AAAAAA
Results:
1-12
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Results: 12
Authors:
Meuleman, J
Pou-Serradell, A
Lofgren, A
Ceuterick, C
Martin, JJ
Timmerman, V
Van Broeckhoven, C
De Jonghe, P
Citation: J. Meuleman et al., A novel 3 '-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies, NEUROMUSC D, 11(4), 2001, pp. 400-403
Authors:
Venken, K
Meuleman, J
Irobi, J
Ceuterick, C
Martini, R
De Jonghe, P
Timmerman, V
Citation: K. Venken et al., CasprI/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies, NEUROREPORT, 12(11), 2001, pp. 2609-2614
Authors:
Kumar-Singh, S
Dewachter, I
Moechars, D
Lubke, U
De Jonghe, C
Ceuterick, C
Checler, F
Naidu, A
Cordell, B
Cras, P
Van Broeckhoven, C
Van Leuven, F
Citation: S. Kumar-singh et al., Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutation, NEUROBIOL D, 7(1), 2000, pp. 9-22
Authors:
Palmeri, S
Villanova, M
Malandrini, A
van Diggelen, OP
Huijmans, JGM
Ceuterick, C
Rufa, A
DeFalco, D
Ciacci, G
Martin, JJ
Guazzi, G
Citation: S. Palmeri et al., Type I sialidosis: A clinical, biochemical and neuroradiological study, EUR NEUROL, 43(2), 2000, pp. 88-94
Authors:
Martin, JJ
Ceuterick, C
Citation: Jj. Martin et C. Ceuterick, NCL in different European countries, BIOM HLTH R, 33, 1999, pp. 128-141
Authors:
Mauger, C
Del-Favero, J
Ceuterick, C
Lubke, U
van Broeckhoven, C
Martin, JJ
Citation: C. Mauger et al., Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody, MOL BRAIN R, 74(1-2), 1999, pp. 35-43
Authors:
Timmerman, V
De Jonghe, P
Ceuterick, C
De Vriendt, E
Lofgren, A
Nelis, E
Warner, LE
Lupski, JR
Martin, JJ
Van Broeckhoven, C
Citation: V. Timmerman et al., Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype, NEUROLOGY, 52(9), 1999, pp. 1827-1832
Authors:
De Jonghe, P
Timmerman, V
Ceuterick, C
Nelis, E
De Vriendt, E
Lofgren, A
Vercruyssen, A
Verellen, C
Van Maldergem, L
Martin, JJ
Van Broeckhoven, C
Citation: P. De Jonghe et al., The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene isassociated with a clinically distinct Charcot-Marie-Tooth phenotype, BRAIN, 122, 1999, pp. 281-290
Authors:
De Jonghe, P
Timmerman, V
Nelis, E
De Vriendt, E
Lofgren, A
Ceuterick, C
Martin, JJ
Van Broeckhoven, C
Citation: P. De Jonghe et al., A novel type of hereditary motor and sensory neuropathy characterized by amild phenotype, ARCH NEUROL, 56(10), 1999, pp. 1283-1288
Authors:
Villanova, M
Ceuterick, C
Dotti, MT
Santorelli, FM
Casali, C
Malandrini, A
De Stefano, N
Lubke, U
Martin, JJ
Guazzi, GC
Federico, A
Citation: M. Villanova et al., Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjogren), ACT NEUROP, 98(1), 1999, pp. 78-84
Authors:
Deprez, M
D'Hooge, M
Misson, JP
de Leval, L
Ceuterick, C
Reznik, M
Martin, JJ
Citation: M. Deprez et al., Infantile and juvenile presentations of Alexander's disease: a report of two cases, ACT NEUR SC, 99(3), 1999, pp. 158-165
Authors:
Deprez, M
D'Hooghe, M
Misson, JP
de Leval, L
Ceuterick, C
Reznik, M
Martin, JJ
Citation: M. Deprez et al., Infantile and juvenile presentations of Alexander's disease: a report of two cases (vol 99, pg 158, 1999), ACT NEUR SC, 100(5), 1999, pp. 354-354
Risultati:
1-12
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