المؤلفون: Diamandis, Carolina

مصطلحات موضوعية: adrenaline blocker, endocrinology, adrenaline inhibition, HFE gene H63D mutation, rare diseases, metabolic disorders, iron metabolism, adrenal gland dysfunction, stress axes

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1dc78485667ddf4732bb322c2c73198cTest

المؤلفون: Cordeiro, Bruna Silva

المساهمون: Porto, Maria da Graça Beça Gonçalves, Marcos, Jorge Martinez, Nunes, Célia Maria Pinto

مصطلحات موضوعية: C282y, H63d, Hemocromatose, Hfe, Motivos de Referenciação, Domínio/Área Científica::Ciências Médicas::Ciências da Saúde::Medicina

العلاقة: http://hdl.handle.net/10400.6/12759Test; 203182405

الإتاحة: http://hdl.handle.net/10400.6/12759Test

المؤلفون: Simonas Juzėnas, Juozas Kupčinskas, Irena Valantienė, Jolanta Šumskienė, Vitalija Petrenkienė, Jūrate Kondrackienė, Laimutis Kučinskas, Gediminas Kiudelis, Jurgita Skiecevičienė, Limas Kupčinskas

المصدر: Medicina, Vol 52, Iss 5, Pp 269-275 (2016)

مصطلحات موضوعية: HFE, C282Y, H63D, Liver cirrhosis, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: http://www.sciencedirect.com/science/article/pii/S1010660X16300593Test; https://doaj.org/toc/1010-660XTest

الوصول الحر: https://doaj.org/article/bc564c93787749559efb66685afc8cc6Test

المؤلفون: Rodriguez, Libia M, Giraldo, Mabel C, Velasquez, Laura I, Alvarez, Cristiam M, Garcia, Luis F, Jimenez-Del-Rio, Marlene, Velez-Pardo, Carlos

المصدر: Genetics and Molecular Biology. March 2015 38(1)

مصطلحات موضوعية: hereditary hemochromatosis, HLA class I genes, HFE gene, H63D, C282Y

وصف الملف: text/html

الوصول الحر: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572015000100008Test

المؤلفون: PDW Kiely

المصدر: The Journal of the Royal College of Physicians of Edinburgh, Vol 48, Iss 3, Pp 233-238 (2018)

مصطلحات موضوعية: C282Y, H63D, haemochromatosis, hepcidin, HFE, osteoarthritis, Medicine (General), R5-920

العلاقة: https://www.rcpe.ac.uk/sites/default/files/jrcpe_48_3_kiely.pdfTest; https://doaj.org/toc/1478-2715Test; https://doaj.org/toc/2042-8189Test; https://doaj.org/article/e4e7be0e2a824b00809a34ad44be4933Test

الإتاحة: https://doi.org/10.4997/JRCPE.2018.307Test
https://doaj.org/article/e4e7be0e2a824b00809a34ad44be4933Test

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

المؤلفون: Nada, Starčević Čizmarević, Božena, Ćurko-Cofek, Vesna, Barac-Latas, Borut, Peterlin, Smiljana, Ristić

المصدر: Biomedical Reports
Volume 16
Issue 2
Biomed Rep

مصطلحات موضوعية: General Neuroscience, nutritional and metabolic diseases, Articles, General Medicine, multiple sclerosis, General Biochemistry, Genetics and Molecular Biology, meta‑analysis, C282Y, iron, BIOMEDICINE AND HEALTHCARE. Basic Medical Sciences. Human Genetics, Genomics and Proteomics, HFE, multiple sclerosis, C282Y, H63D, iron, meta‑analysis, HFE, H63D, General Pharmacology, Toxicology and Pharmaceutics, BIOMEDICINA I ZDRAVSTVO. Temeljne medicinske znanosti. Genetika, genomika i proteomika čovjeka

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32069497033033b84b899cfbd2f7dc1aTest
https://doi.org/10.3892/br.2021.1495Test

المؤلفون: Smith, Lucas, Seideman, David, Diamandis, Carolina

مصطلحات موضوعية: defect, the other mutation, homozygous mutation, H63D, genetic, mutation, HFE gene, H63D syndrome, hemochromatosis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa7f8785aa0cd1ca0e6bc0c8d0a5ad37Test
https://doi.org/10.22541/au.163820567.76952749/v1Test

المؤلفون: Libia M Rodriguez, Mabel C Giraldo, Laura I Velasquez, Cristiam M Alvarez, Luis F Garcia, Marlene Jimenez-Del-Rio, Carlos Velez-Pardo

المصدر: Genetics and Molecular Biology, Vol 38, Iss 1, Pp 8-13 (2015)

مصطلحات موضوعية: hereditary hemochromatosis, HLA class I genes, HFE gene, H63D, C282Y, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572015000100008&lng=en&tlng=enTest; https://doaj.org/toc/1678-4685Test

الوصول الحر: https://doaj.org/article/13fdbf24aa784c4a9f601af5fef7bc1bTest

المؤلفون: Gaus, Fabian Alfons

المساهمون: Malek, Nisar Peter (Prof. Dr.)

مصطلحات موضوعية: C282Y, Hereditary Hemochromatosis, Neonatale Hämochromatose, GALD, Therapy, Ultraschall, H63D, Therapie, primäre Hämochromatose, Neonatal Hemochromatosis, Ultrasonography

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______707::df918dbdca8b176db3e3919912a9ac27Test
https://hdl.handle.net/10900/129350Test