-
3
-
-
0034062698
-
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
-
(2000)
Nat. Genet.
, vol.25
, pp. 17-19
-
-
Bolino, A.1
Muglia, M.2
Conforti, F.L.3
LeGuern, E.4
Salih, M.A.M.5
Georgiou, A.-M.6
Christodoulou, K.7
Hausmanowa-Petrusewicz, I.8
Mandich, P.9
Schenone, A.10
Gambardella, A.11
Bono, F.12
Quattrone, A.13
Devoto, M.14
Monaco, A.P.15
-
5
-
-
0035931751
-
The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in P0
-
(2001)
J. Cell Biol.
, vol.152
, pp. 301-308
-
-
Carenini, S.1
Mäurer, M.2
Werner, A.3
Blazyca, H.4
Toyka, K.V.5
Schmid, C.6
Raivich, G.7
Martini, R.8
-
7
-
-
0000365860
-
Morphometrical and ultrastructural evaluation of the sural nerve in children with Charcot-Marie-Tooth: Implication for pathogenesis and treatment
-
(1991)
Ann. Neurol.
, vol.30
, pp. 500
-
-
Crawford, T.O.1
Griffin, J.W.2
-
11
-
-
0015297040
-
Control of myelin formation by axon caliber (with a model of the control mechanism)
-
(1972)
J. Comp. Neurol.
, vol.144
, pp. 233-252
-
-
Friede, R.L.1
-
16
-
-
0035864930
-
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 415-421
-
-
Guilbot, A.1
Williams, A.2
Ravise, N.3
Verny, C.4
Brice, A.5
Sherman, D.6
Brophy, P.7
LeGuern, E.8
Delague, V.9
Bareil, C.10
Megarbane, A.11
Claustres, M.12
-
20
-
-
0033910767
-
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 47-58
-
-
Kalaydjieva, L.1
Gresham, D.2
Gooding, R.3
Heather, L.4
Baas, F.5
De Jonge, R.6
Blechschmidt, K.7
Angelicheva, D.8
Chandler, D.9
Worsley, P.10
Rosenthal, A.11
King, R.H.M.12
Thomas, P.K.13
-
21
-
-
0033560646
-
Motor neuropathy in porphobilinogen deaminase-deficient mice imitiates the peripheral neuropathy of human acute porphyria
-
(1999)
J. Clin. Invest.
, vol.103
, pp. 1127-1134
-
-
Lindberg, R.L.P.1
Martini, R.2
Baumgartner, M.3
Erne, B.4
Borg, J.5
Zielasek, J.6
Ricker, K.7
Steck, A.8
Toyka, K.V.9
Meyer, U.A.10
-
24
-
-
0030696172
-
Animal models for inherited peripheral neuropathies
-
(1997)
J. Anat.
, vol.191
, pp. 321-336
-
-
Martini, R.1
-
25
-
-
0034254710
-
Animal models for inherited peripheral neuropathies: Chances to find treatment strategies
-
(2000)
J. Neurosci. Res.
, vol.61
, pp. 244-250
-
-
Martini, R.1
-
26
-
-
0033911099
-
A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 37-46
-
-
Mersiyanova, I.V.1
Perepelov, A.V.2
Polyakov, A.V.3
Sidnikov, V.F.4
Dadli, E.L.5
Oparin, R.B.6
Petrin, A.N.7
Evgrafov, O.V.8
-
34
-
-
0033808344
-
Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT1A
-
(2000)
J. Peripher. Nerv. Syst.
, vol.5
, pp. 158-162
-
-
Rajabally, Y.1
Vital, A.2
Ferrer, X.3
Vital, C.4
Julien, J.5
Latour, P.6
Vandenberghe, A.7
Lagueny, A.8
-
35
-
-
18144436151
-
Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and aquired neuropathies
-
(2000)
J. Neuroimmunol.
, vol.104
, pp. 155-163
-
-
Ritz, M.-F.1
Lechner-Scott, J.2
Scott, R.J.3
Fuhr, P.4
Malik, N.5
Erne, B.6
Taylor, V.7
Suter, U.8
Schaeren-Wiemers, N.9
Steck, A.J.10
-
37
-
-
0034651089
-
Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance
-
(2000)
J. Neurosci.
, vol.20
, pp. 729-735
-
-
Schmid, C.D.1
Stienekemeier, M.2
Oehen, S.3
Bootz, F.4
Zielasek, J.5
Gold, R.6
Toyka, K.V.7
Schachner, M.8
Martini, R.9
-
38
-
-
0030611992
-
Heterozygous P0 knock-out mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy
-
J. Neuropathol. Exp. Neurol.
, vol.56
, pp. 811-821
-
-
Shy, M.E.1
Arroyo, E.2
Sladky, J.3
Menichella, D.4
Jiang, H.5
Xu, W.6
Kamholz, J.7
Scherer, S.S.8
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