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Academic Journal

The novel form of amyloidosis derived from EGF-containing fibulin-like extracellular matrix protein 1 (EFEMP1) preferentially affects the lower gastrointestinal tract of elderly females a .

  • Authors : Dao LN; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.; Kurtin PJ

Subjects: Amyloidosis*/Amyloidosis*/Amyloidosis*/diagnosis ; Amyloidosis*/Amyloidosis*/Amyloidosis*/pathology; Extracellular Matrix Proteins/Extracellular Matrix Proteins/Extracellular Matrix Proteins/*metabolism

  • Source: Histopathology [Histopathology] 2021 Feb; Vol. 78 (3), pp. 459-463. Date of Electronic Publication: 2020 Nov 28.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 7704136 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

A novel age-related venous amyloidosis derived from EGF-containing fibulin-like extracellular matrix protein 1.

  • Authors : Tasaki M; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.; Department of Morphological and Physiological Sciences, Graduate School of Health Sciences, Kumamoto University, Kumamoto, Japan.

Subjects: Amyloidosis/Amyloidosis/Amyloidosis/*etiology ; Extracellular Matrix Proteins/Extracellular Matrix Proteins/Extracellular Matrix Proteins/*metabolism ; Vascular Diseases/Vascular Diseases/Vascular Diseases/*etiology

  • Source: The Journal of pathology [J Pathol] 2019 Apr; Vol. 247 (4), pp. 444-455. Date of Electronic Publication: 2018 Dec 21.Publisher: John Wiley And Sons Country of Publication: England NLM ID: 0204634 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Heavy-chain amyloidosis in TGFBI-negative and gelsolin-negative atypical lattice corneal dystrophy.

  • Authors : Pradhan MA; Department of Ophthalmology, New Zealand National Eye Centre, University of Auckland, New Zealand.; Henderson RA

Subjects: Amyloid/Amyloid/Amyloid/*metabolism ; Amyloidosis/Amyloidosis/Amyloidosis/*diagnosis ; Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/*diagnosis Meretoja syndrome

  • Source: Cornea [Cornea] 2011 Oct; Vol. 30 (10), pp. 1163-6.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8216186 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.

  • Authors : Takács L; Department of Ophthalmology, University of Debrecen, Medical and Health Science Center, Debrecen, Hungary. ; Losonczy G

Subjects: Mutation* ; Phenylalanine* ; Serine*

  • Source: Molecular vision [Mol Vis] 2007 Oct 18; Vol. 13, pp. 1976-83. Date of Electronic Publication: 2007 Oct 18.Publisher: Molecular Vision Country of Publication: United States NLM ID: 9605351 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Keratoepithelin in secondary corneal amyloidosis.

  • Authors : Suesskind D; Department of Ophthalmology, University of Tuebingen, Schleichstrasse 12-16, 72076 Tuebingen, Germany. ; Auw-Haedrich C

Subjects: Amyloidosis/Amyloidosis/Amyloidosis/*metabolism ; Corneal Diseases/Corneal Diseases/Corneal Diseases/*metabolism ; Extracellular Matrix Proteins/Extracellular Matrix Proteins/Extracellular Matrix Proteins/*metabolism

  • Source: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie [Graefes Arch Clin Exp Ophthalmol] 2006 Jun; Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 8205248 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene.

  • Authors : Eifrig DE Jr; Department of Ophthalmology, Duke University Medical Center, Durham, North Carolina, USA.; Afshari NA

Subjects: Mutation, Missense*; Amyloidosis/Amyloidosis/Amyloidosis/*genetics ; Corneal Diseases/Corneal Diseases/Corneal Diseases/*genetics

  • Source: Ophthalmology [Ophthalmology] 2004 Jun; Vol. 111 (6), pp. 1108-14.Publisher: Elsevier Country of Publication: United States NLM ID: 7802443 Publication Model: Print Cited Medium: Print ISSN: 0161-6420 (Print)

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Academic Journal

[BIG-H3 protein: mutation of codon 124 and corneal amyloidosis].

Subjects: Mutation*; Amyloidosis/Amyloidosis/Amyloidosis/*genetics ; Codon/Codon/Codon/*genetics

  • Source: Journal francais d'ophtalmologie [J Fr Ophtalmol] 2004 May; Vol. 27 (5), pp. 510-22.Publisher: Masson Country of Publication: France NLM ID: 7804128 Publication Model: Print Cited Medium: Print ISSN: 0181-5512 (Print) Linking

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Academic Journal

Corneal amyloidosis caused by Leu518Pro mutation of betaig-h3 gene.

  • Authors : Hirano K; Department of Ophthalmology, Nagoya University School of Medicine, Aichi, Japan. ; Hotta Y

Subjects: Extracellular Matrix Proteins* ; Point Mutation* ; Transforming Growth Factor beta*

  • Source: The British journal of ophthalmology [Br J Ophthalmol] 2000 Jun; Vol. 84 (6), pp. 583-5.Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 0421041 Publication Model: Print Cited Medium: Print ISSN: 0007-1161 (Print)

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Academic Journal

Unique TGFBI protein in lattice corneal dystrophy.

  • Authors : Han YP; Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri 63110, USA.; Sim AJ

Subjects: Amyloidosis/Amyloidosis/Amyloidosis/*metabolism ; Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/*metabolism ; Extracellular Matrix Proteins/Extracellular Matrix Proteins/Extracellular Matrix Proteins/*metabolism

  • Source: Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2011 Oct 28; Vol. 52 (11), pp. 8401-6. Date of Electronic Publication: 2011 Oct 28.Publisher: Association For Research In Vision And Ophthalmology (Arvo) Country of Publication: United States NLM ID: 7703701 Publication Model: Electronic

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