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Results: 1-25/148
Authors:
TALEB A
PETIT C
PILENI MP
Citation: A. Taleb et al., OPTICAL-PROPERTIES OF SELF-ASSEMBLED 2D AND 3D SUPERLATTICES OF SILVER NANOPARTICLES, JOURNAL OF PHYSICAL CHEMISTRY B, 102(12), 1998, pp. 2214-2220
Authors:
BRUNBUISSON C
SOLLET JP
SCHWEICH H
BRIERE S
PETIT C
Citation: C. Brunbuisson et al., TREATMENT OF VENTILATOR-ASSOCIATED PNEUMONIA WITH PIPERACILLIN-TAZOBACTAM AMIKACIN VERSUS CEFTAZIDIME/AMIKACIN - A MULTICENTER, RANDOMIZED CONTROLLED TRIAL/, Clinical infectious diseases, 26(2), 1998, pp. 346-354
Authors:
MUSTAPHA M
CHARDENOUX S
NIEDER A
SALEM N
WEISSENBACH J
ELZIR E
LOISELET J
PETIT C
Citation: M. Mustapha et al., A SENSORINEURAL PROGRESSIVE AUTOSOMAL RECESSIVE FORM OF ISOLATED DEAFNESS, DFNB13, MAPS TO CHROMOSOME 7Q34-Q36, European journal of human genetics, 6(3), 1998, pp. 245-250
Authors:
AYADI H
DRIRA M
CHAKER F
WEIL D
BOULILAELGAIED A
CHAABOUNI M
PETIT C
Citation: H. Ayadi et al., PHENOTYPIC HETEROGENEITY IN NON SYNDROMIC DEAFNESS DFNB2, European journal of human genetics, 6, 1998, pp. 4277-4277
Authors:
KALATZIS V
PETIT C
Citation: V. Kalatzis et C. Petit, THE FUNDAMENTAL AND MEDICAL IMPACTS OF RECENT PROGRESS IN RESEARCH ONHEREDITARY HEARING-LOSS, Human molecular genetics (Print), 7(10), 1998, pp. 1589-1597
Authors:
MARLIN S
TOUBLANC JE
PETIT C
Citation: S. Marlin et al., 2 CASES OF TOWNES-BROCKS-SYNDROME WITH PREVIOUSLY UNDESCRIBED ANOMALIES, Clinical dysmorphology, 7(4), 1998, pp. 295-298
Authors:
PETIT C
TALEB A
PILENI MP
Citation: C. Petit et al., SELF-ORGANIZATION OF MAGNETIC NANOSIZED COBALT PARTICLES, Advanced materials, 10(3), 1998, pp. 259
Authors:
PETIT C
TALEB A
PILENI MP
Citation: C. Petit et al., SELF-ORGANIZATION OF MAGNETIC NANOSIZED COBALT PARTICLES, Chemical engineering & technology, 21(8), 1998, pp. 679-681
Authors:
PERES JM
BOUHALLAB S
PETIT C
BUREAU F
MAUBOIS JL
ARHAN P
BOUGLE D
Citation: Jm. Peres et al., IMPROVEMENT OF ZINC INTESTINAL-ABSORPTION AND REDUCTION OF ZINC IRON INTERACTION USING METAL-BOUND TO THE CASEINOPHOSPHOPEPTIDE-1-25 OF BETA-CASEIN/, Reproduction, nutrition, development (1989), 38(4), 1998, pp. 465-472
Authors:
DODE C
WEIL D
LEVILLIERS J
CROZET F
CHAIB H
LEVIACOBAS F
GUILFORD P
PETIT C
Citation: C. Dode et al., SEQUENCE CHARACTERIZATION OF A NEWLY IDENTIFIED HUMAN ALPHA-TUBULIN GENE (TUBA2), Genomics, 47(1), 1998, pp. 125-130
Authors:
PETIT C
MARLIN S
DENOYELLE F
Citation: C. Petit et al., HUMAN HEREDITARY DEAFNESS - NUL NEST PROPHETE..., MS. Medecine sciences, 14(8-9), 1998, pp. 1000-1000
Authors:
SAOUDA M
MANSOUR A
MOGLABEY YB
ELZIR E
MUSTAPHA M
CHAIB H
NEHME A
MEGARBANE A
LOISELET J
PETIT C
SLIM R
Citation: M. Saouda et al., THE USHER-SYNDROME IN THE LEBANESE POPULATION AND FURTHER REFINEMENT OF THE USH2A CANDIDATE REGION, Human genetics, 103(2), 1998, pp. 193-198
Authors:
PILENI MP
TALEB A
PETIT C
Citation: Mp. Pileni et al., SILVER METAL NANOSIZED PARTICLES - CONTROL OF PARTICLE-SIZE, SELF-ASSEMBLIES IN 2D AND 3D SUPERLATTICES AND OPTICAL-PROPERTIES, Journal of dispersion science and technology, 19(2-3), 1998, pp. 185-206
Authors:
MARLIN S
DENOYELLE F
BUSQUET D
GARABEDIAN N
PETIT C
Citation: S. Marlin et al., A PARTICULAR CASE OF DEAFNESS-OLIGODONTIA SYNDROME, International journal of pediatric otorhinolaryngology, 44(1), 1998, pp. 63-69
Authors:
PETIT C
KOULAKOV I
DEVERCHERE J
Citation: C. Petit et al., VELOCITY STRUCTURE AROUND THE BAIKAL RIFT-ZONE FROM TELESEISMIC AND LOCAL EARTHQUAKE TRAVEL-TIMES AND GEODYNAMIC IMPLICATIONS, Tectonophysics, 296(1-2), 1998, pp. 125-144
Authors:
THRESHER RJ
VITATERNA MH
MIYAMOTO Y
KAZANTSEV A
HSU DS
PETIT C
SELBY CP
DAWUT L
SMITHIES O
TAKAHASHI JS
SANCAR A
Citation: Rj. Thresher et al., ROLE OF MOUSE CRYPTOCHROME BLUE-LIGHT PHOTORECEPTOR IN CIRCADIAN PHOTORESPONSES, Science, 282(5393), 1998, pp. 1490-1494
Authors:
DENOYELLE F
LINAGRANADE G
PLAUCHU H
BRUZZONE R
CHAIB H
LEVIACOBAS F
WEIL D
PETIT C
Citation: F. Denoyelle et al., CONNEXIN-26 GENE LINKED TO A DOMINANT DEAFNESS, Nature, 393(6683), 1998, pp. 319-320
Authors:
MEINERTZHAGEN A
PETIT C
YARD G
JOURDAIN M
MONDON F
Citation: A. Meinertzhagen et al., EFFECT OF THE DISCHARGING AND RECHARGING OF THE STRESS GENERATED OXIDE CHARGE IN METAL-OXIDE-SEMICONDUCTOR CAPACITORS ON THE LOW-FIELD LEAKAGE CURRENT, Microelectronics and reliability, 38(2), 1998, pp. 221-225
Authors:
MAMMANO F
PETIT C
CLAVEL F
Citation: F. Mammano et al., RESISTANCE-ASSOCIATED LOSS OF VIRAL FITNESS IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 - PHENOTYPIC ANALYSIS OF PROTEASE AND GAG COEVOLUTION INPROTEASE INHIBITOR-TREATED PATIENTS, Journal of virology, 72(9), 1998, pp. 7632-7637
Authors:
PETIT C
THOMPSON JD
Citation: C. Petit et Jd. Thompson, PHENOTYPIC SELECTION AND POPULATION DIFFERENTIATION IN RELATION TO HABITAT HETEROGENEITY IN ARRHENATHERUM-ELATIUS (POACEAE), Journal of Ecology, 86(5), 1998, pp. 829-840
Authors:
SOUSSIYANICOSTAS N
FAIVRESARRAILH C
HARDELIN JP
LEVILLIERS J
ROUGON G
PETIT C
Citation: N. Soussiyanicostas et al., ANOSMIN-1 UNDERLYING THE X-CHROMOSOME-LINKED KALLMANN-SYNDROME IS AN ADHESION MOLECULE THAT CAN MODULATE NEURITE GROWTH IN A CELL-TYPE-SPECIFIC MANNER, Journal of Cell Science, 111, 1998, pp. 2953-2965
Authors:
TROMM A
GRIGA T
PETIT C
GREVING I
ECKER KW
MAY B
Citation: A. Tromm et al., REVERSIBILITY OF SEVERE OSTEOPENIA IN ULCERATIVE-COLITIS AFTER COLECTOMY, Gastroenterology, 114(4), 1998, pp. 4507-4507
Authors:
TROMM A
PETIT C
GRIGA T
GREVING I
MAY B
Citation: A. Tromm et al., SHORT-TERM FOLLOW-UP OF MINERAL BONE-DENSITY IN PATIENTS WITH CROHNS-DISEASE, Gastroenterology, 114(4), 1998, pp. 4508-4508
Authors:
WEIL D
KUSSEL P
BLANCHARD S
LEVY G
LEVIACOBAS F
DRIRA M
AYADI H
PETIT C
Citation: D. Weil et al., THE AUTOSOMAL RECESSIVE ISOLATED DEAFNESS, DFNB2, AND THE USHER 1B SYNDROME ARE ALLELIC DEFECTS OF THE MYOSIN-VIIA GENE, Nature genetics, 16(2), 1997, pp. 191-193
Authors:
ABDELHAK S
KALATZIS V
HEILIG R
COMPAIN S
SAMSON D
VINCENT C
WEIL D
CRUAUD C
SAHLY I
LEIBOVICI M
BITNERGLINDZICZ M
FRANCIS M
LACOMBE D
VIGNERON J
CHARACHON R
BOVEN K
BEDBEDER P
VANREGEMORTER N
WEISSENBACH J
PETIT C
Citation: S. Abdelhak et al., A HUMAN HOMOLOG OF THE DROSOPHILA EYES ABSENT GENE UNDERLIES BRANCHIOOTORENAL (BOR) SYNDROME AND IDENTIFIES A NOVEL GENE FAMILY, Nature genetics, 15(2), 1997, pp. 157-164