Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Bekri

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
International Journal of Clinical Practice|February 1, 2007
Clinical results of enzyme replacement therapy in Fabry disease: a comprehensive review of literatureO Lidove, D Joly, F Barbey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 7, 2017
[A case of neonatal hypotonia]A Hedjoudje, S Torre, S Bekri, et al.
Revue Neurologique|October 29, 2011
[Stroke and cornea verticillata revealing Fabry's disease in a female]D Fetter, A Bagan-Triquenot, E Guegan-Massardier, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Arginase deficiency in two brothersM Candito, B Bebin, C Vianey-Saban, et al.
Mucosal Immunology|June 27, 2013
Antigen-bearing dendritic cells from the sublingual mucosa recirculate to distant systemic lymphoid organs to prime mucosal CD8 T cellsC Hervouet, C Luci, S Bekri, et al.
Genes, Chromosomes & Cancer|October 1, 1993
Expanded range of 11q13 breakpoints with differing patterns of cyclin D1 expression in B-cell malignanciesS D Raynaud, S Bekri, D Leroux, et al.
Alimentary Pharmacology & Therapeutics|March 4, 2011
Plasma carnitine is associated with fatigue in chronic hepatitis C but not in the irritable bowel syndromeR Anty, S Marjoux, S Bekri, et al.
The Science of the Total Environment|August 17, 2019
Integrating MAES implementation into protected area management under climate change: A fine-scale application in GreeceIoannis P Kokkoris, Eleni S Bekri, Dimitrios Skuras, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.
Annales De Biologie Clinique|June 26, 2004
[Hereditary sideroblastic anemia: a rare diagnosis]N Brahem-Jmili, N Salem, S Abdelkefi, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
International Journal of Clinical Practice|February 1, 2007
Clinical results of enzyme replacement therapy in Fabry disease: a comprehensive review of literatureO Lidove, D Joly, F Barbey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 7, 2017
[A case of neonatal hypotonia]A Hedjoudje, S Torre, S Bekri, et al.
Revue Neurologique|October 29, 2011
[Stroke and cornea verticillata revealing Fabry's disease in a female]D Fetter, A Bagan-Triquenot, E Guegan-Massardier, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Arginase deficiency in two brothersM Candito, B Bebin, C Vianey-Saban, et al.
Mucosal Immunology|June 27, 2013
Antigen-bearing dendritic cells from the sublingual mucosa recirculate to distant systemic lymphoid organs to prime mucosal CD8 T cellsC Hervouet, C Luci, S Bekri, et al.
Genes, Chromosomes & Cancer|October 1, 1993
Expanded range of 11q13 breakpoints with differing patterns of cyclin D1 expression in B-cell malignanciesS D Raynaud, S Bekri, D Leroux, et al.
Alimentary Pharmacology & Therapeutics|March 4, 2011
Plasma carnitine is associated with fatigue in chronic hepatitis C but not in the irritable bowel syndromeR Anty, S Marjoux, S Bekri, et al.
The Science of the Total Environment|August 17, 2019
Integrating MAES implementation into protected area management under climate change: A fine-scale application in GreeceIoannis P Kokkoris, Eleni S Bekri, Dimitrios Skuras, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.
Annales De Biologie Clinique|June 26, 2004
[Hereditary sideroblastic anemia: a rare diagnosis]N Brahem-Jmili, N Salem, S Abdelkefi, et al.
Pageof 4