Gentamicin treatment in McArdle disease : Failure to correct myophosphorylase deficiency

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Bibliographische Detailangaben
Veröffentlicht in:	Neurology 2006-01, Vol.66 (2), p.285-286
Hauptverfasser:	SCHROERS, A, KLEY, R. A, STACHON, A, HORVATH, R, LOCHMÜLLER, H, ZANGE, J, VORGERD, M
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Biological and medical sciences Cells, Cultured Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Energy Metabolism Female Gentamicins - administration & dosage Gentamicins - pharmacology Gentamicins - therapeutic use Glycogen Phosphorylase, Muscle Form - deficiency Glycogen Phosphorylase, Muscle Form - genetics Glycogen Phosphorylase, Muscle Form - metabolism Glycogen Storage Disease Type V - drug therapy Glycogen Storage Disease Type V - enzymology Glycogen Storage Disease Type V - genetics Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Magnetic Resonance Spectroscopy Male Medical sciences Middle Aged Muscle, Skeletal - enzymology Mutation Myoblasts - drug effects Myoblasts - enzymology Nervous system (semeiology, syndromes) Neurology Osmolar Concentration Phosphorylases - metabolism
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