Prevalence of hereditary motor and sensory neuropathy in Cantabria
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O. Combarros | J. Berciano | J. Polo | J. M. Polo | J Berciano | J Calleja | O Combarros | J M Polo | J. Calleja
[1] U. Selldén,et al. HEREDITARY MOTOR AND SENSORY NEUROPATHIES IN SWEDISH CHILDREN , 1983 .
[2] P K Thomas,et al. The clinical features of hereditary motor and sensory neuropathy types I and II. , 1980, Brain : a journal of neurology.
[3] L. Kurland,et al. Patterns of neurologic diseases on guam. , 1968, Archives of neurology.
[4] W. Bradley,et al. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification. , 1978, Journal de genetique humaine.
[5] W. Trojaborg. MOTOR NERVE CONDUCTION VELOCITIES IN NORMAL SUBJECTS WITH PARTICULAR REFERENCE TO THE CONDUCTION IN PROXIMAL AND DISTAL SEGMENTS OF MEDIAN AND ULNAR NERVE. , 1964, Electroencephalography and clinical neurophysiology.
[6] L. Kurland. Descriptive epidemiology of selected neurologic and myopathic disorders with particular reference to a survey in Rochester, Minnesota. , 1958, Journal of chronic diseases.
[7] P. Dyck,et al. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations. , 1968, Archives of neurology.
[8] R. Lovelace,et al. CLINICAL AND ELECTRODIAGNOSTIC FEATURES OF CHARCOT‐MARIE‐TOOTH SYNDROME , 1978, Acta neurologica Scandinavica. Supplementum.
[9] H. Skre,et al. Genetic and clinical aspects of Charcot‐Marie‐Tooth's disease , 1974, Clinical genetics.
[10] Fritz Buchthal,et al. Evoked action potentials and conduction velocity in human sensory nerves , 1966 .
[11] P. Bouche,et al. Peroneal muscular atrophy Part 1. Clinical and electrophysiological study , 1983, Journal of the Neurological Sciences.
[12] A. Harding,et al. Genetic aspects of hereditary motor and sensory neuropathy (types I and II) , 1980, Journal of medical genetics.
[13] Herndon Cn. Three North Carolina surveys. , 1954 .
[14] H Miller,et al. Neurological disease in an English city. , 1966, Acta neurologica Scandinavica.
[15] P. Dyck,et al. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. , 1968, Archives of neurology.
[16] O. Combarros,et al. Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family. , 1986, Brain : a journal of neurology.
[17] F. Buchthal,et al. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography. , 1977, Brain : a journal of neurology.
[18] F Buchthal,et al. Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves. , 1977, Brain : a journal of neurology.
[19] A. Emery,et al. A family study of Charcot-Marie-Tooth disease. , 1982, Journal of medical genetics.
[20] A. Hansen,et al. Clinical restitution following cerebral ischemia in hypo‐, normo‐ and hyperglycemic rats , 1978, Acta neurologica Scandinavica.
[21] K. Gudmundsson,et al. PREVALENCE AND OCCURRENCE OF SOME RARE NEUROLOGICAL DISEASES IN ICELAND , 1969, Acta neurologica Scandinavica.
[22] P K Thomas,et al. Autosomal recessive forms of hereditary motor and sensory neuropathy. , 1980, Journal of neurology, neurosurgery, and psychiatry.
[23] B. Hagberg,et al. HEREDITARY MOTOR AND SENSORY NEUROPATHIES IN SWEDISH CHILDREN I , 1983, Acta paediatrica Scandinavica.
[24] A. Harding,et al. Hereditary distal spinal muscular atrophy A report on 34 cases and a review of the literature , 1980, Journal of the Neurological Sciences.
[25] C. Herndon. Three North Carolina surveys. , 1954, American journal of human genetics.