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P Cochat

Showing results (221-230 of 243) with videos related to

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Eye (London, England)|January 16, 2010
New ocular phenotype associated with a mutation in the PAX2 geneF Beby, O Roche, P Cochat, et al.
European Journal of Pediatrics|December 22, 1999
Combined liver-kidney transplantation in primary hyperoxaluria type 1P Cochat, J M Gaulier, P C Koch Nogueira, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1K Latta, N V Jamieson, J I Scheinman, et al.
Pediatric Nephrology (Berlin, Germany)|June 1, 1996
Body composition in children with renal disease: use of dual energy X-ray absorptiometryP Cochat, P Braillon, J Feber, et al.
Pediatrie|January 1, 1991
[Resuscitation during renal transplantation in children]P Cochat, D Long, D Floret, et al.
American Journal of Human Genetics|October 30, 1998
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndromeE Boye, G Mollet, L Forestier, et al.
Bone Marrow Transplantation|September 1, 1989
Systemic interleukin-2 therapy in children with progressive neuroblastoma after high dose chemotherapy and bone marrow transplantationM C Favrot, D Floret, S Negrier, et al.
Presse Medicale (Paris, France : 1983)|June 11, 1988
[Hemoperfusion on charcoal and hemodialysis in acute poisoning caused by methotrexate]D Frappaz, E Bouffet, P Cochat, et al.
Lupus|April 4, 2007
Overexpression of the antiapoptotic gene Bfl-1 in B cells from patients with familial systemic lupus erythematosusJ- M Andre, R Cimaz, B Ranchin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2003
[Childhood-onset systemic lupus erythematosus]B Bader-Meunier, P Quartier, G Deschênes, et al.
Pageof 25

Showing results (221-230 of 243) with videos related to

Sort By:
Pageof 25
Eye (London, England)|January 16, 2010
New ocular phenotype associated with a mutation in the PAX2 geneF Beby, O Roche, P Cochat, et al.
European Journal of Pediatrics|December 22, 1999
Combined liver-kidney transplantation in primary hyperoxaluria type 1P Cochat, J M Gaulier, P C Koch Nogueira, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1K Latta, N V Jamieson, J I Scheinman, et al.
Pediatric Nephrology (Berlin, Germany)|June 1, 1996
Body composition in children with renal disease: use of dual energy X-ray absorptiometryP Cochat, P Braillon, J Feber, et al.
Pediatrie|January 1, 1991
[Resuscitation during renal transplantation in children]P Cochat, D Long, D Floret, et al.
American Journal of Human Genetics|October 30, 1998
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndromeE Boye, G Mollet, L Forestier, et al.
Bone Marrow Transplantation|September 1, 1989
Systemic interleukin-2 therapy in children with progressive neuroblastoma after high dose chemotherapy and bone marrow transplantationM C Favrot, D Floret, S Negrier, et al.
Presse Medicale (Paris, France : 1983)|June 11, 1988
[Hemoperfusion on charcoal and hemodialysis in acute poisoning caused by methotrexate]D Frappaz, E Bouffet, P Cochat, et al.
Lupus|April 4, 2007
Overexpression of the antiapoptotic gene Bfl-1 in B cells from patients with familial systemic lupus erythematosusJ- M Andre, R Cimaz, B Ranchin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2003
[Childhood-onset systemic lupus erythematosus]B Bader-Meunier, P Quartier, G Deschênes, et al.
Pageof 25