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Histological and Histochemical Stains and Reactions
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2B fibres acid appearance arrows associated ATPase pH 9-4 ATPase preincubated atrophic fibres band cellular central core disease clinical Congenital fibre type dehydrogenase demonstrated denervation dermatomyositis diagnosis disorders Dubowitz electron microscopy Engel Fiber fibre atrophy fibre diameter fibre predominance fibre type disproportion fibres Fig fibres were seen fibrosis filaments glycogen glycogenosis histochemical reactions histological intermyofibrillar network internal nuclei large fibres large group atrophy legs limb girdle dystrophy membrane mild mitochondria modified ATPase moth-eaten motor neuron disease motor units Muscle biopsy Muscle biopsy biceps muscle fibres muscle weakness muscular dystrophy myofibrils myotonic dystrophy nemaline myopathy nerve neuromuscular Oxidative enzyme reactions patients pattern peripheral neuropathy phagocytosis phosphorylase polymyositis preincubated at pH present reaction Fig reactions showed Ring fibres rods routine ATPase pH routine stains sarcoplasmic reticulum skeletal muscle small angulated fibres small fibres spinal muscular atrophy stains showed structures target fibres trichrome type 1 fibres type 2B vacuoles variability