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M P Roth

Showing results (61-70 of 97) with videos related to

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Prenatal Diagnosis|October 1, 1983
Paternal age and Down's syndrome diagnosed prenatally: no association in French dataM P Roth, C Stoll, J L Taillemite, et al.
European Journal of Epidemiology|September 1, 1989
Risk factors in congenital heart diseaseC Stoll, Y Alembik, M P Roth, et al.
BMJ (Clinical Research Ed.)|July 19, 2003
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenariansHélène Coppin, M Bensaid, S Fruchon, et al.
Journal of Neuroimmunology|September 1, 1995
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOGM P Roth, L Dolbois, N Borot, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|January 1, 1990
[Maternal oligo-elements and fetal malformations]C Stoll, R Zawislak, B Dott, et al.
Gastroenterology|October 1, 1989
Geographic origins of Jewish patients with inflammatory bowel diseaseM P Roth, G M Petersen, C McElree, et al.
Genes and Immunity|January 22, 2004
A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the ratH Coppin, M-T Ribouchon, B Fontaine, et al.
Journal of Neuroimmunology|April 1, 1994
Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLAM P Roth, L Nogueira, H Coppin, et al.
Digestive Diseases and Sciences|June 1, 1992
Risk factors for gallstone formation during rapid loss of weightH Yang, G M Petersen, M P Roth, et al.
Gut|April 1, 1993
Familial empirical risks for inflammatory bowel disease: differences between Jews and non-JewsH Yang, C McElree, M P Roth, et al.
Pageof 10

Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|October 1, 1983
Paternal age and Down's syndrome diagnosed prenatally: no association in French dataM P Roth, C Stoll, J L Taillemite, et al.
European Journal of Epidemiology|September 1, 1989
Risk factors in congenital heart diseaseC Stoll, Y Alembik, M P Roth, et al.
BMJ (Clinical Research Ed.)|July 19, 2003
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenariansHélène Coppin, M Bensaid, S Fruchon, et al.
Journal of Neuroimmunology|September 1, 1995
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOGM P Roth, L Dolbois, N Borot, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|January 1, 1990
[Maternal oligo-elements and fetal malformations]C Stoll, R Zawislak, B Dott, et al.
Gastroenterology|October 1, 1989
Geographic origins of Jewish patients with inflammatory bowel diseaseM P Roth, G M Petersen, C McElree, et al.
Genes and Immunity|January 22, 2004
A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the ratH Coppin, M-T Ribouchon, B Fontaine, et al.
Journal of Neuroimmunology|April 1, 1994
Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLAM P Roth, L Nogueira, H Coppin, et al.
Digestive Diseases and Sciences|June 1, 1992
Risk factors for gallstone formation during rapid loss of weightH Yang, G M Petersen, M P Roth, et al.
Gut|April 1, 1993
Familial empirical risks for inflammatory bowel disease: differences between Jews and non-JewsH Yang, C McElree, M P Roth, et al.
Pageof 10