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L De Meirleir

Showing results (1-10 of 68) with videos related to

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Acta Neurologica Belgica|December 1, 2000
Mitochondrial cytopathies and neuromuscular disordersR Van Coster, L De Meirleir
Human Genetics|March 1, 1992
Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunitL De Meirleir, W Lissens, E Vamos, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Pyruvate dehydrogenase E1 alpha deficiency in a family: different clinical presentation in two siblingsL De Meirleir, N Specola, S Seneca, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Importance of sequence analysis in NARP syndromeS Seneca, L De Meirleir, I Liebaers, et al.
Pediatric Research|December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiencyA K Cardozo, L De Meirleir, I Liebaers, et al.
Nucleic Acids Research|August 25, 1990
Characterisation of a cDNA for porcine PDH-E1 alpha and comparison with the human cDNAK Sermon, L De Meirleir, I Elpers, et al.
Pediatric Neurology|November 1, 1989
Unexpected diagnosis of Candida albicans meningitis in a premature neonateP Lenoir, L De Meirleir, A Bougatef, et al.
Pediatric Neurology|October 1, 1995
Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 geneL De Meirleir, S Seneca, W Lissens, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
A novel mitochondrial transfer RNA proline mutationS Seneca, C Ceuterik-De Groote, R Van Coster, et al.
The Journal of Pediatrics|March 1, 1994
Acrodermatitis enteropathica-like cutaneous lesions in organic aciduriaL De Raeve, L De Meirleir, J Ramet, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Acta Neurologica Belgica|December 1, 2000
Mitochondrial cytopathies and neuromuscular disordersR Van Coster, L De Meirleir
Human Genetics|March 1, 1992
Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunitL De Meirleir, W Lissens, E Vamos, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Pyruvate dehydrogenase E1 alpha deficiency in a family: different clinical presentation in two siblingsL De Meirleir, N Specola, S Seneca, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Importance of sequence analysis in NARP syndromeS Seneca, L De Meirleir, I Liebaers, et al.
Pediatric Research|December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiencyA K Cardozo, L De Meirleir, I Liebaers, et al.
Nucleic Acids Research|August 25, 1990
Characterisation of a cDNA for porcine PDH-E1 alpha and comparison with the human cDNAK Sermon, L De Meirleir, I Elpers, et al.
Pediatric Neurology|November 1, 1989
Unexpected diagnosis of Candida albicans meningitis in a premature neonateP Lenoir, L De Meirleir, A Bougatef, et al.
Pediatric Neurology|October 1, 1995
Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 geneL De Meirleir, S Seneca, W Lissens, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
A novel mitochondrial transfer RNA proline mutationS Seneca, C Ceuterik-De Groote, R Van Coster, et al.
The Journal of Pediatrics|March 1, 1994
Acrodermatitis enteropathica-like cutaneous lesions in organic aciduriaL De Raeve, L De Meirleir, J Ramet, et al.
Pageof 7