-
1
-
-
34447256798
-
Skin denervation and cutaneous vasculitis in eosinophilia-associated neuropathy
-
Chao C-C, Hsieh S-T, Shun C-T, Hsieh S-C. Skin denervation and cutaneous vasculitis in eosinophilia-associated neuropathy. Arch Neurol. 2007;64(7):959-965.
-
(2007)
Arch Neurol
, vol.64
, Issue.7
, pp. 959-965
-
-
Chao, C.-C.1
Hsieh, S.-T.2
Shun, C.-T.3
Hsieh, S.-C.4
-
2
-
-
0025091391
-
The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis)
-
Masi AT, Hunder GG, Lie JT, et al. The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis). Arthritis Rheum. 1990;33(8):1094-1100.
-
(1990)
Arthritis Rheum
, vol.33
, Issue.8
, pp. 1094-1100
-
-
Masi, A.T.1
Hunder, G.G.2
Lie, J.T.3
-
3
-
-
34447260902
-
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene
-
Miltenberger-Miltenyi G, Janecke AR, Wanschitz JV, et al. Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene. Arch Neurol. 2007;64(7):966-970.
-
(2007)
Arch Neurol
, vol.64
, Issue.7
, pp. 966-970
-
-
Miltenberger-Miltenyi, G.1
Janecke, A.R.2
Wanschitz, J.V.3
-
4
-
-
0037370894
-
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease
-
Jordanova A, De Jonghe P, Boerkoel CF, et al. Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease. Brain. 2003;126(Pt 3):590-597.
-
(2003)
Brain
, vol.126
, Issue.PART 3
, pp. 590-597
-
-
Jordanova, A.1
De Jonghe, P.2
Boerkoel, C.F.3
-
5
-
-
34447263764
-
Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies
-
Li J, Ghandour K, Radovanovic D, et al. Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies. Arch Neurol. 2007;64(7):974-978.
-
(2007)
Arch Neurol
, vol.64
, Issue.7
, pp. 974-978
-
-
Li, J.1
Ghandour, K.2
Radovanovic, D.3
-
6
-
-
0027509953
-
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
-
Chance PF, Alderson MK, Leppig KA, et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell. 1993;72(1):143-151.
-
(1993)
Cell
, vol.72
, Issue.1
, pp. 143-151
-
-
Chance, P.F.1
Alderson, M.K.2
Leppig, K.A.3
-
7
-
-
0034830932
-
The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes
-
Inoue K, Dewar K, Katsanis N, et al. The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes. Genome Res. 2001;11(6):1018-1033.
-
(2001)
Genome Res
, vol.11
, Issue.6
, pp. 1018-1033
-
-
Inoue, K.1
Dewar, K.2
Katsanis, N.3
-
8
-
-
21044457652
-
Skin biopsies in myelin-related neuropathies: Bringing molecular pathology to the bedside
-
Li J, Bai Y, Ghandour K, et al. Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside. Brain. 2005;128(pt 5):1168-1177.
-
(2005)
Brain
, vol.128
, Issue.PART 5
, pp. 1168-1177
-
-
Li, J.1
Bai, Y.2
Ghandour, K.3
-
9
-
-
26444544500
-
Skin denervation in vasculitic neuropathy
-
Lee J-E, Shun C-T, Hsieh S-C, Hsieh S-T. Skin denervation in vasculitic neuropathy. Arch Neurol. 2005;62(10):1570-1573.
-
(2005)
Arch Neurol
, vol.62
, Issue.10
, pp. 1570-1573
-
-
Lee, J.-E.1
Shun, C.-T.2
Hsieh, S.-C.3
Hsieh, S.-T.4
-
10
-
-
0031704145
-
Epidermal nerve fiber density: Normative reference range and diagnostic efficiency
-
McArthur JC, Stocks A, Hauer P, et al. Epidermal nerve fiber density: normative reference range and diagnostic efficiency. Arch Neurol. 1998;55(12):1513-1520.
-
(1998)
Arch Neurol
, vol.55
, Issue.12
, pp. 1513-1520
-
-
McArthur, J.C.1
Stocks, A.2
Hauer, P.3
-
11
-
-
33746854437
-
Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration
-
Li J, Bai Y, Ianakova E, et al. Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration. J Comp Neurol. 2006;498(2):252-265.
-
(2006)
J Comp Neurol
, vol.498
, Issue.2
, pp. 252-265
-
-
Li, J.1
Bai, Y.2
Ianakova, E.3
-
12
-
-
0031909629
-
A prospective quantitative study of sensory deficits after whole sural nerve biopsies in diabetic and nondiabetic patients: Surgical approach and the role of collateral sprouting
-
Theriault M, Dort J, Surtherland G, Zochodne DW. A prospective quantitative study of sensory deficits after whole sural nerve biopsies in diabetic and nondiabetic patients: surgical approach and the role of collateral sprouting. Neurology. 1998;50(2):480-484.
-
(1998)
Neurology
, vol.50
, Issue.2
, pp. 480-484
-
-
Theriault, M.1
Dort, J.2
Surtherland, G.3
Zochodne, D.W.4
-
13
-
-
0033004562
-
Clinical outcome of sural nerve biopsy: A retrospective study
-
Flachenecker P, Janka M, Goldbrunner R, Toyka KV. Clinical outcome of sural nerve biopsy: a retrospective study. J Neurol. 1999;246(2):93-96.
-
(1999)
J Neurol
, vol.246
, Issue.2
, pp. 93-96
-
-
Flachenecker, P.1
Janka, M.2
Goldbrunner, R.3
Toyka, K.V.4
-
14
-
-
0025663652
-
Postoperative effects and value of sural nerve biopsies: A retrospective study
-
Neundorfer B, Grahmann F, Engelhardt A, Harte U. Postoperative effects and value of sural nerve biopsies: a retrospective study. Eur Neurol. 1990;30(6):350-352.
-
(1990)
Eur Neurol
, vol.30
, Issue.6
, pp. 350-352
-
-
Neundorfer, B.1
Grahmann, F.2
Engelhardt, A.3
Harte, U.4
-
15
-
-
0023932396
-
Discomfort after fascicular sural nerve biopsy
-
Solders G. Discomfort after fascicular sural nerve biopsy. Acta Neurol Scand. 1988;77(6):503-504.
-
(1988)
Acta Neurol Scand
, vol.77
, Issue.6
, pp. 503-504
-
-
Solders, G.1
|