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2. [Progressive neuropathic muscular atrophy with pattern reversal visual evoked potentials]. Cao PZ. Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1987 Oct; 20(5):286-9. PubMed ID: 3450486 [No Abstract] [Full Text] [Related]
3. Heterogeneity of hereditary motor and sensory neuropathy type I (HMSN I): electroneurographical findings, visual evoked potentials and blood group markers in a family with Charcot-Marie-Tooth disease (CMT). Leblhuber F, Reisecker F, Mayr WR, Deisenhammer E. Acta Neurol Scand; 1986 Aug; 74(2):145-9. PubMed ID: 3022527 [Abstract] [Full Text] [Related]
4. Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system. Hisama FM, Lee HH, Vashlishan A, Tekumalla P, Russell DS, Auld E, Goldstein JM. Arch Neurol; 2001 Nov; 58(11):1891-6. PubMed ID: 11709000 [Abstract] [Full Text] [Related]
7. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review. Berciano J, García A, Gallardo E, Peeters K, Pelayo-Negro AL, Álvarez-Paradelo S, Gazulla J, Martínez-Tames M, Infante J, Jordanova A. J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294 [Abstract] [Full Text] [Related]
8. Peripheral and central sensory nerve conduction in Charcot-Marie-Tooth disease and comparison with Friedreich's ataxia. Jones SJ, Carroll WM, Halliday AM. J Neurol Sci; 1983 Sep; 61(1):135-48. PubMed ID: 6631449 [Abstract] [Full Text] [Related]
9. Pattern shift visual evoked potentials in Charcot-Marie-Tooth disease, HMSN type I. Tackmann W, Radü EW. J Neurol; 1980 Sep; 224(1):71-4. PubMed ID: 6157801 [Abstract] [Full Text] [Related]
10. Clinical and electrophysiological studies of a family with probable X-linked dominant Charcot-Marie-Tooth neuropathy and ptosis. Wu T, Wang HL, Chu CC, Yu JM, Chen JY, Huang CC. Chang Gung Med J; 2004 Jul; 27(7):489-500. PubMed ID: 15508871 [Abstract] [Full Text] [Related]
11. [Visual, auditory and somatosensory pathway involvement in Charcot-Marie-Tooth disease]. Tang XF, Werner T. Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1984 Oct; 6(5):357-62. PubMed ID: 6241088 [No Abstract] [Full Text] [Related]
16. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Chan CK, Mohsenin V, Loke J, Virgulto J, Sipski ML, Ferranti R. Chest; 1987 Apr; 91(4):567-70. PubMed ID: 3829750 [Abstract] [Full Text] [Related]
17. Pattern-reversal visual evoked potentials in the hereditary ataxias and spinal degenerations. Bird TD, Crill WE. Ann Neurol; 1981 Mar; 9(3):243-50. PubMed ID: 7224589 [Abstract] [Full Text] [Related]
18. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy. McLeod JG, Low PA, Morgan JA. Proc Aust Assoc Neurol; 1975 Mar; 12():23-5. PubMed ID: 1215391 [Abstract] [Full Text] [Related]
19. Phenotype of Charcot-Marie-Tooth disease Type 2. Bienfait HM, Baas F, Koelman JH, de Haan RJ, van Engelen BG, Gabreëls-Festen AA, Ongerboer de Visser BW, Meggouh F, Weterman MA, De Jonghe P, Timmerman V, de Visser M. Neurology; 2007 May 15; 68(20):1658-67. PubMed ID: 17502546 [Abstract] [Full Text] [Related]