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    1. Goudeau, B; Dagvadorj, A; Rodrigues-Lima, F; Nedellec, P; Casteras-Simon, M; Perret, E; Langlois, S; Goldfarb, L; Vicart, P
      Structural and functional analysis of a new desmin variant causing desmin-related myopathy

      HUMAN MUTATION
    2. Hiller, HH; Langlois, S
      The most important books/articles in Canadian sociology in the twentieth century: A report

      CANADIAN JOURNAL OF SOCIOLOGY-CAHIERS CANADIENS DE SOCIOLOGIE
    3. Kuchinka, BD; Barrett, IJ; Moya, G; Sanchez, JM; Langlois, S; Yong, SL; Kalousek, DK; Robinson, WP
      Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy

      PRENATAL DIAGNOSIS
    4. Gingras, D; Bousquet-Gagnon, N; Langlois, S; Lachambre, MP; Annabi, B; Beliveau, R
      Activation of the extracellular signal-regulated protein kinase (ERK) cascade by membrane-type-1 matrix metalloproteinase (MT1-MMP)

      FEBS LETTERS
    5. Guenais-Langlois, S; Bouyer, C; Broudic, JC; Coq, B
      The role of Pt/SiO2 in the catalytic denitration by HCO2H of HNO3 concentrated media

      APPLIED CATALYSIS B-ENVIRONMENTAL
    6. Langlois, S
      A productive decade in the tradition of Canadian sociology

      CANADIAN JOURNAL OF SOCIOLOGY-CAHIERS CANADIENS DE SOCIOLOGIE
    7. Langlois, S
      Paul Lazarsicia (1901-1976). Sociology from Vienna to New York

      CANADIAN JOURNAL OF SOCIOLOGY-CAHIERS CANADIENS DE SOCIOLOGIE
    8. Lestou, VS; Desilets, V; Lomax, BL; Barrett, IJ; Wilson, RD; Langlois, S; Kalousek, DK
      Comparative genomic hybridization: A new approach to screening for intrauterine complete or mosaic aneuploidy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Cogny-Van Weydevelt, F; Dandavino, R; Langlois, S; Boucher, A
      Cost analysis of kidney transplantation with cyclosporin A

      TRANSPLANTATION PROCEEDINGS
    10. Bendahhou, S; Cummins, TR; Hahn, AF; Langlois, S; Waxman, SG; Ptacek, LJ
      A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

      JOURNAL OF CLINICAL INVESTIGATION
    11. Penaherrera, MS; Barrett, IJ; Brown, CJ; Langlois, S; Yong, SL; Lewis, S; Bruyere, H; Howard-Peebles, PN; Kalousek, DK; Robinson, WP
      An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta

      CLINICAL GENETICS
    12. McFadden, DE; Langlois, S
      Parental and meiotic origin of triploidy in the embryonic and fetal periods

      CLINICAL GENETICS
    13. Gardes, F; Gaubert, P; Langlois, S
      Poverty and convergence of convergence of consumers in Canada

      CANADIAN REVIEW OF SOCIOLOGY AND ANTHROPOLOGY-REVUE CANADIENNE DE SOCIOLOGIE ET D ANTHROPOLOGIE
    14. Langlois, S; Desvignes, M; Constans, JM; Revenu, M
      MRI geometric distortion: A simple approach to correcting the effects of non-linear gradient fields

      JMRI-JOURNAL OF MAGNETIC RESONANCE IMAGING
    15. Toffelmire, EB; Barrett, BJ; Fenton, SS; Ferguson, B; Halligan, P; Langlois, S; McCready, WG; Muirhead, N; Weir, RV
      Chapter 2: Clinical practice guidelines for the management of anemia coexistent with chronic renal failure

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    16. Fang, P; Lev-Lehman, E; Tsai, TF; Matsuura, T; Benton, CS; Sutcliffe, JS; Christian, SL; Kubota, T; Halley, DJ; Meijers-Heijboer, H; Langlois, S; Graham, JM; Beuten, J; Willems, PJ; Ledbetter, DH; Beaudet, AL
      The spectrum of mutations in UBE3A causing Angelman syndrome

      HUMAN MOLECULAR GENETICS
    17. Dollfus, S; Brazo, P; Langlois, S; Gourevitch, R; Dassa, D; Besse, F; Van der Elst, A; Thibaut, F; Delamillieure, P; Chabot, B; Guelfi, JD; Petit, M
      Month of birth in deficit and non-deficit schizophrenic patients

      EUROPEAN PSYCHIATRY
    18. Langlois, S; Lit, JWY
      S-resonator with an end reflector

      JOURNAL OF LIGHTWAVE TECHNOLOGY
    19. Bernard, LE; Penaherrera, MS; Van Allen, MI; Wang, MS; Yong, SL; Gareis, F; Langlois, S; Robinson, WP
      Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Bruyere, H; Lewis, MES; Wood, S; MacLeod, P; Langlois, S
      Increasing evidence for a new X-linked mental retardation/epilepsy gene localized to Xp21.3-Xp22.1

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Bruyere, H; Lewis, S; Wood, S; MacLeod, PJ; Langlois, S
      Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1

      CLINICAL GENETICS
    22. Yong, KN; Wadsworth, LD; Langlois, S; Yong, SL; Wilson, RD
      Thalassemia carrier screening and prenatal diagnosis among the British Columbia (Canada) population of Chinese descent

      CLINICAL GENETICS
    23. Lavigne, C; Roblin, A; Outters, V; Langlois, S; Girasole, T; Roze, C
      Comparison of iterative and Monte Carlo methods for calculation of the aureole about a point source in the Earth's atmosphere

      APPLIED OPTICS
    24. LEBEL M; KINGMA I; GROSE JH; LANGLOIS S
      HEMODYNAMIC AND HORMONAL CHANGES DURING ERYTHROPOIETIN THERAPY IN HEMODIALYSIS-PATIENTS

      Journal of the American Society of Nephrology
    25. ROBINSON WP; KUCHINKA BD; BERNASCONI F; PETERSEN MB; SCHULZE A; BRONDUMNIELSEN K; CHRISTIAN SL; LEDBETTER DH; SCHINZEL AA; HORSTHEMKE B; SCHUFFENHAUER S; MICHAELIS RC; LANGLOIS S; HASSOLD TJ
      MATERNAL MEIOSIS-I NONDISJUNCTION OF CHROMOSOME-15 - DEPENDENCE OF THE MATERNAL AGE EFFECT ON LEVEL OF RECOMBINATION

      Human molecular genetics
    26. DOLLFUS S; GERMAINROBIN S; CHABOT B; BRAZO P; DELAMILLIEURE P; LANGLOIS S; VANDERELST A; CAMPION D; PETIT M
      FAMILY HISTORY AND OBSTETRIC COMPLICATIONS IN DEFICIT AND NON-DEFICITSCHIZOPHRENIA - PRELIMINARY-RESULTS

      European psychiatry
    27. DOLLFUS S; BRAZO P; NKAM I; THIBAUT F; MOITY F; LANGLOIS S; GOURREVITCH R; DASSA D; DENISE P; LEVILLAIN D; HALBECQ I; DELAMILLIEURE P; VANDERELST A; SEGARD L; ASSOULYBESSE F; VASSE T; ETARD O; GUELFI JD; LAUNAY C; PETITJEAN F; PETIT M
      DEFICIT AND NEGATIVE SUBTYPES IN SCHIZOPHRENIA - CLINICAL AND BIOLOGICAL DIFFERENCES

      Schizophrenia research
    28. LEBEL M; MOREAU V; GROSE JH; KINGMA I; LANGLOIS S
      PLASMA AND PERITONEAL ENDOTHELIN LEVELS AND BLOOD-PRESSURE IN CAPD PATIENTS WITH OR WITHOUT ERYTHROPOIETIN REPLACEMENT THERAPY

      Clinical nephrology
    29. KINGMA I; LEBEL M; LANGLOIS S; GROSE JH
      HEMODYNAMIC PROFILE AND 24-HR BLOOD-PRESSURE CHANGES INDUCED BY ERYTHROPOIETIN IN THE ABSENCE OF CHANGES IN ANTIHYPERTENSIVE TREATMENTS

      Journal of hypertension
    30. LANGLOIS S
      WOULD THE ALLIES ARRIVE IN TIME - THE 'LIBERATION OF PARIS' ON ABC

      The Journal of popular film and television
    31. MOSLEHI R; LANGLOIS S; YAM I; FRIEDMAN JM
      LINKAGE OF MALIGNANT HYPERTHERMIA AND HYPERKALEMIC PERIODIC PARALYSISTO THE ADULT SKELETAL-MUSCLE SODIUM-CHANNEL (SCN4A) GENE IN A LARGE PEDIGREE

      American journal of medical genetics
    32. LANGLOIS S
      UNTITLED

      Contemporary sociology
    33. KOLLIAS J; GILL PG; BEAMOND B; ROSSI H; LANGLOIS S; VERNONROBERTS E
      CLINICAL AND RADIOLOGICAL PREDICTORS OF COMPLETE EXCISION IN BREAST-CONSERVING SURGERY FOR PRIMARY BREAST-CANCER

      Australian and New Zealand journal of surgery
    34. LANDRY JF; LANGLOIS S
      ACUTE EXPOSURE TO ALIPHATIC-HYDROCARBONS - AN UNUSUAL CAUSE OF ACUTE TUBULAR-NECROSIS

      Archives of internal medicine
    35. HANSEN WF; BERNARD LE; LANGLOIS S; RAO KW; CHESCHEIR NC; AYLSWORTH AS; SMITH DI; ROBINSON WP; BARRETT IJ; KALOUSEK DK
      MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY-2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION,HYPOSPADIAS, AND OLIGOHYDRAMNIOS

      Prenatal diagnosis
    36. FORSE M; LANGLOIS S
      UNTITLED - RESPONSE

      Revue Francaise de Sociologie
    37. KALOUSEK DK; ROBINSON WP; BARRETT I; TELENIUS A; WILSON RD; HOWARDPEEBLES PN; LANGLOIS S
      A MEIOTIC ORIGIN OF TRISOMY IN PREGNANCIES WITH CONFINED PLACENTAL MOSAICISM IS CORRELATED WITH INCREASED RISK OF FETAL INTRAUTERINE GROWTH-RETARDATION AND UNIPARENTAL DISOMY

      Laboratory investigation
    38. MCFADDEN DE; PANTZAR JT; VANALLEN MI; LANGLOIS S
      RENAL TUBULAR DYSGENESIS WITH CALVARIAL HYPOPLASIA - REPORT OF 2 ADDITIONAL CASES AND REVIEW

      Journal of Medical Genetics
    39. LITTLE MT; LANGLOIS S; WILSON RD; LANSDORP PM
      FREQUENCY OF FETAL CELLS IN SORTED SUBPOPULATIONS OF NUCLEATED ERYTHROID AND CD34(-BLOOD() HEMATOPOIETIC PROGENITOR CELLS FROM MATERNAL PERIPHERAL)

      Blood
    40. LAU AW; BROWN CJ; PENAHERRERA M; LANGLOIS S; KALOUSEK DK; ROBINSON WP
      SKEWED X-CHROMOSOME INACTIVATION IS COMMON IN FETUSES OR NEWBORNS ASSOCIATED WITH CONFINED PLACENTAL MOSAICISM

      American journal of human genetics
    41. KUCHINKA BD; HASSOLD TJ; HORSTHEMKE B; LANGLOIS S; LEDBETTER DH; MICHAELIS RC; SCHINZEL A; SCHUFFENHAUER S; ROBINSON WP
      MATERNAL AGE AND RECOMBINATION DISTRIBUTION ASSOCIATED WITH CHROMOSOME-15 NONDISJUNCTION

      American journal of human genetics
    42. ROBINSON WP; LAU AW; BROWN CJ; LANGLOIS S; KALOUSEK DK
      SKEWED X-CHROMOSOME INACTIVATION IS COMMON IN FETUSES OR NEWBORNS ASSOCIATED WITH CONFINED PLACENTAL MOSAICISM

      American journal of human genetics
    43. LANGLOIS S; HUNTSMAN D; RUPPS R; KWONG LC; MACLEOD P; FREIDMAN JM
      NEUROFIBROMATOSIS TYPE-1 (NF1) IN COUSINS WITH UNAFFECTED PARENTS - NON-PENETRANCE OR COINCIDENTAL NEW MUTATIONS

      American journal of human genetics
    44. DESILETS VA; YONG SL; KALOUSEK DK; PANTZAR TJ; KWONG LC; SIEMENS C; LANGLOIS S
      MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-14

      American journal of human genetics
    45. WILSON RD; YONG SL; YONG K; WADSWORTH LD; KWONG LC; LANGLOIS S
      THALASSEMIA CARRIER SCREENING AND PRENATAL-DIAGNOSIS IN BRITISH-COLUMBIAS HIGH-RISK POPULATION

      American journal of human genetics
    46. BERNARD LE; HUNTSMAN D; RAHEMTULLAH A; MCGILLIVRAY BC; LANGLOIS S
      13 NOVEL FIBRILLIN-1 MUTATIONS DETECTED USING HETERODUPLEX ANALYSIS IN A SCREEN OF 44 INDIVIDUALS WITH CLASSICAL MARFAN-SYNDROME

      American journal of human genetics
    47. ROBINSON WP; BARRETT IJ; BERNARD L; TELENIUS A; BERNASCONI F; WILSON RD; BEST RG; HOWARDPEEBLES PN; LANGLOIS S; KALOUSEK DK
      MEIOTIC ORIGIN OF TRISOMY IN CONFINED PLACENTAL MOSAICISM IS CORRELATED WITH PRESENCE OF FETAL UNIPARENTAL DISOMY, HIGH-LEVELS OF TRISOMY IN TROPHOBLAST, AND INCREASED RISK OF FETAL INTRAUTERINE GROWTH RESTRICTION

      American journal of human genetics
    48. OGILVIE RI; ELLIS E; LANGLOIS S; MACKENZIE R; SPENCE JD
      RECOMMENDATIONS FOR SICK-LEAVE FROM WORK FOR PATIENTS WITH HYPERTENSION

      Canadian journal of cardiology
    49. ROBINSON WP; LANGLOIS S; SCHUFFENHAUER S; HORSTHEMKE B; MICHAELIS RC; CHRISTIAN S; LEDBETTER DH; SCHINZEL A
      CYTOGENETIC AND AGE-DEPENDENT RISK-FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY-15

      Prenatal diagnosis
    50. SHAFFER LG; LANGLOIS S; MCCASKILL C; MAIN DM; ROBINSON WP; BARRETT IJ; KALOUSEK DK
      ANALYSIS OF 9 PREGNANCIES WITH CONFINED PLACENTAL MOSAICISM FOR TRISOMY-2

      Prenatal diagnosis
    51. CORON B; CAMPION D; THIBAUT F; DOLLFUS S; PRETERRE P; LANGLOIS S; VASSE T; MOREAU V; MARTIN C; CHARBONNIER F; LAURENT C; MALLET J; PETIT M; FREBOURG T
      ASSOCIATION STUDY BETWEEN SCHIZOPHRENIA AND MONOAMINE-OXIDASE-A AND MONOAMINE-OXIDASE-B DNA POLYMORPHISMS

      Psychiatry research
    52. GARDES F; LANGLOIS S; RICHAUDEAU D
      CROSS-SECTION VERSUS TIME-SERIES INCOME ELASTICITIES OF CANADIAN CONSUMPTION

      Economics letters
    53. ROBINSON WP; LANGLOIS S
      PHENOTYPE OF MATERNAL UPD(14)

      American journal of medical genetics
    54. KALOUSEK DK; LANGLOIS S; ROBINSON WP; TELENIUS A; BERNARD L; BARRETT IJ; HOWARDPEEBLES PN; WILSON RD
      TRISOMY-7 CVS MOSAICISM - PREGNANCY OUTCOME, PLACENTAL AND DNA ANALYSIS IN 14 CASES

      American journal of medical genetics
    55. MITCHELL J; SCHINZEL A; LANGLOIS S; GILLESSENKAESBACH G; SCHUFFENHAUER S; MICHAELIS R; ABELIOVICH D; LERER I; CHRISTIAN S; GUITART M; MCFADDEN DE; ROBINSON WP
      COMPARISON OF PHENOTYPE IN UNIPARENTAL DISOMY AND DELETION PRADER-WILLI-SYNDROME - SEX-SPECIFIC DIFFERENCES

      American journal of medical genetics
    56. ROBINSON WP; LANGLOIS S; BERNASCONI F; CLARK S; CHRISTIAN S; LEDBETTER DH; GILLESSENKAESBACH G; HORSTHEMKE B; LERER I; ABELIOVICH D; MICHAELIS R; SCHUFFENHAUER S; SCHINZEL AA
      THE ORIGIN OF MATERNAL UNIPARENTAL DISOMY-15

      American journal of medical genetics
    57. MITCHELL J; LANGLOIS S; GILLESSENKAESBACH G; HORSTHEMKE B; MICHAELIS R; SCHINZEL AA; ABELOVICH S; LERER I; SCHUFFENHAUER S; GUITART M; ROBINSON WP
      A COMPARISON OF PHENOTYPE IN PATIENTS WITH PRADER-WILLI-SYNDROME (PWS) RESULTING FROM INTERSTITIAL DELETION AND UNIPARENTAL DISOMY

      American journal of medical genetics
    58. LANGLOIS S
      AMERICAN STANDARDS OF LIVING, 1918-1988 - BROWN,C

      Contemporary sociology
    59. LANGLOIS S
      QUEBEC - STATE AND SOCIETY - FRENCH - GAG NON,AG

      Revue d'histoire de l'Amerique francaise
    60. LAMBERT M; LUPIEN PJ; GAGNE C; LEVY E; BLAICHMAN S; LANGLOIS S; HAYDEN M; ROSE V; CLARKE JTR; WOLFE BMJ; CLARSON C; PARSONS H; STEPHURE DK; POTVIN D; LAMBERT J; VANVLIET G; LEFEVRE Y; DESROCHERS M; GODARD M; SZOTS F; ROY N; NAVRATIL O; TKACHUK A; JOHNSON F; MCINTYRE S; DONNELLY D; CANN M; PAULI P; MARCHAND A; GREBENC K; FROLICH J; MCGUINNESS C; DEBELDER M; DUCHARME AM
      TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA IN CHILDREN AND ADOLESCENTS - EFFECT OF LOVASTATIN

      Pediatrics
    61. BERNARD LE; CHITAYAT D; WEKSBERG R; VANALLEN MI; LANGLOIS S
      LINKAGE ANALYSIS OF 2 CANADIAN FAMILIES SEGREGATING FOR X-LINKED SPONDYLOEPIPHYSEAL DYSPLASIA

      Journal of Medical Genetics
    62. BENLIAN P; FOUBERT L; GAGNE E; BERNARD L; DEGENNES JL; LANGLOIS S; ROBINSON W; HAYDEN M
      COMPLETE PATERNAL ISODISOMY FOR CHROMOSOME-8 UNMASKED BY LIPOPROTEIN-LIPASE DEFICIENCY

      American journal of human genetics
    63. LEBEL M; KINGMA I; GROSE JH; LANGLOIS S
      AMBULATORY VS CASUAL BLOOD-PRESSURE RESPONSE DURING ERYTHROPOIETIN THERAPY IN ANEMIC HEMODIALYSIS-PATIENTS

      Journal of the American Society of Nephrology
    64. LEBEL M; KINGMA I; GROSE JH; LANGLOIS S
      EFFECT OF RECOMBINANT-HUMAN-ERYTHROPOIETIN THERAPY ON AMBULATORY BLOOD-PRESSURE IN NORMOTENSIVE AND IN UNTREATED BORDERLINE HYPERTENSIVE HEMODIALYSIS-PATIENTS

      American journal of hypertension
    65. LANGLOIS S
      THE EUROPE OF COMMUNISTS - FRENCH - GOTOV ITCH,J, DELWIT,P, DEWAELE,JM

      Labour
    66. GENIES EM; LANGLOIS S
      POLYPYRROLE-LATEX COATING ON ITO WINDOWS ELECTROCHEMICAL, AND SPECTROELECTROCHEMICAL STUDIES

      Synthetic metals
    67. RIVIERE P; LANGLOIS S; SOUFIANI A; TAINE J
      AN APPROXIMATE DATA-BASE OF H2O INFRARED LINES FOR HIGH-TEMPERATURE APPLICATIONS AT LOW-RESOLUTION - STATISTICAL NARROW-BAND MODEL PARAMETERS

      Journal of quantitative spectroscopy & radiative transfer
    68. LANGLOIS S; YONG SL; WILSON RD; KWONG LC; KALOUSEK DK
      PRENATAL AND POSTNATAL-GROWTH FAILURE ASSOCIATED WITH MATERNAL HETERODISOMY FOR CHROMOSOME-7

      Journal of Medical Genetics
    69. LITTLE MT; LANGLOIS S; WILSON RD; LANSDORP PM
      ENRICHMENT OF FETAL CELLS FROM MATERNAL PERIPHERAL-BLOOD IN SORTED SUBPOPULATIONS OF NUCLEATED ERYTHROID-CELLS AND CD34(+) HEMATOPOIETIC PROGENITOR CELLS

      Blood
    70. BERNARD LE; KALOUSEK DK; LANGLOIS S; BARRETT IJ; HANSEN WF; AYLSWORTH AS; SMITH DI; RAO KW
      CONFINED PLACENTAL MOSAICISM FOR TRISOMY-2 WITH FETAL MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME

      American journal of human genetics
    71. ROBINSON WP; LANGLOIS S; BARRETT I; CLARK S; BERNARD L; KALOUSEK DK
      THE ORIGIN OF TRISOMY CONFINED TO THE PLACENTA

      American journal of human genetics
    72. BENLIAN P; FOUBERT L; BERNARD L; GAGNE E; FORSYTHE I; LAGARDE IP; TELENIUS H; LANGLOIS S; DEGENNES IL; HAYDEN MR
      COMPLETE PATERNAL ISODISOMY OF CHROMOSOME-8 UNMASKED BY THE MOLECULARCHARACTERIZATION OF LIPOPROTEIN-LIPASE DEFICIENCY

      American journal of human genetics
    73. TELENIUS A; KALOUSEK DK; BARRETT IJ; LANGLOIS S; YONG SL
      TRISOMY-7 CVS MOSAICISM, PREGNANCY OUTCOME AND DNA ANALYSIS OF 9 CASES

      American journal of human genetics
    74. LEBEL M; GROSE JH; KINGMA I; LANGLOIS S
      PLASMA ENDOTHELIN LEVELS AND BLOOD-PRESSURE IN HEMODIALYSIS AND IN CAPD PATIENTS - EFFECT OF SUBCUTANEOUS ERYTHROPOIETIN REPLACEMENT THERAPY

      Clinical and experimental hypertension
    75. LEBEL M; KINGMA I; GROSE JH; LANGLOIS S
      CIRCADIAN BLOOD-PRESSURE AND ERYTHROPOIETIN THERAPY IN NORMOTENSIVE AND IN UNTREATED BORDERLINE HYPERTENSIVE HEMODIALYSIS-PATIENTS

      Journal of the American Society of Nephrology
    76. KARLINSKY H; SADOVNICK AD; BURGESS MM; LANGLOIS S; HAYDEN MR; BERG JM
      ISSUES IN MOLECULAR-GENETIC TESTING OF INDIVIDUALS WITH SUSPECTED EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE

      Alzheimer disease and associated disorders
    77. LANGLOIS S
      GENOMIC IMPRINTING - A NEW MECHANISM FOR DISEASE

      Pediatric pathology
    78. KARLINSKY H; SADOVNICK AD; BURGESS MM; LANGLOIS S; BERG JM
      ISSUES IN MOLECULAR-GENETIC DIAGNOSTIC TESTING IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE, WITH AN ILLUSTRATIVE CASE VIGNETTE

      Neurobiology of aging
    79. MCFADDEN DE; PANTZAR JT; LANGLOIS S
      PARENTAL ORIGIN OF TRIPLOIDY - DIGYNY, NOT DIANDRY

      Laboratory investigation
    80. KALOUSEK DK; LANGLOIS S; BARRETT I; WILSON D
      TRISOMIC ZYGOTE RESCUE AND INTRAUTERINE DEVELOPMENT

      Laboratory investigation
    81. LANGLOIS S; BIRBECK TP; HANSON RK
      TEMPERATURE-DEPENDENT COLLISION-BROADENING PARAMETERS OF H2O LINES INTHE 1.4-MU-M REGION USING DIODE-LASER ABSORPTION-SPECTROSCOPY

      Journal of molecular spectroscopy
    82. LANGLOIS S; BIRBECK TP; HANSON RK
      DIODE-LASER MEASUREMENTS OF H2O LINE-INTENSITIES AND SELF-BROADENING COEFFICIENTS IN THE 1.4-MU-M REGION

      Journal of molecular spectroscopy
    83. COLLOMBDUNANDSAUTHIER MN; LANGLOIS S; GENIES E
      SPECTROELECTROCHEMICAL BEHAVIOR OF POLY(3-OCTYLTHIOPHENE) - APPLICATION TO ELECTROCHROMIC WINDOWS WITH POLYANILINE AND IRIDIUM OXIDE

      Journal of Applied Electrochemistry
    84. VANALLEN MI; MCGILLIVRAY BC; LANGLOIS S
      DIZYGOTIC TWINS DISCORDANT FOR STRUCTURAL ANOMALIES FROM VASCULAR DISRUPTION

      Clinical research
    85. ARROYO MP; LANGLOIS S; HANSON RK
      DIODE-LASER ABSORPTION TECHNIQUE FOR SIMULTANEOUS MEASUREMENTS OF MULTIPLE GASDYNAMIC PARAMETERS IN HIGH-SPEED FLOWS CONTAINING WATER-VAPOR

      Applied optics
    86. FROHLICH J; BRUN LD; BLANK D; CAMPEAU L; CROCKFORD P; CURNEW G; DAFOE W; DAVIGNON J; DUFOUR R; EMERY G; FERGUSSON J; FILIPCHUK N; GAGNE C; HAYDEN MR; LANGLOIS S; LEITER L; LERMAN S; LUPIEN PJ; MA P; MCPHERSON R; MCQUEEN M; MISHKEL M; MONTIGNY M; NAKHLE G; OOI TT; ROEDERER G; ROLEAU JL; ROY M; SECCOMBE D; SNIDERMAN AD; DUSOUICH P; STEINER G; VLAHOS WD; XHIGNESSE M; YOKOYAMA S
      COMPARISON OF THE SHORT-TERM EFFICACY AND TOLERABILITY OF LOVASTATIN AND SIMVASTATIN IN THE MANAGEMENT OF PRIMARY HYPERCHOLESTEROLEMIA

      Canadian journal of cardiology
    87. MCFADDEN DE; KWONG LC; YAM IYL; LANGLOIS S
      PARENTAL ORIGIN OF TRIPLOIDY IN HUMAN FETUSES - EVIDENCE FOR GENOMIC IMPRINTING

      Human genetics
    88. VANALLEN MI; KALOUSEK DK; CHERNOFF GF; JURILOFF D; HARRIS M; MCGILLIVRAY BC; YONG SL; LANGLOIS S; MACLEOD PM; CHITAYAT D; FRIEDMAN JM; WILSON RD; MCFADDEN D; PANTZAR J; RITCHIE S; HALL JG
      EVIDENCE FOR MULTISITE CLOSURE OF THE NEURAL-TUBE IN HUMANS

      American journal of medical genetics
    89. LANGLOIS S; WILSON RD
      NONINVASIVE PRENATAL FETAL TESTING BY ANALYSIS OF MATERNAL BLOOD

      Clinical and investigative medicine
    90. NANZER J; LANGLOIS S; COEURET F
      PREPARATION AND USE OF A NICKEL FOAM ELECTRODE FOR THE PRODUCTION OF DIACETONE-2-KETO-L-GULONIC ACID FROM DIACETONE-L-SORBOSE IN VITAMIN-C PRODUCTION

      Journal of Applied Electrochemistry
    91. NANZER J; LANGLOIS S; COEURET F
      ELECTROLYTIC OXIDATION OF DIACETONE-L-SORBOSE (DAS) TO DIACETONE-2-KETO-L-GULONIC ACID (DAG) AT A NICKEL FOAM ELECTRODE

      Journal of Applied Electrochemistry
    92. LANGLOIS S; JUNKER A; YONG SL; YAM I; LIVINGSTON J; SIMINOVITCH K
      CARRIER FEMALES FOR X-LINKED-DYSKERATOSIS-CONGENITA SHOW NONRANDOM X-INACTIVATION

      American journal of human genetics
    93. MCFADDEN DE; PANTZAR JT; LANGLOIS S
      PARTIAL HYDATIDIFORM MOLE IN TRIPLOID CONCEPTUSES

      American journal of human genetics
    94. WILSON RD; LANGLOIS S; DANSEREAU J; MCGILLIVRAY B; VANALLEN M
      FETAL INTRAABDOMINAL HYPERECHOGENICITY - ETIOLOGY AND PROPOSED PROTOCOL

      American journal of human genetics
    95. ROBINSON WP; BERNASCONI F; MUTIRANGURA A; LEDBETTER DH; LANGLOIS S; MALCOLM S; MORRIS MA; SCHINZEL AA
      NONDISJUNCTION OF CHROMOSOME-15 - ORIGIN AND RECOMBINATION

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/05/20 alle ore 18:13:54