Meuleman J - Search Results

1

Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.

Irobi J, Nelis E, Meuleman J, Venken K, De Jonghe P, Van Broeckhoven C, Timmerman V. Irobi J, et al. Among authors: meuleman j. Ann Hum Genet. 2001 Nov;65(Pt 6):517-29. doi: 10.1017/S0003480001008910. Ann Hum Genet. 2001. PMID: 11851982

2

Molecular genetics of inherited peripheral neuropathies: who are the actors?

Meuleman J, Timmerman V, Nelis E, De Jonghe P. Meuleman J, et al. Acta Neurol Belg. 2000 Sep;100(3):171-80. Acta Neurol Belg. 2000. PMID: 11098291 Review.

3

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. Hum Genet. 2001 May;108(5):390-3. doi: 10.1007/s004390100510. Hum Genet. 2001. PMID: 11409865

4

Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.

Venken K, Meuleman J, Irobi J, Ceuterick C, Martini R, De Jonghe P, Timmerman V. Venken K, et al. Among authors: meuleman j. Neuroreport. 2001 Aug 8;12(11):2609-14. doi: 10.1097/00001756-200108080-00063. Neuroreport. 2001. PMID: 11496158

5

Hereditary neuralgic amyotrophy.

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

6

Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA).

Kuhlenbaeumer G, Meuleman J, Schirmacher A, Stoegbauer F, Ringelstein EB, Wehnert M, Hoeltzenbein M, Broeckhoven CV, Timmerman V. Kuhlenbaeumer G, et al. Among authors: meuleman j. Ann Hum Genet. 1998 Sep;62(Pt 5):397-400. doi: 10.1046/j.1469-1809.1998.6250397.x. Ann Hum Genet. 1998. PMID: 10088036

7

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. Ann N Y Acad Sci. 1999 Sep 14;883:443-4. Ann N Y Acad Sci. 1999. PMID: 10586268 No abstract available.

8

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: meuleman j. Genomics. 1999 Dec 1;62(2):242-50. doi: 10.1006/geno.1999.5991. Genomics. 1999. PMID: 10610718

9

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. Neuromuscul Disord. 2001 May;11(4):400-3. doi: 10.1016/s0960-8966(00)00214-5. Neuromuscul Disord. 2001. PMID: 11369192

10

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. Ann N Y Acad Sci. 1999 Oct;883(1):443-444. doi: 10.1111/j.1749-6632.1999.tb08605.x. Ann N Y Acad Sci. 1999. PMID: 29086982 No abstract available.

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