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Different cortical excitability profiles in hereditary brain iron and copper accumulation.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders.
- Published in:
- Journal of Gastroenterology, 2010, v. 45, n. 11, p. 1163, doi. 10.1007/s00535-010-0259-8
- By:
- Publication type:
- Article
Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 1, p. 91, doi. 10.15252/emmm.201708361
- By:
- Publication type:
- Article
Hereditary Hyperferritinemia.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2560, doi. 10.3390/ijms24032560
- By:
- Publication type:
- Article
HIF1A: A Putative Modifier of Hemochromatosis.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1245, doi. 10.3390/ijms22031245
- By:
- Publication type:
- Article
Hepcidin response to acute iron intake and chronic iron loading in dysmetabolic iron overload syndrome.
- Published in:
- Liver International, 2011, v. 31, n. 7, p. 994, doi. 10.1111/j.1478-3231.2011.02520.x
- By:
- Publication type:
- Article
Effects of venesections and restricted diet in patients with the insulin-resistance hepatic iron overload syndrome.
- Published in:
- Liver International, 2004, v. 24, n. 5, p. 471, doi. 10.1111/j.1478-3231.2004.0988.x
- By:
- Publication type:
- Article
Mental Well-Being in Patients with Transfusion-Dependent Anemias and Hemochromatosis during the SARS-CoV-2 Pandemic.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2021, v. 13, n. 1, p. 1, doi. 10.4084/MJHID.2021.024
- By:
- Publication type:
- Article
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato‐Oncologia Pediatrica) study group.
- Published in:
- British Journal of Haematology, 2024, v. 204, n. 1, p. 306, doi. 10.1111/bjh.19208
- By:
- Publication type:
- Article
Hepcidin Expression in Iron Overload Diseases Is Variably Modulated by Circulating Factors.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0036425
- By:
- Publication type:
- Article
Prolonged exposure to welding fumes as a novel cause of systemic iron overload.
- Published in:
- Liver International, 2021, v. 41, n. 7, p. 1600, doi. 10.1111/liv.14874
- By:
- Publication type:
- Article
Hepcidin regulation in a mouse model of acute hypoxia.
- Published in:
- European Journal of Haematology, 2018, v. 100, n. 6, p. 636, doi. 10.1111/ejh.13062
- By:
- Publication type:
- Article
Case report Type 3 hemochromatosis and β-thalassemia trait.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Unusual Iron and Copper Studies in a Patient with Liver Injury and Normocytic Anemia: Commentary.
- Published in:
- Clinical Chemistry, 2020, v. 66, n. 2, p. 281, doi. 10.1093/clinchem/hvz009
- By:
- Publication type:
- Article
Intravenous iron therapy improves the hypercapnic ventilatory response and sleep disordered breathing in chronic heart failure.
- Published in:
- European Journal of Heart Failure, 2022, v. 24, n. 10, p. 1940, doi. 10.1002/ejhf.2628
- By:
- Publication type:
- Article
GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors.
- Published in:
- Annals of Hepatology: Official Journal of the Mexican Association of Hepatology, 2017, v. 16, n. 3, p. 451, doi. 10.5604/01.3001.0009.8601
- By:
- Publication type:
- Article
Hepatocellular carcinoma in Gaucher disease: an international case series.
- Published in:
- Journal of Inherited Metabolic Disease, 2018, v. 41, n. 5, p. 819, doi. 10.1007/s10545-018-0142-y
- By:
- Publication type:
- Article
Olfactory impairment and pathology in neurodegenerative disorders with brain iron accumulation.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Hyperferritinemia and diagnosis of type 1 Gaucher disease.
- Published in:
- American Journal of Hematology, 2020, v. 95, n. 5, p. 570, doi. 10.1002/ajh.25752
- By:
- Publication type:
- Article
Unexplained isolated hyperferritinemia without iron overload.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 4, p. 338, doi. 10.1002/ajh.24641
- By:
- Publication type:
- Article
Transferrin Receptor 2 mutations in patients with juvenile hemochromatosis phenotype.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 12, p. E226, doi. 10.1002/ajh.24202
- By:
- Publication type:
- Article
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemia.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Natural history of juvenile haemochromatosis.
- Published in:
- British Journal of Haematology, 2002, v. 117, n. 4, p. 973, doi. 10.1046/j.1365-2141.2002.03509.x
- By:
- Publication type:
- Article
Haemochromatosis in patients with β-thalassaemia trait.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 3, p. 908, doi. 10.1046/j.1365-2141.2000.02436.x
- By:
- Publication type:
- Article
New Mutations in HFE2 and TFR2 Genes Causing Non HFE -Related Hereditary Hemochromatosis.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Identification of Novel Mutations by Targeted NGS Panel in Patients with Hyperferritinemia.
- Published in:
- Genes, 2021, v. 12, n. 11, p. 1778, doi. 10.3390/genes12111778
- By:
- Publication type:
- Article
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: a microneurographic study.
- Published in:
- European Heart Journal, 2016, v. 37, n. 12, p. 988, doi. 10.1093/eurheartj/ehv696
- By:
- Publication type:
- Article
Changes in 24 h ambulatory blood pressure and effects of angiotensin II receptor blockade during acute and prolonged high-altitude exposure: a randomized clinical trial.
- Published in:
- European Heart Journal, 2014, v. 35, n. 44, p. 3113, doi. 10.1093/eurheartj/ehu275
- By:
- Publication type:
- Article
The use of esketamine in comorbid treatment resistant depression and obsessive compulsive disorder following extensive pharmacogenomic testing: a case report.
- Published in:
- Annals of General Psychiatry, 2021, v. 20, n. 1, p. 1, doi. 10.1186/s12991-021-00365-z
- By:
- Publication type:
- Article
Progressive supranuclear palsy-like phenotype caused by progranulin p.Thr272fs mutation.
- Published in:
- Movement Disorders, 2011, v. 26, n. 10, p. 1964, doi. 10.1002/mds.23749
- By:
- Publication type:
- Article
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis.
- Published in:
- Journal of Gastroenterology & Hepatology, 2016, v. 31, n. 7, p. 1342, doi. 10.1111/jgh.13315
- By:
- Publication type:
- Article
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 5, p. 571
- By:
- Publication type:
- Article
Iron overload in subjects with beta-thalassaemia trait: role of idiopathic haemochromatosis gene.
- Published in:
- British Journal of Haematology, 1985, v. 61, n. 3, p. 487, doi. 10.1111/j.1365-2141.1985.tb02852.x
- By:
- Publication type:
- Article