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J Yaouanq

Showing results (1-10 of 34) with videos related to

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Revue D'Epidemiologie Et De Sante Publique|February 12, 1998
[Should we screen for hemochromatosis? Critical analysis of the literature]S Charvet-Protat, J Yaouanq, F Fleurette
Human Heredity|January 1, 1990
Serum ferritin as a marker of affection for genetic hemochromatosisI B Borecki, D C Rao, J Yaouanq, et al.
American Journal of Medical Genetics|July 1, 1990
Percent transferrin saturation in segregating hemochromatosisI B Borecki, D C Rao, J Yaouanq, et al.
American Journal of Human Genetics|September 1, 1989
Segregation of genetic hemochromatosis indexed by latent capacity of transferrinI B Borecki, D C Rao, J Yaouanq, et al.
Journal of Medical Genetics|December 1, 1998
Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosisS Pinson, J Yaouanq, A M Jouanolle, et al.
European Journal of Neurology|December 18, 2014
Ten-year prognosis in multiple sclerosis: a better outcome in relapsing-remitting patients but not in primary progressive patientsA Kerbrat, S Hamonic, E Leray, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 4, 2012
'Clinically definite benign multiple sclerosis', an unwarranted conceptual hodgepodge: evidence from a 30-year observational studyE Leray, M Coustans, E Le Page, et al.
American Journal of Human Genetics|September 1, 1990
Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLAI B Borecki, G M Lathrop, G E Bonney, et al.
American Journal of Human Genetics|August 1, 1987
A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA associationM Simon, L Le Mignon, R Fauchet, et al.
Human Genetics|October 28, 1997
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutationsA M Jouanolle, P Fergelot, G Gandon, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Revue D'Epidemiologie Et De Sante Publique|February 12, 1998
[Should we screen for hemochromatosis? Critical analysis of the literature]S Charvet-Protat, J Yaouanq, F Fleurette
Human Heredity|January 1, 1990
Serum ferritin as a marker of affection for genetic hemochromatosisI B Borecki, D C Rao, J Yaouanq, et al.
American Journal of Medical Genetics|July 1, 1990
Percent transferrin saturation in segregating hemochromatosisI B Borecki, D C Rao, J Yaouanq, et al.
American Journal of Human Genetics|September 1, 1989
Segregation of genetic hemochromatosis indexed by latent capacity of transferrinI B Borecki, D C Rao, J Yaouanq, et al.
Journal of Medical Genetics|December 1, 1998
Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosisS Pinson, J Yaouanq, A M Jouanolle, et al.
European Journal of Neurology|December 18, 2014
Ten-year prognosis in multiple sclerosis: a better outcome in relapsing-remitting patients but not in primary progressive patientsA Kerbrat, S Hamonic, E Leray, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 4, 2012
'Clinically definite benign multiple sclerosis', an unwarranted conceptual hodgepodge: evidence from a 30-year observational studyE Leray, M Coustans, E Le Page, et al.
American Journal of Human Genetics|September 1, 1990
Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLAI B Borecki, G M Lathrop, G E Bonney, et al.
American Journal of Human Genetics|August 1, 1987
A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA associationM Simon, L Le Mignon, R Fauchet, et al.
Human Genetics|October 28, 1997
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutationsA M Jouanolle, P Fergelot, G Gandon, et al.
Pageof 4