Literature DB >> 6183406

Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy.

M Rimoldi, E Bottacchi, L Rossi, F Cornelio, G Uziel, S Di Donato.   

Abstract

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Year:  1982        PMID： 6183406     DOI： 10.1007/bf00313387

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  14 in total

1.  Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue.

Authors:  J L Willems; L A Monnens; J M Trijbels; J H Veerkamp; A E Meyer; K van Dam; U van Haelst
Journal:  Pediatrics       Date:  1977-12       Impact factor: 7.124

2.  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

3.  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

4.  Carnitine palmityltransferase. Location of two enzymatic activities in rat liver mitochondria.

Authors:  C L Hoppel; R J Tomec
Journal:  J Biol Chem       Date:  1972-02-10       Impact factor: 5.157

5.  A simple method for preparation of methyl-labelled (-) carnitine.

Authors:  O Stokke; J Bremer
Journal:  Biochim Biophys Acta       Date:  1970-12-15

6.  Fatal ataxic encephalopathy and carnitine acetyltransferase deficiency: a functional defect of pyruvate oxidation?

Authors:  S DiDonato; M Rimoldi; A Moise; B Bertagnoglio; G Uziel
Journal:  Neurology       Date:  1979-12       Impact factor: 9.910

7.  Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.

Authors:  S DiMauro; J R Mendell; Z Sahenk; D Bachman; A Scarpa; R M Scofield; C Reiner
Journal:  Neurology       Date:  1980-08       Impact factor: 9.910

Review 8.  Congenital hypotonia revisited.

Authors:  M H Brooke; J E Carroll; S P Ringel
Journal:  Muscle Nerve       Date:  1979 Mar-Apr       Impact factor: 3.217

9.  Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency.

Authors:  S Di Donato; F Cornelio; M R Balestrini; B Bertagnolio; D Peluchetti
Journal:  Neurology       Date:  1978-11       Impact factor: 9.910

10.  Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

Authors:  A M Seligman; M J Karnovsky; H L Wasserkrug; J S Hanker
Journal:  J Cell Biol       Date:  1968-07       Impact factor: 10.539
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  18 in total

1.  Foamy myocardial transformation in a child with a disturbed respiratory chain.

Authors:  H Böhles; H Singer; W Ruitenbeek; J M Trijbels; R C Sengers; U P Ketelsen; E Wagner-Thiessen; H Wick
Journal:  Eur J Pediatr       Date:  1987-11       Impact factor: 3.183

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

Review 3.  Primary lipid cardiomyopathy.

Authors:  A Zimmermann; P Wyss; F Stocker
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

4.  Cytochrome c oxidase deficiency in infancy.

Authors:  A Oldfors; H Sommerland; E Holme; M Tulinius; B Kristiansson
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

5.  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

6.  Muscle pathology in cytochrome c oxidase deficiency.

Authors:  I Nonaka; Y Koga; K Shikura; M Kobayashi; N Sugiyama; E Okino; K Nihei; M Tojo; M Segawa
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

7.  Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency.

Authors:  R C Sengers; J M Trijbels; J A Bakkeren; W Ruitenbeek; J C Fischer; A J Janssen; A M Stadhouders; H J ter Laak
Journal:  Eur J Pediatr       Date:  1984-01       Impact factor: 3.183

8.  Localization of PTP-1B, SHP-2, and Src exclusively in rat brain mitochondria and functional consequences.

Authors:  Amal Arachiche; Olivier Augereau; Marion Decossas; Claire Pertuiset; Etienne Gontier; Thierry Letellier; Jeanne Dachary-Prigent
Journal:  J Biol Chem       Date:  2008-06-26       Impact factor: 5.157

9.  Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.

Authors:  J Müller-Höcker; H Ibel; I Paetzke; T Deufel; W Endres; B Kadenbach; J M Gokel; G Hübner
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

Review 10.  Primary (genetic) cardiomyopathies in infancy. A survey of possible disorders and guidelines for diagnosis.

Authors:  A Kohlschütter; G Hausdorf
Journal:  Eur J Pediatr       Date:  1986-12       Impact factor: 3.183
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