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 *

183 related articles for article (PubMed ID: 3779373)

  • 1. The clinical features of mitochondrial myopathy.
    Petty RK; Harding AE; Morgan-Hughes JA
    Brain; 1986 Oct; 109 ( Pt 5)():915-38. PubMed ID: 3779373
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.
    Holt IJ; Harding AE; Cooper JM; Schapira AH; Toscano A; Clark JB; Morgan-Hughes JA
    Ann Neurol; 1989 Dec; 26(6):699-708. PubMed ID: 2604380
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial dysfunction in adult-onset myopathies with structural abnormalities.
    Naumann M; Reiners K; Gold R; Schindler R; Paulus W; Klopstock T; Reichmann H
    Acta Neuropathol; 1995; 89(2):152-7. PubMed ID: 7732787
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Myopathies with abnormal mitochondria: a clinicopathologic classification.
    Kamieniecka Z; Schmalbruch H
    Muscle Nerve; 1978; 1(5):413-5. PubMed ID: 263980
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial myopathy: a genetic study of 71 cases.
    Harding AE; Petty RK; Morgan-Hughes JA
    J Med Genet; 1988 Aug; 25(8):528-35. PubMed ID: 3050098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Early mitochondrial changes in chronic progressive ocular myopathy.
    Aasly J; Lindal S; Torbergsen T; Borud O; Mellgren SI
    Eur Neurol; 1990; 30(6):314-8. PubMed ID: 1963142
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial myopathies.
    Harding AE; Holt IJ
    Br Med Bull; 1989 Jul; 45(3):760-71. PubMed ID: 2688827
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Mitochondrial myopathies: clinical defects.
    Morgan-Hughes JA; Cooper JM; Holt IJ; Harding AE; Schapira AH; Clark JB
    Biochem Soc Trans; 1990 Aug; 18(4):523-6. PubMed ID: 2276423
    [No Abstract]   [Full Text] [Related]  

  • 10. [Mitochondrial myopathy: report of 12 cases with histochemical study of the skeletal muscle].
    Kiyomoto BH; Gabbai AA; Oliveira AS; Schmidt B; Lima JG
    Arq Neuropsiquiatr; 1991 Sep; 49(3):272-8. PubMed ID: 1807226
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies.
    Truong DD; Harding AE; Scaravilli F; Smith SJ; Morgan-Hughes JA; Marsden CD
    Mov Disord; 1990; 5(2):109-17. PubMed ID: 2325672
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles.
    Van Biervliet JP; Bruinvis L; Ketting D; De Bree PK; Van der Heiden C; Wadman SK
    Pediatr Res; 1977 Oct; 11(10 Pt 2):1088-93. PubMed ID: 904972
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.
    Morgan-Hughes JA; Hayes DJ; Clark JB; Landon DN; Swash M; Stark RJ; Rudge P
    Brain; 1982 Sep; 105 (Pt 3)():553-82. PubMed ID: 7104666
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia.
    Okamoto Y; Higuchi I; Sakiyama Y; Tokunaga S; Watanabe O; Arimura K; Nakagawa M; Takashima H
    Ann Neurol; 2011 Sep; 70(3):486-92. PubMed ID: 21905081
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency.
    Puñal JE; Rodríguez E; Pintos E; Campos Y; Castro-Gago M
    Brain Dev; 1998 Apr; 20(3):175-8. PubMed ID: 9628194
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial myopathy with a defect of mitochondrial-protein transport.
    Schapira AH; Cooper JM; Morgan-Hughes JA; Landon DN; Clark JB
    N Engl J Med; 1990 Jul; 323(1):37-42. PubMed ID: 2113185
    [No Abstract]   [Full Text] [Related]  

  • 18. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.
    Holt IJ; Harding AE; Morgan-Hughes JA
    Nature; 1988 Feb; 331(6158):717-9. PubMed ID: 2830540
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Histopathologic and Biochemical Evidence for Mitochondrial Disease Among 279 Patients with Severe Statin Myopathy.
    Hou T; Li Y; Chen W; Heffner RR; Vladutiu GD
    J Neuromuscul Dis; 2017; 4(1):77-87. PubMed ID: 28269789
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Elucidation of the mechanism of atorvastatin-induced myopathy in a rat model.
    El-Ganainy SO; El-Mallah A; Abdallah D; Khattab MM; Mohy El-Din MM; El-Khatib AS
    Toxicology; 2016 Jun; 359-360():29-38. PubMed ID: 27345130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.