Immunohistochemical analysis of lattice corneal dystrophies types I and II. (Q37304076)

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25 October 2019

title

Immunohistochemical analysis of lattice corneal dystrophies types I and II (English)

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25 October 2019

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1

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25 October 2019

author name string

A Tarkkanen

2

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25 October 2019

I McLean

3

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25 October 2019

J Ghiso

4

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25 October 2019

B Frangione

5

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25 October 2019

M Haltia

6

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25 October 2019

language of work or name

English

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publication date

1 December 1993

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25 October 2019

number of pages

6

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British Journal of Ophthalmology

inferred from page(s)

published in

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25 October 2019

volume

77

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25 October 2019

issue

12

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25 October 2019

page(s)

799-804

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Unilateral lattice dystrophy of the cornea

25 October 2019

cites work

1 reference

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Lattice corneal dystrophy: a source of confusion

6 September 2017

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The actin filament-severing domain of plasma gelsolin

6 September 2017

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Genomic organization and biosynthesis of secreted and cytoplasmic forms of gelsolin

6 September 2017

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

6 September 2017

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Mutation in gelsolin gene in Finnish hereditary amyloidosis

6 September 2017

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

6 September 2017

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

6 September 2017

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

6 September 2017

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Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I

6 September 2017

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

6 September 2017

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

6 September 2017

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Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

6 September 2017

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6 September 2017

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Immunohistochemical identification of the AA protein in lattice dystrophy

14 September 2017

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Corneal dystrophies. I. Dystrophies of the epithelium, Bowman's layer and stroma

28 September 2017

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Lack of evidence for protein AA reactivity in amyloid deposits of lattice corneal dystrophy and amyloid corneal degeneration.

28 September 2017

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Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy

26 June 2018

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Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome

26 June 2018

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Lattice corneal dystrophy. An inherited variety of amyloidosis restricted to the cornea

26 June 2018

1 reference

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An hereditary syndrome consisting of peripheral polyneuropathy, skin changes and lattice-shaped corneal dystrophy

26 June 2018

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Histopathologic and immunochemical features of lattice corneal dystrophy type III.

26 June 2018

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

26 June 2018

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Human serum amyloid P is a multispecific adhesive protein whose ligands include 6-phosphorylated mannose and the 3-sulphated saccharides galactose, N-acetylgalactosamine and glucuronic acid

26 June 2018

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Antigenic profile of the human lacrimal gland

26 June 2018

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Protein AA and lattice corneal dystrophy.

26 June 2018

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Clinical and histopathologic studies of two families with lattice corneal dystrophy and familial systemic amyloidosis (Meretoja syndrome).

2 September 2018

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

2 September 2018

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12 December 2020

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

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12 December 2020

Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin

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12 December 2020

Clinical features of a newly recognized type of lattice corneal dystrophy

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12 December 2020

Primary hereditary systemic amyloidosis (Meretoja's syndrome): clinical features and treatment by plastic surgery

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12 December 2020

Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline

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12 December 2020

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II

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12 December 2020

Creation of amyloid fibrils from mutant Asn187 gelsolin peptides

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12 December 2020

An Immunohistochemical Study of Gelsolin Immunoreactivity in Corneal Amyloidosis

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12 December 2020

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

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12 December 2020

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12 December 2020

Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation. Report on three cases

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12 December 2020

Comparative histopathological and clinical findings in eyes with lattice corneal dystrophy of two different types

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12 December 2020

Three forms of dominant amyloid neuropathy

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12 December 2020

Recurrence of lattice corneal dystrophy type 1 in the corneal grafts of two siblings

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12 December 2020

C-reactive protein in human lattice corneal dystrophy

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12 December 2020

Lattice corneal dystrophy associated with familial systemic amyloidosis (Meretoja's syndrome)

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12 December 2020

Identifiers

DOI

10.1136/BJO.77.12.799

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8110676 AND SRC:MED&resulttype=core&format=json

25 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8110676 AND SRC:MED&resulttype=core&format=json

25 October 2019

PubMed publication ID

8110676

1 reference