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C Rouzier

Showing results (1-10 of 14) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Molecular diagnosis and genetic counseling for spinal muscular atrophy (SMA)C Rouzier, A Chaussenot, V Paquis-Flucklinger
Revue Neurologique|July 13, 2004
[Lumbar epidural lipomatosis]H Husson, C Rouzier, N Ammar, et al.
Revue Neurologique|March 6, 2003
[Malignant externa otitis]S Sangla, C Rouzier, H Lacombe, et al.
Clinical Genetics|March 18, 2006
A novel homozygous MMP2 mutation in a family with Winchester syndromeC Rouzier, R Vanatka, S Bannwarth, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 2014
[Familial Wolfram syndrome]M Bessahraoui, V Paquis, C Rouzier, et al.
Annals of Hematology|February 9, 2000
Ex vivo expansion of CD34+/CD41+ late progenitors from enriched peripheral blood CD34+ cellsP Halle, C Rouzier, J Kanold, et al.
Medical and Pediatric Oncology|January 26, 1999
Large-volume leukapheresis procedure for peripheral blood progenitor cell collection in children weighing 15 kg or less: efficacy and safety evaluationJ Kanold, P Halle, M Berger, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndromeA Cano, C Rouzier, S Monnot, et al.
Clinical Genetics|June 4, 2014
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disordersA Chaussenot, C Rouzier, M Quere, et al.
Revue Neurologique|October 16, 2018
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase DeficiencyE Kaphan, H Bou Ali, M Gastaldi, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Molecular diagnosis and genetic counseling for spinal muscular atrophy (SMA)C Rouzier, A Chaussenot, V Paquis-Flucklinger
Revue Neurologique|July 13, 2004
[Lumbar epidural lipomatosis]H Husson, C Rouzier, N Ammar, et al.
Revue Neurologique|March 6, 2003
[Malignant externa otitis]S Sangla, C Rouzier, H Lacombe, et al.
Clinical Genetics|March 18, 2006
A novel homozygous MMP2 mutation in a family with Winchester syndromeC Rouzier, R Vanatka, S Bannwarth, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 2014
[Familial Wolfram syndrome]M Bessahraoui, V Paquis, C Rouzier, et al.
Annals of Hematology|February 9, 2000
Ex vivo expansion of CD34+/CD41+ late progenitors from enriched peripheral blood CD34+ cellsP Halle, C Rouzier, J Kanold, et al.
Medical and Pediatric Oncology|January 26, 1999
Large-volume leukapheresis procedure for peripheral blood progenitor cell collection in children weighing 15 kg or less: efficacy and safety evaluationJ Kanold, P Halle, M Berger, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndromeA Cano, C Rouzier, S Monnot, et al.
Clinical Genetics|June 4, 2014
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disordersA Chaussenot, C Rouzier, M Quere, et al.
Revue Neurologique|October 16, 2018
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase DeficiencyE Kaphan, H Bou Ali, M Gastaldi, et al.
Pageof 2