Timmerman V - Search Results

1

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy.

Hünermund G, Schirmacher A, Ringelstein B, Young P, Watts GD, Meuleman J, Nelis E, Chance PF, Timmerman V, Stögbauer F, Kuhlenbäumer G. Hünermund G, et al. Among authors: timmerman v. Muscle Nerve. 2004 Apr;29(4):601-4. doi: 10.1002/mus.20009. Muscle Nerve. 2004. PMID: 15052627

2

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.

Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C. Nelis E, et al. Among authors: timmerman v. Hum Genet. 1994 Dec;94(6):653-7. doi: 10.1007/BF00206959. Hum Genet. 1994. PMID: 7527371

3

Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.

Nelis E, Timmerman V, De Jonghe P, Muylle L, Martin JJ, Van Broeckhoven C. Nelis E, et al. Among authors: timmerman v. J Med Genet. 1994 Oct;31(10):811-5. doi: 10.1136/jmg.31.10.811. J Med Genet. 1994. PMID: 7530774 Free PMC article.

4

A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients.

Silander K, Meretoja P, Nelis E, Timmerman V, Van Broeckhoven C, Aula P, Savontaus ML. Silander K, et al. Among authors: timmerman v. Hum Mutat. 1996;8(4):304-10. doi: 10.1002/(SICI)1098-1004(1996)8:4<304::AID-HUMU2>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8956034

5

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25.

Stögbauer F, Young P, Timmerman V, Spoelders P, Ringelstein EB, Van Broeckhoven C, Kurlemann G. Stögbauer F, et al. Among authors: timmerman v. Hum Genet. 1997 May;99(5):685-7. doi: 10.1007/s004390050430. Hum Genet. 1997. PMID: 9150742

6

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.

Bort S, Nelis E, Timmerman V, Sevilla T, Cruz-Martínez A, Martínez F, Millán JM, Arpa J, Vílchez JJ, Prieto F, Van Broeckhoven C, Palau F. Bort S, et al. Among authors: timmerman v. Hum Genet. 1997 Jun;99(6):746-54. doi: 10.1007/s004390050442. Hum Genet. 1997. PMID: 9187667

7

Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q.

Wehnert M, Timmerman V, Spoelders P, Meuleman J, Nelis E, Van Broeckhoven C. Wehnert M, et al. Among authors: timmerman v. Neurology. 1997 Jun;48(6):1719-21. doi: 10.1212/wnl.48.6.1719. Neurology. 1997. PMID: 9191796

8

Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome.

Stögbauer F, Young P, Wiebusch H, Timmerman V, Kuhlenbäumer G, Nelis E, Ringelstein EB, Kurlemann G, Assmann G, Van Broeckhoven C, Funke H. Stögbauer F, et al. Among authors: timmerman v. Neurosci Lett. 1998 Jan 2;240(1):1-4. doi: 10.1016/s0304-3940(97)00887-2. Neurosci Lett. 1998. PMID: 9488160

9

PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A.

Young P, Stögbauer F, Wiebusch H, Löfgren A, Timmerman V, Van Broeckhoven C, Ringelstein EB, Assmann G, Funke H. Young P, et al. Among authors: timmerman v. Neurology. 1998 Mar;50(3):760-3. doi: 10.1212/wnl.50.3.760. Neurology. 1998. PMID: 9521270

10

[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis].

Stögbauer F, Young P, Kuhlenbäumer G, Meuleman J, Timmerman V, van Broeckhoven C, Kurlemann G, Ringelstein EB. Stögbauer F, et al. Among authors: timmerman v. Fortschr Neurol Psychiatr. 1998 Jan;66(1):10-4. doi: 10.1055/s-2007-995234. Fortschr Neurol Psychiatr. 1998. PMID: 9530552 German.

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