Quantitation of meissner’s corpuscles in hereditary neurologic disorders: Charcot-marie-tooth disease, roussy-levy syndrome, dejerine-sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia

Peter J. Dyck; R. K. Winkelmann; Charles F. Bolton

doi:10.1212/wnl.16.1.10

Quantitation of meissner’s corpuscles in hereditary neurologic disorders: Charcot-marie-tooth disease, roussy-levy syndrome, dejerine-sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia

Peter J. Dyck, R. K. Winkelmann, Charles F. Bolton

Neurology

Research output: Contribution to journal › Article › peer-review

32 Scopus citations

Original language	English (US)
Pages (from-to)	10-17
Number of pages	8
Journal	Neurology
Volume	16
Issue number	1
DOIs	https://doi.org/10.1212/wnl.16.1.10
State	Published - Jan 1966

ASJC Scopus subject areas

Clinical Neurology

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10.1212/wnl.16.1.10

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Quantitation of meissner’s corpuscles in hereditary neurologic disorders: Charcot-marie-tooth disease, roussy-levy syndrome, dejerine-sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia. / Dyck, Peter J.; Winkelmann, R. K.; Bolton, Charles F.
In: Neurology, Vol. 16, No. 1, 01.1966, p. 10-17.

Research output: Contribution to journal › Article › peer-review

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Quantitation of meissner’s corpuscles in hereditary neurologic disorders: Charcot-marie-tooth disease, roussy-levy syndrome, dejerine-sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia

ASJC Scopus subject areas

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