AAAAAA

   
Results: 1-10 |
Results: 10
Retrospective study of topiramate in a paediatric population with intractable epilepsy showing promising effects in the West syndrome patients
Authors: Thijs, J Verhelst, H Van Coster, R
Citation: J. Thijs et al., Retrospective study of topiramate in a paediatric population with intractable epilepsy showing promising effects in the West syndrome patients, ACT NEUR BE, 101(3), 2001, pp. 171-176
Blue native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects
Authors: Van Coster, R Smet, J George, E De Meirleir, L Seneca, S Van Hove, J Sebire, G Verhelst, H De Bleecker, J Van Vlem, B Verloo, P Leroy, J
Citation: R. Van Coster et al., Blue native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects, PEDIAT RES, 50(5), 2001, pp. 658-665
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome
Authors: Seneca, S Verhelst, H De Meirleir, L Meire, F Groote, CCD Lissens, W Van Coster, R
Citation: S. Seneca et al., A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome, ARCH NEUROL, 58(7), 2001, pp. 1113-1118
Ultrastructural localization of cytochrome c in apoptosis demonstrates mitochondrial heterogeneity
Authors: D'Herde, K De Prest, B Mussche, S Schotte, P Beyaert, R Van Coster, R Roels, F
Citation: K. D'Herde et al., Ultrastructural localization of cytochrome c in apoptosis demonstrates mitochondrial heterogeneity, CELL DEAT D, 7(4), 2000, pp. 331-337
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2
Authors: Sue, CM Karadimas, C Checcarelli, N Tanji, K Papadopoulou, LC Pallotti, F Guo, FL Shanske, S Hirano, M De Vivo, DC Van Coster, R Kaplan, P Bonilla, E DiMauro, S
Citation: Cm. Sue et al., Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2, ANN NEUROL, 47(5), 2000, pp. 589-595
Mitochondrial cytopathies and neuromuscular disorders
Authors: Van Coster, R De Meirleir, L
Citation: R. Van Coster et L. De Meirleir, Mitochondrial cytopathies and neuromuscular disorders, ACT NEUR BE, 100(3), 2000, pp. 156-161
A novel mitochondrial transfer RNA proline mutation
Authors: Seneca, S Lissens, W Ceuterick-De Groote, C Van Coster, R De Meirleir, L
Citation: S. Seneca et al., A novel mitochondrial transfer RNA proline mutation, J INH MET D, 23(8), 2000, pp. 853-854
Arg-Cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndrome
Authors: Lambert, J Naeyaert, JM De Paepe, A Van Coster, R Ferster, A Song, M Messiaen, L
Citation: J. Lambert et al., Arg-Cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndrome, J INVES DER, 114(4), 2000, pp. 731-733
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene
Authors: Budde, SMS van den Heuvel, LPWJ Janssen, AJ Smeets, RJP Buskens, CAF DeMeirleir, L Van Coster, R Baethmann, M Voit, T Trijbels, JMF Smeitink, JAM
Citation: Sms. Budde et al., Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene, BIOC BIOP R, 275(1), 2000, pp. 63-68
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
Authors: Papadopoulou, LC Sue, CM Davidson, MM Tanji, K Nishino, I Sadlock, JE Krishna, S Walker, W Selby, J Glerum, DM Van Coster, R Lyon, G Scalais, E Lebel, R Kaplan, P Shanske, S De Vivo, DC Bonilla, E Hirano, M DiMauro, S Schon, EA
Citation: Lc. Papadopoulou et al., Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene, NAT GENET, 23(3), 1999, pp. 333-337
Risultati: 1-10 |