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Results: 1-13 |
Results: 13

Authors: FELDMANN D ALESSANDRI JL DESCHENES G
Citation: D. Feldmann et al., LARGE DELETION OF THE 5'-END OF THE ROMK1 GENE CAUSES ANTENATAL BARTTER-SYNDROME, Journal of the American Society of Nephrology, 9(12), 1998, pp. 2357-2359

Authors: MONTBRUN A SAMPERIZ S RIVIERE J ATTALI T PILORGET H ALESSANDRI JL
Citation: A. Montbrun et al., ACUTE LETHAL PANCREATITIS DUE TO ASCARIS INFESTATION IN A 4-YEAR-OLD INFANT, Archives de pediatrie, 5(8), 1998, pp. 928-929

Authors: DUBERN B ALESSANDRI JL MONTBRUN A ATTALI T PILORGET H SAMPERIZ S
Citation: B. Dubern et al., REYES-SYNDROME IN A CHILD HAVING RECEIVED CHEMOTHERAPY, Archives de pediatrie, 5(3), 1998, pp. 342-343

Authors: GRABER D ALESSANDRI JL COMBES JC PONSOT G
Citation: D. Graber et al., SEVERE INFANTILE ANOREXIA WITH PROGRESSIV E NEUROLOGICAL CHANGES (8 CASES) - HIGH PREVALENCE OF THIS HEREDITARY DISORDERS ON REUNION ISLAND, Archives de pediatrie, 5(1), 1998, pp. 90-92

Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPWJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997), Human molecular genetics, 6(4), 1997, pp. 650-650

Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 6(1), 1997, pp. 17-26

Authors: GRABER D JAFFARBANDJEE MC ATTALI T POISSON J RENOUIL M ALESSANDRI JL COMBES JC
Citation: D. Graber et al., EOSINOPHILIC MENINGITIS IN REUNION AND MA YOTTE ISLANDS CAUSED BY ANGIOSTRONGYLUS-CANTONENSIS - 3 CASES IN INFANCY INCLUDING ONE WITH FATALRADICULOMYELOENCEPHALITIS AND HYDROCEPHALUS, Archives de pediatrie, 4(5), 1997, pp. 424-429

Authors: GRABER D JAFFAR MC ATTALI T POISSON J RENOUIL M ALESSANDRI JL COMBES JC
Citation: D. Graber et al., ANGIOSTRONGYLUS EOSINOPHILIC MENINGITIS I N REUNION AND MAYOTTE ISLANDS - REPORT OF 3 CASES IN INFANTS INCLUDING 1 FATAL RADICULOMYELOENCEPHALITIS WITH HYDROCEPHALUS, Bulletin de la Societe de pathologie exotique et de ses filiales, 90(5), 1997, pp. 331-331

Authors: ALESSANDRI JL BRETON A MONTBRUN A BRATZLAWSKY C TUAILLON J TILMONT P
Citation: Jl. Alessandri et al., BONE CHANGES IN CONGENITAL CYTOMEGALOVIRU S-INFECTION, Archives de pediatrie, 2(7), 1995, pp. 650-653

Authors: TILMONT P ROGEWOLTER M ALESSANDRI JL BRATZLAWSKY C
Citation: P. Tilmont et al., SURVIVAL RATE AND SHORT-TERM OUTCOME OF V ERY-LOW-BIRTH-WEIGHT INFANTS (1500 G OR LESS), Archives de pediatrie, 2(6), 1995, pp. 598-600

Authors: ALESSANDRI JL GUIONNET N SERRES H MONTBRUN A TILMONT P COMBES JC
Citation: Jl. Alessandri et al., MYXEDEMA PERICARDITIS IN CHILDREN, Archives de pediatrie, 2(4), 1995, pp. 382-383

Authors: TILMONT P ALESSANDRI JL DUTHOIT G ROSSIFARRER C ROGEWOLTER M
Citation: P. Tilmont et al., POSTOPERATIVE CHYLOUS EFFUSION AFTER BOCH DALEK HERNIORRHAPHY IN 2 NEONATES, Archives francaises de pediatrie, 50(9), 1993, pp. 783-786

Authors: TILMONT P ALESSANDRI JL DUTHOIT G ROSSIFARRER C ROGEWOLTER M
Citation: P. Tilmont et al., POSTOPERATIVE CHYLOUS EFFUSION AFTER BOCH DALEK HERNIORRHAPHY IN 2 NEONATES, Archives francaises de pediatrie, 50(9), 1993, pp. 783-786
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