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Authors: DESPORTES V FRANCIS F PINARD JM DESGUERRE I MOUTARD ML SNOECK I MEINERS LC CAPRON F CUSMAI R RICCI S MOTTE J ECHENNE B PONSOT G DULAC O CHELLY J BELDJORD C
Citation: V. Desportes et al., DOUBLECORTIN IS THE MAJOR GENE CAUSING X-LINKED SUBCORTICAL LAMINAR HETEROTOPIA (SCLH), Human molecular genetics (Print), 7(7), 1998, pp. 1063-1070

Authors: DESCAMPS P LEWIN F BODY G MOUTARD ML
Citation: P. Descamps et al., OBSTETRICAL MANAGEMENT OF AGENESIS OF THE CORPUS-CALLOSUM, Neuro-chirurgie, 44, 1998, pp. 93-95

Authors: MOUTARD ML LEWIN F BARON JM KIEFFER V DESCAMPS P
Citation: Ml. Moutard et al., PROGNOSIS OF ISOLATED AGENESIS OF THE COR PUS-CALLOSUM, Neuro-chirurgie, 44, 1998, pp. 96-98

Authors: DESPORTES V CARRIE A BILLUART P KIEFFER V BIENVENU T VINET MC BELDJORD C KAHN A PONSOT G CHELLY J MOUTARD ML
Citation: V. Desportes et al., INHERITED MICRODELETION IN XP21.3-22.1 INVOLVED IN NONSPECIFIC MENTAL-RETARDATION, Clinical genetics, 53(2), 1998, pp. 136-141

Authors: CONSTANT I DUBOIS MC PIAT V MOUTARD ML MURAT I
Citation: I. Constant et al., ELECTROENCEPHALOGRAPHIC CHANGES DURING INDUCTION OF ANESTHESIA WITH HALOTHANE OR SEVOFLURANE IN CHILDREN, Anesthesiology, 89(3A), 1998, pp. 1254-1254

Authors: DEGOUL F FRANCOIS D DIRY M PONSOT G DESGUERRE I HERON B MARSAC C MOUTARD ML
Citation: F. Degoul et al., A NEAR HOMOPLASMIC T8993G MTDNA MUTATION IN A PATIENT WITH ATYPIC LEIGH-SYNDROME NOT PRESENT IN THE MOTHERS TISSUES, Journal of inherited metabolic disease, 20(1), 1997, pp. 49-53

Authors: RODRIGUEZ D DESGUERRE I ADAMSBAUM C MOUTARD ML PONSOT G
Citation: D. Rodriguez et al., ACUTE POSTINFECTIOUS LEUKOENCEPHALITIS IN PEDIATRIC-PATIENTS - A REVIEW OF 5 CASES, Annales de pediatrie, 44(1), 1997, pp. 15-19

Authors: DESPORTES V PINARD JM SMADJA D MOTTE J BOESPFLUGTANGUY O MOUTARD ML DESGUERRE I BILLUART P CARRIE A BIENVENU T VINET MC BACHNER L BELDJORD C DULAC O KAHN A PONSOT G CHELLY J
Citation: V. Desportes et al., DOMINANT X-LINKED SUBCORTICAL LAMINAR HETEROTOPIA AND LISSENCEPHALY SYNDROME (XSCLH LIS) - EVIDENCE FOR THE OCCURRENCE OF MUTATION IN MALESAND MAPPING OF A POTENTIAL LOCUS IN XQ22/, Journal of Medical Genetics, 34(3), 1997, pp. 177-183

Authors: BILLUART P VINET MC PORTES VD LLENSE S RICHARD L MOUTARD ML RECAN D BRULS T BIENVENU T KAHN A BELDJORD C CHELLY J
Citation: P. Billuart et al., IDENTIFICATION BY STS PCR SCREENING OF A MICRODELETION IN XP21.3-22.1ASSOCIATED WITH NONSPECIFIC MENTAL-RETARDATION, Human molecular genetics, 5(7), 1996, pp. 977-979

Authors: LEMERLE J DAOUD P MOUTARD ML DESGUERRE I RODRIGUEZ D
Citation: J. Lemerle et al., INTRAVENOUS MIDAZOLAM FOR THE TREATMENT O F STATUS EPILEPTICUS IN CHILDREN, Archives de pediatrie, 2(9), 1995, pp. 848-853
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