Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Chevet

Showing results (61-70 of 71) with videos related to

Pageof 8
Sort By:
The Journal of Clinical Investigation|July 1, 1994
Interleukin 10 induces B lymphocytes from IgA-deficient patients to secrete IgAF Brière, J M Bridon, D Chevet, et al.
Annales De Medecine Interne|January 1, 1990
[Anti-basement-membrane antibody mediated, rapidly progressive, glomerulonephritis. Diagnostic and therapeutic strategy based on a retrospective study of 14 cases]J Bouget, P Le Pogamp, G Perrier, et al.
Transplantation Proceedings|April 1, 1995
Azathioprine-induced pancytopenia in homozygous thiopurine methyltransferase-deficient renal transplant recipients: a family studyA Escousse, C Mousson, L Santona, et al.
Intensive Care Medicine|January 1, 1990
Acute renal failure following collective intoxication by Cortinarius orellanusJ Bouget, J Bousser, B Pats, et al.
Pathologie-Biologie|March 1, 1983
Serum angiotensin-converting enzyme levels in patients with chronic renal failureA Le Treut, D Chevet, L Guenet, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French familyL Hamidi Asl, V Fournier, C Billerey, et al.
Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire|April 1, 1974
[Bony densitometry by Cameron's method in the supervision of osteoporosis in patients on chronic hemodialysis (authors's transl)]J Simon, M Laval-Jeantet, P Lautridou, et al.
Human Genetics|July 1, 1990
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locusL Bachner, M C Vinet, R Lacave, et al.
Lancet (London, England)|October 21, 1989
Cyclosporin in idiopathic steroid-resistant membranous glomerulonephritisG Rostoker, L Toro, A Ben Maadi, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1988
[15 years of renal transplantation under conventional immunosuppressive treatment]B Launois, J P Campion, E Bardaxoglou, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
The Journal of Clinical Investigation|July 1, 1994
Interleukin 10 induces B lymphocytes from IgA-deficient patients to secrete IgAF Brière, J M Bridon, D Chevet, et al.
Annales De Medecine Interne|January 1, 1990
[Anti-basement-membrane antibody mediated, rapidly progressive, glomerulonephritis. Diagnostic and therapeutic strategy based on a retrospective study of 14 cases]J Bouget, P Le Pogamp, G Perrier, et al.
Transplantation Proceedings|April 1, 1995
Azathioprine-induced pancytopenia in homozygous thiopurine methyltransferase-deficient renal transplant recipients: a family studyA Escousse, C Mousson, L Santona, et al.
Intensive Care Medicine|January 1, 1990
Acute renal failure following collective intoxication by Cortinarius orellanusJ Bouget, J Bousser, B Pats, et al.
Pathologie-Biologie|March 1, 1983
Serum angiotensin-converting enzyme levels in patients with chronic renal failureA Le Treut, D Chevet, L Guenet, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French familyL Hamidi Asl, V Fournier, C Billerey, et al.
Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire|April 1, 1974
[Bony densitometry by Cameron's method in the supervision of osteoporosis in patients on chronic hemodialysis (authors's transl)]J Simon, M Laval-Jeantet, P Lautridou, et al.
Human Genetics|July 1, 1990
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locusL Bachner, M C Vinet, R Lacave, et al.
Lancet (London, England)|October 21, 1989
Cyclosporin in idiopathic steroid-resistant membranous glomerulonephritisG Rostoker, L Toro, A Ben Maadi, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1988
[15 years of renal transplantation under conventional immunosuppressive treatment]B Launois, J P Campion, E Bardaxoglou, et al.
Pageof 8