Literature DB >> 6151084

Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

E Nikoskelainen, I E Hassinen, L Paljärvi, H Lang, H Kalimo.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1984        PMID： 6151084     DOI： 10.1016/s0140-6736(84)91669-6

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  9 in total

1.  Deficiency of thiosulphate sulphurtransferase (rhodanese) in Leber's hereditary optic neuropathy.

Authors:  C J Poole; P R Kind
Journal:  Br Med J (Clin Res Ed)       Date:  1986-05-10

2.  Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy.

Authors:  A Federico; L Manneschi; M Meloni; C Alessandrini; A M Bardelli; M T Dotti; P Sabatelli
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.

Authors:  J Vilkki; M L Savontaus; E K Nikoskelainen
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

4.  Magnetic resonance imaging in Leber's optic neuropathy.

Authors:  A G Kermode; I F Moseley; B E Kendall; D H Miller; D G MacManus; W I McDonald
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-05       Impact factor: 10.154

5.  Leber's hereditary optic atrophy: further evidence for a defect of cyanide metabolism?

Authors:  T A Berninger; L von Meyer; E Siess; O Schon; F D Goebel
Journal:  Br J Ophthalmol       Date:  1989-04       Impact factor: 4.638

6.  Rhodanese isozymes in three subjects with Leber's optic neuropathy.

Authors:  D B Whitehouse; C J Poole; P R Kind; D A Hopkinson
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 7.  Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.

Authors:  P Riordan-Eva; A E Harding
Journal:  J Med Genet       Date:  1995-02       Impact factor: 6.318

8.  Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy.

Authors:  J Vilkki; M L Savontaus; H Kalimo; E K Nikoskelainen
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

Review 9.  Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review.

Authors:  C Geny; V Cormier; C Meyrignac; P Cesaro; J D Degos; R Gherardi; A Rötig
Journal:  J Neurol       Date:  1991-06       Impact factor: 4.849
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.