Literature DB >> 7483605

MELAS syndrome.

S J Koga1, M Hodges, C Markin, P Gorman.   

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Year:  1995        PMID： 7483605      PMCID： PMC1303144     

Source DB:  PubMed          Journal:  West J Med        ISSN： 0093-0415


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  24 in total

1.  MELAS syndrome with mitochondrial tRNA(Leu)(UUR) mutation: correlation of clinical state, nerve conduction, and muscle 31P magnetic resonance spectroscopy during treatment with nicotinamide and riboflavin.

Authors:  A M Penn; J W Lee; P Thuillier; M Wagner; K M Maclure; M R Menard; L D Hall; N G Kennaway
Journal:  Neurology       Date:  1992-11       Impact factor: 9.910

2.  Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases.

Authors:  T P KEARNS; G P SAYRE
Journal:  AMA Arch Ophthalmol       Date:  1958-08

3.  Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.

Authors:  D N Hu; W Q Qui; B T Wu; L Z Fang; F Zhou; Y P Gu; Q H Zhang; J H Yan; Y Q Ding; H Wong
Journal:  J Med Genet       Date:  1991-02       Impact factor: 6.318

4.  A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors:  Y Goto; I Nonaka; S Horai
Journal:  Nature       Date:  1990-12-13       Impact factor: 49.962

5.  Inborn errors of metabolism: a new purview of internal medicine.

Authors:  S Segal; K S Roth
Journal:  Ann Intern Med       Date:  1994-02-01       Impact factor: 25.391

6.  Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Authors:  M Zeviani; C Gellera; C Antozzi; M Rimoldi; L Morandi; F Villani; V Tiranti; S DiDonato
Journal:  Lancet       Date:  1991-07-20       Impact factor: 79.321

7.  Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Authors:  C T Moraes; S DiMauro; M Zeviani; A Lombes; S Shanske; A F Miranda; H Nakase; E Bonilla; L C Werneck; S Servidei
Journal:  N Engl J Med       Date:  1989-05-18       Impact factor: 91.245

8.  The syndrome of mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes presenting without stroke.

Authors:  R K Mosewich; J R Donat; S DiMauro; E Ciafaloni; S Shanske; M Erasmus; D George
Journal:  Arch Neurol       Date:  1993-03

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.  Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.

Authors:  N Fukuhara; S Tokiguchi; K Shirakawa; T Tsubaki
Journal:  J Neurol Sci       Date:  1980-07       Impact factor: 3.181
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  1 in total

1.  MELAS syndrome associated with a new mitochondrial tRNA-Val gene mutation (m.1616A>G).

Authors:  Yuka Toyoshima; Yuji Tanaka; Kazuo Satomi
Journal:  BMJ Case Rep       Date:  2017-09-11
  1 in total

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