J Hum Genet. 1991 Sep;49(3):522-8. Am J Hum Genet. 1991. PMID: 1652889 Free PMC article.

3

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.

Maury CP, Kere J, Tolvanen R, de la Chapelle A. Maury CP, et al. FEBS Lett. 1990 Dec 10;276(1-2):75-7. doi: 10.1016/0014-5793(90)80510-p. FEBS Lett. 1990. PMID: 2176164 Free article.

4

Mutation in gelsolin gene in Finnish hereditary amyloidosis.

Levy E, Haltia M, Fernandez-Madrid I, Koivunen O, Ghiso J, Prelli F, Frangione B. Levy E, et al. J Exp Med. 1990 Dec 1;172(6):1865-7. doi: 10.1084/jem.172.6.1865. J Exp Med. 1990. PMID: 2175344 Free PMC article.

5

Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187.

de la Chapelle A, Tolvanen R, Boysen G, Santavy J, Bleeker-Wagemakers L, Maury CP, Kere J. de la Chapelle A, et al. Nat Genet. 1992 Oct;2(2):157-60. doi: 10.1038/ng1092-157. Nat Genet. 1992. PMID: 1338910

6

Gelsolin gene mutation--at codon 187--in familial amyloidosis, Finnish: DNA-diagnostic assay.

Haltia M, Levy E, Meretoja J, Fernandez-Madrid I, Koivunen O, Frangione B. Haltia M, et al. Am J Med Genet. 1992 Feb 1;42(3):357-9. doi: 10.1002/ajmg.1320420321. Am J Med Genet. 1992. PMID: 1311149

7

Demonstration of a circulating 65K gelsolin variant specific for familial amyloidosis, Finnish type.

Maury CP, Rossi H. Maury CP, et al. Biochem Biophys Res Commun. 1993 Feb 26;191(1):41-4. doi: 10.1006/bbrc.1993.1181. Biochem Biophys Res Commun. 1993. PMID: 8383491

8

Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis.

Paunio T, Kiuru S, Hongell V, Mustonen E, Syvänen AC, Bengström M, Palo J, Peltonen L. Paunio T, et al. Genomics. 1992 May;13(1):237-9. doi: 10.1016/0888-7543(92)90235-k. Genomics. 1992. PMID: 1315718 No abstract available.

9

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.

Maury CP, Kere J, Tolvanen R, de la Chapelle A. Maury CP, et al. Genomics. 1992 Jul;13(3):902-3. doi: 10.1016/0888-7543(92)90183-s. Genomics. 1992. PMID: 1322360 No abstract available.

10

Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.

Ghiso J, Haltia M, Prelli F, Novello J, Frangione B. Ghiso J, et al. Biochem J. 1990 Dec 15;272(3):827-30. doi: 10.1042/bj2720827. Biochem J. 1990. PMID: 2176481 Free PMC article.

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