Works matching DE "HEMOCHROMATOSIS"
Results: 1351
Repulsive guidance molecule is a structural bridge between neogenin and bone morphogenetic protein.
- Published in:
- Nature Structural & Molecular Biology, 2015, v. 22, n. 6, p. 458, doi. 10.1038/nsmb.3016
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- Publication type:
- Article
Successful pregnancy outcome with the use of antenatal high-dose intravenous immunoglobulin following previous neonatal death associated with neonatal haemochromatosis.
- Published in:
- 2010
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- Publication type:
- Case Study
Nonmalignant Diseases and Treatments Associated with Primary Ovarian Failure: An Expanded Role for Fertility Preservation.
- Published in:
- 2011
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- Publication type:
- Journal Article
Analysis of Hand Joint Space Morphology in Women and Men with Hereditary Hemochromatosis.
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- Calcified Tissue International, 2023, v. 112, n. 4, p. 440, doi. 10.1007/s00223-022-01050-3
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- Publication type:
- Article
Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications.
- Published in:
- 2020
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- Publication type:
- journal article
Neonatal haemochromatosis with reversible pituitary involvement.
- Published in:
- Transplant International, 2014, v. 27, n. 8, p. e76, doi. 10.1111/tri.12336
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- Publication type:
- Article
Divalent metal-ion transporter DMT1 mediates both H<sup>+</sup> -coupled Fe<sup>2+</sup> transport and uncoupled fluxes.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2006, v. 451, n. 4, p. 544, doi. 10.1007/s00424-005-1494-3
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- Publication type:
- Article
Exogenous BMP7 corrects plasma iron overload and bone loss in Bmp6-/- mice.
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- International Orthopaedics, 2015, v. 39, n. 1, p. 161, doi. 10.1007/s00264-014-2550-4
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- Publication type:
- Article
Screening for Iron Overload in the Turkish Population.
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- Digestive Diseases, 2003, v. 21, n. 3, p. 279, doi. 10.1159/000073985
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- Publication type:
- Article
Juvenile Hemochromatosis Connecting Cardiac Arrest and Hypogonadotropic Hypogonadism in a Young Woman.
- Published in:
- 2024
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- Publication type:
- Case Study
A RARE CASE OF GASTROINTESTINAL BLEEDING: NEONATAL HEMOCHROMATOSIS.
- Published in:
- 2018
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- Publication type:
- Case Study
Genetic background of Japanese patients with adult-onset storage diseases in the liver.
- Published in:
- Hepatology Research, 2007, v. 37, n. 10, p. 777, doi. 10.1111/j.1872-034X.2007.00114.x
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- Publication type:
- Article
Hepatocellular carcinoma associated with secondary haemochromatosis in non-cirrhotic liver: a case report
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- Hepatology Research, 2003, v. 26, n. 3, p. 254, doi. 10.1016/S1386-6346(03)00109-8
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- Publication type:
- Article
AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis
- Published in:
- Hepatology Research, 2003, v. 26, n. 2, p. 154, doi. 10.1016/S1386-6346(03)00086-X
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- Publication type:
- Article
Iron metabolism in mice with partial frataxin deficiency.
- Published in:
- Cerebellum, 2003, v. 2, n. 2, p. 146, doi. 10.1080/14734220309408
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- Publication type:
- Article
HFE H63D, C282Y and AGTR1 A1166C Polymorphisms and Brain White Matter Lesions in the Aging Brain.
- Published in:
- Journal of Neurogenetics, 2011, v. 25, n. 1/2, p. 7, doi. 10.3109/01677063.2011.556206
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- Publication type:
- Article
AGENTS DE CHANGEMENT.
- Published in:
- Canadian Journal of Medical Laboratory Science, 2021, v. 83, n. 2, p. 22
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- Publication type:
- Article
Dental pigmentation and hemochromatosis: A case report.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Can two‐dimensional speckle tracking echocardiography be useful for left ventricular assessment in the early stages of hereditary haemochromatosis?
- Published in:
- Echocardiography, 2018, v. 35, n. 11, p. 1772, doi. 10.1111/echo.14141
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- Publication type:
- Article
Research progress in role of iron overload in non - alcoholic fatty liver disease.
- Published in:
- Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi, 2013, v. 29, n. 12, p. 897, doi. 10.3969/j.issn.1001-5256.2013.12.006
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- Publication type:
- Article
A Simple RFLP-Based Method for HFE Gene Multiplex Amplification and Determination of Hereditary Hemochromatosis-Causing Mutation C282Y and H63D Variant with Highly Sensitive Determination of Contamination.
- Published in:
- BioMed Research International, 2020, p. 1, doi. 10.1155/2020/9396318
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- Publication type:
- Article
Hemochromatosis Presenting with Ascites in a Newborn Infant.
- Published in:
- 2022
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- Publication type:
- Case Study
An improved structural model of the human iron exporter ferroportin. Insight into the role of pathogenic mutations in hereditary hemochromatosis type 4.
- Published in:
- Bio-Algorithms & Med-Systems, 2017, v. 13, n. 4, p. 215, doi. 10.1515/bams-2017-0029
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- Publication type:
- Article
HFE-Related Hemochromatosis in a Chinese Patient: The First Reported Case.
- Published in:
- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00077
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- Publication type:
- Article
Hereditary Hemochromatosis Predisposes Mice to Yersinia pseudotuberculosis Infection Even in the Absence of the Type III Secretion System.
- Published in:
- Frontiers in Cellular & Infection Microbiology, 2016, v. 6, p. 1, doi. 10.3389/fcimb.2016.00069
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- Publication type:
- Article
Lack of association between the C2 allele of transferrin and age-related macular degeneration in the Israeli population.
- Published in:
- Ophthalmic Genetics, 2009, v. 30, n. 4, p. 161, doi. 10.3109/13816810903147998
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- Publication type:
- Article
Renal tubular dysgenesis and neonatal hemochromatosis without pulmonary hypoplasia.
- Published in:
- Pediatric Nephrology, 2004, v. 19, n. 3, p. 341
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- Publication type:
- Article
Brucellosis with very high ferritin levels: report of five cases.
- Published in:
- 2012
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- Publication type:
- Case Study
Therapeutic management of neonatal hemochromatosis: Report of four cases and literature review.
- Published in:
- Human & Experimental Toxicology, 2011, v. 30, n. 10, p. 1728, doi. 10.1177/0960327110396534
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- Publication type:
- Article
Comparative study of the protective effect between deferoxamine and deferiprone on chronic iron overload induced cardiotoxicity in rats.
- Published in:
- Human & Experimental Toxicology, 2006, v. 25, n. 7, p. 375, doi. 10.1191/0960327106ht637oa
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- Publication type:
- Article
The Cost-Effectiveness of Screening for Hereditary Hemochromatosis in Germany: A Remodeling Study.
- Published in:
- Medical Decision Making, 2009, v. 29, n. 2, p. 224, doi. 10.1177/0272989X08327112
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- Publication type:
- Article
In vivo adenine base editing reverts C282Y and improves iron metabolism in hemochromatosis mice.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32906-9
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- Publication type:
- Article
'Eyeing' the Cause of Heart Failure: Visible Telltale Clues.
- Published in:
- Texas Heart Institute Journal, 2016, v. 43, n. 6, p. 552, doi. 10.14503/THIJ-16-6085.1
- Publication type:
- Article
Genetic haemochromatosis and sexual health in men.
- Published in:
- Trends in Urology & Men's Health, 2013, v. 4, n. 1, p. 32, doi. 10.1002/tre.312
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- Publication type:
- Article
The Allele Frequency of the HFE gene mutation H63D (rs1799945) and Its Relationship to a Hereditary Hemochromatosis Diagnosis in Metabolic Nutrition Students at Virginia Tech.
- Published in:
- American Journal of Undergraduate Research, 2020, v. 16, n. 4, p. 51, doi. 10.33697/ajur.2020.006
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- Publication type:
- Article
Twenty-Five Years of Contemplating Genotype-Based Hereditary Hemochromatosis Population Screening.
- Published in:
- Genes, 2022, v. 13, n. 9, p. 1622, doi. 10.3390/genes13091622
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- Publication type:
- Article
Mixed-Etiology Restrictive Cardiomyopathy (Desminopathy and Hemochromatosis) with Complex Liver Lesions.
- Published in:
- Genes, 2022, v. 13, n. 4, p. 577, doi. 10.3390/genes13040577
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- Publication type:
- Article
Quality of Life Scores Remained Different among the Genotypic Groups of Patients with Suspected Hemochromatosis, Even after Treatment Period.
- Published in:
- Genes, 2022, v. 13, n. 1, p. 118, doi. 10.3390/genes13010118
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- Publication type:
- Article
HFE Genotype, Ferritin Levels and Transferrin Saturation in Patients with Suspected Hereditary Hemochromatosis.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1162, doi. 10.3390/genes12081162
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- Publication type:
- Article
Distribution and Quantitation of Skin Iron in Primary Haemochromatosis: Correlation with Total Body Iron Stores in Patients Undergoing Phlebotomy.
- Published in:
- Acta Dermato-Venereologica, 2014, v. 94, n. 1, p. 14, doi. 10.2340/00015555-1601
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- Publication type:
- Article
Summaries for patients. Low serum ferritin level rules out advanced liver disease in hemochromatosis.
- Published in:
- 2003
- Publication type:
- journal article
Serum ferritin level predicts advanced hepatic fibrosis among U.S. patients with phenotypic hemochromatosis.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Low Serum Ferritin Level Rules Out Advanced Liver Disease in Hemochromatosis.
- Published in:
- Annals of Internal Medicine, 2003, v. 138, n. 8, p. i-30, doi. 10.7326/0003-4819-138-8-200304150-00003
- By:
- Publication type:
- Article
Hereditary hemochromatosis.
- Published in:
- 2001
- By:
- Publication type:
- Case Study
Hereditary hemochromatosis.
- Published in:
- 2001
- By:
- Publication type:
- commentary
Update in hepatology.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Update in hematology.
- Published in:
- 2001
- By:
- Publication type:
- journal article
The Frequency of Genes for Hemochromatosis in Patients Attending a Health Appraisal Clinic.
- Published in:
- Annals of Internal Medicine, 2000, v. 133, n. 5, p. I-28, doi. 10.7326/0003-4819-133-5-200009050-00003
- Publication type:
- Article
HFE genotype in patients with hemochromatosis and other liver diseases.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Research priorities in hereditary hemochromatosis.
- Published in:
- 1998
- By:
- Publication type:
- journal article