Literature DB >> 6493496

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease.

E Nikoskelainen.   

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Year:  1984        PMID： 6493496     DOI： 10.1212/wnl.34.11.1482

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  12 in total

1.  Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).

Authors:  C Weiller; A Ferbert
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

Review 2.  Mitochondrial DNA and genetic disease.

Authors:  J Poulton
Journal:  Arch Dis Child       Date:  1988-08       Impact factor: 3.791

3.  Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis.

Authors:  J D Chen; I Cox; M J Denton
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

4.  Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.

Authors:  I J Holt; D H Miller; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-08       Impact factor: 10.154

5.  Central nervous system involvement in Leber's optic neuropathy.

Authors:  W Paulus; A Straube; W Bauer; A E Harding
Journal:  J Neurol       Date:  1993       Impact factor: 4.849

6.  Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.

Authors:  Y Kobayashi; H Sharpe; N Brown
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

7.  An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.

Authors:  N Howell; D McCullough
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

8.  Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

Authors:  A E Harding; M G Sweeney; G G Govan; P Riordan-Eva
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

Review 9.  Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and non-hereditary neuropathies, and review of the literature.

Authors:  J M Schröder; C Sommer
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

10.  Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy.

Authors:  B A Kormann; H Schuster; T A Berninger; B Leo-Kottler
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132
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