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 *

142 related articles for article (PubMed ID: 166198)

  • 1. Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria.
    Bonilla E; Schotland DL; DiMauro S; Aldover B
    J Ultrastruct Res; 1975 Jun; 51(3):404-8. PubMed ID: 166198
    [No Abstract]   [Full Text] [Related]  

  • 2. [Contributions to clinical myology. The role of electron microscopy].
    Lehmann J
    Psychiatr Neurol Med Psychol Beih; 1987; 38():108-19. PubMed ID: 2841706
    [No Abstract]   [Full Text] [Related]  

  • 3. Neuromuscular disorder associated with a defect in mitochondrial energy supply.
    Schotland DL; DiMauro S; Bonilla E; Scarpa A; Lee CP
    Arch Neurol; 1976 Jul; 33(7):475-9. PubMed ID: 180936
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Nemaline myopathy and a mitochondrial neuromuscular disorder in one family.
    Shapira YA; Yarom R; Blank A
    Neuropediatrics; 1981 May; 12(2):152-65. PubMed ID: 6267500
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ultrastructural study of globular inclusions in human skeletal muscle mitochondria.
    Bonilla E; Schotland DL; Di Mauro S
    Acta Neuropathol; 1980; 52(1):35-40. PubMed ID: 6254319
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Myoencephalopathies with abnormal mitochondria: a review.
    Walter GF
    Clin Neuropathol; 1983; 2(3):101-13. PubMed ID: 6354540
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electron microscopy and histochemistry in primary and secondary neuromuscular mitochondriopathies.
    Walter GF
    Acta Histochem Suppl; 1983; 28():249-52. PubMed ID: 6412305
    [No Abstract]   [Full Text] [Related]  

  • 9. Mitochondrial encephalomyopathies.
    DiMauro S; Bonilla E; Lombes A; Shanske S; Minetti C; Moraes CT
    Neurol Clin; 1990 Aug; 8(3):483-506. PubMed ID: 2170831
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. Variability of mitochondrial cytochemistry in human neuromuscular diseases.
    Shah A; Sahgal V; Sahgal S; Subramani V; Kochar H
    J Submicrosc Cytol Pathol; 1988 Apr; 20(2):287-95. PubMed ID: 3395968
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial intermembrane inclusion bodies: the common denominator between human mitochondrial myopathies and creatine depletion, due to impairment of cellular energetics.
    O'Gorman E; Piendl T; Müller M; Brdiczka D; Wallimann T
    Mol Cell Biochem; 1997 Sep; 174(1-2):283-9. PubMed ID: 9309701
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new mitochondrial myopathy. Biochemical studies revealing a deficiency in the cytochrome b-c1 complex (complex III) of the respiratory chain.
    Hayes DJ; Lecky BR; Landon DN; Morgan-Hughes JA; Clark JB
    Brain; 1984 Dec; 107 ( Pt 4)():1165-77. PubMed ID: 6095966
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new myopathy with tubulomembranous inclusions.
    Fukuhara N; Kumamoto T; Hirahara H; Tsubaki T
    J Neurol Sci; 1981 Apr; 50(1):95-107. PubMed ID: 6262462
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Intercostal muscle biopsy in human neuromuscular disease. Histochemical and electron microscopic studies.
    Stern LZ; Payne CM; Gruener R; Anderson RM; Hannapel LK
    J Neurol Neurosurg Psychiatry; 1975 Sep; 38(9):900-10. PubMed ID: 127018
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Muscle, nerve, and skin biopsy.
    Jaradeh SS; Ho H
    Neurol Clin; 2004 Aug; 22(3):539-61, v. PubMed ID: 15207875
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and "fingerprint" inclusions.
    Julien J; Vital C; Vallat JM; Vallat M; Le Blanc M
    J Neurol Sci; 1974 Feb; 21(2):165-9. PubMed ID: 4374513
    [No Abstract]   [Full Text] [Related]  

  • 19. [Electron microscopic study of mitochondrial diseases].
    Nonaka I
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():249-55. PubMed ID: 12013859
    [No Abstract]   [Full Text] [Related]  

  • 20. Intracytoplasmic inclusions in the atrophic muscle fibers in Werdnig-Hoffmann disease.
    Miike T; Tamari H; Ohtani Y; Kondo Y
    Brain Dev; 1983; 5(3):315-9. PubMed ID: 6311038
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.