Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia
- 1 December 2004
- journal article
- research article
- Published by Springer Science and Business Media LLC in Zeitschrift für Neurologie
- Vol. 251 (12), 1491-1497
- https://doi.org/10.1007/s00415-004-0578-x
Abstract
Hereditary motor and sensory neuropathy type Ia (HMSN Ia) is known as a primarily demyelinating peripheral nerve disease. Evidence is accumulating that axonal involvement determines the course of the disease process.Keywords
This publication has 43 references indexed in Scilit:
- Coexistent hereditary and inflammatory neuropathyBrain, 2004
- Inflammatory demyelination in a patient with CMT1AMuscle & Nerve, 2003
- Motor unit number estimate of distal and proximal muscles in Charcot–Marie–Tooth diseaseMuscle & Nerve, 2003
- Genetic neuromuscular diseaseJournal of Neurology, Neurosurgery & Psychiatry, 2002
- Psychometric evaluation of a new handicap scale in immune‐mediated polyneuropathiesMuscle & Nerve, 2002
- Immunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a)Journal of Neurology, Neurosurgery & Psychiatry, 2002
- No Adjustments Are Needed for Multiple ComparisonsEpidemiology, 1990
- Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1Muscle & Nerve, 1989
- The Sickness Impact Profile: Development and Final Revision of a Health Status MeasureMedical Care, 1981
- THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND IIBrain, 1980