Literature DB >> 4910907

Subacute necrotizing encephalomyelopathy (LEIGH).

K Jellinger, F Seitelberger.   

Abstract

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Year:  1970        PMID： 4910907     DOI： 10.1007/978-3-642-95138-1_4

Source DB:  PubMed          Journal:  Ergeb Inn Med Kinderheilkd        ISSN： 0071-111X


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  10 in total

1.  Wernicke's encephalopathy: an experimental study in the rhesus monkey.

Authors:  N K Blank; N A Vick; S Schulman
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

2.  A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.

Authors:  P M Van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; H J Ter Laak; A M Stadhouders
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-05       Impact factor: 10.154

3.  Acute gliopathy in spinal cord and brain stem induced by 6-aminonicotinamide.

Authors:  H Schneider; J Cervos-Navarro
Journal:  Acta Neuropathol       Date:  1974-02-07       Impact factor: 17.088

4.  [Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing encephalopathy].

Authors:  F Goutieres; J Aicardi; E Farkas-Bargeton
Journal:  Acta Neuropathol       Date:  1974       Impact factor: 17.088

5.  Spongy glio-neuronal dystrophy in infancy and childhood.

Authors:  K Jellinger; F Seitelberger
Journal:  Acta Neuropathol       Date:  1970       Impact factor: 17.088

6.  Adult form of Leigh's disease: a clinico pathological case with CT scan examination.

Authors:  F Gray; F Louarn; R Gherardi; J F Eizenbaum; C Marsault
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-11       Impact factor: 10.154

7.  [Juvenile type of subacute necrotizing encephalomyelinopathy (Leigh) with unusual CNS-localisation].

Authors:  R Lahl
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

8.  Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome.

Authors:  Martine Tetreault; Somayyeh Fahiminiya; Hana Antonicka; Grant A Mitchell; Michael T Geraghty; Matthew Lines; Kym M Boycott; Eric A Shoubridge; John J Mitchell; Jacques L Michaud; Jacek Majewski
Journal:  Hum Genet       Date:  2015-06-23       Impact factor: 4.132

9.  Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.

Authors:  P M van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; K J Lamers; J L Sloof
Journal:  J Neurol       Date:  1987-05       Impact factor: 4.849

10.  Microcephaly with peculiar demyelination mimicking Pelizaeus-Merzbacher disease.

Authors:  S Kamoshita; M Igarashi; R Kono
Journal:  Acta Neuropathol       Date:  1977-09-26       Impact factor: 17.088
  10 in total

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