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    1. Gili, R; Bonneau, D
      CCD measurements of visual double stars made with the 74 cm and 50 cm refractors of the Nice Observatory (2nd series)

      ASTRONOMY & ASTROPHYSICS
    2. Le Contel, D; Valtier, JC; Bonneau, D
      SIDONIE: A gateway for visual double stars studies

      ASTRONOMY & ASTROPHYSICS
    3. Mourard, D; Thureau, N; Abe, L; Berio, P; Blazit, A; Bonneau, D; Petrov, R; Vakili, F
      The G12T/REGAIN interferometer

      COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE IV PHYSIQUE ASTROPHYSIQUE
    4. Crisponi, L; Deiana, M; Loi, A; Chiappe, F; Uda, M; Amati, P; Bisceglia, L; Zelante, L; Nagaraja, R; Porcu, S; Ristaldi, MS; Marzella, R; Rocchi, M; Nicolino, M; Lienhardt-Roussie, A; Nivelon, A; Verloes, A; Schlessinger, D; Gasparini, P; Bonneau, D; Cao, A; Pilia, G
      The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

      NATURE GENETICS
    5. Nishimura, DY; Searby, CC; Carmi, R; Elbedour, K; Van Maldergem, L; Fulton, AB; Lam, BL; Powell, BR; Swiderski, RE; Bugge, KE; Haider, NB; Kwitek-Black, AE; Ying, LH; Duhl, DM; Gorman, SW; Heon, E; Iannaccone, A; Bonneau, D; Biesecker, LG; Jacobson, SG; Stone, EM; Sheffield, VC
      Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

      HUMAN MOLECULAR GENETICS
    6. Giraudeau, F; Taine, L; Biancalana, V; Delobel, B; Journel, H; Missirian, C; Lacombe, D; Bonneau, D; Parent, P; Aubert, D; Hauck, Y; Croquette, MF; Toutain, A; Mattei, MG; Loiseau, HA; David, A; Vergnaud, G
      Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation

      JOURNAL OF MEDICAL GENETICS
    7. Bonneau, D; Longy, M
      Mutations of the human PTEN gene

      HUMAN MUTATION
    8. Optasanu, V; Bonneau, D
      Finite element mass-conserving cavitation algorithm in pure squeeze motion. Validation/application to a connecting-rod small end bearing

      JOURNAL OF TRIBOLOGY-TRANSACTIONS OF THE ASME
    9. Piffeteau, S; Souchet, D; Bonneau, D
      Influence of thermal and elastic deformations on connecting-rod big end bearing lubrication under dynamic loading

      JOURNAL OF TRIBOLOGY-TRANSACTIONS OF THE ASME
    10. Sarfati, R; Hubert, A; Dugue-Marechaud, M; Biran-Mucignat, V; Pierre, F; Bonneau, D
      Prenatal diagnosis of Gaucher's disease type 2. Ultrasonographic, biochemical and histological aspects

      PRENATAL DIAGNOSIS
    11. Merlini, L; Kaplan, JC; Navarro, C; Barois, A; Bonneau, D; Brasa, J; Echenne, B; Gallano, P; Jarre, L; Jeanpierre, M; Kalaydjieva, L; Leturcq, F; Levi-Gomes, A; Toutain, A; Tournev, I; Urtizberea, A; Vallat, JM; Voit, T; Warter, JM
      Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

      NEUROLOGY
    12. Berio, P; Mourard, D; Bonneau, D; Chesneau, O; Stee, P; Thureau, N; Vakili, F; Borgnino, J
      Spectrally resolved Michelson stellar interferometry. I. Exact formalism in the multispeckle mode

      JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION
    13. Garnier, T; Bonneau, D; Grente, C
      Three-dimensional EHD behavior of the engine block/crankshaft assembly fora four cylinder inline automotive engine

      JOURNAL OF TRIBOLOGY-TRANSACTIONS OF THE ASME
    14. Goizet, C; Bonneau, D; Lacombe, D
      W syndrome: Report of three cases and review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Bonneau, D; Roume, J; Gonzalez, M; Toutain, A; Carles, D; Marechaud, M; Biran-Mucignat, V; Amati, P; Moraine, C
      Splenogonadal fusion limb defect syndrome: Report of five new cases and review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Bonneau, D; Marechaud, M; Odent, S; Piegay, I; Godard, A; Amati, P
      Heterotaxy-neural tube defect and holoprosencephaly occurring independently in two sib fetuses

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. Kraimps, JL; Canzian, F; Jost, C; Menet, E; Amati, P; Levillian, P; Harach, R; Lesueur, F; Barbier, J; Romeo, G; Bonneau, D
      Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene

      SURGERY
    18. Harach, HR; Lesueur, F; Amati, P; Brown, A; Canzian, F; Kraimps, JL; Levillain, P; Menet, E; Romeo, G; Bonneau, D
      Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2

      JOURNAL OF PATHOLOGY
    19. Berio, P; Stee, P; Vakili, F; Mourard, D; Bonneau, D; Chesneau, O; Thureau, N; Le Mignant, D; Hirata, R
      Interferometric insight into gamma Cassiopeiae long-term variability

      ASTRONOMY AND ASTROPHYSICS
    20. Thomas, JC; Basson, S; Gardner-Bonneau, D
      Universal access and assistive technology

      HUMAN FACTORS AND VOICE INTERACTIVE SYSTEMS
    21. Gardner-Bonneau, D
      Guidelines for speech-enabled IVR application design

      HUMAN FACTORS AND VOICE INTERACTIVE SYSTEMS
    22. Gardner-Bonneau, D
      The future of voice interactive applications

      HUMAN FACTORS AND VOICE INTERACTIVE SYSTEMS
    23. Gardner-Bonneau, D
      Ergonomics, work, and health.

      ASSISTIVE TECHNOLOGY
    24. AMATI P; BONNEAU D; CANZIAN F; KITZIS A; KRAIMPS JI; BARBIER J; ROMEO G; BONNEAU D
      SEVERAL GENES ACCOUNT FOR FAMILIAL PAPILLARY THYROID-CANCER

      European journal of human genetics
    25. BONNEAU D; DAVID A; BOTTANI A; LACOMBE D; LONGY M
      MUTATIONS OF PTEN IN PATIENTS WITH BANNAYAN-RILEY-RUVALCABA PHENOTYPE

      European journal of human genetics
    26. BISCEGLIA L; DAMBROSIO L; PIEMONTESE MR; CARELLA M; AMATI P; BONNEAU D; PILIA G; GASPARINI P; ZELANTE L
      MOLECULAR-GENETICS OF EPHAROPHIMOSIS-PTOSIS-EPICANTHUS-INVERSUS-SYNDROME (BPES) - LOCUS REFINEMENT AND EXCLUSION OF CANDIDATE GENES

      European journal of human genetics
    27. BISCEGLIA L; DAMBROSIO L; PIEMONTESE MR; CARELLA M; AMATI P; BONNEAU D; PILIA G; GASPARINI P; ZELANTE L
      CELLULAR RETINOL-BINDING PROTEIN-1 (RBP1) - A FREQUENT POLYMORPHISM, REFINED MAP POSITION AND EXCLUSION AS THE BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS-INVERSUS SYNDROME GENE

      Molecular and cellular probes
    28. BERIO P; VAKILI F; MOURARD D; BONNEAU D
      REMOVING THE PHOTON-CENTROIDING HOLE IN OPTICAL STELLAR INTERFEROMETRY

      Astronomy & Astrophysics. Supplement series
    29. LONGY M; COULON V; DUBOUE B; DAVID A; LARREGUE M; ENG C; AMATI P; KRAIMPS JL; BOTTANI A; LACOMBE D; BONNEAU D
      MUTATIONS OF PTEN IN PATIENTS WITH BANNAYAN-RILEY-RUVALCABA PHENOTYPE

      Journal of Medical Genetics
    30. VAKILI F; MOURARD D; STEE P; BONNEAU D; BERIO P; CHESNEAU O; THUREAU N; MORAND F; LABEYRIE A; TALLONBOSC I
      EVIDENCE FOR ONE-ARMED OSCILLATIONS IN THE EQUATORIAL DISK OF ZETA-TAURI FROM GI2T SPECTRALLY RESOLVED INTERFEROMETRY

      Astronomy and astrophysics (Berlin)
    31. STEE P; VAKILI F; BONNEAU D; MOURARD D
      ON THE INNER ENVELOPE OF THE BE STAR GAMMA-CASSIOPEIAE

      Astronomy and astrophysics
    32. Canzian, F; Amati, P; Harach, HR; Kraimps, JL; Lesueur, F; Barbier, J; Levillain, P; Romeo, G; Bonneau, D
      A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. PIEMONTESE MR; MEMEO E; CARELLA M; AMATI P; CHOMEL JC; BONNEAU D; PILIA G; CAO A; DRABKIN H; GEMMILL R; ROMMENS J; ZELANTE L; GASPARINI P; BISCEGLIA L
      A YAC CONTIG SPANNING THE BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS INVERSUSSYNDROME AND PROPIONIC ACIDEMIA LOCI

      European journal of human genetics
    34. CANDELIER JJ; BONNEAU D; MENNESSON B; COULLIN P
      TISSUE EXPRESSION OF A GENE POTENTIALLY I MPLICATED IN SOME DISEASES INVOLVING THE RETINA AND THE KIDNEY

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    35. ROUSSELETPERRAUT K; VAKILI F; MOURARD D; MORAND F; BONNEAU D; STEE P
      AN ATTEMPT TO DETECT POLARIZATION EFFECTS IN THE ENVELOPE OF GAMMA-CASSIOPEIAE WITH THE GI2T INTERFEROMETER

      Astronomy & Astrophysics. Supplement series
    36. ABDELMALKI A; MERINO D; BONNEAU D; BIGARD AX; GUEZENNEC CY
      ADMINISTRATION OF A GABA(B) AGONIST BACLOFEN BEFORE RUNNING TO EXHAUSTION IN THE RAT - EFFECTS ON PERFORMANCE AND ON SOME INDICATORS OF FATIGUE

      International journal of sports medicine
    37. CORMIERDAIRE V; WOLF C; LEMERRER M; NIVELON A; BONNEAU D; JOURNEL H; FELLMANN F; MUNNICH A; ROUX C
      ABNORMAL CHOLESTEROL-BIOSYNTHESIS IN THE SMITH-LEMLI-OPITZ AND THE LETHAL ACRODYSGENITAL SYNDROMES

      American journal of medical genetics
    38. KRAIMPS JL; BOUINPINEAU MH; AMATI P; MOTHES D; BONNEAU D; MARECHAUD R; BARBIER J
      FAMILIAL PAPILLARY CARCINOMA OF THE THYROID

      Surgery
    39. VAKILI F; MOURARD D; BONNEAU D; MORAND F; STEE P
      SUBTLE STRUCTURES IN THE WIND OF P-CYGNI

      Astronomy and astrophysics
    40. MOURARD D; BONNEAU D; KOECHLIN L; LABEYRIE A; MORAND F; STEE P; TALLONBOSC I; VAKILI F
      THE MEAN ANGULAR DIAMETER OF DELTA-CEPHEI MEASURED BY OPTICAL LONG-BASE-LINE INTERFEROMETRY

      Astronomy and astrophysics
    41. BONNEAU D; AMATI P; DESMONS C; FONTANEL JP; KLOSSEK JM
      AUTOSOMAL-DOMINANT INHERITANCE OF NASAL POLYPS

      American journal of human genetics
    42. AMATI P; CHOMEL JC; KITZIS A; BONNEAU D; NICOLINO M
      GENE FOR PREMATURE OVARIAN FAILURE ASSOCI ATED WITH EYELID MALFORMATION MAPS TO CHROMOSOME 3Q22-Q23

      MS. Medecine sciences
    43. BEAUMONT C; BONNEAU D
      HIGH SERUM FERRITIN AND CATARACT - A NEW MUTATION FOR A NEW SYNDROME

      MS. Medecine sciences
    44. DOIRON A; BLAIS C; BONNEAU D
      SPONTANEOUS CEREBRAL EMBOLUS FROM A CALCIFIED AORTIC-VALVE

      American journal of roentgenology
    45. CORMIERDAIRE V; WOLF C; MUNNICH A; LEMERRER M; NIVELON A; BONNEAU D; JOURNEL H; FELLMANN F; CHEVY F; ROUX C
      ABNORMAL CHOLESTEROL-BIOSYNTHESIS IN THE SMITH-LEMLI-OPITZ AND THE LETHAL ACRODYSGENITAL SYNDROMES

      European journal of pediatrics
    46. CAMUZAT A; ROZET JM; DOLLFUS H; GERBER S; PERRAULT I; BONNEAU D; GHAZI I; DUFIER JL; MUNNICH A; KAPLAN J
      EVIDENCE FOR GENETIC-HETEROGENEITY IN LEBERS CONGENITAL AMAUROSIS ANDFINE MAPPING OF LCA1 TO CHROMOSOME 17P13

      Investigative ophthalmology & visual science
    47. BONNEAU D; SOUIED EH; ROZET JM; GERBER S; CAMUZAT A; DHAENS E; MUNNICH A; KAPLAN J
      NO EVIDENCE OF GENETIC-HETEROGENEITY IN DOMINANT OPTIC ATROPHY

      Investigative ophthalmology & visual science
    48. GERBER S; LARGETPIET D; ROZET JM; BONNEAU D; MATHIEU M; DERKALOUSTIAN V; MUNNICH A; KAPLAN J
      EVIDENCE FOR A FOURTH LOCUS IN USHER SYNDROME TYPE-I

      Journal of Medical Genetics
    49. TELLIER AL; LYONNET S; CORMIERDAIRE V; DELONLAY P; ABADIE V; BAUMANN C; BONNEAU D; LABRUNE P; LACOMBE D; LEMERRER M; NIVELON A; PHILIP N; BRIARD ML; MUNNICH A
      INCREASED PATERNAL AGE IN CHARGE ASSOCIATION

      Clinical genetics
    50. HARMANEC P; MORAND F; BONNEAU D; JIANG Y; YANG S; GUINAN EF; HALL DS; MOURARD D; HADRAVA P; BOZIC H; STERKEN C; TALLONBOSC I; WALKER GAH; MCCOOK GP; VAKILI F; STEE P; LECONTEL JM
      JET-LIKE STRUCTURES IN BETA-LYRAE - RESULTS OF OPTICAL INTERFEROMETRY, SPECTROSCOPY AND PHOTOMETRY

      Astronomy and astrophysics
    51. KOECHLIN L; LAWSON PR; MOURARD D; BLAZIT A; BONNEAU D; MORAND F; STEE P; TALLONBOSC I; VAKILI F
      DISPERSED FRINGE TRACKING WITH THE MULTI-R(O) APERTURES OF THE GRAND-INTERFEROMETRE-A-2-TELESCOPES

      Applied optics
    52. AMATI P; GASPARINI P; ZLOTOGORA J; ZELANTE L; CHOMEL JC; KITZIS A; KAPLAN J; BONNEAU D
      A GENE FOR PREMATURE OVARIAN FAILURE ASSOCIATED WITH EYELID MALFORMATION MAPS TO CHROMOSOME 3Q22-Q23

      American journal of human genetics
    53. BEAUMONT C; LENEUVE P; DEVAUX I; SCOAZEC JY; BERTHIER M; LOISEAU MN; GRANDCHAMP B; BONNEAU D
      MUTATION IN THE IRON-RESPONSIVE ELEMENT OF THE L-FERRITIN MESSENGER-RNA IN A FAMILY WITH DOMINANT HYPERFERRITINEMIA AND CATARACT

      Nature genetics
    54. CAMUZAT A; DOLLFUS H; ROZET JM; GERBER S; BONNEAU D; BONNEMAISON M; BRIARD ML; DUFIER JL; GHAZI I; LEOWSKI C; WEISSENBACH J; FREZAL J; MUNNICH A; KAPLAN J
      A GENE FOR LEBERS CONGENITAL AMAUROSIS MAPS TO CHROMOSOME 17P

      Human molecular genetics
    55. CHEVREL J; BERTHIER M; BONNEAU D; CARDONA J; ORIOT D
      HYPEREXPLEXIA

      Archives de pediatrie
    56. BERTHIER M; ORIOT D; BONNEAU D; JAEKEN J
      DOES A MUTATION OF THE GLYCINE RECEPTOR MODIFY GABA-METABOLISM IN STARTLE DISEASE

      Acta paediatrica
    57. KAPLAN J; ROZET JM; GERBER S; CAMUZAT A; SOUIED E; BONNEAU D; LARGETPIET D; DOLLFUS H; DUFIER JL; BRIARD ML; FREZAL J; MUNNICH A
      GENES FOR CHILDHOOD RETINAL DYSTROPHIES

      MS. Medecine sciences
    58. BONNEAU D; GUINES D; FRENE J; TOPLOSKY J
      EHD ANALYSIS, INCLUDING STRUCTURAL INERTIA EFFECTS AND A MASS-CONSERVING CAVITATION MODEL

      Journal of tribology
    59. AMATI P; CHOMEL JC; NIVELONCHEVALIER A; GILGENKRANTZ S; KITZIS A; KAPLAN J; BONNEAU D
      A GENE FOR BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS INVERSUS SYNDROME MAPS TO CHROMOSOME 3Q23

      Human genetics
    60. GERBER S; ROZET JM; BONNEAU D; SOUIED E; WEISSENBACH J; FREZAL J; MUNNICH A; KAPLAN J
      EXCLUSION OF THE CONE-SPECIFIC ALPHA-SUBUNIT OF THE TRANSDUCIN GENE IN STARGARDTS-DISEASE

      Human genetics
    61. BOUSSEMART T; BONNEAU D; LEVARD G; BERTHIER M; ORIOT D
      OMPHALOCELE IN A NEWBORN BABY EXPOSED TO SODIUM VALPROATE IN-UTERO

      European journal of pediatrics
    62. LUCCIONI R; SEVER PS; DIPERRI T; REDON J; LAURANDIN I; BRAULT Y; CHASTANG C; GUEZ D; ANDREJAK M; ARAUD JM; AUPY JM; BACLET JL; BAIXAS JP; BAUD J; BILLAUT P; BIN E; BIOULAC B; BLANCHE M; BLONDEL D; BOGETTO D; BONNEAU D; BONTEMPS P; BOUCHER L; BOURNEUF P; BOUVET P; BOYE A; CABOT JM; CAHOREAU R; CALMET G; CAMPARD JC; CASES B; CASSIN H; CASTELLANI J; CLERSON P; COGNEE F; COLLROTGER J; CONSTENSOUX JP; COPERE C; COZIC JA; DAHAN G; DALLERIVE MC; DESAINTELORETTE E; DELTOUR LC; DRUGEON M; DUBOURG D; DUPONT S; CIRICA NE; ELSAWY A; EOCHE R; ETCHEGARAY G; FAUCHEY PM; FAUVEL P; FLEURY M; FOURAGE JF; FOURE Y; FRESSINAUD P; GABILLY I; GACIOCH M; GIRARDIER G; GOULESQUE X; GOUNAUD A; GRIMARD E; GUICHARD G; GUILLOT P; HERMAN D; HUIN P; HUMEZ JP; IGIGABEL P; JACQUIER P; JANTET R; JAVELOT T; KASSIANIDES A; KERHARONICOLAS A; KOWNATOR S; LAHOUSSINE S; VANLETHI N; LECLER L; LEQUEUX Y; LESAGE JF; LESCROART JC; LLORY P; LOURY P; MALFOY A; MALLET P; MARESCHAL J; MARIN D; MARTIN Y; MARTY J; MASSE JF; MORISSETMELARA B; MOUDOULAUD M; MOZZICONACCI JG; MUSSAT P; NALPAS P; OLIER P; OLLIVIER JP; PARMENTIER D; PERIMONY C; PERROT M; PESQUIE M; PIEAUD M; POURCHER JL; RAPOUD JP; REYNES F; ROBIN C; ROUMAGNAC M; ROUSSEL C; SALEMBIER A; SANCHEZ PY; SAVARY N; SEBBAH A; SEBBAH R; SIVERY B; SOUSMANNE M; THUILLIER G; TIBERGHIEN P; TILLY C; TISSOT F; TONDUT J; TRAVERSAT J; VANDAMME P; ARORA A; BACKHOUSE C; SELFRIDGE DI; SMITHERS A; THOMAS H; GIANNUZZI U; GUIDERI R; GORETTI P; CAMARRI E; HONORATO J; GOMEZ CC; MARIN R
      AN EQUIVALENCE STUDY OF THE SAFETY AND EFFICACY OF A FIXED-DOSE COMBINATION OF PERINDOPRIL WITH INDAPAMIDE VERSUS FIXED-DOSE COMBINATIONS OF CAPTOPRIL WITH HYDROCHLOROTHIAZIDE AND ENALAPRIL WITH HYDROCHLOROTHIAZIDE IN THE TREATMENT OF HYPERTENSION

      Journal of hypertension
    63. GERBER S; ROZET JM; BONNEAU D; SOUIED E; CAMUZAT A; DUFIER JL; AMALRIC P; MUNNICH A; KAPLAN J
      A GENE FOR LATE-ONSET FUNDUS-FLAVIMACULATUS WITH MACULAR DYSTROPHY MAPS TO CHROMOSOME-1P13

      Investigative ophthalmology & visual science
    64. ROZET JM; GERBER S; BONNEAU D; SOUIED E; FREZAL J; MUNNICH A; KAPLAN J
      EXCLUSION OF THE CONE-SPECIFIC ALPHA-SUBUNIT OF THE TRANSDUCIN GENE IN STARGARDTS-DISEASE

      Investigative ophthalmology & visual science
    65. LARGETPIET D; GERBER S; ROZET JM; BONNEAU D; MATHIEU M; DERKALOUSTIAN V; MUNNICH A; KAPLAN J
      EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER SYNDROME TYPE-I (USID)

      Vision research
    66. KAPLAN J; CAMUZAT A; DOLLFUS H; ROZET JM; GERBER S; BONNEAU D; GHAZI I; DUFIER JL; MUNNICH A
      A GENE FOR LEBERS CONGENITAL AMAUROSIS MAPS TO CHROMOSOME 17P

      Vision research
    67. BERTHIER M; BONNEAU D; MURA P; PIRIOU A; ORIOT D
      BENZATHINE AS A CAUSE FOR A FALSE-POSITIVE TEST RESULT FOR AMPHETAMINES

      The Journal of pediatrics
    68. BONNEAU D; SOUIED E; GERBER S; ROZET JM; DHAENS E; JOURNEL H; PLESSIS G; WEISSENBACH J; MUNNICH A; KAPLAN J
      NO EVIDENCE OF GENETIC-HETEROGENEITY IN DOMINANT OPTIC ATROPHY

      Journal of Medical Genetics
    69. BONNEAU D; WINTERFUSEAU I; LOISEAU MN; AMATI P; BERTHIER M; ORIOT D; BEAUMONT C
      BILATERAL CATARACT AND HIGH SERUM FERRITIN - A NEW DOMINANT GENETIC DISORDER

      Journal of Medical Genetics
    70. ZAHARIA F; PEK B; TETRAULT JP; PLANTE GE; SIROIS P; BONNEAU D; TEIJEIRA J
      APROTININ, TRANEXAMIC ACID, AND MEDIASTINAL AUTOTRANSFUSION IN ELECTIVE CORONARY-ARTERY SURGERY

      British Journal of Anaesthesia
    71. THIEBAUT E; BALEGA Y; BALEGA I; BELKINE I; BOUVIER J; FOY R; BLAZIT A; BONNEAU D
      ORBITAL MOTION OF DF TAURI FROM SPECKLE INTERFEROMETRY

      Astronomy and astrophysics
    72. THIEBAUT E; BOUVIER J; BLAZIT A; BONNEAU D; FOY FC
      THE COMPANION OF Z-CANIS-MAJORIS DETECTED IN THE VISIBLE

      Astronomy and astrophysics
    73. DEVANEY MN; THIEBAUT E; FOY R; BLAZIT A; BONNEAU D; BOUVIER J; DEBATZ B; THOM C
      THE H-ALPHA ENVIRONMENT OF T-TAURI RESOLVED BY SPECKLE INTERFEROMETRY

      Astronomy and astrophysics
    74. STEE P; DEARAUJO FX; VAKILI F; MOURARD D; ARNOLD L; BONNEAU D; MORAND F; TALLONBOSC I
      GAMMA-CASSIOPEIAE REVISITED BY SPECTRALLY RESOLVED INTERFEROMETRY

      Astronomy and astrophysics
    75. BONNEAU D; LENEUVE P; BEAUMONT C
      MUTATION IN THE IRON-RESPONSIVE ELEMENT OF THE L-FERRITINE MESSENGER-RNA IN A FAMILY WITH DOMINANT CATARACT AND HYPERFERRITINEMIA

      American journal of human genetics
    76. JEANPIERRE M; BECKMANN JS; AZIBI K; ELKERCH F; LETURCQ F; RECAN D; MERLINI L; TOUTAIN A; BONNEAU D; TOME FMS; FARDEAU M; KAPLAN JC; DODE C
      REFINED MAPPING OF THE LGMD2C LOCUS TO A 1-CENTIMORGAN INTERVAL

      American journal of human genetics
    77. KAPLAN J; CAMUZAT A; DOLLFUS H; ROZET JM; GERBER S; BONNEAU D; GHAZI I; DUFIER JL; MUNNICH A
      A GENE FOR LEBERS CONGENITAL AMAUROSIS MAPS TO CHROMOSOME 17P

      American journal of human genetics
    78. LARGETPIET D; GERBER S; ROZET JM; BONNEAU D; MATHIEU M; DERKALOUSTIAN V; MUNNICH A; KAPLAN J
      EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER-SYNDROME TYPE-I (USID)

      American journal of human genetics
    79. GERBER S; ROZET JM; BONNEAU D; SOUIED E; CAMUZAT A; DUFIER JL; AMALRIC P; WEISSENBACH J; MUNNICH A; KAPLAN J
      A GENE FOR LATE-ONSET FUNDUS FLAVIMACULATUS WITH MACULAR DYSTROPHY MAPS TO CHROMOSOME 1P13

      American journal of human genetics
    80. GILBERTDUSSARDIER B; BONNEAU D; GIGAREL N; LEMERRER M; BONNET D; PHILIP N; SERVILLE F; VERLOES A; ROSSI A; AYME S; WEISSENBACH J; MATTEI MG; LYONNET S; MUNNICH A
      A NOVEL MICROSATELLITE DNA MARKER AT LOCUS D7S1870 DETECTS HEMIZYGOSITY IN 75-PERCENT OF PATIENTS WITH WILLIAMS-SYNDROME

      American journal of human genetics
    81. SAUGIERVEBER P; MUNNICH A; BONNEAU D; ROZET JM; LEMERRER M; GIL R; BOESPFLUGTANGUY O
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      Acta paediatrica
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 00:09:45