Literature DB >> 4107704

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

J Meretoja, L Teppo.   

Abstract

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Year:  1971        PMID： 4107704     DOI： 10.1111/j.1699-0463.1971.tb01841.x

Source DB:  PubMed          Journal:  Acta Pathol Microbiol Scand A        ISSN： 0365-4184


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  9 in total

1.  Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.

Authors:  G Boysen; G Galassi; Z Kamieniecka; J Schlaeger; W Trojaborg
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-11       Impact factor: 10.154

Review 2.  Genetic factors in amyloidosis.

Authors:  P K Thomas
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

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

Authors:  M Haltia; J Ghiso; F Prelli; G Gallo; S Kiuru; H Somer; J Palo; B Frangione
Journal:  Am J Pathol       Date:  1990-06       Impact factor: 4.307

Review 4.  The cornea--structure and macromolecules in health and disease. A review.

Authors:  G K Klintworth
Journal:  Am J Pathol       Date:  1977-12       Impact factor: 4.307

5.  Bilateral amyloidosis of the vitreous body without systemic involvement.

Authors:  T W Lieberman; A P Ferry
Journal:  Trans Am Ophthalmol Soc       Date:  1974

6.  Idiopathic AA amyloidosis manifested by autonomic neuropathy, vestibulocochleopathy, and lattice corneal dystrophy.

Authors:  I Tsunoda; H Awano; H Kayama; T Tsukamoto; S Ueno; T Fujiwara; M Watanabe; T Yamamoto
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-05       Impact factor: 10.154

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

Authors:  J Ghiso; M Haltia; F Prelli; J Novello; B Frangione
Journal:  Biochem J       Date:  1990-12-15       Impact factor: 3.857

8.  Immunohistochemical analysis of lattice corneal dystrophies types I and II.

Authors:  T Kivelä; A Tarkkanen; I McLean; J Ghiso; B Frangione; M Haltia
Journal:  Br J Ophthalmol       Date:  1993-12       Impact factor: 4.638

9.  Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases.

Authors:  Shuichiro Yamanaka; Yoichi Miyazaki; Kenji Kasai; Shu-Ichi Ikeda; Sari Kiuru-Enari; Tatsuo Hosoya
Journal:  Clin Kidney J       Date:  2013-04
  9 in total

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