Works matching Hemochromatosis
Results: 2986
Juvenile Hemochromatosis Connecting Cardiac Arrest and Hypogonadotropic Hypogonadism in a Young Woman.
- Published in:
- 2024
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- Publication type:
- Case Study
Haemochromatosis: a clinical update for the practising physician.
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- Internal Medicine Journal, 2018, v. 48, n. 5, p. 509, doi. 10.1111/imj.13784
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- Publication type:
- Article
Idiopathic hand osteoarthritis vs haemochromatosis arthropathy—a clinical, functional and radiographic study.
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- Rheumatology, 2013, v. 52, n. 5, p. 910, doi. 10.1093/rheumatology/kes392
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- Publication type:
- Article
An unfortunate case of acquired hemochromatosis: a case report review of the clinical presentation, diagnosis, management, and prognosis.
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- International Medical Case Reports Journal, 2016, v. 9, p. 385, doi. 10.2147/imcrj.s117322
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- Publication type:
- Article
Serum ferritin concentration predicts hepatic fibrosis better than hepatic iron concentration in human HFE-Haemochromatosis.
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- Liver International, 2017, v. 37, n. 9, p. 1382, doi. 10.1111/liv.13395
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- Publication type:
- Article
Magnetic resonance imaging of neonatal hemochromatosis.
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- Pediatric Radiology, 2022, v. 52, n. 2, p. 334, doi. 10.1007/s00247-021-05008-9
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- Publication type:
- Article
Juvenile Hemochromatosis in Iran: A Case Report with 5-Year Follow-up after Treatment.
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- Middle East Journal of Digestive Diseases, 2016, v. 8, n. 2, p. 143, doi. 10.15171/mejdd.2016.20
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- Publication type:
- Article
Novel homozygote variant in the HJV gene leading to juvenile hemochromatosis: a case report.
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- Gastroenterology & Hepatology from Bed to Bench, 2023, v. 16, n. 4, p. 441, doi. 10.22037/ghfbb.v16i4.2721
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- Publication type:
- Article
Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping Barton et al. Hemochromatosis survival and HLA-A*03, B*14
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- European Journal of Haematology, 2010, v. 85, n. 5, p. 439, doi. 10.1111/j.1600-0609.2010.01511.x
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- Publication type:
- Article
Homeopathy and Hemochromatosis: A Classic Case of Hypochondriasis or a Modern Case for Bloodletting?
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- American Journal of Homeopathic Medicine, 2005, v. 98, n. 4, p. 243
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- Publication type:
- Article
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis.
- Published in:
- 2003
- By:
- Publication type:
- journal article
The Clinical Expression of Hemochromatosis in Oslo, Norway: Excessive Oral Iron Intake May Lead to Secondary Hemochromatosis Even in HFE C282Y Mutation Negative Subjects.
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- Scandinavian Journal of Gastroenterology, 2000, v. 35, n. 12, p. 1301, doi. 10.1080/003655200453665
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- Publication type:
- Article
Panhypopituitarism Due to Hemochromatosis.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Successful pregnancy outcome with the use of antenatal high-dose intravenous immunoglobulin following previous neonatal death associated with neonatal haemochromatosis.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
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
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
A RARE CASE OF GASTROINTESTINAL BLEEDING: NEONATAL HEMOCHROMATOSIS.
- Published in:
- 2018
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- Publication type:
- Case Study
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
Hemochromatosis Presenting with Ascites in a Newborn Infant.
- Published in:
- 2022
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- Publication type:
- Case Study
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
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.
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- 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.
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- 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.
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- 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
A farewell to phlebotomy—use of placenta-derived drugs Laennec and Porcine for improving hereditary hemochromatosis without phlebotomy: a case report.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
A farewell to phlebotomy-use of placenta-derived drugs Laennec and Porcine for improving hereditary hemochromatosis without phlebotomy: a case report.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Recurrent BMP4 variants in exon 4 cause non-HFE-associated hemochromatosis via the BMP/SMAD signaling pathway.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03439-9
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- Publication type:
- Article
The role of hereditary hemochromatosis in aseptic loosening following primary total hip arthroplasty
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- Journal of Orthopaedic Research, 2005, v. 23, n. 3, p. 542, doi. 10.1016/j.orthres.2004.11.004
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- Publication type:
- Article
Endocrinopathy of HFE-related hemochromatosis.
- Published in:
- Expert Review of Endocrinology & Metabolism, 2007, v. 2, n. 2, p. 277, doi. 10.1586/17446651.2.2.277
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- Publication type:
- Article
Hemochromatosis: Ferroptosis, ROS, Gut Microbiome, and Clinical Challenges with Alcohol as Confounding Variable.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 5, p. 2668, doi. 10.3390/ijms25052668
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- Publication type:
- Article
PATHOLOGY TEACH AND TELL: NEONATAL HEMOCHROMATOSIS WITH MASSIVE HEPATIC NECROSIS.
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- Fetal & Pediatric Pathology, 2004, v. 23, n. 5/6, p. 345, doi. 10.1080/15227950490952406
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- Publication type:
- Article
Hereditary haemochromatosis and diabetes.
- Published in:
- Journal of Diabetes Nursing, 2018, v. 22, n. 4, p. 1
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- Publication type:
- Article
French Retrospective Multicentric Study of Neonatal Hemochromatosis: Importance of Autopsy and Autoimmune Maternal Manifestations.
- Published in:
- 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
Surgery for Hepatocellular Carcinoma Arising in Hereditary Hemochromatosis.
- Published in:
- European Surgical Research, 2006, v. 38, n. 4, p. 371, doi. 10.1159/000094532
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- Publication type:
- Article
Hereditary hemochromatosis: Retrospective study on clinical data from Emergency County Hospital Mures.
- Published in:
- Acta Marisiensis. Seria Medica, 2022, v. 68, n. 4, p. 179, doi. 10.2478/amma-2022-0031
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- Publication type:
- Article
Phlebotomy-Mobilized Iron as a Surrogate for Liver Iron Content in Hemochromatosis Patients.
- Published in:
- Hematology, 2003, v. 8, n. 6, p. 429, doi. 10.1080/1024533032000158832
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- Publication type:
- Article
Patient-focused outcomes following detection in a hospital-based screening programme for C282Y haemochromatosis.
- Published in:
- Internal Medicine Journal, 2008, v. 38, n. 8, p. 651, doi. 10.1111/j.1445-5994.2007.01578.x
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- Publication type:
- Article
Successful treatment of hemochromatosis with renal tubular dysgenesis in a preterm infant.
- Published in:
- Clinical Case Reports, 2015, v. 3, n. 8, p. 690, doi. 10.1002/ccr3.306
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- Publication type:
- Article
Secondary Haemochromatosis in a Patient with Thalassemia Intermedia.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Infectious Mononucleosis Causing Acute Liver Failure and Hemolytic Anemia in a Patient with Underlying Hereditary Hemochromatosis.
- Published in:
- Case Reports in Oncology, 2020, v. 13, n. 3, p. 1232, doi. 10.1159/000509742
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- Publication type:
- Article
Discrepancy between Serum Ferritin and Liver Iron Concentration in a Patient with Hereditary Hemochromatosis – The Value of T2* MRI.
- Published in:
- Case Reports in Oncology, 2020, v. 13, n. 2, p. 712, doi. 10.1159/000507756
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- Publication type:
- Article
Appropriate Clinical Genetic Testing of Hemochromatosis Type 2–4, Including Ferroportin Disease.
- Published in:
- Application of Clinical Genetics, 2021, v. 14, p. 353, doi. 10.2147/TACG.S269622
- By:
- Publication type:
- Article
Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Periodontal status and serum biomarker levels in HFE haemochromatosis patients. A case-series study.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Brain iron deposition and movement disorders in hereditary haemochromatosis without liver failure: A cross‐sectional study.
- Published in:
- European Journal of Neurology, 2022, v. 29, n. 5, p. 1417, doi. 10.1111/ene.15242
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- Publication type:
- Article
Two-dimensional Strain Echocardiography in the Evaluation of Ventricular Function in Patients with Newly Diagnosed Hereditary Hemochromatosis.
- Published in:
- Revista Argentina de Cardiología, 2019, v. 87, n. 6, p. 429, doi. 10.7775/rac.v87.i6.16590
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- Publication type:
- Article
Cenário das políticas públicas para hemocromatose hereditária no Brasil.
- Published in:
- Saúde e Sociedade, 2023, v. 32, n. 4, p. 1, doi. 10.1590/S0104-12902023210915pt
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- Publication type:
- Article
Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
- Published in:
- Annals of Hematology, 2012, v. 91, n. 4, p. 491, doi. 10.1007/s00277-011-1338-5
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- Publication type:
- Article