-
1
-
-
0027270106
-
Hereditary demyelinating motor and sensory neuropathies
-
Gabreëls-Festen A, Gabreëls F. Hereditary demyelinating motor and sensory neuropathies. Brain Pathol 1993;3:135-146.
-
(1993)
Brain Pathol
, vol.3
, pp. 135-146
-
-
Gabreëls-Festen, A.1
Gabreëls, F.2
-
2
-
-
0030900182
-
A clinical, electrophysiologic, neuropathologic, and genetic study of two Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease
-
Kessali M, Zemmouri R, Guilbot A, et al. et al. A clinical, electrophysiologic, neuropathologic, and genetic study of two Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease. Neurology 1997;48:867-873.
-
(1997)
Neurology
, vol.48
, pp. 867-873
-
-
Kessali, M.1
Zemmouri, R.2
Guilbot, A.3
-
3
-
-
0027491703
-
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
-
Ben Othmane K, Hentati F, Lennon F, et al. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet 1993;2:1625-1628.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1625-1628
-
-
Ben Othmane, K.1
Hentati, F.2
Lennon, F.3
-
4
-
-
9344241377
-
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. Clinical, elctrophysiologic, and genetic aspects of a large family
-
Quattrone A, Gambardella A, Bono F, et al. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. Clinical, elctrophysiologic, and genetic aspects of a large family. Neuorology 1996;46:1318-1324.
-
(1996)
Neuorology
, vol.46
, pp. 1318-1324
-
-
Quattrone, A.1
Gambardella, A.2
Bono, F.3
-
5
-
-
0029849358
-
Homozygosity mapiping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33
-
LeGuern E, Guilbot A, Kessali M, et al. Homozygosity mapiping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. Hum Mol Genet 1996;5:1685-1688.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1685-1688
-
-
LeGuern, E.1
Guilbot, A.2
Kessali, M.3
-
6
-
-
0030015647
-
Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing
-
Bolino A, Brancolini V, Bono F, et al. Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing. Hum Mol Genet 1996;5:1051-1054.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1051-1054
-
-
Bolino, A.1
Brancolini, V.2
Bono, F.3
-
7
-
-
0027317609
-
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
-
Ben Othmane K, Middleton LT, Loprest LJ, et al. Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. Genomics 1993;17:370-375.
-
(1993)
Genomics
, vol.17
, pp. 370-375
-
-
Ben Othmane, K.1
Middleton, L.T.2
Loprest, L.J.3
-
8
-
-
0029150128
-
Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q
-
Kwon JM, Elliott JL, Yee WC, et al. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q. Am J Hum Genet 1995;57:853-858.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 853-858
-
-
Kwon, J.M.1
Elliott, J.L.2
Yee, W.C.3
-
9
-
-
0029831478
-
Autosomal dominant Chartcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)
-
Ionanesu V, Searby C, Sheffield VC, Roklina T, Nishimura D, Ionanescu R, Autosomal dominant Chartcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D). Hum Mol Genet 1996;5:1373-1375.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1373-1375
-
-
Ionanesu, V.1
Searby, C.2
Sheffield, V.C.3
Roklina, T.4
Nishimura, D.5
Ionanescu, R.6
-
10
-
-
0029058673
-
From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myeloin protein
-
Harding AE. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myeloin protein. Brain 1995;118: 809-818.
-
(1995)
Brain
, vol.118
, pp. 809-818
-
-
Harding, A.E.1
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