Works matching DE "HEMOCHROMATOSIS"
Results: 1356
Hemochromatosis.
- Published in:
- Radiologic Technology, 2025, v. 96, n. 4, p. 295
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- Publication type:
- Article
Clinical characteristics of endocrinopathies in Chinese patients with hereditary haemochromatosis.
- Published in:
- 2021
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- Publication type:
- journal article
French Retrospective Multicentric Study of Neonatal Hemochromatosis: Importance of Autopsy and Autoimmune Maternal Manifestations.
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- Pediatric & Developmental Pathology, 2012, v. 15, n. 6, p. 450, doi. 10.2350/12-02-1155-OA.1
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- Publication type:
- Article
Elevated mean corpuscular volume in patients with hereditary hemochromatosis.
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- Comparative Clinical Pathology, 2009, v. 18, n. 2, p. 145, doi. 10.1007/s00580-008-0761-z
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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
Localization of the iron-regulatory proteins hemojuvelin and transferrin receptor 2 to the basolateral membrane domain of hepatocytes.
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- Histochemistry & Cell Biology, 2007, v. 127, n. 2, p. 221, doi. 10.1007/s00418-006-0229-7
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- Publication type:
- Article
Applying an Age-specific Definition to Better Characterize Etiologies and Outcomes in Neonatal Acute Liver Failure.
- Published in:
- 2021
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- Publication type:
- journal article
Magnetic Resonance Imaging Findings in Neonatal Hemochromatosis.
- Published in:
- 2018
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- Publication type:
- journal article
Fetal Magnetic Resonance Imaging Detection of Liver Iron Deposition in Neonatal Hemochromatosis During Prenatal Therapy.
- Published in:
- 2016
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- Publication type:
- Case Study
Hemochromatosis as a Preventable Cause of Heart Failure: A Rare Case.
- Published in:
- 2024
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- Publication type:
- Case Study
Intestinal perforation after pediatric liver transplantation: risk factors and management.
- Published in:
- Cirugía Pediátrica (English Edition), 2023, v. 36, n. 2, p. 73, doi. 10.54847/cp.2023.02.14
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- Publication type:
- Article
Red Blood Cell Exchange in Sickle Cell Disease: A Single Center Experience.
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- Global Journal of Transfusion Medicine, 2021, v. 6, n. 2, p. 156, doi. 10.4103/gjtm.gjtm_13_21
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- Publication type:
- Article
Hereditary Hemochromatosis and Alpha-Thalassemia Presenting with Diabetes Mellitus: A Rare Case Report.
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- Case Reports in Clinical Practice, 2022, v. 7, n. 3, p. 144
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- Publication type:
- Article
Hemochromatosis Gene Mutations, Body Iron Stores, Dietary Iron, and Risk of Colorectal Adenoma in Women.
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- JNCI: Journal of the National Cancer Institute, 2005, v. 97, n. 12, p. 917, doi. 10.1093/jnci/dji165
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- Publication type:
- Article
Recognition and management of pancreatogenic (type 3c) diabetes.
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- Diabetes & Primary Care, 2020, v. 22, n. 5, p. 111
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- Publication type:
- Article
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 3, p. 525, doi. 10.1007/s10072-011-0504-9
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- Publication type:
- Article
Interaction of the H63D Mutation in the Hemochromatosis Gene with the Apolipoprotein E Epsilon 4 Allele Modulates Age at Onset of Alzheimers Disease.
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- Dementia & Geriatric Cognitive Disorders, 2003, v. 15, n. 3, p. 151, doi. 10.1159/000068480
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- Publication type:
- Article
Allelic Diversity of the Hemochromatosis Gene (HFE) in Malays, Chinese and Indians.
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- Malaysian Journal of Medicine & Health Sciences, 2021, n. 3, p. 49
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- Publication type:
- Article
Cardiac Hemochromatosis Treated With Prolonged Extracorporeal Membrane Oxygenation Support and Chelation Therapy.
- Published in:
- 2018
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- Publication type:
- Case Study
Hemochromatosis Presenting with Ascites in a Newborn Infant.
- Published in:
- 2022
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- Publication type:
- Case Study
HYPERSOMNIA AND HEMOCHROMATOSIS: A CASE REPORT.
- Published in:
- 2000
- Publication type:
- Abstract
Utility of HbA<sub>1c</sub> assessment in people with diabetes awaiting liver transplantation.
- Published in:
- Diabetic Medicine, 2019, v. 36, n. 11, p. 1444, doi. 10.1111/dme.13870
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- Publication type:
- Article
THE CLINICAL SIGNIFICANCE OF PIGMENTATION OF THE SKIN.
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- British Journal of Dermatology, 1957, v. 69, n. 6, p. 235
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- Publication type:
- Article
CLINICAL FEATURES, PATHOLOGY, AND THERAPY OF HAEMOCHROMATOSIS.
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- British Journal of Dermatology, 1955, v. 67, n. 12, p. 461
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- Publication type:
- Article
A REVIEW OF SOME CASES WITH HAEMOSIDEROSIS.
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- British Journal of Dermatology, 1954, v. 66, n. 2, p. 71
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- Publication type:
- Article
CURRENT LITERATURE.
- Published in:
- British Journal of Dermatology, 1951, v. 63, n. 3, p. 121, doi. 10.1111/j.1365-2133.1951.tb13701.x
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- Publication type:
- Article
Icariin Protects Bone Marrow Mesenchymal Stem Cells Against Iron Overload Induced Dysfunction Through Mitochondrial Fusion and Fission, PI3K/AKT/mTOR and MAPK Pathways.
- Published in:
- Frontiers in Pharmacology, 2019, p. N.PAG, doi. 10.3389/fphar.2019.00163
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- Publication type:
- Article
Autoimmune Hepatitis: Diagnostic Dilemma in the Setting of Suspected Iron Overload.
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- Case Reports in Gastrointestinal Medicine, 2013, p. 1, doi. 10.1155/2013/872987
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- Publication type:
- Article
Unexplained Findings of Kayser-Fleischer-Like Rings in a Patient with Cryptogenic Cirrhosis.
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- Case Reports in Gastrointestinal Medicine, 2012, p. 1, doi. 10.1155/2012/438525
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- Publication type:
- Article
Use of High Dose Defroxamine and Nocturnal Home Hemodialysis to Reduce Secondary Hemochromatosis: A Case Study.
- Published in:
- 2018
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- Publication type:
- Abstract
The effect of therapeutic phlebotomy for hemochromatosis on non-suicidal self-injury: A case report.
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- International Journal of Psychiatry in Medicine, 2019, v. 54, n. 1, p. 74, doi. 10.1177/0091217418791451
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- Publication type:
- Article
'Eyeing' the Cause of Heart Failure: Visible Telltale Clues.
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- Texas Heart Institute Journal, 2016, v. 43, n. 6, p. 552, doi. 10.14503/THIJ-16-6085.1
- Publication type:
- Article
Circulating ferritin concentrations and risk of type 2 diabetes in Japanese individuals.
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- Journal of Diabetes Investigation, 2017, v. 8, n. 4, p. 462, doi. 10.1111/jdi.12617
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- Publication type:
- Article
Calcific arteriolopathy beyond chronic kidney disease. The role of hemochromatosis and vitamin K antagonists.
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- Clinical Cases in Mineral & Bone Metabolism, 2018, v. 15, n. 1, p. 85
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- Publication type:
- Article
NEONATAL HEMOCHROMATOSIS - A FULMINANT CAUSE OF NEONATAL CHOLESTASIS.
- Published in:
- Pediatric Oncall Journal, 2022, v. 19, n. 3, p. 1, doi. 10.7199/ped.oncall.2022.34
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- Publication type:
- Article
Periodontal pathogens and clinical parameters in chronic periodontitis.
- Published in:
- 2020
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- Publication type:
- journal article
Sixty-two hepatocellular carcinomas arising in otherwise-healthy livers are shown to display larger size and more vascular invasion, but no difference in pT stage or WHO grade, as compared to their counterparts arising in diseased livers.
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- Canadian Journal of Pathology, 2017, v. 9, p. 7
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- Publication type:
- Article
HFE GENE MUTATIONS; FREQUENCY OF TWO COMMON HFE GENE MUTATIONS (C282Y & H63D) IN AN IMMIGRANT POPULATION (BRITISH PAKISTANIS) IN UK.
- Published in:
- Professional Medical Journal, 2018, v. 25, n. 1, p. 129, doi. 10.29309/TPMJ/18.4462
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- Publication type:
- Article
Appropriate Clinical Genetic Testing of Hemochromatosis Type 2–4, Including Ferroportin Disease.
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- Application of Clinical Genetics, 2021, v. 14, p. 353, doi. 10.2147/TACG.S269622
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- Publication type:
- Article
Is the role of liver biopsy changing in hemochromatosis? A non invasive approach is ready.
- Published in:
- 2012
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- Publication type:
- Letter
HFE Gene C282Y, H63D and S65C Mutations Frequency in the Transylvania Region, Romania.
- Published in:
- Journal of Gastrointestinal & Liver Diseases, 2012, v. 21, n. 2, p. 177
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- Publication type:
- Article
Combined Cardiac Surgery and Liver Transplantation: Three Decades of Worldwide Results.
- Published in:
- Journal of Gastrointestinal & Liver Diseases, 2011, v. 20, n. 4, p. 415
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- Publication type:
- Article
Clinical penetrance of C282Y homozygous HFE hemochromatosis in a western Romanian population.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Homozygous G320V Mutation in the HJV Gene Causing Juvenile Hereditary Haemochromatosis Type A. A Case Report.
- Published in:
- Journal of Gastrointestinal & Liver Diseases, 2010, v. 19, n. 2, p. 191
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- Publication type:
- Article
Elevated Serum Ferritin.
- Published in:
- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 7, p. 743, doi. 10.1001/jama.2014.302
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- Publication type:
- Article
Do Your Genes Make You Absorb Too Much Iron?
- Published in:
- Agricultural Research, 2005, v. 53, n. 5, p. 17
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- Publication type:
- Article
Superficial siderosis of the central nervous system: pathogenetic heterogeneity and therapeutic approaches.
- Published in:
- Acta Neurologica Scandinavica, 2003, v. 107, n. 1, p. 54, doi. 10.1034/j.1600-0404.2003.02001.x
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- Publication type:
- Article
Diagnosis of Hereditary Spherocytosis and Secondary Hemochromatosis in a Patient with Jaundice.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Hepcidin: Homeostasis and Diseases Related to Iron Metabolism.
- Published in:
- Acta Haematologica, 2017, v. 137, n. 4, p. 220, doi. 10.1159/000471838
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- Publication type:
- Article
HAMP Gene Mutation Associated with Juvenile Hemochromatosis in Brazilian Patients.
- Published in:
- Acta Haematologica, 2016, v. 135, n. 4, p. 228, doi. 10.1159/000444119
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- Publication type:
- Article