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V Laugel

Showing results (21-30 of 28) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 20, 2019
Lyme neuroborreliosis in children: Report of nine cases and a review of the literatureH Guet-Revillet, C Levy, C Vallet, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|January 23, 2008
Peritoneal dialysis in children: consider the membrane for optimal prescriptionM Fischbach, C Dheu, A C Michallat, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.
Journal of Human Genetics|December 20, 2019
Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth diseaseJ Mortreux, J Bacquet, A Boyer, et al.
Journal of Inherited Metabolic Disease|May 31, 2012
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 casesS Koene, R J Rodenburg, M S van der Knaap, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|April 9, 2020
The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central BrazilL P Castro, M Sahbatou, F S G Kehdy, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 20, 2019
Lyme neuroborreliosis in children: Report of nine cases and a review of the literatureH Guet-Revillet, C Levy, C Vallet, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|January 23, 2008
Peritoneal dialysis in children: consider the membrane for optimal prescriptionM Fischbach, C Dheu, A C Michallat, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.
Journal of Human Genetics|December 20, 2019
Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth diseaseJ Mortreux, J Bacquet, A Boyer, et al.
Journal of Inherited Metabolic Disease|May 31, 2012
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 casesS Koene, R J Rodenburg, M S van der Knaap, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|April 9, 2020
The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central BrazilL P Castro, M Sahbatou, F S G Kehdy, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Pageof 3