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FONTAN

Showing results (471-480 of 814) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1988
Glomerular nephropathy associated with chronic Q feverM Perez-Fontan, E Huarte, A Tellez, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|April 29, 1974
[Attenuation of the antigenic characteristics of human aortic valves intended for transplantation]P Ruffié, J J Berjon, E Baudet, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|May 27, 1974
[Study of survival, after preservation at low temperature, of human aortic valves for transplantation]P Ruffié, F Fontan, C Dulong de Rosnay, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|May 16, 2021
Development and implementation of an analytical procedure for the quantification of natural and synthetic steroid hormones in whole surface watersE Mirmont, A Bœuf, M Charmel, et al.
AJR. American Journal of Roentgenology|October 1, 1984
Radionuclide studies in postoperative evaluation of the Fontan procedureA J Brendel, S Wynchank, A Choussat, et al.
Scandinavian Journal of Haematology|November 1, 1982
Hereditary myeloperoxidase deficiency: study of 12 casesC Larrocha, M Fernández de Castro, G Fontan, et al.
Pediatrie|January 1, 1973
[Karyotype 49, XXXXY in an infant]F Serville, J M Guillard, C de Joigny, et al.
Hybridoma (2005)|April 25, 2007
Generation of a new monoclonal antibody against MALT1 by genetic immunizationLorena Maestre, Lorena Fontan, Jose Angel Martinez-Climent, et al.
Archives Francaises De Pediatrie|July 1, 1979
[Results of brain tomography in acute lymphoblastic leukemia in children]J M Guillard, D Candito, P Constant, et al.
Journal of Human Genetics|December 24, 2005
A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signalsNuria Andreu, Maricruz García-Rodríguez, Victor Volpini, et al.
Pageof 82

Showing results (471-480 of 814) with videos related to

Sort By:
Pageof 82
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1988
Glomerular nephropathy associated with chronic Q feverM Perez-Fontan, E Huarte, A Tellez, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|April 29, 1974
[Attenuation of the antigenic characteristics of human aortic valves intended for transplantation]P Ruffié, J J Berjon, E Baudet, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|May 27, 1974
[Study of survival, after preservation at low temperature, of human aortic valves for transplantation]P Ruffié, F Fontan, C Dulong de Rosnay, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|May 16, 2021
Development and implementation of an analytical procedure for the quantification of natural and synthetic steroid hormones in whole surface watersE Mirmont, A Bœuf, M Charmel, et al.
AJR. American Journal of Roentgenology|October 1, 1984
Radionuclide studies in postoperative evaluation of the Fontan procedureA J Brendel, S Wynchank, A Choussat, et al.
Scandinavian Journal of Haematology|November 1, 1982
Hereditary myeloperoxidase deficiency: study of 12 casesC Larrocha, M Fernández de Castro, G Fontan, et al.
Pediatrie|January 1, 1973
[Karyotype 49, XXXXY in an infant]F Serville, J M Guillard, C de Joigny, et al.
Hybridoma (2005)|April 25, 2007
Generation of a new monoclonal antibody against MALT1 by genetic immunizationLorena Maestre, Lorena Fontan, Jose Angel Martinez-Climent, et al.
Archives Francaises De Pediatrie|July 1, 1979
[Results of brain tomography in acute lymphoblastic leukemia in children]J M Guillard, D Candito, P Constant, et al.
Journal of Human Genetics|December 24, 2005
A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signalsNuria Andreu, Maricruz García-Rodríguez, Victor Volpini, et al.
Pageof 82