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1
المؤلفون: Francesca Mangialasche, Grégoria Kalpouzos, Goran Papenberg, Farshad Falahati, Erika J. Laukka
المصدر: Neuropsychopharmacology Reports
مصطلحات موضوعية: cognition, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Iron Overload, Genotype, brain, Iron, Transferrin receptor, blood, Internal medicine, medicine, Humans, Pharmacology (medical), H63D, Hemochromatosis Protein, Episodic memory, Pharmacology, chemistry.chemical_classification, Transferrin saturation, Working memory, business.industry, Putamen, aging, QSM, Histocompatibility Antigens Class I, Transferrin, nutritional and metabolic diseases, Membrane Proteins, Quantitative susceptibility mapping, Cognition, Original Articles, Psychiatry and Mental health, Clinical Psychology, Endocrinology, C282Y, chemistry, Original Article, business, HFE gene
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e59d4a6982203902af590bd83526fcdfTest
http://europepmc.org/articles/PMC8411306Test -
2
المؤلفون: Yu Wu, Ting Liu, Yan Lun, Jinjun Yang, Xiao Shuai
المصدر: Internal Medicine
مصطلحات موضوعية: Liver Cirrhosis, Male, China, Heterozygote, hereditary hemochromatosis (HH), congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Iron Overload, Cirrhosis, Thalassemia, Case Report, Late onset, Intestinal absorption, 03 medical and health sciences, 0302 clinical medicine, Hepcidins, Hepcidin, hemic and lymphatic diseases, H63D heterozygous mutation, Epidemiology, Internal Medicine, medicine, Humans, Age of Onset, Hemochromatosis Protein, Hemochromatosis, Aged, biology, business.industry, beta-Thalassemia, General Medicine, medicine.disease, Pedigree, 030220 oncology & carcinogenesis, Hereditary hemochromatosis, Mutation, β-thalassemia, Immunology, biology.protein, HFE gene, business, 030215 immunology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aecbf480b9fc16c0d41b44f74a9799dTest
https://doi.org/10.2169/internalmedicine.8628-16Test -
3
المؤلفون: P Dw Kiely
المصدر: The Journal of the Royal College of Physicians of Edinburgh, Vol 48, Iss 3, Pp 233-238 (2018)
مصطلحات موضوعية: 0301 basic medicine, Genotype, Cardiomyopathy, Osteoarthritis, Bioinformatics, medicine.disease_cause, Education, 03 medical and health sciences, Hepcidin, Arthropathy, medicine, Humans, H63D, Hemochromatosis Protein, lcsh:R5-920, Mutation, biology, business.industry, Cartilage, General Medicine, medicine.disease, C282Y, Phenotype, 030104 developmental biology, medicine.anatomical_structure, haemochromatosis, Joint pain, biology.protein, hepcidin, HFE, Hemochromatosis, medicine.symptom, lcsh:Medicine (General), Hepatic fibrosis, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed4a7bcf2764bcaa2dd35675c4b7b272Test
https://doi.org/10.4997/jrcpe.2018.307Test -
4
المؤلفون: Eugenia Quiros-Roldan, Francesco Castelli, Melania Degli-Antoni, Emanuele Focà, Isabella Zanella
مصطلحات موضوعية: CD4-Positive T-Lymphocytes, case report, elite controller, H63D, HFE variant, HIV, Aged, 80 and over, CD8-Positive T-Lymphocytes, Female, Genes, Regulator, HLA-B Antigens, Humans, Iron, Neuroinflammatory Diseases, RNA, Viral Load, Virus Replication, Elite Controllers, HIV Infections, HIV Seropositivity, HIV-1, Hemochromatosis Protein, Regulator, Context (language use), Immune system, 80 and over, Medicine, Gene, Regulator gene, Aged, Innate immune system, business.industry, General Medicine, Acquired immune system, Viral replication, Genes, Immunology, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0038a720a26b3832957c29e5f060ce4cTest
http://hdl.handle.net/11379/554022Test -
5
المؤلفون: Mattias Ekstedt, Nelson Ndegwa, Iris Posserud, Hannes Hagström, Johan Askling, Per Stål, Fredrik Rorsman, Hanns-Ulrich Marschall, Nils Nyhlin, Daniel Klintman, Mårten Werner, Molly Jalmeus
المصدر: Liver international : official journal of the International Association for the Study of the LiverREFERENCES. 41(3)
مصطلحات موضوعية: Male, medicine.medical_specialty, Carcinoma, Hepatocellular, Colorectal cancer, Population, Gastroenterology and Hepatology, hemochromatosis, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Internal medicine, medicine, Gastroenterologi, Humans, Cumulative incidence, C282Y, epidemiology, H63D, prognosis, education, Hemochromatosis Protein, Hemochromatosis, Sweden, education.field_of_study, Hepatology, business.industry, Hazard ratio, Histocompatibility Antigens Class I, Liver Neoplasms, Absolute risk reduction, Cancer, medicine.disease, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, 030220 oncology & carcinogenesis, Other Clinical Medicine, Mutation, Annan klinisk medicin, 030211 gastroenterology & hepatology, Female, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc52d32b21cc848e0742d1c5c9cc0690Test
https://pubmed.ncbi.nlm.nih.gov/33450138Test -
6
المؤلفون: Mehfooz Hussain, Lubna Danish, Muhammad Ismail, Aqib Iqbal, Ruqiya Pervaiz, Fakhar Zaman, Maryam Shah, Najeeb U. Khan
المصدر: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)مصطلحات موضوعية: 0301 basic medicine, Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, Thalassemia, Hepcidin, Mutation, Missense, 030105 genetics & heredity, Gene mutation, medicine.disease_cause, 03 medical and health sciences, Gene Frequency, Hepcidins, hemic and lymphatic diseases, HAMP, Genetics, medicine, Humans, Pakistan, H63D, Hemochromatosis Protein, Molecular Biology, Genetics (clinical), Hemochromatosis, Mutation, biology, business.industry, beta-Thalassemia, Beta thalassemia, nutritional and metabolic diseases, beta thalassemia major, Original Articles, medicine.disease, Ferritin, lcsh:Genetics, 030104 developmental biology, Ferritins, biology.protein, Original Article, Female, HFE, business, G71D
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7e5983545e73cdd9672c9cdbca30816Test
http://europepmc.org/articles/PMC7507326Test -
7
المصدر: Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-4 (2020)مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Iron Overload, Ferroportin, Venesection, lcsh:Medicine, Transferrin receptor, Case Report, Phlebotomy, Hepcidin, H63D homozygosity, Medicine, Humans, Hemochromatosis Protein, Hemojuvelin, Sri Lanka, biology, Transferrin saturation, business.industry, lcsh:R, nutritional and metabolic diseases, General Medicine, Ferritin, Hereditary hemochromatosis, Immunology, Ferritins, Mutation, biology.protein, HAMP, Hemochromatosis, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b53e1f45ade84b58098436d33903d374Test
https://pubmed.ncbi.nlm.nih.gov/32641120Test -
8دورية أكاديمية
المؤلفون: Oliveira, T. M., Souza, F. P., Jardim, A. C. G., Cordeiro, J. A., Pinho, J. R. R., Sitnik, R., Estevão, J. F., Bonini-Domingos, C. R., Rahal, Paula
المساهمون: Universidade Estadual Paulista (UNESP)
مصطلحات موضوعية: C282Y, H63D, HFE, S65C, Thalassemia, HFE protein, alpha thalassemia, beta thalassemia, Brazil, chi square test, clinical feature, controlled study, female, Fisher exact test, gene frequency, gene mutation, hemoglobinopathy, heterozygote, human, inheritance, major clinical study, male, prevalence, alpha-Thalassemia, beta-Thalassemia, Case-Control Studies, Genotype, Histocompatibility Antigens Class I, Humans, Membrane Proteins
وصف الملف: 1575-1580
العلاقة: Brazilian Journal of Medical and Biological Research; 1.492; http://dx.doi.org/10.1590/S0100-879X2006001200008Test; http://dx.doi.org/10.1590/S0100-879X2006005000041Test; Brazilian Journal of Medical and Biological Research, v. 39, n. 12, p. 1575-1580, 2006.; http://hdl.handle.net/11449/69283Test; S0100-879X2006001200008; WOS:000243103300008; 2-s2.0-33847656226; 2-s2.0-33847656226.pdf; 7991082362671212; 3279428066176719; orcid:0000-0001-5693-6148; orcid:0000-0002-4603-9467
الإتاحة: https://doi.org/10.1590/S0100-879X2006001200008Test
https://doi.org/10.1590/S0100-879X2006005000041Test
http://hdl.handle.net/11449/69283Test -
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المؤلفون: Rui-Xi Hua, Gang Meng, Xi Zhang, Xian Chang, Guang-Ning Yan, Xiao‐Yu Liao, Yang-Fan Lv, Qiao-Nan Guo
المصدر: Journal of Cellular and Molecular Medicine
مصطلحات موضوعية: Oncology, medicine.medical_specialty, Colorectal cancer, Bioinformatics, Polymorphism, Single Nucleotide, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Risk Factors, Neoplasms, Internal medicine, Genetic model, Odds Ratio, hereditary haemochromatosis, cancer, Humans, Medicine, Missense mutation, Genetic Predisposition to Disease, H63D, Allele, Hemochromatosis Protein, business.industry, Case-control study, Cancer, Original Articles, Cell Biology, Odds ratio, medicine.disease, C282Y, meta‐analysis, Case-Control Studies, 030220 oncology & carcinogenesis, Mutation, Molecular Medicine, Original Article, 030211 gastroenterology & hepatology, HFE, business, Publication Bias
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df41233e478c29f77b57bf25fff54ef7Test
https://doi.org/10.1111/jcmm.12764Test -
10
المؤلفون: James R. Connor, Ian A. Simpson, Elizabeth B. Neely, Anne M. Nixon
المصدر: Journal of Neuroinflammation, Vol 15, Iss 1, Pp 1-11 (2018)
Journal of Neuroinflammationمصطلحات موضوعية: Male, 0301 basic medicine, Genotype, Iron, Immunology, Bone Marrow Cells, Mice, Transgenic, Inflammation, Biology, lcsh:RC346-429, Mice, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, H67D, medicine, Animals, Humans, Macrophage, Gene Knock-In Techniques, H63D, Hemochromatosis Protein, Cells, Cultured, lcsh:Neurology. Diseases of the nervous system, Cell Proliferation, chemistry.chemical_classification, Microglia, Research, Macrophages, General Neuroscience, Wild type, Phenotype, Cell biology, Mice, Inbred C57BL, Bone morphogenetic protein 6, 030104 developmental biology, medicine.anatomical_structure, Neurology, chemistry, Transferrin, HFE, medicine.symptom, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f2b709f3064d0d88c7114bd276cd9cTest
https://doi.org/10.1186/s12974-018-1057-0Test