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Results:
1-9
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Results: 9
Authors:
De Jonghe, P
Mersivanova, I
Nelis, E
Del Favero, J
Martin, JJ
Van Broeckhoven, C
Evgrafov, OC
Timmerman, V
Citation: P. De Jonghe et al., Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E, ANN NEUROL, 49(2), 2001, pp. 245-249
Authors:
De Jonghe, P
Timmerman, V
Nelis, E
Citation: P. De Jonghe et al., Hereditary peripheral neuropathies, MG CLIN NEU, 18, 2000, pp. 128-146
Authors:
Mersiyanova, IV
Ismailov, SM
Polyakov, AV
Dadali, EL
Fedotov, VP
Nelis, E
Lofgren, A
Timmerman, V
Van Broeckhoven, C
Evgrafov, OV
Citation: Iv. Mersiyanova et al., Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32(GJB1) in Russian Charcot-Marie-Tooth neuropathy patients (vol 15, pg 340,2000), HUM MUTAT, 16(2), 2000, pp. 175-175
Authors:
Mersiyanova, IV
Ismailov, SM
Polyakov, AV
Dadali, EL
Fedotov, VP
Nelis, E
Lofgren, A
Timmerman, V
Van Broeckhoven, C
Evgrafov, OV
Citation: Iv. Mersiyanova et al., Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32(GJB1) in Russian Charcot-Marie-Tooth neuropathy patients, HUM MUTAT, 15(4), 2000, pp. 340-347
Authors:
Meuleman, J
Timmerman, V
Nelis, E
De Jonghe, P
Citation: J. Meuleman et al., Molecular genetics of inherited peripheral neuropathies: who are the actors?, ACT NEUR BE, 100(3), 2000, pp. 171-180
Authors:
Nelis, E
Haites, N
Van Broeckhoven, C
Citation: E. Nelis et al., Mutations in the peripheral myelin genes and associated genes in inheritedperipheral neuropathies, HUM MUTAT, 13(1), 1999, pp. 11-28
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
Risultati:
1-9
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