Literature DB >> 7574881

Investigation of mitochondrial disease.

J Poulton1, G K Brown.   

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Year:  1995        PMID： 7574881      PMCID： PMC1511186          DOI： 10.1136/adc.73.2.94-a

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


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  24 in total

Review 1.  Biogenesis of mitochondria.

Authors:  G Attardi; G Schatz
Journal:  Annu Rev Cell Biol       Date:  1988

2.  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

3.  A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.

Authors:  D D de Vries; B G van Engelen; F J Gabreëls; W Ruitenbeek; B A van Oost
Journal:  Ann Neurol       Date:  1993-09       Impact factor: 10.422

4.  Noninvasive diagnosis of the MELAS syndrome from blood DNA.

Authors:  J Poulton; K Morten
Journal:  Ann Neurol       Date:  1993-07       Impact factor: 10.422

5.  Multiple deletions of mtDNA in two brothers with sideroblastic anemia and mitochondrial myopathy and in their asymptomatic mother.

Authors:  J Casademont; A Barrientos; F Cardellach; A Rötig; J M Grau; J Montoya; B Beltrán; F Cervantes; C Rozman; X Estivill
Journal:  Hum Mol Genet       Date:  1994-11       Impact factor: 6.150

6.  Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.

Authors:  T R Prezant; J V Agapian; M C Bohlman; X Bu; S Oztas; W Q Qiu; K S Arnos; G A Cortopassi; L Jaber; J I Rotter
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

Review 7.  The expanding clinical spectrum of mitochondrial diseases.

Authors:  D C De Vivo
Journal:  Brain Dev       Date:  1993 Jan-Feb       Impact factor: 1.961

8.  Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.

Authors:  N Fischel-Ghodsian; T R Prezant; X Bu; S Oztas
Journal:  Am J Otolaryngol       Date:  1993 Nov-Dec       Impact factor: 1.808

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.  Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

Authors:  J Poulton; K J Morten; K Weber; G K Brown; L Bindoff
Journal:  Hum Mol Genet       Date:  1994-06       Impact factor: 6.150
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  3 in total

1.  Pulmonary hypertension--a new manifestation of mitochondrial disease.

Authors:  A R Barclay; G Sholler; J Christodolou; A Shun; S Arbuckle; S Dorney; M O Stormon
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

Review 2.  Advances in genetics.

Authors:  M M Lees; R M Winter
Journal:  Arch Dis Child       Date:  1996-10       Impact factor: 3.791

Review 3.  Pulmonary hypertension as a manifestation of mitochondrial disease: A case report and review of the literature.

Authors:  Shan Xu; Xiaoling Xu; Jisong Zhang; Kejing Ying; Yuquan Shao; Ruifeng Zhang
Journal:  Medicine (Baltimore)       Date:  2017-11       Impact factor: 1.889
  3 in total

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