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Literature DB >> 8936364

Characterization of basal ganglia dysfunction in Leber 'plus' disease.

C O Hanemann, H Hefter, G Schlaug, R J Seitz, H J Freund, R Benecke.

Abstract

Entities: Disease

Mesh：

Year: 1996 PMID： 8936364 DOI： 10.1007/bf00868531

Source DB: PubMed Journal: J Neurol ISSN： 0340-5354 Impact factor: 4.849

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19 in total

1. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.

Authors: A E Harding; M G Sweeney; D H Miller; C J Mumford; H Kellar-Wood; D Menard; W I McDonald; D A Compston
Journal: Brain Date: 1992-08 Impact factor: 13.501

2. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.

Authors: D R Johns; J Berman
Journal: Biochem Biophys Res Commun Date: 1991-02-14 Impact factor: 3.575

Review 3. The functional anatomy of basal ganglia disorders.

Authors: R L Albin; A B Young; J B Penney
Journal: Trends Neurosci Date: 1989-10 Impact factor: 13.837

4. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors: D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal: Science Date: 1988-12-09 Impact factor: 47.728

5. Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

Authors: B Obermaier-Kusser; B Lorenz; S Schubring; A Paprotta; K Zerres; T Meitinger; F Meire; P Cochaux; A Blankenagel; G Kommerell
Journal: Am J Hum Genet Date: 1994-11 Impact factor: 11.025

6. Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes.

Authors: R Benecke; P Strümper; H Weiss
Journal: Brain Date: 1993-12 Impact factor: 13.501

Characterization of basal ganglia dysfunction in Leber 'plus' disease.

1. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.

2. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.

Review 3. The functional anatomy of basal ganglia disorders.

4. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

5. Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

6. Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes.

Review 7. Leber's hereditary optic neuropathy. New genetic considerations.

8. Atypical Leber's hereditary optic neuropathy with molecular confirmation.

9. Platelet mitochondrial function in Leber's hereditary optic neuropathy.

10. Leber's hereditary optic neuropathy and complex I deficiency in muscle.

1. Varying Clinical Phenotypes of Mitochondrial DNA T12811C Mutation: A Case Series Report.