-
1
-
-
0013878073
-
Ultrastructural appearance of glycogen in the B-neurons of the lumbar spinal ganglia of the frog
-
Berthold C-H, (1966). Ultrastructural appearance of glycogen in the B-neurons of the lumbar spinal ganglia of the frog. J Ultrastruct Res 14: 254-267.
-
(1966)
J Ultrastruct Res
, vol.14
, pp. 254-267
-
-
Berthold, C.-H.1
-
2
-
-
0017286744
-
Peripheral nerve fibre changes in asymptomatic children of patients with familial amyloid polyneuropathy
-
Carvalho J, Coimbra A, Andrade C, (1976). Peripheral nerve fibre changes in asymptomatic children of patients with familial amyloid polyneuropathy. Brain 99: 1-10.
-
(1976)
Brain
, vol.99
, pp. 1-10
-
-
Carvalho, J.1
Coimbra, A.2
Andrade, C.3
-
3
-
-
0027509953
-
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
-
DOI 10.1016/0092-8674(93)90058-X
-
Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Bird TD, (1993). DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 72: 143-151. (Pubitemid 23029701)
-
(1993)
Cell
, vol.72
, Issue.1
, pp. 143-151
-
-
Chance, P.F.1
Alderson, M.K.2
Leppig, K.A.3
Lensch, M.W.4
Matsunami, N.5
Smith, B.6
Swanson, P.D.7
Odelberg, S.J.8
Disteche, C.M.9
Bird, T.D.10
-
4
-
-
58149147512
-
Schwann cell to axon transfer of ribosomes: Toward a novel understanding of the role of glia in the nervous system
-
Court FA, Hendriks WT, Macgillavry HD, Alvarez J, van Minnen J, (2008). Schwann cell to axon transfer of ribosomes: toward a novel understanding of the role of glia in the nervous system. J Neurosci 28: 11024-11029.
-
(2008)
J Neurosci
, vol.28
, pp. 11024-11029
-
-
Court, F.A.1
Hendriks, W.T.2
MacGillavry, H.D.3
Alvarez, J.4
Van Minnen, J.5
-
5
-
-
0036257516
-
Dejerine-Sottas syndrome grown to maturity: Overview of genetic and morphologicl heterogeneity and follow-up of 25 patients
-
DOI 10.1046/j.1469-7580.2002.00043.x
-
Gabreels-Festen A, (2002). Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients. J Anat 200: 341-356. (Pubitemid 34498529)
-
(2002)
Journal of Anatomy
, vol.200
, Issue.4
, pp. 341-356
-
-
Gabreels-Festen, A.1
-
6
-
-
0037370894
-
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease
-
DOI 10.1093/brain/awg059
-
Jordanova A, De Jonghe P, Boerkoel CF, Takashima H, De Vriendt E, Ceuterick C, Martin JJ, Butler IJ, Mancias P, Papasozomenos S, Terespolsky D, Potocki L, Brown CW, Shy M, Rita DA, Tournev I, Kremensky I, Lupski JR, Timmerman V, (2003). Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease. Brain 126: 590-597. (Pubitemid 36240860)
-
(2003)
Brain
, vol.126
, Issue.3
, pp. 590-597
-
-
Jordanova, A.1
De Jonghe, P.2
Boerkoel, C.F.3
Takashima, H.4
De Vriendt, E.5
Ceuterick, C.6
Martin, J.-J.7
Butler, I.J.8
Mancias, P.9
Papasozomenos, S.Ch.10
Terespolsky, D.11
Potocki, L.12
Brown, C.W.13
Shy, M.14
Rita, D.A.15
Tournev, I.16
Kremensky, I.17
Lupski, J.R.18
Timmerman, V.19
-
7
-
-
34547439282
-
Ribosomal distributions in axons of mammalian myelinated fibers
-
DOI 10.1002/jnr.21340
-
Kun A, Otero L, Sotelo-Silveira JR, Sotelo JR, (2007). Ribosomal distributions in axons of mammalian myelinated fibers. J Neurosci Res 85: 2087-2098. (Pubitemid 47172141)
-
(2007)
Journal of Neuroscience Research
, vol.85
, Issue.10
, pp. 2087-2098
-
-
Kun, A.1
Otero, L.2
Sotelo-Silveira, J.R.3
Sotelo, J.R.4
-
8
-
-
0025868571
-
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
-
Lupski JR, de Oca-Luna RM, Slaugenhaupt S, Pentao L, Guzzetta V, Trask BJ, Saucedo-Cardenas O, Barker DF, Killian JM, Garcia CA, Chakravarti A, Patel PI, (1991). DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 66: 219-232. (Pubitemid 121001361)
-
(1991)
Cell
, vol.66
, Issue.2
, pp. 219-232
-
-
Lupski, J.R.1
De Oca-Luna, R.M.2
Slaugenhaupt, S.3
Pentao, L.4
Guzzetta, V.5
Trask, B.J.6
Saucedo-Cardenas, O.7
Barker, D.F.8
Killian, J.M.9
Garcia, C.A.10
Chakravarti, A.11
Patel, P.I.12
-
9
-
-
0035078628
-
The effect of myelinating Schwann cells on axons
-
DOI 10.1002/mus.1027
-
Martini R, (2001). The effect of myelinating Schwann cells on axons. Muscle Nerve 24: 456-466. (Pubitemid 32246780)
-
(2001)
Muscle and Nerve
, vol.24
, Issue.4
, pp. 456-466
-
-
Martini, R.1
-
10
-
-
60149083988
-
Molecular mechanisms of inherited demyelinating neuropathies
-
Scherer SS, Wrabetz L, (2008). Molecular mechanisms of inherited demyelinating neuropathies. Glia 56: 1578-1589.
-
(2008)
Glia
, vol.56
, pp. 1578-1589
-
-
Scherer, S.S.1
Wrabetz, L.2
-
11
-
-
0141833983
-
Disease mechanisms in inherited neuropathies
-
DOI 10.1038/nrn1196
-
Suter U, Scherer SS, (2003). Disease mechanisms in inherited neuropathies. Nat Rev Neurosci 4: 714-726. (Pubitemid 37280151)
-
(2003)
Nature Reviews Neuroscience
, vol.4
, Issue.9
, pp. 714-726
-
-
Suter, U.1
Scherer, S.S.2
-
12
-
-
2442589922
-
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
-
DOI 10.1038/ng1341
-
Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battologlu E, Polyakov AV, Timmerman V, Schroder JM, Vance JM., (2004) Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nat Genet 36: 449-451. (Pubitemid 38620027)
-
(2004)
Nature Genetics
, vol.36
, Issue.5
, pp. 449-451
-
-
Zuchner, S.1
Mersiyanova, I.V.2
Muglia, M.3
Bissar-Tadmouri, N.4
Rochelle, J.5
Dadali, E.L.6
Zappia, M.7
Nelis, E.8
Patitucci, A.9
Senderek, J.10
Parman, Y.11
Evgrafov, O.12
De Jonghe, P.13
Takahashi, Y.14
Tsuji, S.15
Pericak-Vance, M.A.16
Quattrone, A.17
Battologlu, E.18
Polyakov, A.V.19
Timmerman, V.20
Schroder, J.M.21
Vance, J.M.22
more..
|