Lissens W - Search Results

1

Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene.

Buysse K, Vergult S, Mussche S, Ceuterick-de Groote C, Speleman F, Menten B, Lissens W, Van Coster R. Buysse K, et al. Among authors: lissens w. Am J Med Genet A. 2010 Nov;152A(11):2802-4. doi: 10.1002/ajmg.a.33508. Am J Med Genet A. 2010. PMID: 20949505

2

Proteomic analysis in giant axonal neuropathy: new insights into disease mechanisms.

Mussche S, De Paepe B, Smet J, Devreese K, Lissens W, Rasic VM, Murnane M, Devreese B, Van Coster R. Mussche S, et al. Among authors: lissens w. Muscle Nerve. 2012 Aug;46(2):246-56. doi: 10.1002/mus.23306. Muscle Nerve. 2012. PMID: 22806374

3

Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II.

Van Coster R, Seneca S, Smet J, Van Hecke R, Gerlo E, Devreese B, Van Beeumen J, Leroy JG, De Meirleir L, Lissens W. Van Coster R, et al. Among authors: lissens w. Am J Med Genet A. 2003 Jul 1;120A(1):13-8. doi: 10.1002/ajmg.a.10202. Am J Med Genet A. 2003. PMID: 12794685

4

Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene.

De Meirleir L, Seneca S, Damis E, Sepulchre B, Hoorens A, Gerlo E, García Silva MT, Hernandez EM, Lissens W, Van Coster R. De Meirleir L, et al. Among authors: lissens w. Am J Med Genet A. 2003 Aug 30;121A(2):126-31. doi: 10.1002/ajmg.a.20171. Am J Med Genet A. 2003. PMID: 12910490

5

A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.

Seneca S, Verhelst H, De Meirleir L, Meire F, Ceuterick-De Groote C, Lissens W, Van Coster R. Seneca S, et al. Among authors: lissens w. Arch Neurol. 2001 Jul;58(7):1113-8. doi: 10.1001/archneur.58.7.1113. Arch Neurol. 2001. PMID: 11448301 Review.

6

Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12.

De Meirleir L, Seneca S, Lissens W, De Clercq I, Eyskens F, Gerlo E, Smet J, Van Coster R. De Meirleir L, et al. Among authors: lissens w. J Med Genet. 2004 Feb;41(2):120-4. doi: 10.1136/jmg.2003.012047. J Med Genet. 2004. PMID: 14757859 Free PMC article.

7

Array comparative genomic hybridization in male infertility.

Stouffs K, Vandermaelen D, Massart A, Menten B, Vergult S, Tournaye H, Lissens W. Stouffs K, et al. Among authors: lissens w. Hum Reprod. 2012 Mar;27(3):921-9. doi: 10.1093/humrep/der440. Epub 2012 Jan 11. Hum Reprod. 2012. PMID: 22238114

8

A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis.

Meulemans A, Seneca S, Smet J, De Paepe B, Lissens W, Van Coster R, Debeer A, De Meirleir L, Jaeken J. Meulemans A, et al. Among authors: lissens w. Eur J Paediatr Neurol. 2007 Jan;11(1):17-20. doi: 10.1016/j.ejpn.2006.10.004. Epub 2006 Dec 11. Eur J Paediatr Neurol. 2007. PMID: 17161635

9

A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure.

Meulemans A, Seneca S, Lagae L, Lissens W, De Paepe B, Smet J, Van Coster R, De Meirleir L. Meulemans A, et al. Among authors: lissens w. Arch Neurol. 2006 Aug;63(8):1194-8. doi: 10.1001/archneur.63.8.1194. Arch Neurol. 2006. PMID: 16908752

10

Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA.

Smet J, Seneca S, De Paepe B, Meulemans A, Verhelst H, Leroy J, De Meirleir L, Lissens W, Van Coster R. Smet J, et al. Among authors: lissens w. Electrophoresis. 2009 Oct;30(20):3565-72. doi: 10.1002/elps.200900213. Electrophoresis. 2009. PMID: 19862739

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