Van Broeckhoven C - Search Results

1

Meuleman J, Timmerman V, Van Broeckhoven C, De Jonghe P. Meuleman J, et al. Among authors: van broeckhoven c. Neurogenetics. 2001 Jul;3(3):115-8. doi: 10.1007/s100480100109. Neurogenetics. 2001. PMID: 11523561 Review.

2

Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24.

Timmerman V, De Jonghe P, Simokovic S, Löfgren A, Beuten J, Nelis E, Ceuterick C, Martin JJ, Van Broeckhoven C. Timmerman V, et al. Among authors: van broeckhoven c. Hum Mol Genet. 1996 Jul;5(7):1065-9. doi: 10.1093/hmg/5.7.1065. Hum Mol Genet. 1996. PMID: 8817349

3

Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.

Nelis E, Timmerman V, De Jonghe P, Van Broeckhoven C, Rautenstrauss B. Nelis E, et al. Among authors: van broeckhoven c. Neurogenetics. 1999 Sep;2(3):137-48. doi: 10.1007/s100480050074. Neurogenetics. 1999. PMID: 10541586 Review.

4

Distal hereditary motor neuropathy type II (distal HMN type II): phenotype and molecular genetics.

Timmerman V, Beuten J, Irobi J, De Jonghe P, Martin JJ, Van Broeckhoven C. Timmerman V, et al. Among authors: van broeckhoven c. Ann N Y Acad Sci. 1999 Sep 14;883:60-4. Ann N Y Acad Sci. 1999. PMID: 10586231

5

Hereditary neuralgic amyotrophy: mutation analysis of candidate genes.

Meuleman J, Kuhlenbäumer G, Schirmacher A, Wehnert M, Young P, Stögbauer F, Ringelstein EB, Van Broeckhoven C, Timmerman V. Meuleman J, et al. Among authors: van broeckhoven c. Ann N Y Acad Sci. 1999 Sep 14;883:443-4. Ann N Y Acad Sci. 1999. PMID: 10586268 No abstract available.

6

Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.

Meulemann J, Kuhlenbäumer G, Schirmacher A, Wehnert M, De Jonghe P, De Vriendt E, Young P, Airaksinen E, Pou-Serradell A, Prats JM, Ringelstein B, Stögbauer F, Van Broeckhoven C, Timmerman V. Meulemann J, et al. Among authors: van broeckhoven c. Eur J Hum Genet. 1999 Dec;7(8):920-7. doi: 10.1038/sj.ejhg.5200384. Eur J Hum Genet. 1999. PMID: 10602368

7

A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.

Kuhlenbäumer G, Schirmacher A, Meuleman J, Tissir F, Del-Favero J, Stögbauer F, Young P, Ringelstein B, Van Broeckhoven C, Timmerman V. Kuhlenbäumer G, et al. Among authors: van broeckhoven c. Genomics. 1999 Dec 1;62(2):242-50. doi: 10.1006/geno.1999.5991. Genomics. 1999. PMID: 10610718

8

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies.

Meuleman J, Pou-Serradell A, Löfgren A, Ceuterick C, Martin JJ, Timmerman V, Van Broeckhoven C, De Jonghe P. Meuleman J, et al. Among authors: van broeckhoven c. Neuromuscul Disord. 2001 May;11(4):400-3. doi: 10.1016/s0960-8966(00)00214-5. Neuromuscul Disord. 2001. PMID: 11369192

9

Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).

Meuleman J, Kuhlenbäumer G, Audenaert D, Hünermund G, Hor H, Young P, Stögbauer F, Ringelstein EB, Van Broeckhoven C, De Jonghe P, Timmerman V. Meuleman J, et al. Among authors: van broeckhoven c. Hum Genet. 2001 May;108(5):390-3. doi: 10.1007/s004390100510. Hum Genet. 2001. PMID: 11409865

10

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: van broeckhoven c. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522

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