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 *

135 related articles for article (PubMed ID: 619006)

  • 1. Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease.
    Scarlato G; Pellegrini G; Veicsteinas A
    J Neuropathol Exp Neurol; 1978 Jan; 37(1):1-12. PubMed ID: 619006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial oculoskeletal myopathy: case report.
    Colombo A; Merelli E; Sola P; Panzetti P; Quaglino D; Fornieri C
    Ital J Neurol Sci; 1988 Aug; 9(4):385-9. PubMed ID: 2851565
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Childhood mitochondrial myopathy with ophthalmoplegia.
    Land JM; Hockaday JM; Hughes JT; Ross BD
    J Neurol Sci; 1981 Sep; 51(3):371-82. PubMed ID: 7276984
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of oculocraniosomatic neuromuscular disease with "ragged-red" fibers].
    Matsubara S; Yasuda A; Komai K; Okumura S; Takamori M
    Rinsho Shinkeigaku; 1984 Mar; 24(3):221-9. PubMed ID: 6467743
    [No Abstract]   [Full Text] [Related]  

  • 5. Oculo cranio-somatic syndrome: mitochondrial alterations and lactic acidemia.
    Angelini C; Armani M; Lücke S; Negrin P
    Acta Neurol (Napoli); 1979 Feb; 1(1):59-63. PubMed ID: 433682
    [No Abstract]   [Full Text] [Related]  

  • 6. Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.
    Egger J; Lake BD; Wilson J
    Arch Dis Child; 1981 Oct; 56(10):741-52. PubMed ID: 7305411
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial abnormalities in progressive external ophthalmoplegia.
    Hyman BN; Patten BM; Dodson RF
    Am J Ophthalmol; 1977 Mar; 83(3):362-71. PubMed ID: 848542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myopathy with mitochondrial inclusion bodies: histological and metabolic studies.
    Sulaiman WR; Doyle D; Johnson RH; Jennett S
    J Neurol Neurosurg Psychiatry; 1974 Nov; 37(11):1236-46. PubMed ID: 4376164
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis].
    Beyenburg S; von Wersebe O; Zierz S
    Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A familial mitochondrial myopathy with central defect in neural transmission.
    Barron SA; Heffner RR; Zwirecki R
    Arch Neurol; 1979 Sep; 36(9):553-6. PubMed ID: 224846
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria.
    Tamura K; Santa T; Kuroiwa Y
    Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795
    [No Abstract]   [Full Text] [Related]  

  • 12. Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism.
    Reske-Nielsen E; Lou HC; Lowes M
    Acta Ophthalmol (Copenh); 1976 Oct; 54(5):553-73. PubMed ID: 185877
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neuropathy and mitochondrial myopathy.
    Peyronnard JM; Charron L; Bellavance A; Marchand L
    Ann Neurol; 1980 Mar; 7(3):262-8. PubMed ID: 6252825
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuromuscular disorders with abnormal muscle mitochondria.
    Kamieniecka Z; Schmalbruch H
    Int Rev Cytol; 1980; 65():321-57. PubMed ID: 6993406
    [No Abstract]   [Full Text] [Related]  

  • 15. Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven cases.
    Pellegrini G; Scarlato G; Moggio M
    Acta Neuropathol Suppl; 1981; 7():317-9. PubMed ID: 6939262
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Morphological study of muscle fibers stained red by modified Gomori trichrome staining with special reference to smooth red fibers].
    Yoshida K
    Hokkaido Igaku Zasshi; 1997 Mar; 72(2):163-80. PubMed ID: 9145310
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial myopathy in Marinesco-Sjögren syndrome.
    Torbergsen T; Aasly J; Borud O; Lindal S; Mellgren SI
    J Ment Defic Res; 1991 Apr; 35 ( Pt 2)():154-9. PubMed ID: 2072394
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Oculocraniosomatic neuromuscular disease, a multisystem disease with abnormal mitochondria demonstrated in skeletal muscle and liver (author's transl)].
    Shima K; Hamada T; Tashiro K; Matsumoto H
    Nihon Naika Gakkai Zasshi; 1982 Mar; 71(3):357-63. PubMed ID: 7108326
    [No Abstract]   [Full Text] [Related]  

  • 19. Muscle fiber hypotrophy with intact neuromuscular junctions. A study of a patient with congenital neuromuscular disease and ophthalmoplegia.
    Bender AN; Bender MB
    Neurology; 1977 Mar; 27(3):206-12. PubMed ID: 557754
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sporadic oculopharyngeal myopathy with abnormal mitochondria.
    Palmucci L; Bertolotto A; Cavicchioli D; Monga G; Schiffer D
    Acta Neurol Belg; 1978; 78(6):373-82. PubMed ID: 749515
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.