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    1. Fenton, PA; Clarke, SEM; Owen, W; Hibbert, J; Hodgson, SV
      Cribriform variant papillary thyroid cancer: A characteristic of familial adenomatous polyposis

      THYROID
    2. Kerr, TP; Durward, A; Hodgson, SV; Hughes, E; Robb, SA
      Hyperkalaemic cardiac arrest in a manifesting carrier of Duchenne musculardystrophy following general anaesthesia

      EUROPEAN JOURNAL OF PEDIATRICS
    3. Ogilvie, CM; Harrison, RH; Horsley, SW; Hodgson, SV; Kearney, L
      A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

      CYTOGENETICS AND CELL GENETICS
    4. Evans, HS; Lewis, CM; Robinson, D; Bell, CMJ; Moller, H; Hodgson, SV
      Cancer risks in women with 2 breast or ovarian cancers: Clues to genetic cancer susceptibility

      INTERNATIONAL JOURNAL OF CANCER
    5. Evans, HS; Lewis, CM; Robinson, D; Bell, CMJ; Moller, H; Hodgson, SV
      Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England

      BRITISH JOURNAL OF CANCER
    6. Zhou, XP; Woodford-Richens, K; Lehtonen, R; Kurose, K; Aldred, M; Hampel, H; Launonen, V; Virta, S; Pilarski, R; Salovaara, R; Bodmer, WF; Conrad, BA; Dunlop, M; Hodgson, SV; Iwama, T; Jarvinen, H; Kellokumpu, I; Kim, JC; Leggett, B; Markie, D; Mecklin, JP; Neale, K; Phillips, R; Piris, J; Rozen, P; Houlston, RS; Aaltonen, LA; Tomlinson, IPM; Eng, C
      Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. Olavesen, MG; Hampe, J; Mirza, MM; Saiz, R; Lewis, CM; Bridger, S; Teare, D; Easton, DF; Herrmann, T; Scott, G; Hirst, J; Sanderson, J; Hodgson, SV; Lee, J; MacPherson, A; Schreiber, S; Lennard-Jones, JE; Curran, ME; Mathew, CG
      Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease

      IMMUNOGENETICS
    8. Hodgson, SV; Haites, NE; Caligo, M; Chang-Claude, J; Eccles, D; Evans, G; Moller, P; Morrison, P; Steel, CM; Stoppa-Lyonnet, D; Vasen, H
      A survey of the current clinical facilities for the management of familialcancer in Europe

      JOURNAL OF MEDICAL GENETICS
    9. Woodford-Richens, K; Bevan, S; Churchman, M; Dowling, B; Jones, D; Norbury, CG; Hodgson, SV; Desai, D; Neale, K; Phillips, RKS; Young, J; Leggett, B; Dunlop, M; Rozen, P; Eng, C; Markie, D; Rodriguez-Bigas, MA; Sheridan, E; Iwama, T; Eccles, D; Smith, GT; Kim, JC; Kim, KM; Sampson, JR; Evans, G; Tejpar, S; Bodmer, WF; Tomlinson, IPM; Houlston, RS
      Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

      GUT
    10. Izatt, L; Vessey, C; Hodgson, SV; Solomon, E
      Rapid and efficient ATM mutation detection by fluorescent chemical cleavage of mismatch: identification of four novel mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. Marsh, DJ; Kum, JB; Lunetta, KL; Bennett, MJ; Gorlin, RJ; Ahmed, SF; Bodurtha, J; Crowe, C; Curtis, MA; Dasouki, M; Dunn, T; Feit, H; Geraghty, MT; Graham, JM; Hodgson, SV; Hunter, A; Korf, BR; Manchester, D; Miesfeldt, S; Murday, VA; Nathanson, KL; Parisi, M; Pober, B; Romano, C; Tolmie, JL; Trembath, R; Winter, RM; Zackai, EH; Zori, RT; Weng, LP; Dahia, PLM; Eng, C
      PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

      HUMAN MOLECULAR GENETICS
    12. Hodgson, SV
      Cancer genetics services in the UK

      DISEASE MARKERS
    13. Hodgson, SV; Heap, E; Cameron, J; Ellis, D; Mathew, CG; Eeles, RA; Solomon, E; Lewis, CM
      Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer

      JOURNAL OF MEDICAL GENETICS
    14. MARSH DJ; DAHIA PLM; COULON V; ZHENG ZM; DORIONBONNET F; CALL KM; LITTLE R; LIN AY; EELES RA; GOLDSTEIN AM; HODGSON SV; RICHARDSON AL; ROBINSON BG; WEBER HC; LONGY M; ENG C
      ALLELIC IMBALANCE, INCLUDING DELETION OF PTEN MMACI, AT THE COWDEN DISEASE LOCUS ON 10Q22-23, IN HAMARTOMAS FROM PATIENTS WITH COWDEN SYNDROME AND GERMLINE PTEN MUTATION/

      Genes, chromosomes & cancer
    15. IZATT L; HODGSON SV; SOLOMON E
      A STUDY OF THE FREQUENCY OF GERMLINE ATAXIA-TELANGIECTASIA MUTATED MUTATIONS IN YOUNG BREAST-CANCER PATIENTS

      European journal of human genetics
    16. MARSH DJ; COULON V; LUNETTA KL; ROCCASERRA P; DAHIA PLM; ZHENG ZM; LIAW D; CARON S; DUBOUE B; LIN AY; RICHARDSON AL; BONNETBLANC JM; BRESSIEUX JM; CABARROTMOREAU A; CHOMPRET A; DEMANGE L; EELES RA; YAHANDA AM; FEARON ER; FRICKER JP; GORLIN RJ; HODGSON SV; HUSON S; LACOMBE D; LEPRAT F; ODENT S; TOULOUSE C; OLOPADE OI; SOBOL H; TISHLER S; WOODS CG; ROBINSON BG; WEBER HC; PARSONS R; PEACOCKE M; LONGY M; ENG C
      MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION

      Human molecular genetics
    17. FRAYLING IM; BECK NE; ILYAS M; DOVEEDWIN I; GOODMAN P; PACK K; BELL JA; WILLIAMS CB; HODGSON SV; THOMAS HJW; TALBOT IC; BODMER WF; TOMLINSON IPM
      THE APC VARIANTS I1307K AND E1317Q ARE ASSOCIATED WITH COLORECTAL TUMORS, BUT NOT ALWAYS WITH A FAMILY HISTORY

      Proceedings of the National Academy of Sciences of the United Statesof America
    18. DESAI DC; MURDAY V; PHILLIPS RKS; NEALE KF; MILLA P; HODGSON SV
      A SURVEY OF PHENOTYPIC FEATURES IN JUVENILE POLYPOSIS

      Journal of Medical Genetics
    19. MIRZA MM; LEE J; TEARE D; HUGOT JP; LAURENTPUIG P; COLOMBEL JF; HODGSON SV; THOMAS G; EASTON DF; LENNARDJONES JE; MATHEW CG
      EVIDENCE OF LINKAGE OF THE INFLAMMATORY BOWEL-DISEASE SUSCEPTIBILITY LOCUS ON CHROMOSOME-16 (IBD1) TO ULCERATIVE-COLITIS

      Journal of Medical Genetics
    20. MARSH DJ; DAHIA PLM; CARON S; KUM JB; FRAYLING IM; TOMLINSON IPM; HUGHES KS; EELES RA; HODGSON SV; MURDAY VA; HOULSTON R; ENG C
      GERMLINE PTEN MUTATIONS IN COWDEN-SYNDROME-LIKE FAMILIES

      Journal of Medical Genetics
    21. HODGSON SV
      THE GENETICS OF LEARNING-DISABILITIES

      Developmental Medicine and Child Neurology
    22. OGILVIE CM; ROONEY SC; HODGSON SV; BERRY AC
      DELETION OF CHROMOSOME 3Q PROXIMAL REGION GIVES RISE TO A VARIABLE PHENOTYPE

      Clinical genetics
    23. MOHAMMED SN; SMITH P; HODGSON SV; FENTIMAN IS; MILES DW; BARNES DM; MILLIS RR; RUBENS RD
      FAMILY HISTORY AND SURVIVAL IN PREMENOPAUSAL BREAST-CANCER

      British Journal of Cancer
    24. TOMLINSON IPM; BECK NE; HOMFRAY T; HAROCOPOS CJ; ADAMS M; HODGSON SV; MARKIE D; BODMER WF
      MOLECULAR AND CLINICOPATHOLOGICAL FEATURES OF 2 FAMILIES WITH THE HNPCC SYNDROME AND UNUSUAL PHENOTYPES

      GI cancer
    25. HODGSON SV
      GENETIC SUSCEPTIBILITY TO BREAST AND OVARIAN-CANCER

      Cancer gene therapy
    26. BECK NE; TOMLINSON IPM; HOMFRAY T; FRAYLING I; HODGSON SV; HAROCOPOS C; BODMER WF
      USE OF SSCP ANALYSIS TO IDENTIFY GERMLINE MUTATIONS IN HNPCC FAMILIESFULFILLING THE AMSTERDAM CRITERIA

      Human genetics
    27. TOMLINSON IPM; BECK NE; WILLIAMSON J; HAROCOPOS CJ; MITCHELL VE; HODGSON SV; BODMER WF
      CLINICAL-FEATURES AND MOLECULAR ANALYSIS OF A FAMILY WITH MULTIPLE COLON TUMORS AND REDUCED PLASMINOGEN-ACTIVATOR ACTIVITY

      International journal of colorectal disease
    28. CLARK SK; PACK K; PRITCHARD J; HODGSON SV
      FAMILIAL ADENOMATOUS POLYPOSIS PRESENTING WITH CHILDHOOD DESMOIDS

      Lancet
    29. BECK NE; TOMLINSON IPM; HOMFRAY TFR; FRAYLING IM; HODGSON SV; BODMER WF
      FREQUENCY OF GERMLINE HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER GENE-MUTATIONS IN PATIENTS WITH MULTIPLE OR EARLY-ONSET COLORECTAL ADENOMAS

      Gut
    30. NOVELLI MR; WILLIAMSON JA; TOMLINSON IPM; ELIA G; HODGSON SV; TALBOT IC; BODMER WF; WRIGHT NA
      DETERMINATION OF THE CLONALITY OF COLORECTAL TUMORS - CLUES TO THE ORIGIN OF HUMAN CANCER

      Gut
    31. WHITELAW SC; MURDAY VA; TOMLINSON IPM; THOMAS HJW; COTTRELL S; GINSBERG A; BUKOFZER S; HODGSON SV; SKUDOWITZ RB; JASS JR; TALBOT IC; NORTHOVER JMA; BODMER WF; SOLOMON E
      CLINICAL AND MOLECULAR-FEATURES OF THE HEREDITARY MIXED POLYPOSIS SYNDROME

      Gastroenterology
    32. PATCHETT SE; ALSTEAD EM; SAUNDERS BP; HODGSON SV; FARTHING MJG
      REGIONAL PROLIFERATIVE PATTERNS IN THE COLON OF PATIENTS AT RISK FOR HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER

      Diseases of the colon & rectum
    33. MARSH DJ; ROTH S; LUNETTA KL; HEMMINKI A; DAHIA PLM; SISTONEN P; ZHENG ZM; CARON S; VANORSOUW NJ; BODMER WF; COTTRELL SE; DUNLOP MG; ECCLES D; HODGSON SV; JARVINEN H; KELLOKUMPU I; MARKIE D; NEALE K; PHILLIPS R; ROZEN P; SYNGAL S; VIJG J; TOMLINSON IPM; AALTONEN LA; ENG C
      EXCLUSION OF PTEN AND 10Q22-24 AS THE SUSCEPTIBILITY LOCUS FOR JUVENILE POLYPOSIS SYNDROME

      Cancer research
    34. BECK NE; TOMLINSON IPM; HOMFRAY T; HODGSON SV; HAROCOPOS CJ; BODMER WF
      GENETIC TESTING IS IMPORTANT IN FAMILIES WITH A HISTORY SUGGESTIVE OFHEREDITARY NONPOLYPOSIS COLORECTAL-CANCER EVEN IF THE AMSTERDAM CRITERIA ARE NOT FULFILLED

      British Journal of Surgery
    35. JARMAN PR; DAVIS MB; HODGSON SV; MARSDEN CD; WOOD NW
      PAROXYSMAL DYSTONIC CHOREOATHETOSIS - GENETIC-LINKAGE STUDIES IN A BRITISH FAMILY

      Brain
    36. SCOTT RJ; FROGGATT NJ; TREMBATH RC; EVANS DGR; HODGSON SV; MAHER ER
      FAMILIAL INFILTRATIVE FIBROMATOSIS (DESMOID TUMORS) (MIM135290) CAUSED BY A RECURRENT 3'-APC GENE MUTATION

      Human molecular genetics
    37. NOVELLI MR; WILLIAMSON JA; TOMLINSON IPM; ELIA G; HODGSON SV; TALBOT IC; BODMER WF; WRIGHT NA
      POLYCLONAL ORIGIN OF COLONIC ADENOMAS IN AN XO XY PATIENT WITH FAP/

      Science
    38. MATHEW CG; SOLOMON E; HODGSON SV
      BREAST-CANCER AND BRCA1 MUTATIONS

      The New England journal of medicine
    39. FROGGATT NJ; BRASSETT C; KOCH DJ; EVANS DGR; HODGSON SV; PONDER BAJ; MAHER ER
      MUTATION SCREENING OF MSH2 AND MLH1 MESSENGER-RNA IN HEREDITARY NONPOLYPOSIS COLON-CANCER SYNDROME

      Journal of Medical Genetics
    40. WHITELAW S; NORTHOVER JM; HODGSON SV
      ATTITUDES TO PREDICTIVE DNA TESTING IN FAMILIAL ADENOMATOUS POLYPOSIS

      Journal of Medical Genetics
    41. THOMAS HJW; WHITELAW SC; COTTRELL SE; MURDAY VA; TOMLINSON IPM; MARKIE D; JONES T; BISHOP DT; HODGSON SV; SHEER D; NORTHOVER JMA; TALBOT IC; SOLOMON E; BODMER WF
      HEREDITARY MIXED POLYPOSIS SYNDROME - GENETIC-MAPPING TO CHROMOSOME

      Gastroenterology
    42. PACK K; SMITHRAVIN J; PHILLIPS RKS; HODGSON SV
      EXCEPTIONS TO THE RULE - INDIVIDUALS WITH FAP SPECIFIC CHRPE AND MUTATIONS IN EXON-6 OF THE APC GENE

      Clinical genetics
    43. NAOM I; LEE J; FORD D; BOWMAN SJ; LANCHBURY JS; HARIS I; HODGSON SV; EASTON D; LENNARDLONES J; MATHEW CG
      ANALYSIS OF THE CONTRIBUTION OF HLA GENES TO GENETIC PREDISPOSITION IN INFLAMMATORY BOWEL-DISEASE

      American journal of human genetics
    44. THOMAS HJW; WHITELAW SC; COTTRELL SE; MURDAY VA; TOMLINSON IPM; MARKIE D; JONES T; BISHOP DT; HODGSON SV; SHEER D; NORTHOVER JMA; TALBOT IC; SOLOMON E; BODMER WF
      MAPPING OF THE HEREDITARY MIXED POLYPOSIS SYNDROME TO CHROMOSOME 6Q

      American journal of human genetics
    45. JOHNSON N; LANCASTER T; FULLER A; HODGSON SV
      THE PREVALENCE OF A FAMILY HISTORY OF CANCER IN GENERAL-PRACTICE

      Family practice
    46. FROGGATT NJ; KOCH J; DAVIES R; EVANS DGR; CLAMP A; QUARRELL OWJ; WEISSENBACH J; HODGSON SV; PONDER BAJ; BARTON DE; MAHER ER
      GENETIC-LINKAGE ANALYSIS IN HEREDITARY NONPOLYPOSIS COLON-CANCER SYNDROME

      Journal of Medical Genetics
    47. FROGGATT NJ; KOCH DJ; DAVIES R; EVANS DGR; PARSONS R; VOGELSTEIN B; HODGSON SV; PONDER BAJ; BARTON DE; MAHER ER
      MOLECULAR-GENETIC ANALYSIS OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER SYNDROME

      Journal of Medical Genetics
    48. GAGLIA P; ATKIN WS; WHITELAW S; TALBOT IC; WILLIAMS CB; NORTHOVER JMA; HODGSON SV
      VARIABLES ASSOCIATED WITH THE RISK OF COLORECTAL ADENOMAS IN ASYMPTOMATIC PATIENTS WITH A FAMILY HISTORY OF COLORECTAL-CANCER

      Gut
    49. HODGSON SV; BERRY AC; DUNBAR HM
      2 BROTHERS WITH AN UNBALANCED 8-17-TRANSLOCATION AND INFANTILE PYLORIC-STENOSIS

      Clinical genetics
    50. DESAI DC; NEALE KF; TALBOT IC; HODGSON SV; PHILLIPS RKS
      JUVENILE POLYPOSIS

      British Journal of Surgery
    51. CAMPLEJOHN RS; PERRY P; HODGSON SV; TURNER G; WILLIAMS A; UPTON C; MACGEOCH C; MOHAMMED S; BARNES DM
      A POSSIBLE SCREENING-TEST FOR INHERITED P53-RELATED DEFECTS BASED ON THE APOPTOTIC RESPONSE OF PERIPHERAL-BLOOD LYMPHOCYTES TO DNA-DAMAGE

      British Journal of Cancer
    52. HODGSON SV; MOHAMMED SN
      SCREENING FOR BREAST-CANCER - CONSIDER FAMILY HISTORY ALSO

      BMJ. British medical journal
    53. ENG C; MURDAY V; SEAL S; MOHAMMED S; HODGSON SV; CHAUDARY MA; FENTIMAN IS; PONDER BAJ; EELES RA
      COWDEN SYNDROME AND LHERMITTE-DUCLOS DISEASE IN A FAMILY - A SINGLE GENETIC SYNDROME WITH PLEIOTROPY

      Journal of Medical Genetics
    54. HODGSON SV; FAGG NLK; TALBOT IC; WILKINSON M
      DELETIONS OF THE ENTIRE APC GENE ARE ASSOCIATED WITH SESSILE COLONIC ADENOMAS

      Journal of Medical Genetics
    55. NUGENT KP; PHILLIPS RKS; HODGSON SV; COTTRELL S; SMITHRAVIN J; PACK K; BODMER WF
      MUTATION ANALYSIS IN FAMILIAL ADENOMATOUS POLYPOSIS (FAP) - PARTIAL PREDICTION OF PHENOTYPE

      Journal of Medical Genetics
    56. MOHAMMED SN; BARNES DM; GILLETT CE; MCGEOCH C; TURNER G; LANE DP; HODGSON SV
      A VARIANT OF THE LI-FRAUMENI SYNDROME - AN ANALYSIS OF 2 FURTHER FAMILIES

      Journal of Medical Genetics
    57. MUNTONI F; GOBBI P; SEWRY C; SHERRATT T; TAYLOR J; SANDHU SK; ABBS S; ROBERTS R; HODGSON SV; BOBROW M; DUBOWITZ V
      DELETIONS IN THE 5' REGION OF DYSTROPHIN AND RESULTING PHENOTYPES

      Journal of Medical Genetics
    58. HODGSON SV; BISHOP DT; JAY B
      GENETIC-HETEROGENEITY OF CONGENITAL HYPERTROPHY OF THE RETINAL-PIGMENT EPITHELIUM (CHRPE) IN FAMILIES WITH FAMILIAL ADENOMATOUS POLYPOSIS

      Journal of Medical Genetics
    59. NUGENT KP; PHILLIPS RKS; HODGSON SV; COTTRELL S; SMITHRAVIN J; PACK K; BODMER WF
      PHENOTYPIC-EXPRESSION IN FAMILIAL ADENOMATOUS POLYPOSIS - PARTIAL PREDICTION BY MUTATION ANALYSIS

      Gut
    60. NUGENT KP; PHILLIPS RKS; HODGSON SV; COTTRELL S; SMITHRAVIN J; PACK K; BODMER WF
      PHENOTYPIC-EXPRESSION IN FAMILIAL ADENOMATOUS POLYPOSIS - PARTIAL PREDICTION BY MUTATION ANALYSIS

      Gut
    61. THOMAS HJW; COTTRELL S; WHITELAW S; HODGSON SV; MURDAY V; SOLOMON E; BODMER WF
      GENETIC-LINKAGE IN A PEDIGREE WITH HEREDITARY MIXED POLYPOSIS SYNDROME

      Gastroenterology
    62. MACGEOCH C; BARNES DM; NEWTON JA; MOHAMMED S; HODGSON SV; NG M; BISHOP DT; SPURR NK
      P53 PROTEIN DETECTED BY IMMUNOHISTOCHEMICAL STAINING IS NOT ALWAYS MUTANT

      Disease markers
    63. HODGSON SV; HAROCOPOS C; GAGLIA P
      SCREENING RESULTS IN A FAMILY CANCER CLINIC - 5 YEARS EXPERIENCE

      Anticancer research
    64. HODGSON SV; COONAR AS; HANSON PJV; COTTRELL S; SCRIVEN PN; JONES T; HAWLEY PR; WILKINSON ML
      2 CASES OF 5Q DELETIONS IN PATIENTS WITH FAMILIAL ADENOMATOUS POLYPOSIS - POSSIBLE LINK WITH CAROLIS-DISEASE

      Journal of Medical Genetics
    65. NUGENT KP; TALBOT IC; HODGSON SV; PHILLIPS RKS
      SOLITARY JUVENILE POLYPS - NOT A MARKER FOR SUBSEQUENT MALIGNANCY

      Gastroenterology
    66. PATCHETT SE; SAUNDERS BP; HAROCOPOS C; HODGSON SV; ALSTEAD EM; FARTHING MJG
      MUCOSAL PROLIFERATION ASSESSED BY THE WHOLE CRYPT MITOTIC COUNT IN SUBJECTS WITH THE FAMILY CANCER SYNDROME (FCS)

      Gastroenterology
    67. MAHER ER; MORSON B; BEACH R; HODGSON SV
      PHENOTYPIC VARIATION IN HEREDITARY NONPOLYPOSIS COLON CANCER SYNDROME- ASSOCIATION WITH INFILTRATIVE FIBROMATOSIS (DESMOID TUMOR)

      Cancer


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Documento generato il 11/08/20 alle ore 03:22:33