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La ricerca find articoli where authors phrase all words ' Gelbart, T' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 46 riferimenti
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    1. Beutler, E; Gelbart, T; West, C
      Synergy between TLR2 and TLR4: A safety mechanism

      BLOOD CELLS MOLECULES AND DISEASES
    2. Beutler, E; Felitti, V; Gelbart, T; Ho, N
      Genetics of iron storage and hemochromatosis

      DRUG METABOLISM AND DISPOSITION
    3. Corrons, JLV; Alvarez, R; Pujades, A; Zarza, R; Oliva, E; Lasheras, G; Callis, M; Ribes, A; Gelbart, T; Beutler, E
      Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinicaland molecular studies

      BRITISH JOURNAL OF HAEMATOLOGY
    4. Beutler, E; Gelbart, T
      Large-scale screening for HFE mutations: Methodology and cost

      GENETIC TESTING
    5. Iancovici-Kidon, M; Sthoeger, D; Abrahamov, A; Volach, B; Beutler, E; Gelbart, T; Barak, Y
      A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypes

      BLOOD CELLS MOLECULES AND DISEASES
    6. Beutler, E; Gelbart, T
      A common intron 3 mutation (IVS3-48c -> g) leads to misdiagnosis of the c.845G -> A (C282Y) HFE gene mutation

      BLOOD CELLS MOLECULES AND DISEASES
    7. Ruiz-Arguelles, GJ; Garces-Eisele, J; Gelbart, T; Monroy-Barreto, M; Reyes-Nunez, V; Juarez-Morales, JL; Gonzalez-Garrido, MD; Ramirez-Cisneros, FJ; Gallegos-Antunez, D
      Analysis of HFE-Codon 63/282 (H63D/C282Y) gene variants in Mexican mestizos: Blood donors and patients with hereditary hemochromatosis

      ARCHIVES OF MEDICAL RESEARCH
    8. Valentin, C; Pissard, S; Martin, J; Heron, D; Labrune, P; Livet, MO; Mayer, M; Gelbart, T; Schneider, A; Max-Audit, I; Cohen-Solal, M
      Triose phosphate isomerase deficiency in 3 French families: two novel nullalleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)

      BLOOD
    9. Beutler, E; Gelbart, T; Lee, P; Trevino, R; Fernandez, MA; Fairbanks, VF
      Molecular characterization of a case of atransferrinemia

      BLOOD
    10. Beutler, E; Gelbart, T
      PK deficiency prevalence and the limitations of a population-based survey

      BLOOD
    11. Beutler, E; Gelbart, T
      Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white population

      BLOOD
    12. Beutler, E; Felitti, V; Gelbart, T; Ho, N
      The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

      ANNALS OF INTERNAL MEDICINE
    13. Beutler, E; Liebman, H; Gelbart, T; Stefanski, E
      Three Gaucher-disease-producing mutations in a patient with Gaucher disease: Mechanism and diagnostic implications

      ACTA HAEMATOLOGICA
    14. Beutler, E; Felitti, VJ; Ho, NJ; Gelbart, T
      Commentary on HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors by Naveen Arya, Subrata Chakrabrati,Robert A. Hegele, Paul C. Adams

      BLOOD CELLS MOLECULES AND DISEASES
    15. Beutler, E; Felitti, VJ; Gelbart, T; Ho, N
      Commentary on significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosis by J. Nico P. de Villiers and Maritha J. Kotze

      BLOOD CELLS MOLECULES AND DISEASES
    16. Beutler, E; Gelbart, T; Kondo, T; Matsunaga, AT
      The molecular basis of a case of gamma-glutamylcysteine synthetase deficiency

      BLOOD
    17. Zimran, A; Wasser, G; Forman, L; Gelbart, T; Beutler, E
      Effect of ozone on red blood cell enzymes and intermediates

      ACTA HAEMATOLOGICA
    18. LEE PL; GELBART T; WEST C; HALLORAN C; BEUTLER E
      THE HUMAN NRAMP2 GENE - CHARACTERIZATION OF THE GENE STRUCTURE, ALTERNATIVE SPLICING, PROMOTER REGION AND POLYMORPHISMS

      Blood cells, molecules, & diseases
    19. BEUTLER E; GELBART T
      HEMATOLOGICALLY IMPORTANT MUTATIONS - GAUCHER-DISEASE

      Blood cells, molecules, & diseases
    20. BEUTLER E; GELBART T; DEMINA A
      RACIAL VARIABILITY IN THE UDP-GLUCURONOSYLTRANSFERASE-1 (UGT1A1) PROMOTER - A BALANCED POLYMORPHISM FOR REGULATION OF BILIRUBIN METABOLISM

      Proceedings of the National Academy of Sciences of the United Statesof America
    21. BARTON JC; BEUTLER E; GELBART T
      COINHERITANCE OF ALLELES ASSOCIATED WITH HEMOCHROMATOSIS AND HEREDITARY HYPERFERRITINEMIA-CATARACT SYNDROME

      Blood
    22. BEUTLER E; GELBART T
      HLA-H MUTATIONS IN THE ASHKENAZI JEWISH POPULATION

      Blood cells, molecules, & diseases
    23. BEUTLER E; GELBART T
      HEMATOLOGICALLY IMPORTANT MUTATIONS - GAUCHER-DISEASE

      Blood cells, molecules, & diseases
    24. BEUTLER E; WEST C; GELBART T
      HLA-H AND ASSOCIATED PROTEINS IN PATIENTS WITH HEMOCHROMATOSIS

      Molecular medicine
    25. LEE PL; GELBART T; WEST C; ADAMS M; BLACKSTONE R; BEUTLER E
      3 GENES ENCODING ZINC-FINGER PROTEINS ON HUMAN-CHROMOSOME 6P21.3 - MEMBERS OF A NEW SUBCLASS OF THE KRUPPEL GENE FAMILY CONTAINING THE CONSERVED SCAN BOX DOMAIN

      Genomics
    26. BEUTLER E; GELBART T; BALICKI D; DEMINA A; ADUSUMALLI J; ELSAS L; GRINZAID KA; GITZELMANN R; SUPERTIFURGA A; KATTAMIS C; LIOU BBH
      GAUCHER-DISEASE - 4 FAMILIES WITH PREVIOUSLY UNDESCRIBED MUTATIONS

      Proceedings of the Association of American Physicians
    27. BEUTLER E; GELBART T; WEST C; LEE P; ADAMS M; BLACKSTONE R; POCKROS P; KOSTY M; VENDITTI CP; PHATAK PD; SEESE NK; CHORNEY KA; TENELSHOF AE; GERHARD GS; CHORNEY M
      MUTATION ANALYSIS IN HEREDITARY HEMOCHROMATOSIS

      Blood cells, molecules, & diseases
    28. BEUTLER E; GELBART T; WEST C; LEE P; ADAMS M; BLACKSTONE R; POCKROS P; KOSTY M; VENDITTI CP; PHATAK PD; SEESE NK; CHORNEY KA; TENELSHOF AE; GERHARD GS; CHORNEY M
      MUTATION ANALYSIS IN HEREDITARY HEMOCHROMATOSIS (CORRECTED VERSION OFVF214)

      Blood cells, molecules, & diseases
    29. BEUTLER E; GELBART T
      GLUCOCEREBROSIDASE (GAUCHER DISEASE)

      Human mutation
    30. LIU Y; THORNLEYBROWN D; LOWENTHAL EA; GELBART T; PRCHAL JT
      RAPID-DETERMINATION OF G6PD A--GENOTYPE, A-GENOTYPE, AND B-GENOTYPE()

      Blood
    31. BEUTLER E; GELBART T; WEST C; LEE P; ADAMS M; BLACKSTONE R; POCKROS P; KOSTY M; VENDITTI CP; PHATAK P; SEESE NK; GERHARD G; CHORNEY M
      MOLECULAR DIAGNOSIS OF HEREDITARY HEMOCHROMATOSIS

      Blood
    32. BEUTLER E; GELBART T; WEST C; KUHL W; LEE P
      A STRATEGY FOR CLONING THE HEREDITARY HEMOCHROMATOSIS GENE

      Blood cells, molecules, & diseases
    33. BEUTLER E; DEMINA A; LAUBSCHER K; GARVER P; GELBART T; BALICKI D; VAUGHAN L
      THE CLINICAL COURSE OF TREATED AND UNTREATED GAUCHER-DISEASE - A STUDY OF 45 PATIENTS

      Blood cells, molecules, & diseases
    34. BEUTLER E; GELBART T; DEMINA A; ZIMRAN A; LECOUTRE P
      5 NEW GAUCHER-DISEASE MUTATIONS

      Blood cells, molecules, & diseases
    35. RAHBAR S; NOZARI G; FORREST G; GELBART T; FORMAN SJ; BEUTLER E
      A NOVEL INTRACHROMOSOMAL REARRANGEMENT IN THE BETA-GLOBIN GENE FOUND IN AN AFRICAN-AMERICAN FAMILY

      Hemoglobin
    36. ARGARANA CE; GIVOGRI I; DEKREMER RD; GELBART T; DEBOLDINI CD
      MOLECULAR DIAGNOSIS OF GAUCHER DISEASE IN ARGENTINE PATIENTS

      Medicina
    37. BEUTLER E; DEMINA A; GELBART T
      GLUCOCEREBROSIDASE MUTATIONS IN GAUCHER DISEASE

      Molecular medicine
    38. BEUTLER E; GELBART T
      ERRONEOUS ASSIGNMENT OF GAUCHER DISEASE GENOTYPE AS A CONSEQUENCE OF A COMPLETE GENE DELETION

      Human mutation
    39. LEE P; KUHL W; GELBART T; KAMIMURA T; WEST C; BEUTLER E
      HOMOLOGY BETWEEN A HUMAN PROTEIN AND A PROTEIN OF THE GREEN GARDEN PEA

      Genomics
    40. GLENN D; GELBART T; BEUTLER E
      TIGHT LINKAGE OF PYRUVATE-KINASE (PKLR) AND GLUCOCEREBROSIDASE (GBA) GENES

      Human genetics
    41. BEUTLER E; GELBART T
      2 NEW GAUCHER DISEASE MUTATIONS

      Human genetics
    42. NEWBURGER PE; MALAWISTA SE; DINAUER MC; GELBART T; WOODMAN RC; CHADA S; SHEN QC; VANBLARICOM G; QUIE PG; CURNUTTE JT
      CHRONIC GRANULOMATOUS-DISEASE AND GLUTATHIONE-PEROXIDASE DEFICIENCY, REVISITED

      Blood
    43. BEUTLER E; GELBART T
      GAUCHER DISEASE MUTATIONS IN NON-JEWISH PATIENTS

      British Journal of Haematology
    44. GLENN D; GELBART T; BEUTLER E
      TIGHT LINKAGE BETWEEN GAUCHER DISEASE AND PYRUVATE-KINASE (PK) DEFICIENCY GENES

      Blood
    45. NOZARI G; FORREST G; GELBART T; BEUTLER E; RAHBAR S
      A NOVEL INTRACHROMOSOMAL GENE CONVERSION IN THE BETA-GLOBIN GENE FOUND IN AN AFRICAN-AMERICAN PATIENT WITH BETA-THALASSEMIA-INTERMEDIA IN ASSOCIATION WITH ALPHA-THALASSEMIA-2 (ALPHA-3.7)

      Blood
    46. BEUTLER E; GELBART T; KUHL W; ZIMRAN A; WEST C
      MUTATIONS IN JEWISH PATIENTS WITH GAUCHER DISEASE

      Blood


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/05/20 alle ore 11:30:05