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R Van Coster

Showing results (11-20 of 46) with videos related to

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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.
Journal of Medical Genetics|June 1, 1985
Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndromeE Orye, M Craen, G Laureys, et al.
Acta Clinica Belgica|June 21, 2012
Cyclic vomiting syndrome: case report and short review of the literatureA Van Driessche, E Sermijn, K Paemeleire, et al.
Acta Neurochirurgica|January 1, 1992
Endoscopic treatment of suprasellar arachnoid cystsJ Caemaert, J Abdullah, L Calliauw, et al.
Cell Death and Differentiation|September 3, 2005
Butylated hydroxyanisole is more than a reactive oxygen species scavengerN Festjens, M Kalai, J Smet, et al.
Neurology|July 11, 2007
Limbic encephalitis as presentation of a SAP deficiencyH Verhelst, R Van Coster, N Bockaert, et al.
Ophthalmic Genetics|September 1, 1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutationsF M Meire, R Van Coster, P Cochaux, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiencyA Aeby, Y Sznajer, H Cavé, et al.
The Journal of Investigative Dermatology|March 25, 2000
arg-cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndromeJ Lambert, J M Naeyaert, A De Paepe, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 6, 2017
Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humansS J Vandecasteele, S Seneca, J Smet, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
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.
Journal of Medical Genetics|June 1, 1985
Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndromeE Orye, M Craen, G Laureys, et al.
Acta Clinica Belgica|June 21, 2012
Cyclic vomiting syndrome: case report and short review of the literatureA Van Driessche, E Sermijn, K Paemeleire, et al.
Acta Neurochirurgica|January 1, 1992
Endoscopic treatment of suprasellar arachnoid cystsJ Caemaert, J Abdullah, L Calliauw, et al.
Cell Death and Differentiation|September 3, 2005
Butylated hydroxyanisole is more than a reactive oxygen species scavengerN Festjens, M Kalai, J Smet, et al.
Neurology|July 11, 2007
Limbic encephalitis as presentation of a SAP deficiencyH Verhelst, R Van Coster, N Bockaert, et al.
Ophthalmic Genetics|September 1, 1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutationsF M Meire, R Van Coster, P Cochaux, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiencyA Aeby, Y Sznajer, H Cavé, et al.
The Journal of Investigative Dermatology|March 25, 2000
arg-cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndromeJ Lambert, J M Naeyaert, A De Paepe, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 6, 2017
Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humansS J Vandecasteele, S Seneca, J Smet, et al.
Pageof 5