Peripheral neuropathies of childhood

Physical Medicine and Rehabilitation Clinics of North America

Volumn 12, Issue 2, 2001, Pages 473-490

  McDonald, C M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIA; DISEASE ASSOCIATION; DNA REPAIR; ELECTROMYOGRAPHY; FABRY DISEASE; GLOBOID CELL LEUKODYSTROPHY; GUILLAIN BARRE SYNDROME; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; METACHROMATIC LEUKODYSTROPHY; NERVE BIOPSY; PERIPHERAL NERVE; PERIPHERAL NEUROPATHY; POLYNEUROPATHY; PORPHYRIA; PRIORITY JOURNAL; REFSUM DISEASE; REVIEW; SURAL NERVE; TANGIER DISEASE;

EID: 0035042755     PISSN: 10479651     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1047-9651(18)30803-9     Document Type: Review

References (75)

1. Electrodiagnostic findings in acute porphyric neuropathy
2. Familial dysautonomia: A prospective study of survival
3. Fulminant demyelinating neuropathy mimicking cerebral death
4. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
5. Connexin mutations in X-linked Charcot-Marie-Tooth disease
6. Peripheral neuropathy in globoid cell leucodystrophy (Krabbe's disease): Ultrastructural and histochemical findings
7. First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe
8. Guillain-Barré syndrome in children: Clinical course, electrodiagnosis and prognosis
9. Profiles of neuromuscular diseases: Hereditary motor and sensory neuropathy, Types I and II
10. Molecular basis of neuromuscular disease
11. DNA deletion associated with hereditary neuropathy with liability to pressure palsies
12. Acute arsenic intoxication presenting as Guillian-Barré-like syndrome
13. Peripheral nerve biopsy as an aid to diagnosis in infantile neuroaxonal dystrophy
14. Nerve conduction studies in children with Friedreich's ataxia and ataxia telangiectasia
15. The phenotype of "pure" autosomal dominant spastic paraplegia
16. Chronic inflammatory polyradiculoneuropathy
17. Not "indifference to pain" but varieties of hereditary sensory and autonomic neuropathy
18. Neuronal atrophy and degeneration predominantly affecting peripheral sensory and autonomic neurons
19. Childhood diabetic neuropathy: A clinical and neurophysiological study
20. Childhood diabetic neuropathy: A clinical and electrophysiological study
21. The role of plasmapheresis in childhood Guillain-Barré syndrome
22. Peripheral neuropathy in juvenile diabetes
23. Echocardiographic findings in Friedreich's ataxia
24. Ataxia telangiectasia, a report of two cases in siblings presenting a picture of progressive spinal muscular atrophy
25. Severe vincristine neuropathy in Charcot- Marie-Tooth disease type 1A
26. Radiological manifestation in familial dysautonomia
27. Ultrastructure and electrodiagnosis of peripheral neuropathy in Cockayne's syndrome
28. Peripheral neuropathy in classic Niemann-Pick disease: Ultrastructure of nerves and skeletal muscles
29. Tangier disease
30. Correlates of delayed motor nerve conduction and retinopathy in juvenile-onset diabetes mellitus
31. The peripheral neuropathy of Krabbe's (globoid) leukodystrophy
32. Infantile neuroaxonal dystrophy: Clinical pathologic and histochemical findings in a family with 3 affected siblings
33. Charcot-Marie-Tooth neuropathies: From clinical description to molecular genetics
34. Polyneuropathy following exposure to insecticides: Two cases of polyneuropathy with albuminocytologic dissociation in the spinal fluid following exposure to DDD and aldrin and DT and endrin
35. Guillain-Barré syndrome and plasmapheresis in childhood
36. Peripheral and central somatosensory nerve conduction defects in Friedreich's ataxia
37. Multiple peripheral nerve entrapments: An unusual phenotypic variant of the Hunter syndrome (mucopolysaccharidosis II) in a family
38. Ultrastructural muscle pathology in infantile neuroaxonal dystrophy
39. Peripheral nerve involvement in Fabry's disease
40. o gene in Charcot-Marie-Tooth disease Type 1B
41. Plasmapheresis in children with Guillain Barré syndrome
42. Dominantly transmitted congenital indifference to pain
43. Four-year followup study of use of IVIG in childhood acute inflammatory demyelinating polyneuropathy (GBS)
44. Perinatal neuropathy as an early manifestation of Krabbe's disease
45. Organophosphate polyneuropathy: Pathogenesis and prevention
46. Clinical approach to the diagnostic evaluation of progressive neuromuscular diseases
47. Electrodiagnosis in pediatrics
48. Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A
49. Peripheral neuropathy in Cockayne's syndrome
50. Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts
51. Rehabilitation of an adult with disabilities due to congenital sensory neuropathy
52. The mucopolysaccharidoses
53. The clinical spectrum and morphology of type II hereditary sensory neuropathy
54. Hereditary sensory neuropathy, type II: Clinical, electrophysiologic, histologic and biochemical studies of a Quebec kinship
55. Friedreich's ataxia: Early detection and progression of peripheral nerve abnormalities
56. Genetic diagnosis of Friedreich's ataxia
57. Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease
58. Motor and somatosensory evoked potentials in hereditary spastic paraplegia
59. Congenital hypomyelinating neuropathy: Two patients with long-term followup
60. Patterns of Refsum's disease: Phytanic oxidase deficiency
61. Familial dysautonomia
62. Xeroderma pigmentosum: An inherited disease with sun sensitivity, multiple cutaneous neoplasms and abnormal DNA repair
63. Lead neuropathy in childhood
64. Benefit of intravenously administered immune serum globulin in patients with Guillain-Barré syndrome
65. Phytonic acid storage Disease
66. Peripheral neuropathy in the cherry-red spot myoclonus syndrome (sialidosis type I)
67. Classification and electrodiagnosis of hereditary neuropathies
68. Other inherited neuropathies
69. Neurological manifestations of xeroderma pigmentosum in two siblings
70. Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype
71. Pediatric electrodiagnostic medicine
72. Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
73. Functional consequences of mutations in the early growth response 2 gene (EGR2) correlate with severity of human myelopathies
74. Metal neuropathy