-
1
-
-
0024463835
-
Assessment and management of pes cavus in Charcot Marie Tooth disease
-
Alexander IJ, Johnson KA. Assessment and management of pes cavus in Charcot Marie Tooth disease. Clin Orthop. 1989;246:273-281.
-
(1989)
Clin Orthop
, vol.246
, pp. 273-281
-
-
Alexander, I.J.1
Johnson, K.A.2
-
2
-
-
0028147187
-
Inherited neuropathies: Charcot Marie Tooth disease and related disorders
-
Chance PF, Lupski JR. Inherited neuropathies: Charcot Marie Tooth disease and related disorders. Baillieres Clin Neurol. 1994;3:373-385.
-
(1994)
Baillieres Clin Neurol
, vol.3
, pp. 373-385
-
-
Chance, P.F.1
Lupski, J.R.2
-
3
-
-
0002896804
-
Sur une forme particuliere d'atrophie musculaire progressive, souvant famiele de'butant par les pieds et les jambs et atteignant plus tard les maine
-
Charcot JM, Marie P. Sur une forme particuliere d'atrophie musculaire progressive, souvant famiele de'butant par les pieds et les jambs et atteignant plus tard les maine. Rev Med (Paris). 1886;6:97-138.
-
(1886)
Rev Med (Paris)
, vol.6
, pp. 97-138
-
-
Charcot, J.M.1
Marie, P.2
-
4
-
-
0033170113
-
Guidelines for the diagnosis of Charcot Marie Tooth disease and related neuropathies
-
Crespi V, Fabrizi GM, Mandich P, et al. Guidelines for the diagnosis of Charcot Marie Tooth disease and related neuropathies. Ital J Neurol Sci. 1999;20:207-216.
-
(1999)
Ital J Neurol Sci
, vol.20
, pp. 207-216
-
-
Crespi, V.1
Fabrizi, G.M.2
Mandich, P.3
-
5
-
-
0005457713
-
Congenital and acquired neurological disorders
-
Couglin MJ, Mann RA, eds. St. Louis: Mosby
-
Dehne R. Congenital and acquired neurological disorders. In: Couglin MJ, Mann RA, eds. Surgery of the Foot and Ankle. St. Louis: Mosby, 1999: 525-557.
-
(1999)
Surgery of the Foot and Ankle
, pp. 525-557
-
-
Dehne, R.1
-
6
-
-
0035136847
-
Further evidence that neurofilament light chain gene mutations can cause Charcot Marie Tooth disease type 2E
-
De Jonghe P, Mersivanova I, Nelis E, et al. Further evidence that neurofilament light chain gene mutations can cause Charcot Marie Tooth disease type 2E. Ann Neurol. 2001;49:245-249.
-
(2001)
Ann Neurol
, vol.49
, pp. 245-249
-
-
De Jonghe, P.1
Mersivanova, I.2
Nelis, E.3
-
7
-
-
0032949034
-
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot Marie Tooth phenotype
-
De Jonghe P, Timmerman V, Ceuterick C. et al. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot Marie Tooth phenotype. Brain. 1999;122: 281-290.
-
(1999)
Brain
, vol.122
, pp. 281-290
-
-
De Jonghe, P.1
Timmerman, V.2
Ceuterick, C.3
-
8
-
-
0001768884
-
Inherited neuronal degeneration and atrophy affecting the peripheral motor, sensory and autonomic neurons
-
Dyck PJ, Thomas PK, Lambert EH, eds. Philadelphia and London: WB Saunders
-
Dyek PJ. Inherited neuronal degeneration and atrophy affecting the peripheral motor, sensory and autonomic neurons. In: Dyck PJ, Thomas PK, Lambert EH, eds. Peripheral Neuropathy. Vol. 2. Philadelphia and London: WB Saunders, 1975:825-867.
-
(1975)
Peripheral Neuropathy
, vol.2
, pp. 825-867
-
-
Dyek, P.J.1
-
9
-
-
0023335004
-
Pes valgoplanus in Friedreich and Charcot Marie Tooth Hoffman disease
-
Exner GU. (Pes valgoplanus in Friedreich and Charcot Marie Tooth Hoffman disease). Z Orthop Jhre Grenzgeh. 1987;125:298-301.
-
(1987)
Z Orthop Jhre Grenzgeh
, vol.125
, pp. 298-301
-
-
Exner, G.U.1
-
10
-
-
0026673182
-
Detection of hereditary motor sensory neuropathy type 1 in childhood
-
Feasby TE, Hahn AF, Bolton CF, et al. Detection of hereditary motor sensory neuropathy type 1 in childhood. J Neurol Neurosurg Psychiatry. 1992;55:895-897.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 895-897
-
-
Feasby, T.E.1
Hahn, A.F.2
Bolton, C.F.3
-
11
-
-
0029962096
-
Le pied dans les neuropathies périphériques héréditaires sensitivomotrices chez l'enfant
-
Ghanem I, Zeller R, Seringe R. Le pied dans les neuropathies périphériques héréditaires sensitivomotrices chez l'enfant. Rev Chir Orthop Reparatrice Appar Mot. 1996;82:152-160.
-
(1996)
Rev Chir Orthop Reparatrice Appar Mot
, vol.82
, pp. 152-160
-
-
Ghanem, I.1
Zeller, R.2
Seringe, R.3
-
12
-
-
0027425232
-
Foot and ankle manifestations of Charcot Marie Tooth disease
-
Holmes JR, Hansen ST. Foot and ankle manifestations of Charcot Marie Tooth disease. Foot Ankle. 1993;14:476-486.
-
(1993)
Foot Ankle
, vol.14
, pp. 476-486
-
-
Holmes, J.R.1
Hansen, S.T.2
-
14
-
-
0033400053
-
Inherited peripheral neuropathy
-
Keller MP, Chance PF. Inherited peripheral neuropathy. Semin Neurol. 1999;19:353-362.
-
(1999)
Semin Neurol
, vol.19
, pp. 353-362
-
-
Keller, M.P.1
Chance, P.F.2
-
15
-
-
0018704216
-
Charcot Marie Tooth disease associated with retinal pigment dystrophy and protanopia
-
Khoubesserian P, Regemorter NV, Ohm-Degueldre O, et al. Charcot Marie Tooth disease associated with retinal pigment dystrophy and protanopia. J Neurol. 1979;222:1.
-
(1979)
J Neurol
, vol.222
, pp. 1
-
-
Khoubesserian, P.1
Regemorter, N.V.2
Ohm-Degueldre, O.3
-
16
-
-
0023722767
-
Pathophysiology of Charcot Marie Tooth disease
-
Mann RA. Missirian J. Pathophysiology of Charcot Marie Tooth disease. Clin Orthop. 1988;234:221-228.
-
(1988)
Clin Orthop
, vol.234
, pp. 221-228
-
-
Mann, R.A.1
Missirian, J.2
-
18
-
-
0023127966
-
The hypertrophic forms of the hereditary motor and sensory neuropathy
-
Ouvrier RA, McLeod JG, Conchin TE. The hypertrophic forms of the hereditary motor and sensory neuropathy Brain. 1987;110:121-148.
-
(1987)
Brain
, vol.110
, pp. 121-148
-
-
Ouvrier, R.A.1
McLeod, J.G.2
Conchin, T.E.3
-
19
-
-
0037323130
-
Diagnosis of hereditary neuropathies in adult patients
-
Pareyson D. Diagnosis of hereditary neuropathies in adult patients. J Neurol. 2003;250:148-160.
-
(2003)
J Neurol
, vol.250
, pp. 148-160
-
-
Pareyson, D.1
-
21
-
-
0021138932
-
Pathogenesis of Charcot Marie Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic and enzyme studies in a kinship
-
Sabir M, Lyttle D. Pathogenesis of Charcot Marie Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic and enzyme studies in a kinship. Clin Orthop. 1984;184:223-235.
-
(1984)
Clin Orthop
, vol.184
, pp. 223-235
-
-
Sabir, M.1
Lyttle, D.2
-
22
-
-
0020510453
-
Cavus, cavovarus and calcaneovarus. An update
-
Samilson RL, Dillon W. Cavus, cavovarus and calcaneovarus. An update. Clin Orthop. 1983;177:125-132.
-
(1983)
Clin Orthop
, vol.177
, pp. 125-132
-
-
Samilson, R.L.1
Dillon, W.2
-
23
-
-
0027068223
-
Investigation of muscle imbalance in the leg in symptomatic forefoot pes cavus: A multi disciplinary study
-
Tynan MC, Klenerman L, Helliwell TR. et al. Investigation of muscle imbalance in the leg in symptomatic forefoot pes cavus: a multi disciplinary study. Foot Ankle. 1992;13:489-501.
-
(1992)
Foot Ankle
, vol.13
, pp. 489-501
-
-
Tynan, M.C.1
Klenerman, L.2
Helliwell, T.R.3
-
25
-
-
0024584005
-
Long-term results of triple arthrodesis in Charcot-Marie-Tooth disease
-
Wetmore RS, Drennan JC. Long-term results of triple arthrodesis in Charcot-Marie-Tooth disease. J Bone Joint Surg [Am]. 1989;71:417-422.
-
(1989)
J Bone Joint Surg [Am]
, vol.71
, pp. 417-422
-
-
Wetmore, R.S.1
Drennan, J.C.2
-
26
-
-
0035369084
-
Charcot Marie Tooth disease type 2A caused by mutations in a microtubule motor K1F1 beta
-
Zhao C, Takita J, Tanaka Y, et al. Charcot Marie Tooth disease type 2A caused by mutations in a microtubule motor K1F1 beta. Cell. 2001; 105:587-597.
-
(2001)
Cell
, vol.105
, pp. 587-597
-
-
Zhao, C.1
Takita, J.2
Tanaka, Y.3
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