Hereditary defects of glycogenolysis and glycolysis enzymes in neuromuscular diseases (a review)
Rozenfel'd, E.L.; Popova, I.A.
Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 88(11): 115-122
1988
ISSN/ISBN: 0044-4588 PMID: 2851906 Document Number: 309722
Document emailed within 1 workday
Related Documents
Reznik, B.I.; Soroka, I.A. 1972: The activity of various glycolysis and pentose-phosphate cycle enzymes in the erythrocytes of children with hereditary spherocytosis Voprosy Okhrany Materinstva i Detstva 17(6): 21-24Husain, K.; Matin, M.A. 1986: Cerebral glycolysis and glycogenolysis in diazinon treated animals Arhiv Za Higijenu Rada i Toksikologiju 37(1): 29-34
Potapov, P.P. 1989: The rate of glycolysis and glycogenolysis in the skeletal muscles of rats in the period of readaptation following 30 days' hypokinesia Kosmicheskaia Biologiia i Aviakosmicheskaia Meditsina 23(4): 92-94
Skupchenko, V.V.; Novikova, N.P. 2001: Hereditary neuromuscular diseases in the Samara region Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 101(9): 49-53
Popov, O.G.; Sitnikov, V.F. 1975: Changes in the bone system and muscles in children with certain hereditary neuromuscular diseases, according to roentgenological image Pediatriia 1975(12): 41-45
Shukhova, E.V.; Goriunova, A.V.; Savel'eva, E.A.; Ovnanian, A.A. 1987: Sanatorium-health resort treatment of children with hereditary diseases of the neuromuscular system Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 87(11): 1635-1640
Sitnikov, V.F.; Khrennikov, V.I.; Teselkin, I.O. 1987: Chemiluminescence of blood plasma and functional status of the erythrocytes of patients with various hereditary neuromuscular diseases Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 87(3): 376-381
Brewster, M.A. 1981: Leukocyte Enzymes in birth defects- a review Annals of Clinical and Laboratory Science 11(2): 146-151
Hirnlowa, L.; Kwiatkowska, J.; Rybusińska-Lebuda, J.; Dobryszycka, W.; Wlodarczyk, W. 1971: Glycolysis and the character of red blood cell hemoglobin in hereditary spherocytic anemia Acta Haematologica Polonica 2(2): 121-128
Lukoshiavichius, L.I.; Grigaliunene, V.I.; Prashkiavichius, A.K. 1977: Activity of key enzymes of glycolysis in the rat liver during the development of experimental myocardial necrosis Kardiologiia 17(8): 133-136
Kil'dema, L.A.; Teras, L.E.; Lond, M.E. 1977: Activity of enzymes of glycolysis and gluconeogenesis in primary hepatomas induced by diethylnitrosamine Voprosy Meditsinskoi Khimii 23(4): 490-494
Girard, J. 1996: Regulation of the expression of hepatic genes coding the enzymes of glycolysis and gluconeogenesis Journees Annuelles de Diabetologie de l'Hotel-Dieu 1996: 37-53
Nazarian, K.B.; Gevorkian, E.S.; Kostanian, A.A.; Akopian, N.S.; Panosian, G.A. 1987: Relation between hormonal induction of enzymes regulating glycolysis and convulsive activity in the brain Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 87(6): 870-873
Ginter, E.K.; Budagova, K.A.; Revazov, A.A.; Petrin, A.N.; Bugaeva, E.A. 1986: Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region Genetika 22(7): 1199-1206
Horodnicki, J.M.; Wasik, A.; Firko, M.; Janicka, B. 1979: Effect of lithium ions on the activity of glycolysis enzymes in the brain and peripheral blood leukocytes of rats Psychiatria Polska 13(6): 543-548
Krakhmaleva, I.N.; Vlasov, V.I.; Telesnina, G.N.; Krasnova, T.P.; Vladimirov, A.V.; Sazykin, I.O. 1993: Dynamics of the content of glycolysis enzymes in Streptomyces rimosus as it relates to the problem of regulation of oxytetracycline biosynthesis Antibiotiki i Khimioterapiia 38(8-9): 11-15
Koehn, R.K.; Diehl, W.J.; Scott, T.M. 1988: The differential contribution by individual enzymes of glycolysis and protein catabolism to the relationship between heterozygosity and growth rate in the coot clam, Mulinia lateralis Genetics 118(1): 121-130
Fagoaga, J.; Girabent-Farres, M.; Bagur-Calafat, C. 2017: Translation and validation of the Individualised Neuromuscular Quality of Life scale for the Spanish population: quality of life assessment for persons with neuromuscular diseases Revista de Neurologia 64(5): 194-200
Girabent-Farres, M.; Monne-Guasch, L.; Bagur-Calafat, C.; Fagoaga, J. 2018: Spanish translation and validation of the neuromuscular module of the Pediatric Quality of Life Inventory (PedsQL): evaluation of the quality of life perceived by the parents of 2-4-year-old children with neuromuscular diseases Revista de Neurologia 66(3): 81-88
Kremer, J. 1980: Donor insemination for the prevention of hereditary defects Nederlands Tijdschrift Voor Geneeskunde 124(16): 577-581