Haltia M - Search Results

1

Gelsolin variant and beta-amyloid co-occur in a case of Alzheimer's with Lewy bodies.

Haltia M, Ghiso J, Wisniewski T, Kiuru S, Miller D, Frangione B. Haltia M, et al. Neurobiol Aging. 1991 Jul-Aug;12(4):313-6. doi: 10.1016/0197-4580(91)90007-7. Neurobiol Aging. 1991. PMID: 1660109

2

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

3

Lewy bodies are immunoreactive with antibodies raised to gelsolin related amyloid-Finnish type.

Wisniewski T, Haltia M, Ghiso J, Frangione B. Wisniewski T, et al. Among authors: haltia m. Am J Pathol. 1991 May;138(5):1077-83. Am J Pathol. 1991. PMID: 1850958 Free PMC article.

4

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein.

Haltia M, Prelli F, Ghiso J, Kiuru S, Somer H, Palo J, Frangione B. Haltia M, et al. Biochem Biophys Res Commun. 1990 Mar 30;167(3):927-32. doi: 10.1016/0006-291x(90)90612-q. Biochem Biophys Res Commun. 1990. PMID: 2157434 Free article.

5

Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin.

Haltia M, Ghiso J, Prelli F, Gallo G, Kiuru S, Somer H, Palo J, Frangione B. Haltia M, et al. Am J Pathol. 1990 Jun;136(6):1223-8. Am J Pathol. 1990. PMID: 2162627 Free PMC article.

6

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. Among authors: haltia m. 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.

7

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

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

8

Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome.

Kivelä T, Tarkkanen A, Frangione B, Ghiso J, Haltia M. Kivelä T, et al. Among authors: haltia m. Invest Ophthalmol Vis Sci. 1994 Sep;35(10):3759-69. Invest Ophthalmol Vis Sci. 1994. PMID: 8088963

9

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, Purcell JJ Jr, Rodrigues M, Ghiso J, Levy E, Haltia M, Frangione B. Gorevic PD, et al. Among authors: haltia m. N Engl J Med. 1991 Dec 19;325(25):1780-5. doi: 10.1056/NEJM199112193252505. N Engl J Med. 1991. PMID: 1658654 Free article. No abstract available.

10

Immunohistochemical analysis of lattice corneal dystrophies types I and II.

Kivelä T, Tarkkanen A, McLean I, Ghiso J, Frangione B, Haltia M. Kivelä T, et al. Among authors: haltia m. Br J Ophthalmol. 1993 Dec;77(12):799-804. doi: 10.1136/bjo.77.12.799. Br J Ophthalmol. 1993. PMID: 8110676 Free PMC article.

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