These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 5583094)

  • 1. Myopathy with abnormal structure and function of muscle mitochondria.
    Hulsmann WC; Bethlem J; Meijer AE; Fleury P; Schellens JP
    J Neurol Neurosurg Psychiatry; 1967 Dec; 30(6):519-25. PubMed ID: 5583094
    [No Abstract]   [Full Text] [Related]  

  • 2. Skeletal muscle disease with abnormal mitochondria.
    van Wijngaarden GK; Bethlem J; Meijer AE; Hülsmann WC; Feltkamp CA
    Brain; 1967 Sep; 90(3):577-92. PubMed ID: 6058143
    [No Abstract]   [Full Text] [Related]  

  • 3. Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy.
    Schellens JP; Ossentjuk E
    Virchows Arch B Cell Pathol; 1969; 4(1):21-9. PubMed ID: 4242998
    [No Abstract]   [Full Text] [Related]  

  • 4. Rare muscle diseases.
    van Wijngaarden GK
    S Afr Med J; 1972 Dec; 46(48):1884-9. PubMed ID: 4268850
    [No Abstract]   [Full Text] [Related]  

  • 5. Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency.
    Müller-Höcker J; Paetzke I; Pongratz D; Hübner G
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1985; 48(2):185-96. PubMed ID: 2859691
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Preliminary observations on 2 cases of so-called "mitochondrial myopathy"].
    Mazzarella L; De Giacomo P
    Boll Soc Ital Biol Sper; 1969 Feb; 45(4):230-2. PubMed ID: 5346806
    [No Abstract]   [Full Text] [Related]  

  • 7. [Myopathy with mitochondrial abnormalities localizated in type I fibers. Clinical, histochemical and ultrastructural data apropos of a diffuse atrophic form with ocular onset].
    Castaigne P; Laplane D; Fardeau M; Dordain G; Autret A; Hirt L
    Rev Neurol (Paris); 1972 Feb; 126(2):81-96. PubMed ID: 4654782
    [No Abstract]   [Full Text] [Related]  

  • 8. A new mitochondrial myopathy in a patient with salt craving.
    Spiro AJ; Prineas JW; Moore CL
    Arch Neurol; 1970 Mar; 22(3):259-69. PubMed ID: 4189219
    [No Abstract]   [Full Text] [Related]  

  • 9. Acute alcoholic myopathy. Enzyme histochemistry and electron microscopic findings.
    Martinez AJ; Hooshmand H; Faris AA
    J Neurol Sci; 1973 Nov; 20(3):245-52. PubMed ID: 4357768
    [No Abstract]   [Full Text] [Related]  

  • 10. [A case of congenital myopathy with mitochondrial abnormalities. Clinical and ultrastructural study].
    Vallat JM; Aubertin J; Julien J; Vital C; Leng B; Boget JC
    Sem Hop; 1973 Sep; 49(37):2475-82. PubMed ID: 4359500
    [No Abstract]   [Full Text] [Related]  

  • 11. Abnormal mitochondria on a renal biopsy from a case of mitochondrial myopathy.
    Thorner PS; Balfe JW; Becker LE; Baumal R
    Pediatr Pathol; 1985; 4(1-2):25-35. PubMed ID: 4095040
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Histoenzymatic and ultrastructural aspects of mitochondrial myopathy (mitochondriopathy)].
    Antoci B; Pizzolitto S
    Pathologica; 1984; 76(1046):655-68. PubMed ID: 6537477
    [No Abstract]   [Full Text] [Related]  

  • 13. A cytochrome-related inherited disorder of the nervous system and muscle.
    Spiro AJ; Moore CL; Prineas JW; Strasberg PM; Rapin I
    Arch Neurol; 1970 Aug; 23(2):103-12. PubMed ID: 5430330
    [No Abstract]   [Full Text] [Related]  

  • 14. Late-onset hereditary myopathy with abnormal mitochondria and progressive dementia.
    Vilming ST; Dietrichson P; Isachsen MM; Løvvik L; Heiberg A
    Acta Neurol Scand; 1986 May; 73(5):502-6. PubMed ID: 3727928
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Ultrastructure and topochemistry of giant mitochondria and their inclusions in myopathies].
    Sluga E; Monneron A
    Virchows Arch A Pathol Pathol Anat; 1970; 350(3):250-60. PubMed ID: 4318563
    [No Abstract]   [Full Text] [Related]  

  • 16. Familial myopathy with abnormal muscle mitochondria.
    D'Agostino AN; Ziter FA; Rallison ML; Bray PF
    Arch Neurol; 1968 Apr; 18(4):388-401. PubMed ID: 5638542
    [No Abstract]   [Full Text] [Related]  

  • 17. Fingerprint body myopathy, a newly recognized congenital muscle disease.
    Engel AG; Angelini C; Gomez MR
    Mayo Clin Proc; 1972 Jun; 47(6):377-88. PubMed ID: 4339422
    [No Abstract]   [Full Text] [Related]  

  • 18. [A case of nemaline myopathy with abnormal mitochondria].
    Tanaka T; Yoshimoto M; Shirai K; Kinoshita S; Watanabe M; Yoshimura T; Tsujihata M
    No To Hattatsu; 1984 Nov; 16(6):476-80. PubMed ID: 6097295
    [No Abstract]   [Full Text] [Related]  

  • 19. Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.
    Engel AG; Gomez MR; Groover RV
    Mayo Clin Proc; 1971 Oct; 46(10):666-81. PubMed ID: 5115748
    [No Abstract]   [Full Text] [Related]  

  • 20. Myopathy associated with abnormal lipid metabolism in skeletal muscle.
    Bradley WG; Hudgson P; Gardner-Medwin D; Walton JN
    Lancet; 1969 Mar; 1(7593):495-8. PubMed ID: 4179573
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.