يعرض 1 - 10 نتائج من 56 نتيجة بحث عن '"HLA-A3 Antigen"', وقت الاستعلام: 1.69s تنقيح النتائج
  1. 1
    Clinical, biochemical and histological features of primary haemochromatosis: a report of 67 cases

    المؤلفون: Dario Conte, Alberto Piperno, Clara Mandelli, Silvia Fargion, Marina Cesana, Lucia Brunelli, Luciana Ferrario, Pietro Velio, Maria Grazia Zaramella, Claudio Tiribelli, Gemino Fiorelli, Paolo A. Bianchi

    المساهمون: Conte, D, Piperno, A, Mandelli, C, Fargion, S, Cesana, M, Brunelli, L, Ferrario, L, Velio, P, Zaramella, Mg, Tiribelli, Claudio, Zaramella, M, Tiribelli, C

    المصدر: Liver. 6:310-315

    مصطلحات موضوعية: Liver Cirrhosis, Male, HBsAg, Pathology, Cirrhosis, HLA-A3 Antigen, Gastroenterology, Liver Cirrhosis/complications, Bone Marrow, HLA Antigens, Hemochromatosis*/complications, Skin/metabolism, Medicine, HLA Antigen, Liver Neoplasms/complications, Skin, Mortality rate, Stomach, Liver Neoplasms, Hemochromatosis*/metabolism, Middle Aged, medicine.anatomical_structure, Liver Neoplasm, Hepatocellular carcinoma, Female, Hemochromatosis, Hepatocellular/complications, Human, Adult, medicine.medical_specialty, Carcinoma, Hepatocellular, HLA Antigens/analysis, Duodenum, Liver Cirrhosi, Iron, HLA-B7 Antigen, Internal medicine, Humans, Bone Marrow/metabolism, Carcinoma, Hepatocellular/complications, Duodenum/metabolism, Female, HLA Antigens/analysis, HLA-A3 Antigen, HLA-B7 Antigen, Hemochromatosis*/complications, Hemochromatosis*/metabolism, Hemochromatosis*/pathology, Humans, Iron/metabolism, Liver Cirrhosis/complications, Liver Neoplasms/complications, Male, Middle Aged, Skin/metabolism, Stomach/metabolism, Hemochromatosis*/pathology, Aged, Stomach/metabolism, Bone Marrow/metabolism, Hepatology, business.industry, Transferrin saturation, Carcinoma, Cancer, Duodenum/metabolism, medicine.disease, Gastric Mucosa, business, Iron/metabolism

    وصف الملف: STAMPA

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50aaba5deb080a35ed3e626544ea3917Test
    https://doi.org/10.1111/j.1600-0676.1986.tb00297.xTest


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  2. 2
    HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload

    المؤلفون: K. Sigvard Olsson, Ruma Raha-Chowdhury, Bernd Ritter

    المصدر: European Journal of Haematology. 84:145-153

    مصطلحات موضوعية: Male, Linkage disequilibrium, Population, Mutation, Missense, Pedigree chart, HLA-A3 Antigen, Biology, Linkage Disequilibrium, HLA-A3, medicine, Humans, Family, Allele, Hemochromatosis Protein, education, Alleles, Hemochromatosis, Recombination, Genetic, Sweden, Genetics, education.field_of_study, Histocompatibility Antigens Class I, Homozygote, Haplotype, Membrane Proteins, Hematology, General Medicine, medicine.disease, Founder Effect, Pedigree, Amino Acid Substitution, Haplotypes, Female, Follow-Up Studies, Founder effect

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc4b375f5044250a97e2a3099dd453aeTest
    https://doi.org/10.1111/j.1600-0609.2009.01376.xTest


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  3. 3
    The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?

    المؤلفون: Norbeth Hansson, Bernd Ritter, K. Sigvard Olsson

    المصدر: European Journal of Haematology. 79:429-434

    مصطلحات موضوعية: Adult, Male, Locus (genetics), Human leukocyte antigen, HLA-A3 Antigen, HLA-B8 Antigen, medicine, Humans, Porphyria cutanea tarda, Cysteine, Hemochromatosis Protein, HLA-A1 Antigen, Hemochromatosis, Aged, Sweden, Genetics, biology, Transferrin saturation, HLA A1-B8 haplotype, Histocompatibility Antigens Class I, Haplotype, Membrane Proteins, Iron Deficiencies, Hematology, General Medicine, Middle Aged, medicine.disease, Pedigree, Ferritin, Phenotype, Haplotypes, Ferritins, Mutation, Immunology, biology.protein, Tyrosine, Female

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47064f8c052e549d3456ddfc082fa3fTest
    https://doi.org/10.1111/j.1600-0609.2007.00953.xTest


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  4. 4
    HLA haplotype A*03-B*07 in hemochromatosis probands with C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload

    المؤلفون: Rodney C.P. Go, James C. Barton, Ronald T. Acton, Howard W. Wiener

    المصدر: Blood Cells, Molecules, and Diseases. 34:38-47

    مصطلحات موضوعية: Adult, Male, Proband, medicine.medical_specialty, Adolescent, Iron, Human leukocyte antigen, HLA-A3 Antigen, Gastroenterology, HLA-B7 Antigen, Gene Frequency, Internal medicine, medicine, Humans, Cysteine, Hemochromatosis Protein, Molecular Biology, Hemochromatosis, Aged, Aged, 80 and over, Sex Characteristics, Univariate analysis, HLA-A Antigens, medicine.diagnostic_test, business.industry, Transferrin saturation, Histocompatibility Antigens Class I, Homozygote, Haplotype, Membrane Proteins, Cell Biology, Hematology, Middle Aged, Phlebotomy, medicine.disease, Common Variable Immunodeficiency, Amino Acid Substitution, Haplotypes, HLA-B Antigens, Immunology, Serum iron, Molecular Medicine, Female, business

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a691432096652b97b9468aa122d98398Test
    https://doi.org/10.1016/j.bcmd.2004.08.022Test


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  5. 5
    A Reappraisal of Hepatic Siderosis in Patients With End-Stage Cirrhosis: Practical Implications for the Diagnosis of Hemochromatosis

    المؤلفون: Bernard Launois, M. Messner, Romain Moirand, Yves Deugnier, Daniéle Le Quilleuc, Bruno Turlin, Pierre Brissot, Oliver Loréal, Bernard Meunier

    المصدر: The American Journal of Surgical Pathology. 21:669-675

    مصطلحات موضوعية: Adult, Liver Cirrhosis, Male, medicine.medical_specialty, Pathology, Carcinoma, Hepatocellular, Siderosis, Cirrhosis, Iron, HLA-A3 Antigen, Gastroenterology, Pathology and Forensic Medicine, Diagnosis, Differential, Internal medicine, Humans, Medicine, In patient, Stage (cooking), Practical implications, Hemochromatosis, Aged, business.industry, Liver Neoplasms, Respiratory disease, Middle Aged, medicine.disease, Liver, Female, Surgery, Anatomy, business, Complication, Biomarkers

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f225a2c80b04b676994da3a4708b8aTest
    https://doi.org/10.1097/00000478-199706000-00007Test


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  6. 6
    A new highly polymorphic marker in the 5' untranslated region of HLA-F shows strong allelic association with haemochromatosis

    المؤلفون: Derrick John Bowen, Ruma Raha-Chowdhury, Mark Worwood

    المصدر: Human Genetics. 97:228-231

    مصطلحات موضوعية: Genetic Markers, Male, Heterozygote, Genes, MHC Class I, Locus (genetics), Minisatellite Repeats, HLA-A3 Antigen, Biology, Loss of heterozygosity, Replication slippage, Gene Frequency, Gene mapping, HLA Antigens, Genetics, Humans, Allele, Gene, Alleles, Genetics (clinical), Repetitive Sequences, Nucleic Acid, Histocompatibility Antigens Class I, Molecular biology, Pedigree, Genetic marker, Microsatellite, Chromosomes, Human, Pair 6, Female, Hemochromatosis, Polymorphism, Restriction Fragment Length

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a2cf0522cbff9feaa9aa08bacb5f899Test
    https://doi.org/10.1007/bf02265271Test


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  7. 7
    Screening for Hemochromatosis

    المؤلفون: Jane F. Desforges, Corwin Q. Edwards, James P. Kushner

    المصدر: New England Journal of Medicine. 328:1616-1620

    مصطلحات موضوعية: Adult, Male, Isoantigens, medicine.medical_specialty, Genetic Linkage, Daily intake, Absorption (skin), HLA-A3 Antigen, Intestinal mucosa, Blood loss, Internal medicine, Humans, Medicine, Alleles, Hemochromatosis, Dietary iron, business.industry, General Medicine, Sloughing, medicine.disease, Pedigree, Endocrinology, Hereditary hemochromatosis, Ferritins, business

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c779717199ff078ec0e562e13c34f684Test
    https://doi.org/10.1056/nejm199306033282208Test


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  8. 8
    Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden

    المؤلفون: Inge Hoegh Dufva, Jan Konar, Anne Ricksten, Karl Sigvard Olsson, Ruma Raha-Chowdhury

    المصدر: European journal of haematology. 86(1)

    مصطلحات موضوعية: Proband, Linkage disequilibrium, Genotype, Mutation, Missense, Pedigree chart, Biology, HLA-A3 Antigen, Linkage Disequilibrium, Irish, Gene Frequency, medicine, Humans, Hemochromatosis, Dominance (genetics), Genetics, Sweden, Haplotype, Hematology, General Medicine, medicine.disease, language.human_language, Founder Effect, History, Medieval, Pedigree, Europe, Genetics, Population, Haplotypes, Case-Control Studies, language, Ireland, Founder effect

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b889313d20a438ca30676ec0fe5c925Test
    https://pubmed.ncbi.nlm.nih.gov/21933281Test


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  9. 9
    Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping

    المؤلفون: James C, Barton, J Clayborn, Barton, Ronald T, Acton

    المصدر: European journal of haematology. 85(5)

    مصطلحات موضوعية: Adult, Male, Iron Overload, HLA-A Antigens, Histocompatibility Testing, Histocompatibility Antigens Class I, Homozygote, Mutation, Missense, Membrane Proteins, HLA-A3 Antigen, Middle Aged, Survival Rate, HLA-B14 Antigen, Sex Factors, Haplotypes, HLA-B Antigens, Humans, Female, Hemochromatosis, Hemochromatosis Protein, Aged

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::d82b0ee6c6ec917ef59dfe4d8adf14bbTest
    https://pubmed.ncbi.nlm.nih.gov/20722701Test


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  10. 10
    The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda

    المؤلفون: Jennifer J. Pointon, Sharon D. Whatley, Andrew G. Roberts, George H. Elder, Caroline Stone, Stuart A. Nicklin, Mark Worwood

    المصدر: Hepatology. 25:159-161

    مصطلحات موضوعية: Adult, Male, Porphyria Cutanea Tarda, congenital, hereditary, and neonatal diseases and abnormalities, Iron, Population, HLA-A3 Antigen, Biology, Loss of heterozygosity, medicine, Humans, Porphyria cutanea tarda, Allele, skin and connective tissue diseases, education, Alleles, Hemochromatosis, Aged, Aged, 80 and over, Genetics, education.field_of_study, Hepatology, Haplotype, Transferrin, nutritional and metabolic diseases, Middle Aged, medicine.disease, Porphyria, Haplotypes, Ferritins, Immunology, Female, Siderosis

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c974c5f80185d127ddf10234e52174cTest
    https://doi.org/10.1002/hep.510250129Test


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