Literature DB >> 2846962

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

A Federico1, L Manneschi, M Meloni, C Alessandrini, A M Bardelli, M T Dotti, P Sabatelli.   

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Year:  1988        PMID： 2846962     DOI： 10.1007/bf01804233

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  7 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.  Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

Authors:  E Nikoskelainen; I E Hassinen; L Paljärvi; H Lang; H Kalimo
Journal:  Lancet       Date:  1984-12-22       Impact factor: 79.321

3.  Rhodanese-Mediated sulfur transfer to succinate dehydrogenase.

Authors:  F Bonomi; S Pagani; P Cerletti; C Cannella
Journal:  Eur J Biochem       Date:  1977-01-03

4.  Normal rhodanese activity in leukocytes from Leber patients: enzyme characterization and activity levels.

Authors:  R Pallini; P Martelli; A M Bardelli; G C Guazzi; A Federico
Journal:  Neurology       Date:  1987-12       Impact factor: 9.910

5.  Leber's disease and dystonia: a mitochondrial disease.

Authors:  E J Novotny; G Singh; D C Wallace; L J Dorfman; A Louis; R L Sogg; L Steinman
Journal:  Neurology       Date:  1986-08       Impact factor: 9.910

6.  Decreased thiosulfate sulfur transferase (rhodanese) in Leber's hereditary optic atrophy.

Authors:  B Cagianut; H P Schnebli; K Rhyner; J Furrer
Journal:  Klin Wochenschr       Date:  1984-09-17

7.  Leber's disease with spastic paraplegia and peripheral neuropathy. Case report with nerve biopsy study.

Authors:  M Pagès; A M Pagès
Journal:  Eur Neurol       Date:  1983       Impact factor: 1.710
  7 in total

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