Some muscular manifestations of hypothyroidism.
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Disease↗
Biomedical subjects
J N WALTON
Publications and source records attributed to J N WALTON.
The inheritance of muscular dystrophy.
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Databases, Genetic↗
The amyotonia congenita syndrome.
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Neuromuscular Diseases↗
Amyotonia congenita: a follow-up study.
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Follow-Up Studies↗
The response of the normal, the denervated and the dystrophic muscle-cell to injury.
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Muscle Cells↗
The inheritance of muscular dystrophy: further observations.
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Disease↗
Colour blindness and the Duchenne-type muscular dystrophy.
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Color Perception↗
Two cases of myopathy limited to the quadriceps.
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Disease↗
Benign congenital myopathy with myasthenic features.
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Disease↗
Polymyositis: diagnosis, pathology, prognosis and treatment.
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Humans↗
The prognosis and management of subarachnoid haemorrhage.
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Disease Management↗
On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies.
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Blood Group Antigens↗
Ribosuria in muscular dystrophy.
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Body Fluids↗
The electroencephalogram in pernicious anaemia and subacute combined degeneration of the cord.
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Anemia↗
On the classification, natural history and treatment of the myopathies.
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Disease↗
Osseous changes in myopathy.
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Bone and Bones↗