Literature DB >> 6329761

Mitochondrial myopathies. Clinical, morphological and biochemical aspects.

R C Sengers, A M Stadhouders, J M Trijbels.   

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Year:  1984        PMID： 6329761     DOI： 10.1007/bf00572761

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  105 in total

1.  Enzymic activities of human skeletal muscle mitochondria: a tool in clinical metabolic research.

Authors:  L ERNSTER; D IKKOS; R LUFT
Journal:  Nature       Date:  1959-12-12       Impact factor: 49.962

2.  A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study.

Authors:  R LUFT; D IKKOS; G PALMIERI; L ERNSTER; B AFZELIUS
Journal:  J Clin Invest       Date:  1962-09       Impact factor: 14.808

3.  Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles.

Authors:  J P Van Biervliet; L Bruinvis; D Ketting; P K De Bree; C Van der Heiden; S K Wadman
Journal:  Pediatr Res       Date:  1977-10       Impact factor: 3.756

4.  Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy.

Authors:  F Jerusalem; C Angelini; A G Engel; R V Groover
Journal:  Arch Neurol       Date:  1973-09

5.  Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings.

Authors:  M Worsfold; D C Park; R J Pennington
Journal:  J Neurol Sci       Date:  1973-07       Impact factor: 3.181

6.  An electron-microscope study of muscle degeneration and vascular changes in polymyositis.

Authors:  S A Shafiq; A T Milhorat; M A Gorycki
Journal:  J Pathol Bacteriol       Date:  1967-07

7.  A familial mitochondrial myopathy with central defect in neural transmission.

Authors:  S A Barron; R R Heffner; R Zwirecki
Journal:  Arch Neurol       Date:  1979-09

8.  [Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].

Authors:  G Spalke; R Heene; D Herold
Journal:  J Neurol       Date:  1975       Impact factor: 4.849

9.  Percutaneous needle biopsy of skeletal muscle in childhood.

Authors:  R C Sengers; A M Stadhouders; S L Notermans
Journal:  Eur J Pediatr       Date:  1980-10       Impact factor: 3.183

10.  [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)].

Authors:  J Roger; J F Pellissier; C Dravet; M Bureau-Paillas; M Arnoux; J L Larrieu
Journal:  Rev Neurol (Paris)       Date:  1982       Impact factor: 2.607
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  39 in total

1.  Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.

Authors:  H R Scholte; H F Busch; I E Luyt-Houwen; M H Vaandrager-Verduin; H Przyrembel; W F Arts
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder.

Authors:  A Bardosi; W Creutzfeldt; S DiMauro; K Felgenhauer; R L Friede; H H Goebel; A Kohlschütter; G Mayer; G Rahlf; S Servidei
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

3.  A carnitine/acylcarnitine translocase assay applicable to biopsied muscle specimens without requiring mitochondrial isolation.

Authors:  M S Murthy; V S Kamanna; S V Pande
Journal:  Biochem J       Date:  1986-05-15       Impact factor: 3.857

4.  Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

Authors:  D M Slipetz; J R Aprille; P R Goodyer; R Rozen
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

Review 5.  Mitochondrial disorders and the kidney.

Authors:  P Niaudet
Journal:  Arch Dis Child       Date:  1998-04       Impact factor: 3.791

6.  Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Authors:  C Doriguzzi; L Palmucci; T Mongini; N Bresolin; L Bet; G Comi; R Lala
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-01       Impact factor: 10.154

7.  Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.

Authors:  M Kobayashi; H Morishita; N Sugiyama; K Yokochi; M Nakano; Y Wada; Y Hotta; A Terauchi; I Nonaka
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

8.  A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.

Authors:  P M Van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; H J Ter Laak; A M Stadhouders
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-05       Impact factor: 10.154

9.  Translation rates of isolated liver mitochondria under conditions of hepatic mitochondrial proliferation.

Authors:  E P Brass
Journal:  Biochem J       Date:  1992-11-15       Impact factor: 3.857

10.  Clinical aspects of mitochondrial disorders.

Authors:  A Munnich; P Rustin; A Rötig; D Chretien; J P Bonnefont; C Nuttin; V Cormier; A Vassault; P Parvy; J Bardet
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
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