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    1. Brouwers, P; van Engelen, M; Lalonde, F; Perez, L; de Haan, E; Wolters, P; Martin, A
      Abnormally increased semantic priming in children with symptomatic HIV-1 disease: Evidence for impaired development of semantics?

      JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY
    2. de Haan, E
      The treatment of obsessive-compulsive disorder

      CLINICAL PSYCHOLOGY & PSYCHOTHERAPY
    3. Meiser, B; Butow, P; Barratt, A; Gattas, M; Gaff, C; Haan, E; Gleeson, M; Dudding, T; Tucker, K
      Risk perceptions and knowledge of breast cancer genetics in women at increased risk of developing hereditary breast cancer

      PSYCHOLOGY & HEALTH
    4. van Honk, J; Tuiten, A; de Haan, E; van den Hout, M; Stam, H
      Attentional biases for angry faces: Relationships to trait anger and anxiety

      COGNITION & EMOTION
    5. van Honk, J; Tuiten, A; van den Hout, M; Putman, P; de Haan, E; Stam, H
      Selective attention to unmasked and masked threatening words: relationships to trait anger and anxiety

      PERSONALITY AND INDIVIDUAL DIFFERENCES
    6. Damen, M; Weegink, CJ; Mauser-Bunschoten, EP; Cuypers, HTM; Hermus, MC; Sillekens, P; Haan, E; van den Berg, HM; Bresters, D; Lelie, PN; Chamuleau, RAFM; Reesink, HW
      Sustained virological response in chronic hepatitis C patients after a 6-and a 36-month interferon-alpha 2b treatment schedule - A multicenter, randomized, controlled study

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    7. Cox, TC; Allen, LR; Cox, LL; Hopwood, B; Goodwin, B; Haan, E; Suthers, GK
      New mutations in MID1 provide support for loss of function as the cause ofX-linked Opitz syndrome

      HUMAN MOLECULAR GENETICS
    8. Meiser, B; Butow, P; Friedlander, M; Schnieden, V; Gattas, M; Kirk, J; Suthers, G; Haan, E; Tucker, K
      Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancer

      JOURNAL OF CLINICAL ONCOLOGY
    9. Vlot, AJ; Mauser-Bunschoten, EP; Zarkova, AG; Haan, E; Kruitwagen, CLJJ; Sixma, JJ; van den Berg, HM
      The half-life of infused factor VIII is shorter in hemophiliac patients with blood group O than in those with blood group A

      THROMBOSIS AND HAEMOSTASIS
    10. van Honk, J; Tuiten, A; van den Hout, M; Koppeschaar, H; Thijssen, J; de Haan, E; Verbaten, R
      Conscious and preconscious selective attention to social threat: differentneuroendocrine response patterns

      PSYCHONEUROENDOCRINOLOGY
    11. Schmitt, M; Postma, A; De Haan, E
      Interactions between exogenous auditory and visual spatial attention

      QUARTERLY JOURNAL OF EXPERIMENTAL PSYCHOLOGY SECTION A-HUMAN EXPERIMENTAL PSYCHOLOGY
    12. Meiser, B; Butow, P; Barratt, A; Friedlander, M; Kirk, J; Gaff, C; Haan, E; Aittomaki, K; Tucker, K
      Breast cancer screening uptake in women at increased risk of developing hereditary breast cancer

      BREAST CANCER RESEARCH AND TREATMENT
    13. Thong, MK; Scherer, G; Kozlowski, K; Haan, E; Morris, L
      Acampomelic campomelic dysplasia with SOX9 mutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    14. Kramer, KJM; Dorten, WS; Van het Groenewoud, H; de Haan, E; Kramer, GN; Monteiro, L; Muntau, H; Quevauviller, P
      Collaborative study to improve the quality control of rare earth element determinations in environmental matrices

      JOURNAL OF ENVIRONMENTAL MONITORING
    15. Thong, MK; Thompson, E; Keenan, R; Simmer, K; Harbord, M; Davidson, G; Haan, E
      A child with hemimegalencephaly, hemihypertrophy, macrocephaly, cutaneous vascular malformation, psychomotor retardation and intestinal lymphangiectasia - a diagnostic dilemma

      CLINICAL DYSMORPHOLOGY
    16. van Honk, J; Tuiten, A; Verbaten, R; van den Hout, M; Koppeschaar, H; Thijssen, J; de Haan, E
      Correlations among salivary testosterone, mood, and selective attention tothreat in humans

      HORMONES AND BEHAVIOR
    17. Woffendin, H; Jakins, T; Jouet, M; Stewart, H; Landy, S; Haan, E; Harris, A; Donnai, D; Read, A; Kenwrick, S
      X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation

      CLINICAL GENETICS
    18. DONNELLY A; HAAN E; MANSON J; MULLEY J
      A NOVEL MUTATION IN EXON-B (R253C) OF THE MTM1-GENE IS ASSOCIATED WITH A MILD MYOTUBULAR MYOPATHY

      Human mutation
    19. BATEMAN JF; CHIODO AA; WENG YM; CHAN D; HAAN E
      A TYPE-III COLLAGEN GLY559 TO ARG HELIX MUTATION IN EHLERS-DANLOS-SYNDROME TYPE-IV

      Human mutation
    20. SMITH A; HAAN E; WARNE G; MONTGOMERY P; MACMILLAN J; ELLIOTT E; WILLIAMS K
      PRADER-WILLI-SYNDROME - A NEW STUDY OF THE AUSTRALIAN-PEDIATRIC-SURVEILLANCE-UNIT

      Journal of paediatrics and child health
    21. SMITH A; WARNE G; HAAN E; MONTGOMERY P; WILLIAMS K; ELLIOTT E
      PRADER-WILLI-SYNDROME - A NEW STUDY OF THE AUSTRALIAN PEDIATRIC SURVEILLANCE UNIT (APSU)

      European journal of human genetics
    22. HAAN E; MORRIS L
      SHORT-SYNDROME - DISTINCTIVE RADIOGRAPHIC FEATURES

      Clinical dysmorphology
    23. THOMPSON E; HAAN E; SHEFFIELD L
      AUTOSOMAL-DOMINANT KLIPPEL-FEIL ANOMALY WITH CLEFT-PALATE

      Clinical dysmorphology
    24. van Honk, J; Tuiten, A; van den Hout, M; Koppeschaar, H; Thijssen, J; de Haan, E; Verbaten, R
      Baseline salivary cortisol levels and preconscious selective attention forthreat - A pilot study

      PSYCHONEUROENDOCRINOLOGY
    25. BYRONSCOTT R; HAAN E; CHAN A; BOWER C; SCOTT H; CLARK K
      A POPULATION-BASED STUDY OF ABDOMINAL-WALL DEFECTS IN SOUTH-AUSTRALIAAND WESTERN-AUSTRALIA

      Paediatric and perinatal epidemiology
    26. Haan, E
      From Academia to Amicitia: Milton's Latin writings and the Italian academies

      TRANSACTIONS OF THE AMERICAN PHILOSOPHICAL SOCIETY
    27. Haan, E
      John Milton's 'Ad Patrem' and Hugo Grotius's 'In Natalem Patris'

      NOTES AND QUERIES
    28. GIBSON MA; ELLIS SL; ADES LC; HAAN E; CLEARY EG
      PREFERENTIAL PRE-MESSENGER-RNA UTILIZATION OF AN UPSTREAM CRYPTIC 5'-SPLICE-SITE CREATED BY A SINGLE-BASE DELETION MUTATION IN EXON-37 OF THE FBN-1 GENE

      European journal of biochemistry
    29. BADAWI N; WATSON L; PETTERSON B; BLAIR E; SLEE J; HAAN E; STANLEY F
      WHAT CONSTITUTES CEREBRAL-PALSY

      Developmental Medicine and Child Neurology
    30. THOMPSON PW; SAMPSON JR; MAHESHWAR MM; ASPINWALL P; CHEADLE J; RAVINE D; ROY S; HAAN E; BERNSTEIN J; HARRIS PC
      THE ROLE OF FISH IN INVESTIGATING DELETIONS OF THE TSC2 AND PKD1 GENEREGION AT CHROMOSOME 16P13.3

      Cytogenetics and cell genetics
    31. SHARP P; HAAN E; FLETCHER JM; KHONG TY; CAREY WF
      FIRST-TRIMESTER DIAGNOSIS OF SMITH-LEMLI-OPITZ-SYNDROME

      Prenatal diagnosis
    32. HAAN E
      MILTON,JOHN AMONG THE NEO-LATINISTS - 3 NOTES ON 'MANSUS'

      Notes and queries
    33. HAAN E
      MILTON AND 2 ITALIAN HUMANISTS - SOME HITHERTO UNNOTICED NEO-LATIN ECHOES IN 'IN OBITUM PROCANCELLARII MEDICI' AND 'IN OBITUM PRAESULIS ELIENSIS'

      Notes and queries
    34. SMITH A; MARKS R; HAAN E; DIXON J; TRENT RJ
      CLINICAL-FEATURES IN 4 PATIENTS WITH ANGELMAN-SYNDROME RESULTING FROMPATERNAL UNIPARENTAL DISOMY

      Journal of Medical Genetics
    35. SAVARIRAYAN R; NANCE J; MORRIS L; HAAN E; COUPER R
      OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS - HIGHLY VARIABLE PHENOTYPIC-EXPRESSION WITHIN A FAMILY

      Clinical genetics
    36. VLOT AJ; MAUSERBUNSCHOTEN EP; ZARKOVA AG; HAAN E; KRUITWAGEN CLJJ; SIXMA JJ; VANDENBERG HM
      THE HALF-LIFE OF INFUSED FACTOR-VIII IN PATIENTS WITH HEMOPHILIA-A ISINFLUENCED BY ABO BLOOD-GROUP

      Blood
    37. SAVARIRAYAN R; COUPER R; MORRIS L; HAAN E
      OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS - HIGHLY VARIABLE PHENOTYPIC-EXPRESSION IN 5 FAMILY MEMBERS SPANNING 4 GENERATIONS

      American journal of human genetics
    38. SAMPSON JR; MAHESHWAR MM; ASPINWALL R; THOMPSON P; CHEADLE JP; RAVINE D; ROY S; HAAN E; BERNSTEIN J; HARRIS PC
      RENAL CYSTIC-DISEASE IN TUBEROUS SCLEROSIS - ROLE OF THE POLYCYSTIC KIDNEY-DISEASE-1 GENE

      American journal of human genetics
    39. DADAMO P; FASSONE L; GEDEON A; JANSSEN EAM; BIONE S; BOLHUIS PA; BARTH PG; WILSON M; HAAN E; ORSTAVIK KH; PATTON MA; GREEN AJ; ZAMMARCHI E; DONATI MA; TONIOLO D
      THE X-LINKED GENE G4.5 IS RESPONSIBLE FOR DIFFERENT INFANTILE DILATEDCARDIOMYOPATHIES

      American journal of human genetics
    40. SAMPSON J; MAHESHWAR M; ASPINWALL R; THOMPSON P; CHEADLE J; RAVINE D; ROY S; HAAN E; BERNSTEIN J; HARRIS P
      PKD1 GENE INVOLVEMENT IN RENAL CYSTIC-DISEASE IN PATIENTS WITH TUBEROUS SCLEROSIS

      Journal of the American Society of Nephrology
    41. GEDEON A; MULLEY J; HAAN E
      GENE LOCALIZATION FOR SUTHERLAND-HAAN-SYNDROME (SHS-MIM-309470)

      American journal of medical genetics
    42. SMITH A; WILES C; HAAN E; MCGILL J; WALLACE G; DIXON J; SELBY R; COLLEY A; MARKS R; TRENT RJ
      CLINICAL-FEATURES IN 27 PATIENTS WITH ANGELMAN SYNDROME RESULTING FROM DNA DELETION

      Journal of Medical Genetics
    43. MAUSERBUNSCHOTEN EP; BRESTERS D; REESINK HM; ROOSENDAAL G; CHAMULEAU RAFM; HAAN E; JANSEN PLM; VANDENBERG HM
      EFFECT AND SIDE-EFFECTS OF ALPHA-INTERFERON TREATMENT IN HEMOPHILIA PATIENTS WITH CHRONIC HEPATITIS-C

      Haemophilia
    44. LAING NG; WILTON SD; AKKARI PA; DOROSZ S; BOUNDY K; KNEEBONE C; BLUMBERGS P; WHITE S; WATKINS H; LOVE DR; HAAN E
      A MUTATION IN THE ALPHA-TROPOMYOSIN GENE TPM3 ASSOCIATED WITH AUTOSOMAL-DOMINANT NEMALINE MYOPATHY

      Nature genetics
    45. LAING N; WILTON S; AKKARI P; DOROSZ S; BOUNDY K; KNEEBONE C; BLUMBERGS P; WHITE S; WATKINS H; LOVE D; HAAN E
      A MUTATION IN THE ALPHA-TROPOMYOSIN GENE TPM3 ASSOCIATED WITH AUTOSOMAL-DOMINANT NEMALINE MYOPATHY NEM1 (VOL 9, PG 75, 1995)

      Nature genetics
    46. DEWAN PA; BROWN N; MURTHY DP; DANGACHRISTIAN B; HAAN E; BYARD RW; WATTERS DAK
      HYDROMETROCOLPOS AND SEGMENTAL COLONIC DILATATION IN A GIRL WITH MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME

      Journal of paediatrics and child health
    47. HAAN E
      CICERO-ACADEMICUS - STUDIES ON THE ACADEMICS AND ON CICERONIAN PHILOSOPHY - FRENCH - LEVY,C

      Classical review
    48. HAAN E
      THE LATIN LANGUAGE - LANGUAGE OF PHILOSOPHY - PROCEEDINGS OF THE COLLOQUIUM ORGANIZED BY THE ECOLE-FRANCAISE-DE-ROME IN COLLABORATION WITH THE UNIVERSITE-DE-ROME-LA-SAPIENZA (ROME, MAY 17-19,1990) - FRENCH - GRIMAL,P

      Classical review
    49. VLOT AJ; MAUSERBUNSCHOTEN EP; HAAN E; VANDERSCHOUW YT; BOUMA BN; SIXMA JJ; VANDENBERG HM
      A POSSIBLE GENETIC-BASIS FOR THE PHARMACOKINETICS OF TRANSFUSED FACTOR-VIII IN PATIENTS WITH HEMOPHILIA-A

      Blood
    50. SHANLEY S; RATCLIFFE J; HOCKEY A; HAAN E; OLEY C; RAVINE D; MARTIN N; WICKING C; CHENEVIXTRENCH G
      NEVOID BASAL-CELL CARCINOMA SYNDROME - REVIEW OF 118 AFFECTED INDIVIDUALS

      American journal of medical genetics
    51. HAAN E
      ROMAN EPIC - BOYLE,AJ

      Journal of Roman studies
    52. HAAN E
      EPIC AND EMPIRE - POLITICS AND GENERIC FORM FROM VIRGIL TO MILTON - QUINT,D

      Journal of Roman studies
    53. SINGER SL; HAAN E; SLEE J; GOLDBLATT J
      FAMILIAL HEMIFACIAL MICROSOMIA DUE TO AUTOSOMAL-DOMINANT INHERITANCE - CASE-REPORTS

      Australian dental journal
    54. HAAN E
      HEAVENS-PUREST-LIGHT - MILTON 'PARADISE LOST 3' AND VIDA

      Comparative literature studies
    55. CHENEVIXTRENCH G; WICKING C; BERKMAN J; SHARPE H; HOCKEY A; HAAN E; OLEY C; RAVINE D; TURNER A; GOLDGAR D; SEARLE J; WAINWRIGHT B
      FURTHER LOCALIZATION OF THE GENE FOR NEVOID BASAL-CELL CARCINOMA SYNDROME (NBCCS) IN 15 AUSTRALASIAN FAMILIES - LINKAGE AND LOSS OF HETEROZYGOSITY

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 11/08/20 alle ore 12:41:27