Literature DB >> 7155306

Mitochondrial cytopathy or Leigh's syndrome? Mitochondrial abnormalities in Spongiform encephalopathies.

J Egger, C J Wynne-Williams, M Erdohazi.   

Abstract

A boy with mitochondrial cytopathy and neuropathological changes of subacute necrotizing encephalopathy is reported. Conditions with abnormal mitochondria in muscle and/or brain are reviewed and the role of mitochondrial abnormalities in spongiform encephalopathies is discussed. It is suggested that electronmicroscopical and histochemical investigations of muscle tissue would be of value in patients with Leigh's syndrome or other forms of spongiform encephalopathies.

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Year:  1982        PMID: 7155306     DOI: 10.1055/s-2008-1059627

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  10 in total

Review 1.  Biochemistry and molecular biology of Canavan disease.

Authors:  R Matalon; K Michals-Matalon
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

2.  Cardiomyopathy associated with Leigh's disease.

Authors:  K Langes; H Frenzel; R Seitz; G Kluitmann
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

3.  Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome.

Authors:  P Runge; D Calver; J Marshall; D Taylor
Journal:  Br J Ophthalmol       Date:  1986-10       Impact factor: 4.638

4.  Leukoencephalopathy with swelling in children and adolescents: MRI patterns and differential diagnosis.

Authors:  M S van der Knaap; J Valk; P G Barth; L M Smit; B G van Engelen; P Tortori Donati
Journal:  Neuroradiology       Date:  1995-11       Impact factor: 2.804

5.  Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).

Authors:  B Kustermann-Kuhn; K Harzer; R Schröder; W Permanetter; J Peiffer
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Congenital Leigh's disease: panencephalomyelopathy and peripheral neuropathy.

Authors:  R J Seitz; K Langes; H Frenzel; G Kluitmann; W Wechsler
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

7.  Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase.

Authors:  A W Behbehani; H Goebel; G Osse; M Gabriel; U Langenbeck; J Berden; R Berger; R B Schutgens
Journal:  Eur J Pediatr       Date:  1984-11       Impact factor: 3.183

8.  A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.

Authors:  R S Howard; R Greenwood; J Gawler; F Scaravilli; C D Marsden; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-09       Impact factor: 10.154

9.  Brain lesions of the Leigh-type distribution associated with a mitochondriopathy of Pearson's syndrome: light and electron microscopic study.

Authors:  I Yamadori; A Kurose; S Kobayashi; M Ohmori; T Imai
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

10.  RML prions act through Mahogunin and Attractin-independent pathways.

Authors:  Teresa M Gunn; George A Carlson
Journal:  Prion       Date:  2013-05-31       Impact factor: 3.931

  10 in total

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