(Q40968900)

25 September 2017

1 reference

title

Ocular amyloidosis, with special reference to the hereditary forms with vitreous involvement (English)

1 reference

25 September 2017

Sandgren O

1

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25 September 2017

publication date

1 November 1995

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25 September 2017

published in

Survey of Ophthalmology

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25 September 2017

volume

40

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25 September 2017

issue

3

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25 September 2017

page(s)

173-196

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Hereditary amyloidosis with polyneuropathy

25 September 2017

cites work

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A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves

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7 January 2021

A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family

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7 January 2021

Generalized amyloid in a family of Swedish origin. A study of 426 family members in seven generations of a new kinship with neuropathy, nephropathy, and central nervous system involvement

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7 January 2021

Immunoglobulin deposition in localized conjunctival amyloidosis

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7 January 2021

Incidence of corneal crystals in the monoclonal gammopathies

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7 January 2021

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

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7 January 2021

Ophthalmologic Aspects of Amyloidosis

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7 January 2021

Pathology of ocular tissues in amyloidosis

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation

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7 January 2021

Electron Microscopic Observations on a Fibrous Component in Amyloid of Diverse Origins

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7 January 2021

Primary localized amyloidosis of the lacrimal glands

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7 January 2021

Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation

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7 January 2021

Cotton Wool Exudates in Systemic Amyloidosis

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7 January 2021

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

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7 January 2021

Pars plana vitrectomy for vitreous amyloidosis

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7 January 2021

Immunocytochemical demonstration of prealbumin in the vitreous in heredofamilial amyloidosis

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7 January 2021

Meretoja syndrome. Lattice dystrophy of the cornea with hereditary generalized amyloidosis

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7 January 2021

The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish population

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7 January 2021

Diagnosis of early lattice corneal dystrophy

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7 January 2021

[Retinal periartitis and generalized vasculitis]

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7 January 2021

Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Dissociated sensation in amylidosis. Compound action potential, quantitative histologic and teased-fiber, and electron microscopic studies of sural nerve biopsies

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

X-ray diffraction studies on amyloid filaments

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Orbital amyloidosis involving the extraocular muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Ocular manifestations of hereditary primary systemic amyloidosis

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Bilateral amyloidosis of the vitreous body: report of a case without systemic of familial involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary localized amyloidosis presenting as an eyelid margin tumor

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Clinically Atypical Granular Corneal Dystrophy with Pathologic Features of Lattice-like Amyloid Deposits

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

The Relationship Between Granular, Lattice Type 1, and Avellino Corneal Dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Amyloidosis of the cornea

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary gelatinous drop-like keratopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Amyloidotic Polyneuritis of Type III (Iowa-Van Allen)

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Amyloid deposits and amyloidosis. The beta-fibrilloses (first of two parts).

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Amyloid fibril proteins: proof of homology with immunoglobulin light chains by sequence analyses

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Extraocular muscle involvement in idiopathic primary amyloidosis

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Familial oculoleptomeningeal amyloidosis

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Prealbumin. A major constituent of vitreous amyloid

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7 January 2021

Unusual cause of vitreous opacities. Primary familial amyloidosis

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Secondary localized amyloidosis of the cornea caused by trichiasis

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7 January 2021

Transthyretin: a choroid plexus-specific transport protein in human brain. The 1986 S. Weir Mitchell award

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7 January 2021

Clinical features of a newly recognized type of lattice corneal dystrophy

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7 January 2021

Amyloidosis of corneal stroma in patients with trachoma. A clinicopathologic study of 62 cases.

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7 January 2021

Subepithelial corneal deposits in IgG lambda myeloma

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7 January 2021

Secondary corneal amyloidosis (author's transl)

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Vitreous opacities in primary amyloid disease. A clinical, histochemical, and ultrastructural report

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Avellino Corneal Dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary orbital amyloidosis localised to an extraocular muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Molecular genetics of amyloid neuropathy in Europe

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Chemical and clinical classification of amyloidosis 1985.

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7 January 2021

Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

[Primary isolated amyloidosis--a rare corneal degeneration]

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Familial primary amyloidosis with nervous system involvement

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary familial amyloidosis

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Vitreous Opacities Diagnostic of Familial Primary Amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Immunohistochemical analysis of lattice corneal dystrophies types I and II.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Studies on familial amyloid polyneuropathy in Ogawa Village, Japan

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Secondary corneal amyloidosis: clinical and pathohistological examinations

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7 January 2021

Multiple myeloma and its ocular manifestations

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7 January 2021

Sicca syndrome due to primary amyloidosis

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7 January 2021

Primary systemic amyloidosis

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7 January 2021

[Familial amyloidosis of the Andrade disease type in a Greek family]

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Genetic expression of a transthyretin mutation in a case of amyloidotic polyneuropathy occurring in an African.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Scalloped Pupils in Familial Amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

The Amino Acid Sequence of a Major Nonimmunoglobulin Component of Some Amyloid Fibrils

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Immunologic studies of the major nonimmunoglobulin protein of amyloid. I. Identification and partial characterization of a related serum component

1 reference

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7 January 2021

An Immunohistochemical Study of Gelsolin Immunoreactivity in Corneal Amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Apparent monoclonal origin of lymphocytes and plasma cells infiltrating ocular adnexal amyloid deposits: report of 2 cases

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7 January 2021

A new concept for vitreous surgery. 3. Indications and results

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7 January 2021

External ophthalmoplegia secondary to systemic amyloidosis

1 reference

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7 January 2021

Portuguese-type amyloid neuropathy in an English family

1 reference

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7 January 2021

Polymorphic amyloid degeneration of the cornea. A clinical and histopathologic study

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Localized conjunctival amyloidosis associated with extranodal lymphoma

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Transthyretin is synthesized in the mammalian eye

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7 January 2021

Climatic droplet keratopathy with corneal amyloidosis

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

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

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

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7 January 2021

Some histologic findings in keratoconus

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7 January 2021

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

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7 January 2021

Vitreous amyloidosis. Case report

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary familial amyloidosis of the cornea

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Structurally abnormal transthyretin causing familial amyloidotic polyneuropathy in Sweden

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary localized orbital amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

CONJUNCTIVAL AMYLOIDOSIS. A CASE WITH ASSOCIATED HYPERGLOBULINAEMIA

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary familial amyloidosis with vitreous opacities. Report of an autopsy case

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Pharmacological studies of the pupils in familial amyloid polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary amyloidosis with familial vitreous opacities: an unusual case and family

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Superficial granular corneal dystrophy with amyloid deposits

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Surgical management of advanced ocular adnexal amyloidosis

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https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

A variant of prealbumin from amyloid fibrils in familial polyneuropathy of Jewish origin

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Conjunctival involvement in primary systemic nonfamilial amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Complete Ophthalmoplegia Secondary to Amyloidosis Associated with Multiple Myeloma

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Secondary Amyloidosis in Ocular Leprosy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Gelsolin immunoreactivity in corneal amyloid, wound healing, and macular and granular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Phenotypic variation in combined granular-lattice (Avellino) corneal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Scalloped pupils in familial amyloid polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Vitreous amyloidosis without systemic or familial involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Conjunctival involvement in familial amyloidotic polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Restriction fragment length polymorphism analysis of mutated transthyretin in vitreous amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Vitreous surgery in patients with primary neuropathic amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Relation of vitreous amyloidosis to prealbumin

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Amyloidosis of the vitreous. Fluorescein angiographic findings and association with neovascularization

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Familial amyloid polyneuropathy: report of an autopsy case with neuropathy, vitreous opacities and polycystic kidney

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Peripheral neuropathy in familial primary amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

An unusual case of ocular involvement in primary systemic nonfamilial amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

A new transthyretin mutation associated with amyloidotic vitreous opacities. Asparagine for isoleucine at position 84

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Familial Mediterranean fever. A survey of 470 cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary amyloidosis associated with a novel heavy-chain fragment (AH amyloidosis)

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

CONJUNCTIVAL AMYLOIDOSIS IN ASSOCIATION WITH SYSTEMIC AMYLOID DISEASE. A CASE HISTORY

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Corneal amyloidosis associated with keratoconus

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Lattice corneal dystrophy type IIIA. Clinical and histopathologic correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Three autosomal dominant corneal dystrophies map to chromosome 5q

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese family

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary localized orbital amyloidosis composed of the immunoglobulin gamma heavy chain CH3 domain

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Polymorphic stromal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Occlusion of Choriocapillaris in Primary Nonfamilial Amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Secondary glaucoma accompanied with primary familial amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Fluorographical findings in familial primary amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg)

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Familial oculoleptomeningeal amyloidosis. Report of a new family with unusual features

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary systemic amyloidosis. An electron microscopic study of the vitreous

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Pars plana vitrectomy in a case of amyloidosis of the vitreous.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Sicca syndrome due to amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

[Neurohistological study of a case of reticular corneal dystrophy].

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

1 reference

7 January 2021

Gelatinous drop-like dystrophy. A form of primary corneal amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Fibril in senile systemic amyloidosis is derived from normal transthyretin

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Immunohistochemical identification of the AA protein in lattice dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Primary familial amyloidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Familial amyloid polyneuropathy in Taiwan: identification of transthyretin variant (Leu55-->Pro)

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

Haplotype analysis of familial amyloidotic polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6257%2895%2980025-5

7 January 2021

10.1016/S0039-6257(95)80025-5

Identifiers

DOI

1 reference

25 September 2017

1 reference