Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'C282Y MUTATION' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 47 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Bassett, ML
      Haemochromatosis: iron still matters

      INTERNAL MEDICINE JOURNAL
    2. Jorquera, F; Dominguez, A; Diaz-Golpe, V; Espinel, J; Munoz, F; Herrera, A; Fernandez-Gundin, MJ; Vivas, S; Olcoz, JL
      C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload

      REVISTA ESPANOLA DE ENFERMEDADES DIGESTIVAS
    3. Lucotte, G
      Frequency analysis and allele map in favor of the Celtic origin of the C282Y mutation of hemochromatosis

      BLOOD CELLS MOLECULES AND DISEASES
    4. Andrikovics, H; Kalmar, L; Bors, A; Fandl, B; Petri, I; Kalasz, L; Tordai, A
      Genotype screening for hereditary hemochromatosis among voluntary blood donors in hungary

      BLOOD CELLS MOLECULES AND DISEASES
    5. Emery, C; Rose, P
      Hereditary haemochromatosis: never seen a case?

      BRITISH JOURNAL OF GENERAL PRACTICE
    6. Bauduer, F; Scribans, C; Renoux, M; Borot, N
      Genetic hemochromatosis is a rare disease entity among French Basques: a center-based study from the General Hospital of Basque Country

      ANNALS OF HEMATOLOGY
    7. Tavill, AS
      Diagnosis and management of hemochromatosis

      HEPATOLOGY
    8. Sinclair, PR; Gorman, N; Walton, HS; Bement, WJ; Sinclair, JF; Gerhard, GS; Szakacs, JG; Andrews, NC; Levy, JE
      Uroporphyria in HFE mutant mice given 5-aminolevulinate: A new model of Fe-mediated porphyria cutanea tarda

      HEPATOLOGY
    9. Cardoso, C; Porto, G; Lacerda, R; Resende, D; Rodrigues, P; Bravo, F; Oliveira, JC; Justica, B; de Sousa, M
      T-cell receptor repertoire in hereditary hemochromatosis: A study of 32 hemochromatosis patients and 274 healthy subjects

      HUMAN IMMUNOLOGY
    10. Ellervik, C; Mandrup-Poulsen, T; Nordestgaard, BG; Larsen, LE; Appleyard, M; Frandsen, M; Petersen, P; Schlichting, P; Saermark, T; Tybjaerg-Hansen, A; Birgens, H
      Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective study

      LANCET
    11. Ho, GT; Stanley, AJ
      Haemochromatosis: Where are all the patients?

      SCOTTISH MEDICAL JOURNAL
    12. Fleming, RE; Holden, CC; Tomatsu, S; Waheed, A; Brunt, EM; Britton, RS; Bacon, BR; Roopenian, DC; Sly, WS
      Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    13. Pereira, AC; Mota, GFA; Krieger, JE
      Hemochromatosis gene variants in three different ethnic populations: Effects of admixture for screening programs

      HUMAN BIOLOGY
    14. Sullivan, JL; Zacharski, LR
      Hereditary haemochromatosis and the hypothesis that iron depletion protects against ischemic heart disease

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    15. Jackson, HA; Carter, K; Darke, C; Guttridge, MG; Ravine, D; Hutton, RD; Napier, JA; Worwood, M
      HFE mutations, iron deficiency and overload in 10 500 blood donors

      BRITISH JOURNAL OF HAEMATOLOGY
    16. Dereure, O; Aguilar-Martinez, P; Bessis, D; Perney, P; Vallat, C; Guillot, B; Blanc, F; Guilhou, JJ
      HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France

      BRITISH JOURNAL OF DERMATOLOGY
    17. Worwood, M
      What is the role of genetic testing in diagnosis of haemochromatosis?

      ANNALS OF CLINICAL BIOCHEMISTRY
    18. Hanson, EH; Imperatore, G; Burke, W
      HFE gene and hereditary hemochromatosis: A HuGE review

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    19. Annichino-Bizzacchi, JM; Saad, STO; Arruda, VR; Ramires, JAF; Siqueira, LH; Chiaparini, LC; Mansur, AP
      C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction

      JOURNAL OF CARDIOVASCULAR RISK
    20. Burke, W; Imperatore, G; McDonnell, SM; Baron, RC; Khoury, MJ
      Contribution of different HFE genotypes to iron overload disease: a pooledanalysis

      GENETICS IN MEDICINE
    21. Worwood, M
      Early detection of genetic hemochromatosis: Should all young adults be offered the genetic test?

      GENETIC TESTING
    22. Moirand, R
      Hemochromatosis

      GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
    23. Durupt, S; Durieu, I; Nove-Josserand, R; Bencharif, L; Rousset, H; Durand, DV
      Hereditary hemochromatosis.

      REVUE DE MEDECINE INTERNE
    24. Motulsky, AG; Beutler, E
      Population screening in hereditary hemochromatosis

      ANNUAL REVIEW OF PUBLIC HEALTH
    25. Hohler, T; Leininger, S; Kohler, HH; Schirmacher, P; Galle, PR
      Heterozygosity for the hemochromatosis gene in liver diseases - prevalenceand effects on liver histology

      LIVER
    26. Hohler, T; Gerken, G
      Genetic hemochromatosis - from molecular genetics to the clinical diagnosis

      ZEITSCHRIFT FUR GASTROENTEROLOGIE
    27. Brady, JJ; Jackson, HA; Roberts, AG; Morgan, RR; Whatley, SD; Rowlands, GL; Darby, C; Shudell, E; Watson, R; Paiker, J; Worwood, MW; Elder, GH
      Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    28. Guix, P; Picornell, A; Parera, M; Tomas, C; Muncunill, J; Castro, JA; Rossell, J; Vaquer, P; Ramon, MM; Obrador, A
      Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca

      CLINICAL GENETICS
    29. Robson, KJH; Merryweather-Clark, AT; Pointon, JJ; Shearman, JD; Halsall, DJ; Kelly, A; Cox, TM; Rosenberg, WM; Howell, M; Eccles, D; Patch, C; Fowler, AV; Wallace, DF; Camaschella, C; Roetto, A; Zecchina, G; De Gobbi, M; Gasparini, P; Cadet, E; Vandwalle, JL; Capron, D; Rochette, J; Borot, N; Demangel, C; Dery, R; Vinel, JP; Pascal, JP; Coppin, H; Roth, MP
      Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience

      BRITISH JOURNAL OF HAEMATOLOGY
    30. Moirand, R
      Genetic hemochromatosis and the HFE gene

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    31. Agostinho, MF; Arruda, VR; Basseres, DS; Bordin, S; Soares, MCP; Menezes, RC; Costa, FF; Saad, STO
      Mutation analysis of the HFE gene in Brazilian populations

      BLOOD CELLS MOLECULES AND DISEASES
    32. Crawford, DHG; Ramm, GA
      Haemochromatosis

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    33. Mortimore, M; Merryweather-Clarke, AT; Robson, KJH; Powell, LW
      The haemochromatosis gene: A global perspective and implications for the Asia-Pacific region

      JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    34. Crawford, DHG; Fletcher, LM
      Utility of genotyping in diagnosis of genetic haemochromatosis

      JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    35. Deugnier, Y; Moirand, R; Brissot, P; David, V
      Iron overload in the era of molecular biology.

      PATHOLOGIE BIOLOGIE
    36. Blanc, JF; De Ledinghen, V; Trimoulet, P; Le Bail, B; Bernard, PH; Saric, J; Balabaud, C; Bioulac-Sage, P
      Premalignant lesions and hepatocellular carcinoma in a non-cirrhotic alcoholic patient with iron overload and normal transferrin saturation

      JOURNAL OF HEPATOLOGY
    37. Tavill, AS
      Clinical implications of the hemochromatosis gene

      NEW ENGLAND JOURNAL OF MEDICINE
    38. Szakony, S; Balogh, I; Muszbek, L
      The frequency of the haemochromatosis C282Y mutation in the ethnic Hungarian and Romany populations of eastern Hungary

      BRITISH JOURNAL OF HAEMATOLOGY
    39. Lubin, IM; Yamada, NA; Stansel, RM; Pace, RG; Rohlfs, EM; Silverman, LM
      HFE genotyping using multiplex allele-specific polymerase chain reaction and capillary electrophoresis

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    40. Press, RD
      Hereditary hemochromatosis - Impact of molecular and iron-based testing onthe diagnosis, treatment, and prevention of a common, chronic disease

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    41. Tavill, AS
      Screening for hemochromatosis: Phenotyping or genotyping or both?

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    42. Moirand, R; Deugnier, Y; Brissot, P
      Haemochromatosis and HFE gene

      ACTA GASTRO-ENTEROLOGICA BELGICA
    43. MERCIER G; BATHELIER C; LUCOTTE G
      FREQUENCY OF THE C282Y MUTATION OF HEMOCHROMATOSIS IN 5 FRENCH POPULATIONS

      Blood cells, molecules, & diseases
    44. LUCOTTE G
      CELTIC ORIGIN OF THE C282Y MUTATION OF HEMOCHROMATOSIS

      Blood cells, molecules, & diseases (Print)
    45. BATY D; KWIATKOWSKI AT; MECHAN D; HARRIS A; PIPPARD MJ; GOUDIE D
      DEVELOPMENT OF A MULTIPLEX ARMS TEST FOR MUTATIONS IN THE HFE GENE ASSOCIATED WITH HEREDITARY HEMOCHROMATOSIS

      Journal of Clinical Pathology
    46. DYKES A; GURTLER V; FIRKIN F
      ETIOLOGY OF SEVERE IRON OVERLOAD IN A FAMILY WITH HEREDITARY HEMOLYTIC-ANEMIA

      British Journal of Haematology
    47. GOTTSCHALK R; SEIDL C; LOFFLER T; SEIFRIED E; HELZER D; KALTWASSER JP
      HFE CODON-63 282 (H63D/C282Y) DIMORPHISM IN GERMAN PATIENTS WITH GENETIC HEMOCHROMATOSIS/

      Tissue antigens


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 13/08/20 alle ore 22:46:26