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: 6743800)

  • 1. [Adrenergic structures and monoamine oxidase activity in dystrophic skeletal muscles].
    Badalian LO; Severina IS; Grinio LP; Temin PA; Amanova ZN
    Biull Eksp Biol Med; 1984 Jun; 97(6):660-2. PubMed ID: 6743800
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Fluorescence histochemical study of catecholamine concentrations in the skeletal muscles of patients with different forms of progressive neuromuscular disease].
    Temin PA; Dzhabarov BD; Grinio LP; Kargina-Terent'eva RA; Parshikova MV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):31-4. PubMed ID: 7080773
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Catecholamine concentration in the blood and excretion in the urine in different forms of progressive muscular dystrophy].
    Badalian LO; Temin PA; Dzhabarov BD; Bespalova VA; Kret LA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):339-42. PubMed ID: 6426220
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Mitochondrial monoamine oxidase in progressive Duchenne muscular dystrophy].
    Badalian LO; Amanova ZN; Temin PA; Grinio LP; Severina IS
    Vopr Med Khim; 1985; 31(1):68-71. PubMed ID: 3984276
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Catecholamines in the adrenergic structures of skeletal muscles and in the blood and urine of patients with progressive Duchenne muscular dystrophy].
    Badalian LO; Temin PA; Dzhabarov BD; Grinio LP; Parshchikova MV
    Pediatriia; 1983 Oct; (10):40-2. PubMed ID: 6657350
    [No Abstract]   [Full Text] [Related]  

  • 6. [Vegetative and trophic disorders and functional status of the sympatho-adrenal system in Rossolimo-Curschmann-Batten-Steinert myotonic dystrophy].
    Dzhabarov BD
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(3):333-5. PubMed ID: 3705837
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Serum cytoplasmic and mitochondrial aspartate aminotransferase in Duchenne's progressive muscular dystrophy.
    Janik P; Nowak I; Niebrój-Dobosz I
    Mater Med Pol; 1994; 26(3):101-4. PubMed ID: 7603078
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Chemiluminescence of blood plasma and functional status of the erythrocytes of patients with various hereditary neuromuscular diseases].
    Sitnikov VF; Khrennikov VIu; Teselkin IuO
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(3):376-81. PubMed ID: 3577527
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Metabolism and pathology of catecholamines].
    Traba ML
    Rev Clin Esp; 1981 Jul 15-31; 162(1-2):5-13. PubMed ID: 6117933
    [No Abstract]   [Full Text] [Related]  

  • 10. Cholinesterase and monoamine oxidase activities in skeletal muscle of normal and hereditary dystrophic mice.
    Srivastava U; Berlinguet L
    Can J Biochem; 1967 Apr; 45(4):573-80. PubMed ID: 6033828
    [No Abstract]   [Full Text] [Related]  

  • 11. [Succinic dehydrogenase activity in the skeletal muscles of children in diseases of the locomotor apparatus].
    Iaroshevskaia EN
    Arkh Patol; 1965; 27(7):63-5. PubMed ID: 5865149
    [No Abstract]   [Full Text] [Related]  

  • 12. [Carnosine and anserine content of muscles in the course of progressive muscular dystrophy].
    Stepanova NG; Grinio LP
    Vopr Med Khim; 1968; 14(2):210-4. PubMed ID: 5682163
    [No Abstract]   [Full Text] [Related]  

  • 13. Early changes of muscle mitochondria in Duchenne dystrophy. Partition and activity of mitochondrial enzymes in fractionated muscle of unaffected boys and adults and patients.
    Scholte HR; Busch HF
    J Neurol Sci; 1980 Mar; 45(2-3):217-34. PubMed ID: 6245185
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Myocardial lesions in several forms of progressive muscular atrophy].
    Popov'ian MD; Dubinskaia EE; Proshina OV; Tul'skaia MP; Loginova LA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):330-5. PubMed ID: 6720172
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Absence of a calmitine-specific protease inhibitor in skeletal muscle mitochondria of patients with Duchenne's muscular dystrophy.
    Lucas-Heron B
    Biochem Biophys Res Commun; 1996 Aug; 225(3):701-4. PubMed ID: 8780677
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A drug inhibits the mitochondrial protease inducing calmitine deficiency in skeletal muscle of patients with Duchenne's muscular dystrophy and dy/dy dystrophic mice.
    Lucas-Heron B
    Biochem Biophys Res Commun; 1997 Mar; 232(2):559-61. PubMed ID: 9125222
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Sideremia and muscular myoglobin in progressive muscular dystrophy and other neuromuscular diseases].
    Buscaino GA
    Acta Neurol (Napoli); 1966; 21(1):26-32. PubMed ID: 5999243
    [No Abstract]   [Full Text] [Related]  

  • 18. Skeletal muscle of patients with Duchenne's muscular dystrophy: evidence of a mitochondrial proteolytic factor responsible for calmitine deficiency.
    Lucas-Heron B
    Biochem Biophys Res Commun; 1996 Jun; 223(1):31-5. PubMed ID: 8660374
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Various features of muscle tissue metabolism in various muscular and neuromuscular diseases of a hereditary nature (clinico-histochemical study)].
    Anosov NN; Saĭkova LA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):22-5. PubMed ID: 6952668
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Biochemical studies in progressive muscular dystrophy. II. Changes of glycogen, potassium, and total and residual nitrogen. Oxygen consumption with endogenous and exogenous substrates].
    Duma D; Popoviciu L; Mareş V; Serban M; Pîrvu M; Lazăr TC; Pop R; Băltescu V
    Stud Cercet Neurol; 1967; 12(2):85-91. PubMed ID: 6043564
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.