[Spino-cerebellar heredodegeneration].
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Cerebellum↗
Biomedical subjects
L VAN BOGAERT
Publications and source records attributed to L VAN BOGAERT.
[Hereditary diseases of peripheral neurons and of muscle].
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Humans↗
[Studies on acquired and familial muscular disorders excluding myopathias].
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Disease↗
[I. Acute primary polymyositis in a young child, with favorable evolution].
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Biological Evolution↗
[Studies on familial spastic paraplegia. III. The Tib family...; very early forms of familial spastic paraplegia with idiocy and oligophrenia in collateral branches of the family].
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Heredity↗
[III. An osteoplastic myopathia (Münchmeyer's myositis ossificans progressiva) with a terminal trophoneurotic component].
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Arthrodesis↗
Post-infectious encephalomyelitis and multiple sclerosis; the significance of perivenous encephalomyelitis.
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Encephalomyelitis↗
[Heredity in hepatolenticular degeneration and the problem of the intrinsic relations between Westphal-Strumpell's pseudosclerosis and Wilson's disease; the nosologic location of Kehrer's "abdominal-Wilson" within hepatolenticular degeneration].
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Corpus Striatum↗
[Cerebellar encephalitis in two young cats].
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Animals↗
[Spontaneous and intentional clonic spasms in two atypical forms of general paralysis].
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Humans↗
[Affection manifested by diffused tetanoid contraction with variable hyperkinesia and of subacute fatal evolution].
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Biological Evolution↗
[Approach to pathology of the optical layer].
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Nerve Tissue↗
Hereditary ataxia with optic atrophy of the retrobulbar neuritis type, and latent pallido-luysian degeneration.
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Ataxia↗
Choriorin alterations in two sisters suffering from hereditary Friedreich type.
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Ataxia↗
Neuro-ectodermal pigmentary dysplasias.
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Ectoderm↗
On a hereditary dementia with dementia, epilepsy-myocloma and arachnodactyly.
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Ataxia↗
Study of neural, reactive and inflammatory manifestations, especially in children.
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Central Nervous System Depressants↗