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Genetic analysis of childhood-onset spinal muscular atrophy.
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[The muscular atrophies following facial nerve paralysis. Biochemical and electromyographical data].
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Neurogenic muscular atrophy of infancy with prolonged survival--the variable course of Werdnig-Hoffmann disease.
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Electrophysiological investigation of the skeletal muscle in peroneal muscular atrophy.
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Animal model of human disease: motor neuron disease: spinal muscular atrophy and amyotrophic lateral sclerosis.
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[Hereditary spinal distal muscular atrophy (report of 2 cases)].
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[Association of post-radiation focal muscular atrophy and hypertrophy].
We report a 48 year old woman who had radiotherapy for uterine carcinoma and who developed amyotrophy and muscle hypertrophy in one lower limb. Very few cases of post-radiation monomelic amyotrophy have been reported. On the other hand denervation hypertrophy was presumed to be well known. The seat of the lesions was presumed to be radicular and spinal. The mechanism of atrophy and hypertrophy is discussed.
Juvenile type of distal and segmental muscular atrophy of upper extremities. Description of a case.
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Proximal myotonic dystrophy mimicking progressive muscular atrophy.
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The nosology of the spinal muscular atrophies.
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A predominantly cervical form of spinal muscular atrophy.
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A clinical study on hereditary progressive neurogenic muscular atrophy in Pointer dogs.
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[A family study of the association between X-linked bulbospinal muscular atrophy (Kennedy-Alter-Sung type) and color blindness protan].
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Peroneal muscular atrophy (Charcot-Marie-Tooth disease): a review of three cases.
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Heart block and peroneal muscular atrophy. A family study.
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[Morphometric analysis of oculomotor, trochlear and abducent nerve roots from amyotrophic lateral sclerosis and X-linked recessive bulbar spinal muscular atrophy (author's transl)].
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