Literature DB >> 3046511

Mitochondrial DNA and genetic disease.

J Poulton1.   

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Year:  1988        PMID： 3046511      PMCID： PMC1778996          DOI： 10.1136/adc.63.8.883

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  19 in total

1.  Blood dyscrasias attributed to chloramphenicol. A review of 576 published and unpublished cases.

Authors:  B C Polak; H Wesseling; D Schut; A Herxheimer; L Meyler
Journal:  Acta Med Scand       Date:  1972-11

2.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Authors:  S G Pavlakis; P C Phillips; S DiMauro; D C De Vivo; L P Rowland
Journal:  Ann Neurol       Date:  1984-10       Impact factor: 10.422

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

Authors:  E Nikoskelainen
Journal:  Neurology       Date:  1984-11       Impact factor: 9.910

4.  Visually evoked responses.

Authors:  G Hosking
Journal:  Arch Dis Child       Date:  1984-01       Impact factor: 3.791

5.  A female case of glycogen storage myopathy due to phosphorylase kinase deficiency.

Authors:  Y Ohtani; I Matsuda; T Iwamasa
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

6.  Mitochondrial inheritance in a mitochondrially mediated disease.

Authors:  J Egger; J Wilson
Journal:  N Engl J Med       Date:  1983-07-21       Impact factor: 91.245

7.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

8.  Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

Authors:  H S Rosing; L C Hopkins; D C Wallace; C M Epstein; K Weidenheim
Journal:  Ann Neurol       Date:  1985-03       Impact factor: 10.422

9.  Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

Authors:  I J Holt; A E Harding; J A Morgan-Hughes
Journal:  Nature       Date:  1988-02-25       Impact factor: 49.962

10.  Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance.

Authors:  S E Kearsey; I W Craig
Journal:  Nature       Date:  1981-04-16       Impact factor: 49.962
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  5 in total

1.  Congenital myotonic dystrophy and mtDNA.

Authors:  J Poulton
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

2.  Departure of human mitochondrial DNA variation from neutral expectations: an alternative explanation.

Authors:  M Stoneking
Journal:  J Mol Evol       Date:  1990-10       Impact factor: 2.395

3.  Genetic risks for children of women with myotonic dystrophy.

Authors:  M C Koch; T Grimm; H G Harley; P S Harper
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

4.  Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded protein.

Authors:  P G Barth; P A Bolhuis; F A Wijburg; K M Sinjorgo; W Ruitenbeek; R B Schutgens
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

5.  Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy.

Authors:  J Poulton; H G Harley; J Dasmahapatra; G K Brown; C G Potter; B Sykes
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318
  5 in total

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