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JOYEUX V
MORIN MP
DJEFFAL R
LOMBART ML
RIVALAN J
LEPOGAMP P
CANAUD B
Citation: V. Joyeux et al., SUBJECTIVE GLOBAL ASSESSMENT, UREA KINETIC, BODY-COMPOSITION ANALYSISBY MULTIFREQUENCY BIOIMPEDANCE IN HEMODIALYZED PATIENTS, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1335-1335
Authors:
JOYEUX V
MORIN MP
LOMBART ML
STANESCU C
RIVALAN J
LEPOGAMP P
Citation: V. Joyeux et al., EVOLUTION OF BODY-COMPOSITION IN TRANSPLANT PATIENTS - USEFULNESS OF BIOIMPEDANCE-SCALE IN ROUTINE AND MULTIFREQUENCY BIOIMPEDANCE FOR ACCURATE EVALUATION, Journal of the American Society of Nephrology, 7(9), 1996, pp. 3434-3434
Citation: Mv. Joyeux et P. Lepogamp, POSTTRANSPLANT ERYTHROCYTOSIS TREATMENT WITH LOSARTAN, Journal of the American Society of Nephrology, 7(9), 1996, pp. 3459-3459
Authors:
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NUIJTEN MJC
BAYLE F
CANTAROVICH D
LANG P
LEBRANCHU Y
LEPOGAMP P
TOURAINE JL
VIALTEL P
MONROE T
DEVRIES MJ
Citation: C. Louistouizer et al., ECONOMIC CONTRIBUTION OF PROPHYLACTIC IMM UNOSUPPRESSIVE THERAPY WITHMYCOPHENOLATE MOFETIL IN RENAL CADAVERIC TRANSPLANT RECIPIENTS, La Presse medicale, 25(33), 1996, pp. 1577-1582
Authors:
JOYEUX V
MORIN MP
GUERARD A
RIVALAN J
LEPOGAMP P
Citation: V. Joyeux et al., INTEREST OF SIMULTANEOUS MULTIFREQUENCY BODY AND PLASMATIC EXTRACORPOREAL IMPEDANCEMETRIES IN PATIENTS ON HEMODIALYSIS, Journal of the American Society of Nephrology, 6(3), 1995, pp. 603-603
Authors:
BENKALFATE L
ZEIN K
LEGALL F
CHEVRANTBRETON J
RIVALAN J
LEPOGAMP P
Citation: L. Benkalfate et al., INTERTRIGINOUS CUTANEOUS CALCIFICATION - AN UNUSUAL CASE OF CALCINOSIS CUTIS, Annales de dermatologie et de venereologie, 122(11-12), 1995, pp. 789-792
Authors:
ISLAM MS
BARD JM
LEPOGAMP P
LEGLISE D
BOURBIGOT B
RIVALAN J
CLEDES J
Citation: Ms. Islam et al., SERUM-LIPOPROTEIN (A) IN RENAL-TRANSPLANT RECIPIENTS TREATED WITH CYCLOSPORINE MONOTHERAPY COMPARED TO CONVENTIONAL TREATMENT, Nephrology, dialysis, transplantation, 9(3), 1994, pp. 332-333
Authors:
DORVAL I
JEZEQUEL P
DUBOURG C
CHAUVEL B
LEPOGAMP P
LEGALL JY
Citation: I. Dorval et al., IDENTIFICATION OF THE HOMOZYGOUS MISSENSE MUTATION IN THE LECITHIN-CHOLESTEROL-ACYLTRANSFERASE (LCAT) GENE, CAUSING LCAT FAMILIAL DEFICIENCY IN 2 FRENCH PATIENTS, Atherosclerosis, 105(2), 1994, pp. 251-252