Results
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81.
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Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. [electronic resource] by
- Lenssen, P P
- Gabreëls-Festen, A A
- Valentijn, L J
- Jongen, P J
- van Beersum, S E
- van Engelen, B G
- van Wensen, P J
- Bolhuis, P A
- Gabreëls, F J
- Mariman, E C
Producer: 19980911
In:
Brain : a journal of neurology vol. 121 ( Pt 8)
Availability: No items available.
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82.
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Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological study. [electronic resource] by
- Teunissen, L L
- Notermans, N C
- Franssen, H
- van der Graaf, Y
- Oey, P L
- Linssen, W H
- van Engelen, B G
- Ippel, P F
- van Dijk, G W
- Gabreëls-Festen, A A
- Wokke, J H
Producer: 19970801
In:
Brain : a journal of neurology vol. 120 ( Pt 6)
Availability: No items available.
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83.
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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. [electronic resource] by
- Gabreëls-Festen, A A
- Hoogendijk, J E
- Meijerink, P H
- Gabreëls, F J
- Bolhuis, P A
- van Beersum, S
- Kulkens, T
- Nelis, E
- Jennekens, F G
- de Visser, M
- van Engelen, B G
- Van Broeckhoven, C
- Mariman, E C
Producer: 19961122
In:
Neurology vol. 47
Availability: No items available.
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84.
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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations. [electronic resource] by
- Azzedine, H
- Ravisé, N
- Verny, C
- Gabrëels-Festen, A
- Lammens, M
- Grid, D
- Vallat, J M
- Durosier, G
- Senderek, J
- Nouioua, S
- Hamadouche, T
- Bouhouche, A
- Guilbot, A
- Stendel, C
- Ruberg, M
- Brice, A
- Birouk, N
- Dubourg, O
- Tazir, M
- LeGuern, E
Producer: 20060913
In:
Neurology vol. 67
Availability: No items available.
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85.
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Phenotype of Charcot-Marie-Tooth disease Type 2. [electronic resource] by
- Bienfait, H M E
- Baas, F
- Koelman, J H T M
- de Haan, R J
- van Engelen, B G M
- Gabreëls-Festen, A A W M
- Ongerboer de Visser, B W
- Meggouh, F
- Weterman, M A J
- De Jonghe, P
- Timmerman, V
- de Visser, M
Producer: 20070607
In:
Neurology vol. 68
Availability: No items available.
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86.
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Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy. [electronic resource] by
- Nelis, E
- Erdem, S
- Van Den Bergh, P Y K
- Belpaire-Dethiou, M-C
- Ceuterick, C
- Van Gerwen, V
- Cuesta, A
- Pedrola, L
- Palau, F
- Gabreëls-Festen, A A W M
- Verellen, C
- Tan, E
- Demirci, M
- Van Broeckhoven, C
- De Jonghe, P
- Topaloglu, H
- Timmerman, V
Producer: 20030114
In:
Neurology vol. 59
Availability: No items available.
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87.
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Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT Consortium. [electronic resource] by
- Müller, H W
- Suter, U
- Van Broeckhoven, C
- Hanemann, C O
- Nelis, E
- Timmerman, V
- Sancho, S
- Barrio, L
- Bolhuis, P
- Dermietzel, R
- Frank, M
- Gabreëls-Festen, A
- Gillen, C
- Haites, N
- Levi, G
- Mariman, E
- Martini, R
- Nave, K
- Rautenstrauss, B
- Schachner, M
- Schenone, A
- Schneider, C
- Schröder, M
- Willecke, K
- Haneman, O
Producer: 19971210
In:
Neurobiology of disease vol. 4
Availability: No items available.
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