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Found 4 results Filters: author is Mourad [Clear All Filters]2008
Mycophenolate Mofetil Monotherapy in Membranous Nephropathy: A 1-Year Randomized Controlled Trial.
Dussol, B.; Morange, S.; Burtey, S.; Indreies, M.; Cassuto, E.; Mourad, G.; Villar, E.; Pouteil-Noble, C.; Karaaslan, H.; Sichez, H.; Lasseur, C.; Delmas, Y.; Nogier, M.; Fathallah, M.; Lound, A.
, Mycophenolate Mofetil Monotherapy in Membranous Nephropathy: A 1-Year Randomized Controlled Trial., Jun2008, (2008)
Abstract
Total absence of ST-segment resolution after failed thrombolysis is correlated with unfavorable short- and long-term outcomes despite successful rescue angioplasty.
Rekik, S.; Mnif, S.; Sahnoun, M.; Krichen, S.; Charfeddine, H.; Trabelsi, I.; Triki, F.; Hentati, M.; Kammoun, S.; ,
, Total absence of ST-segment resolution after failed thrombolysis is correlated with unfavorable short- and long-term outcomes despite successful rescue angioplasty., Jun2008, (2008)
Abstract
Partial recovery of delayed graft function due to cholesterol emboli after renal transplantation.
Ackoundou-N& #039, C.; Guessan,; Bismuth, J.; Canet, S.; Iborra, F.; Mourad, G.; ,
, Partial recovery of delayed graft function due to cholesterol emboli after renal transplantation., Jul2008, Volume 19, Issue 4, Saudi Arabia, (2008)
Abstract
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.
Bouhlal, Y.; Zouari, M.; Kefi, M.; Hamida, C.B.; Hentati, F.; Amouri, R.; ,
, Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family., Volume 22, Issue 2, United States, (2008)
Abstract
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