Literature DB >> 5507249

Hereditary amyloidosis with polyneuropathy.

R Andersson.   

Abstract

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Year:  1970        PMID: 5507249     DOI: 10.1111/j.0954-6820.1970.tb08009.x

Source DB:  PubMed          Journal:  Acta Med Scand        ISSN: 0001-6101


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  9 in total

Review 1.  Genetic factors in amyloidosis.

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

2.  A DNA test for Indiana/Swiss hereditary amyloidosis (FAP II).

Authors:  M R Wallace; P M Conneally; M D Benson
Journal:  Am J Hum Genet       Date:  1988-08       Impact factor: 11.025

3.  Ultrastructure of myocardium in familial heart block and peroneal muscular atrophy.

Authors:  J M Kay; W A Littler; J B Meade
Journal:  Br Heart J       Date:  1972-10

Review 4.  A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected.

Authors:  T Coelho; A Sousa; E Lourenço; J Ramalheira
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

5.  The sinoatrial node in familial amyloidosis with polyneuropathy. A clinico-pathological study of nine cases from northern Sweden.

Authors:  A Eriksson; P Eriksson; B O Olofsson; L E Thornell
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1984

Review 6.  Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met 30) gene. Pathological and immunohistochemical similarity to human familial amyloidotic polyneuropathy, type I.

Authors:  S Araki; S Yi; T Murakami; S Watanabe; S Ikegawa; K Takahashi; K Yamarnura
Journal:  Mol Neurobiol       Date:  1994-02       Impact factor: 5.590

7.  Familial amyloid polyneuropathy associated with transthyretin Gly42 mutation: a quantitative light and electron microscopic study of the peripheral nervous system.

Authors:  K Toyooka; H Fujimura; S Ueno; H Yoshikawa; M Kaido; T Nishimura; S Yorifuji; T Yanagihara
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

8.  Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77).

Authors:  M M Reilly; D Adams; M B Davis; G Said; A E Harding
Journal:  J Neurol       Date:  1995-10       Impact factor: 4.849

9.  Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.

Authors:  M R Wallace; F E Dwulet; P M Conneally; M D Benson
Journal:  J Clin Invest       Date:  1986-07       Impact factor: 14.808

  9 in total

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