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C Ropartz

Showing results (91-100 of 117) with videos related to

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Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|March 1, 1987
[Genetic study of a family of subjects with ankylosing spondylitis]P Deshayes, S Demangeon, B Cavelier, et al.
European Journal of Immunology|March 1, 1975
Immunochemical and biochemical study of a human Fcmu-like fragment (mu-chain disease)J P Lebreton, C Ropartz, J Rousseaus, et al.
The American Journal of Medicine|April 1, 1970
Primary antibody deficiency syndrome of adult onset. Evidence for genetic transmissionA Cruchaud, M Robert, J P Girard, et al.
Vox Sanguinis|January 1, 1976
Expression of genetic markers of erythrocyte immunoglobulin G autoantibodies in autoimmune hemolytic anemiaJ C Le Petit, L Rivat, N François, et al.
Tissue Antigens|September 1, 1975
Definition in man of a polymorphic system of the normal colonic secretionsA Zweibaum, R Oriol, J Dausset, et al.
Biochimica Et Biophysica Acta|August 9, 1976
Localization of J-chain and interchain disulfide bonds in a human F(c)5mu-like fragmentJ P Lebreton, J Rousseaux, M Fontaine, et al.
La Presse Medicale|September 26, 1970
[Familial Kahler's disease. Immunological and karyotype study of a case]G Manigand, A Sarrazin, L Demuth, et al.
Lancet (London, England)|February 1, 1975
Heterozygous alpha 1-antitrypsin deficiency and cirrhosis in adults, a fortuitous associationT Morin, J P Martin, G Feldmann, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|April 1, 1978
[Study of a population carrying HLA B27 antigen compared with a population without B27, in the detection of ankylosing spondylitis]J B Thorel, B Cavelier, J C Bonneau, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1972
[Study of a case of severe congenital primary, non-sex-linked hypogammaglobulinemia of probable genetic origin. Familial survey]M L North, L Rodier, G Miech, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|March 1, 1987
[Genetic study of a family of subjects with ankylosing spondylitis]P Deshayes, S Demangeon, B Cavelier, et al.
European Journal of Immunology|March 1, 1975
Immunochemical and biochemical study of a human Fcmu-like fragment (mu-chain disease)J P Lebreton, C Ropartz, J Rousseaus, et al.
The American Journal of Medicine|April 1, 1970
Primary antibody deficiency syndrome of adult onset. Evidence for genetic transmissionA Cruchaud, M Robert, J P Girard, et al.
Vox Sanguinis|January 1, 1976
Expression of genetic markers of erythrocyte immunoglobulin G autoantibodies in autoimmune hemolytic anemiaJ C Le Petit, L Rivat, N François, et al.
Tissue Antigens|September 1, 1975
Definition in man of a polymorphic system of the normal colonic secretionsA Zweibaum, R Oriol, J Dausset, et al.
Biochimica Et Biophysica Acta|August 9, 1976
Localization of J-chain and interchain disulfide bonds in a human F(c)5mu-like fragmentJ P Lebreton, J Rousseaux, M Fontaine, et al.
La Presse Medicale|September 26, 1970
[Familial Kahler's disease. Immunological and karyotype study of a case]G Manigand, A Sarrazin, L Demuth, et al.
Lancet (London, England)|February 1, 1975
Heterozygous alpha 1-antitrypsin deficiency and cirrhosis in adults, a fortuitous associationT Morin, J P Martin, G Feldmann, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|April 1, 1978
[Study of a population carrying HLA B27 antigen compared with a population without B27, in the detection of ankylosing spondylitis]J B Thorel, B Cavelier, J C Bonneau, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1972
[Study of a case of severe congenital primary, non-sex-linked hypogammaglobulinemia of probable genetic origin. Familial survey]M L North, L Rodier, G Miech, et al.
Pageof 12