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Results:
1-11
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Results: 11
Authors:
Meuleman, J
Kuhlenbaumer, G
Audenaert, D
Hunermund, G
Hor, H
Young, P
Stogbauer, F
Ringelstein, EB
Van Broeckhoven, C
De Jonghe, P
Timmerman, V
Citation: J. Meuleman et al., Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy(HNA), HUM GENET, 108(5), 2001, pp. 390-393
Authors:
Young, P
Grote, K
Kuhlenbaumer, G
Debus, O
Kurlemann, H
Halfter, H
Funke, H
Ringelstein, EB
Stogbauer, E
Citation: P. Young et al., Mutation analysis in Charcot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity, J NEUROL, 248(5), 2001, pp. 410-415
Authors:
Kuhlenbaumer, G
Meuleman, J
De Jonghe, P
Falck, B
Young, P
Hunermund, G
Van Broeckhoven, C
Timmerman, V
Stogbauer, F
Citation: G. Kuhlenbaumer et al., Hereditary neuralgic amyotrophy (HNA) is genetically heterogeneous, J NEUROL, 248(10), 2001, pp. 861-865
Authors:
Kuhlenbaumer, G
Kress, W
Ringelstein, EB
Stogbauer, F
Citation: G. Kuhlenbaumer et al., Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals, J NEUROL, 248(1), 2001, pp. 23-26
Authors:
Kuhlenbaumer, G
Stogbauer, F
Timmerman, V
De Jonghe, P
Citation: G. Kuhlenbaumer et al., Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection, NEUROMUSC D, 10(7), 2000, pp. 515-517
Authors:
Young, P
Stogbauer, F
Eller, B
de Jonghe, P
Lofgren, A
Timmerman, V
Rautenstrauss, B
Oexle, K
Grehl, H
Kuhlenbaumer, G
Van Broeckhoven, C
Ringelstein, EB
Funke, H
Citation: P. Young et al., PMP22 Thr118Met is not a clinically relevant CMT1 marker, J NEUROL, 247(9), 2000, pp. 696-700
Authors:
Stogbauer, F
Young, P
Kuhlenbaumer, G
De Jonghe, P
Timmerman, V
Citation: F. Stogbauer et al., Hereditary recurrent focal neuropathies - Clinical and molecular features, NEUROLOGY, 54(3), 2000, pp. 546-551
Authors:
Meuleman, J
Kuhlenbaumer, G
Schirmacher, A
Wehnert, M
De Jonghe, P
De Vriendt, E
Young, P
Airaksinen, E
Pou-Serradell, A
Prats, JM
Ringelstein, B
Stogbauer, F
Van Broeckhoven, C
Timmerman, V
Citation: J. Meuleman et al., Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25, EUR J HUM G, 7(8), 1999, pp. 920-927
Authors:
Kuhlenbaumer, G
Schirmacher, A
Meuleman, J
Tissir, F
Del-Favero, J
Stogbauer, F
Young, P
Ringelstein, B
Van Broeckhoven, C
Timmerman, V
Citation: G. Kuhlenbaumer et al., A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes, GENOMICS, 62(2), 1999, pp. 242-250
Authors:
Liehr, T
Kuhlenbaumer, G
Wulf, P
Taylor, V
Suter, U
Van Broeckhoven, C
Lupski, JR
Claussen, U
Rautenstrauss, B
Citation: T. Liehr et al., Regional localization of the human epithelial membrane protein genes 1, 2,and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3, GENOMICS, 58(1), 1999, pp. 106-108
Authors:
Stogbauer, F
Young, P
Kuhlenbaumer, G
Kiefer, R
Timmerman, V
Ringelstein, EB
Wang, JF
Schroder, JM
Van Broeckhoven, C
Weis, J
Citation: F. Stogbauer et al., Autosomal dominant burning feet syndrome, J NE NE PSY, 67(1), 1999, pp. 78-81
Risultati:
1-11
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