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 *

106 related articles for article (PubMed ID: 5910845)

  • 1. Urinary excretion of histamine in patients with various muscular disorders.
    Sjaastad O
    Acta Med Scand; 1966 Mar; 179(3):269-74. PubMed ID: 5910845
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. [Muscular weakness and creatinine excretion (author's transl)].
    Weisner B; Frerk C; Bernhardt W
    Nervenarzt; 1979 Sep; 50(9):582-6. PubMed ID: 537668
    [No Abstract]   [Full Text] [Related]  

  • 4. Comparative biochemistry of myopathies.
    Weinstock IM
    Ann N Y Acad Sci; 1966 Sep; 138(1):199-212. PubMed ID: 4291234
    [No Abstract]   [Full Text] [Related]  

  • 5. Free fatty acid concentrations in normal and diseased human muscle and in blood sera from patients with neuromuscular disease.
    Susheela AK
    Clin Chim Acta; 1968 Oct; 22(2):219-22. PubMed ID: 5687088
    [No Abstract]   [Full Text] [Related]  

  • 6. [The muscular clearance of Na24 in amyotrophic syndromes].
    Radu H; Blücher G; Gödri I
    Rev Neurol (Paris); 1967 Jan; 116(1):81-4. PubMed ID: 6032289
    [No Abstract]   [Full Text] [Related]  

  • 7. [Histochemical research in various muscular diseases].
    Duma D; Serban M; Popoviciu L; Lazăr T; Mareş V; Tăranu A
    Stud Cercet Neurol; 1965 Jun; 10(3):159-65. PubMed ID: 5828878
    [No Abstract]   [Full Text] [Related]  

  • 8. [Carbohydrate metabolism disorders in hereditary forms of neuromuscular diseases].
    Golubeva VV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1153-9. PubMed ID: 5136819
    [No Abstract]   [Full Text] [Related]  

  • 9. Leakage of enzymes from denervated and dystrophic chicken muscle.
    Dawson DM
    Arch Neurol; 1966 Mar; 14(3):321-5. PubMed ID: 5905082
    [No Abstract]   [Full Text] [Related]  

  • 10. Isotope studies of body composition in neuromuscular diseases.
    Delwaide PA; Delwaide PJ; Penders CA
    J Neurol Sci; 1972 Mar; 15(3):339-49. PubMed ID: 4622483
    [No Abstract]   [Full Text] [Related]  

  • 11. Myoglobinuria.
    Rowland LP; Penn AS
    Med Clin North Am; 1972 Nov; 56(6):1233-56. PubMed ID: 5085857
    [No Abstract]   [Full Text] [Related]  

  • 12. Leucocyte metabolism in hereditary neuromuscular disorders.
    Emery AE; King B; Brock JH
    J Neurol Sci; 1971 Dec; 14(4):463-8. PubMed ID: 5125760
    [No Abstract]   [Full Text] [Related]  

  • 13. Long-term turnover of selenite-Se in children with motor disorders.
    Westermarck T; Rahola T; Kallio AK; Suomela M
    Klin Padiatr; 1982; 194(5):301-2. PubMed ID: 7144043
    [No Abstract]   [Full Text] [Related]  

  • 14. PRIMARY PAROXYSMAL MYOGLOBINURIA. A CASE REPORT ASSOCIATED WITH MUSCULAR WASTING IN THE SHOULDER GIRDLE.
    MIYAZAKI T; UZAWA H; KUROIWA Y; KATSUKI S
    Kyushu J Med Sci; 1963 Dec; 14():421-30. PubMed ID: 14119579
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. [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]  

  • 17. [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]  

  • 18. [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]  

  • 19. Electrophoretic patterns of several dehydrogenases and hydrolases in muscles in human myopathies.
    Kar NC; Pearson CM
    Am J Clin Pathol; 1967 May; 47(5):594-7. PubMed ID: 6022990
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hreditary myopathies].
    Kuhn E
    Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.