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Autofluorescence imaging within the liver: a promising tool for the detection and characterization of primary liver tumors.
- Published in:
- European Radiology, 2022, v. 32, n. 4, p. 2481, doi. 10.1007/s00330-021-08307-9
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- Publication type:
- Article
Erythropoietic protoporphyria.
- Published in:
- 2009
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- Publication type:
- journal article
OCCURRENCE OF HEPATOCELLULAR CARCINOMA IN A CASE OF HEREDITARY COPROPORPHYRIA.
- Published in:
- American Journal of Gastroenterology (Springer Nature), 1997, v. 92, n. 8, p. 1389
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- Publication type:
- Article
Ferroptosis in Liver Diseases: An Overview.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 14, p. 4908, doi. 10.3390/ijms21144908
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- Publication type:
- Article
Crosstalk between Acidosis and Iron Metabolism: Data from In Vivo Studies.
- Published in:
- Metabolites (2218-1989), 2022, v. 12, n. 2, p. N.PAG, doi. 10.3390/metabo12020089
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- Publication type:
- Article
Iron, Heme Synthesis and Erythropoietic Porphyrias: A Complex Interplay.
- Published in:
- Metabolites (2218-1989), 2021, v. 11, n. 12, p. 798, doi. 10.3390/metabo11120798
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- Publication type:
- Article
Fecal calprotectin in inflammatory bowel diseases: update and perspectives.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 4, p. 474, doi. 10.1515/cclm-2016-0522
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- Publication type:
- Article
High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria.
- Published in:
- Kidney International, 2015, v. 88, n. 2, p. 386, doi. 10.1038/ki.2015.97
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- Publication type:
- Article
Hepcidin regulates intrarenal iron handling at the distal nephron.
- Published in:
- Kidney International, 2013, v. 84, n. 4, p. 756, doi. 10.1038/ki.2013.142
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- Publication type:
- Article
Carence martiale sans anémie : première comorbidité curable de l'insuffisance cardiaque.
- Published in:
- Annales de Biologie Clinique, 2022, v. 80, n. 2, p. 109, doi. 10.1684/abc.2022.1719
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- Publication type:
- Article
Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior.
- Published in:
- Nature Genetics, 2012, v. 44, n. 2, p. 174, doi. 10.1038/ng.1070
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- Publication type:
- Article
ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis.
- Published in:
- Nature Genetics, 2012, v. 44, n. 2, p. 170, doi. 10.1038/ng.1069
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- Publication type:
- Article
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 256, doi. 10.1007/s00439-003-1059-5
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- Publication type:
- Article
Correction to: Urinary metabolic profiling of asymptomatic acute intermittent porphyria using a rule-mining-based algorithm.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Urinary metabolic profiling of asymptomatic acute intermittent porphyria using a rule-mining-based algorithm.
- Published in:
- Metabolomics, 2018, v. 14, n. 1, p. 1, doi. 10.1007/s11306-017-1305-9
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- Publication type:
- Article
Reversible atransferrinemia in a patient with chronic enteropathy: is transferrin mandatory for iron transport?
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- Biochemia Medica, 2023, v. 33, n. 1, p. 1, doi. 10.11613/BM.2023.010801
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- Publication type:
- Article
Iron deficiency diagnosed using hepcidin on critical care discharge is an independent risk factor for death and poor quality of life at one year: an observational prospective study on 1161 patients.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Diagnostic accuracy of serum hepcidin for iron deficiency in critically ill patients with anemia.
- Published in:
- 2010
- By:
- Publication type:
- Report
Quantification of Urine and Plasma Porphyrin Precursors Using LC-MS in Acute Hepatic Porphyrias: Improvement in Routine Diagnosis and in the Monitoring of Kidney Failure Patients.
- Published in:
- Clinical Chemistry, 2023, v. 69, n. 10, p. 1186, doi. 10.1093/clinchem/hvad117
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- Publication type:
- Article
Iron deficiency screening is a key issue in chronic inflammatory diseases: A call to action.
- Published in:
- Journal of Internal Medicine, 2022, v. 292, n. 4, p. 542, doi. 10.1111/joim.13503
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- Publication type:
- Article
Iron status and inflammatory biomarkers in patients with acutely decompensated heart failure: early in-hospital phase and 30-day follow-up.
- Published in:
- European Journal of Heart Failure, 2017, v. 19, n. 8, p. 1075, doi. 10.1002/ejhf.837
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- Publication type:
- Article
Kinetics of serum hepcidin and interleukin-6 levels following COVID-19 infection in hemodialysis patients.
- Published in:
- Clinical Kidney Journal, 2022, v. 15, n. 3, p. 582, doi. 10.1093/ckj/sfab254
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- Publication type:
- Article
Porphyria and kidney diseases.
- Published in:
- Clinical Kidney Journal, 2018, v. 11, n. 2, p. 191, doi. 10.1093/ckj/sfx146
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- Publication type:
- Article
Functional erythropoietin‐hepcidin axis in recombinant human erythropoietin independent haemodialysis patients.
- Published in:
- Nephrology, 2019, v. 24, n. 7, p. 751, doi. 10.1111/nep.13485
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- Publication type:
- Article
Late-Onset X-Linked Dominant Protoporphyria: An Etiology of Photosensitivity in the Elderly.
- Published in:
- Journal of Investigative Dermatology, 2013, v. 133, n. 6, p. 1688, doi. 10.1038/jid.2012.467
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- Publication type:
- Article
From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 7, p. 1164, doi. 10.1093/hmg/ddy030
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- Publication type:
- Article
Mitochondrial energetic defects in muscle and brain of a Hmbs<sup>-/-</sup> mouse model of acute intermittent porphyria.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 17, p. 5015, doi. 10.1093/hmg/ddv222
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- Publication type:
- Article
Molecular and functional analysis of the C-terminal region of human erythroid-specific 5-aminolevulinic synthase associated with X-linked dominant protoporphyria (XLDPP).
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 7, p. 1280, doi. 10.1093/hmg/dds531
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- Publication type:
- Article
Cardiac iron overload in chronically transfused patients with thalassemia, sickle cell anemia, or myelodysplastic syndrome.
- Published in:
- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0172147
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- Publication type:
- Article
R eview: Molecular pathogenesis of hepatic acute porphyrias.
- Published in:
- Journal of Gastroenterology & Hepatology, 1996, v. 11, n. 11, p. 1046, doi. 10.1111/j.1440-1746.1996.tb00035.x
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- Publication type:
- Article
The Relevancy of Data Regarding the Metabolism of Iron to Our Understanding of Deregulated Mechanisms in ALS; Hypotheses and Pitfalls.
- Published in:
- Frontiers in Neuroscience, 2019, p. N.PAG, doi. 10.3389/fnins.2018.01031
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- Publication type:
- Article
Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutations.
- Published in:
- Human Mutation, 2011, v. 32, n. 6, p. 590, doi. 10.1002/humu.21455
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- Publication type:
- Article
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 20, p. 3089, doi. 10.1093/hmg/ddi342
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- Publication type:
- Article
TSPO2 translocates 5‐aminolevulinic acid into human erythroleukemia cells.
- Published in:
- Biology of the Cell (Wiley-Blackwell), 2020, v. 112, n. 4, p. 113, doi. 10.1111/boc.201900098
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- Publication type:
- Article
Three novel mutations in the coproporphyrinogen oxidase gene.
- Published in:
- Human Mutation, 1997, v. 9, n. 1, p. 78, doi. 10.1002/(SICI)1098-1004(1997)9:1<78::AID-HUMU17>3.0.CO;2-M
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- Publication type:
- Article
Ancestral Founder of Mutation W283X in the Porphobilinogen Deaminase Gene among Acute Intermittent Porphyria Patients.
- Published in:
- Human Heredity, 2002, v. 54, n. 2, p. 69, doi. 10.1159/000067665
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- Publication type:
- Article
Identification of a Prevalent Nonsense Mutation (W283X) and Two Novel Mutations in the Porphobilinogen Deaminase Gene of Swiss Patients with Acute Intermittent Porphyria.
- Published in:
- Human Heredity, 2000, v. 50, n. 4, p. 247, doi. 10.1159/000022924
- By:
- Publication type:
- Article
Iron status and inflammatory biomarkers in patients with acutely decompensated heart failure: early in-hospital phase and 30-day follow-up.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Molecular characterization of homozygous variegate porphyria.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 12, p. 1921, doi. 10.1093/hmg/7.12.1921
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- Publication type:
- Article
Mutations in the Protoporphyrinogen Oxidase Gene in Patients with Variegate Porphyria.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 3, p. 407, doi. 10.1093/hmg/5.3.407
- By:
- Publication type:
- Article
Neglected Comorbidity of Chronic Heart Failure: Iron Deficiency.
- Published in:
- Nutrients, 2022, v. 14, n. 15, p. 3214, doi. 10.3390/nu14153214
- By:
- Publication type:
- Article
Towards a Common Definition for the Diagnosis of Iron Deficiency in Chronic Inflammatory Diseases.
- Published in:
- Nutrients, 2022, v. 14, n. 5, p. N.PAG, doi. 10.3390/nu14051039
- By:
- Publication type:
- Article
Hepcidin and Iron Deficiency in Women One Year after Sleeve Gastrectomy: A Prospective Cohort Study.
- Published in:
- Nutrients, 2021, v. 13, n. 8, p. 2516, doi. 10.3390/nu13082516
- By:
- Publication type:
- Article