Biomedical subjects
L P ROWLAND
Publications and source records attributed to L P ROWLAND.
MUSCULAR DYSTROPHY. FEATURES OF OCULAR MYOPATHY, DISTAL MYOPATHY, AND MYOTONIC DYSTROPHY.
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MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
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NEUROMUSCULAR DISORDERS ASSOCIATED WITH MALIGNANT NEOPLASTIC DISEASE.
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MCARDLE'S DISEASE: HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
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The formation of isoleucine from beta-methylaspartic acid in Escherichia coli W.
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On the function of the endocrine glands in myotonic muscular dystrophy.
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Acute intermittent porphyria: search for an enzymatic defect with implications for neurology and psychiatry.
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Bassen-Kornweig syndrome. Neuromuscular disorder resembling Friedreich's ataxia associated with retinitis pigmentosa, acanthocytosis, steatorrhea, and an abnormality of lipid metabolism.
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Current concepts of the pathogenesis of myasthenia gavis.
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Neuropathy with malignant tumor metastases.
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Serum enzymes in the myopathies.
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Myasthenia gravis and epilepsy.
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Serum aldolase in muscular dystrophies, neuromuscular disorders, and wasting of skeletal muscle.
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Neurological syndromes associated with congenital absence of the odontoid process.
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Muscular dystrophies, polymyositis, and other myopathies.
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