Works matching DE "HEMOCHROMATOSIS"

Results: 1367

Hemochromatosis gene mutations and treatment of anemia in patients on hemodialysis.

Published in:

Hemodialysis International, 2009, v. 13, n. 4, p. 460, doi. 10.1111/j.1542-4758.2009.00378.x

By:

BROWN, Michaela C.;
GAFFNEY, Dairena;
GEMMELL, Clare;
OAKES, Eleanor;
MORRIS, Scott;
SPOONER, Richard;
JARDINE, Alan G.;
GEDDES, Colin C.

Publication type:

Article

HFE gene mutation is a risk factor for tissue iron accumulation in hemodialysis patients.

Published in:

Hemodialysis International, 2017, v. 21, n. 3, p. 359, doi. 10.1111/hdi.12537

By:

Turkmen, Ercan;
Yildirim, Tolga;
Yilmaz, Rahmi;
Hazirolan, Tuncay;
Eldem, Gonca;
Yilmaz, Engin;
Aybal Kutlugun, Aysun;
Altindal, Mahmut;
Altun, Bulent

Publication type:

Article

Autoantibodies towards HFE and SYT5 in anti-neutrophil cytoplasm antibody-associated vasculitis relapse Open Access.

Published in:

Rheumatology, 2025, v. 64, n. 5, p. 3142, doi. 10.1093/rheumatology/keae540

By:

Bayati, Shaghayegh;
Nazeer, Jamsheela;
Ng, James;
George, Angel M;
Hayes, Michael;
Little, Mark A;
Nilsson, Peter;
Pin, Elisa

Publication type:

Article

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

By:

Healey, Eleanor G;
Bishop, Benjamin;
Elegheert, Jonathan;
Bell, Christian H;
Padilla-Parra, Sergi;
Siebold, Christian

Publication type:

Article

Aging results in iron accumulations in the non-human primate choroid of the eye without an associated increase in zinc, copper or sulphur.

Published in:

BioMetals, 2018, v. 31, n. 6, p. 1061, doi. 10.1007/s10534-018-0147-x

By:

Ugarte, M.;
Geraki, K.;
Jeffery, G.

Publication type:

Article

Genetic modification of iron metabolism in mice affects the gut microbiota.

Published in:

BioMetals, 2012, v. 25, n. 5, p. 883, doi. 10.1007/s10534-012-9555-5

By:

Buhnik-Rosenblau, Keren;
Moshe-Belizowski, Shirly;
Danin-Poleg, Yael;
Meyron-Holtz, Esther

Publication type:

Article

Physiologic implications of metal-ion transport by ZIP14 and ZIP8.

Published in:

BioMetals, 2012, v. 25, n. 4, p. 643, doi. 10.1007/s10534-012-9526-x

By:

Jenkitkasemwong, Supak;
Wang, Chia-Yu;
Mackenzie, Bryan;
Knutson, Mitchell

Publication type:

Article

Effect of dietary iron deficiency and overload on the expression of ZIP metal-ion transporters in rat liver.

Published in:

BioMetals, 2012, v. 25, n. 1, p. 115, doi. 10.1007/s10534-011-9487-5

By:

Nam, Hyeyoung;
Knutson, Mitchell

Publication type:

Article

Iron excess upregulates SPNS2 mRNA levels but reduces sphingosine-1-phosphate export in human osteoblastic MG-63 cells.

Published in:

Osteoporosis International, 2018, v. 29, n. 8, p. 1905, doi. 10.1007/s00198-018-4531-8

By:

Peltier, L.;
Bendavid, C.;
Cavey, T.;
Island, M.-L.;
Doyard, M.;
Leroyer, P.;
Allain, C.;
De Tayrac, M.;
Ropert, M.;
Loréal, O.;
Guggenbuhl, P.

Publication type:

Article

Osteoporosis across chronic liver disease.

Published in:

Osteoporosis International, 2016, v. 27, n. 6, p. 1967, doi. 10.1007/s00198-016-3512-z

By:

Guarino, M.;
Loperto, I.;
Camera, S.;
Cossiga, V.;
Somma, C.;
Colao, A.;
Caporaso, N.;
Morisco, F.

Publication type:

Article

Beyond Human Leukocyte Antigen Class I Antigens: Hereditary Hemochromatosis Gene Mutations in Recurrent Aphthous Oral Ulcers and Behçet Disease in the South of Tunisia.

Published in:

2017

By:

Elaoud, Sahar;
Kamoun, arwa;
Mahfoudh, Nadia;
Charfi, aida;
Snoussi, Mouna;
Hachicha, Hend;
Jerbi, ameni;
Dammak, Chifa;
Frikha, Feten;
Hakim, Faiza;
Gaddour, Lilia;
Bahloul, Zouheir;
Makni, Hafedh

Publication type:

journal article

Screening for Iron Overload in the Turkish Population.

Published in:

Digestive Diseases, 2003, v. 21, n. 3, p. 279, doi. 10.1159/000073985

By:

Barut, Gultekin;
Balci, Huriye;
Bozdayi, Mithat;
Hatemi, Ibrahim;
Ozcelik, Dervis;
Senturk, Hakan

Publication type:

Article

Hereditary hemochromatosis promotes colitis and colon cancer and causes bacterial dysbiosis in mice.

Published in:

Biochemical Journal, 2020, v. 477, n. 19, p. 3867, doi. 10.1042/BCJ20200392

By:

Sivaprakasam, Sathish;
Ristic, Bojana;
Mudaliar, Nithya;
Hamood, Abdul N.;
Colmer-Hamood, Jane;
Wachtel, Mitchell S.;
Nevels, Anna G.;
Kottapalli, Kameswara R.;
Ganapathy, Vadivel

Publication type:

Article

Diamond-Blackfan anemia: a familial case with emphasis on multi-diagnostic approach to diagnosis and treatment.

Published in:

Medical Laboratory Observer (MLO), 2019, v. 51, n. 6, p. 28

By:

Josephat, Floyd;
Goff, Katrina

Publication type:

Article

MRI as a Aiagnostic Tool for Paroxysmal Nocturnal Hemoglobinuria: A Case Report.

Published in:

Medical Bulletin of Sisli Etfal Hospital, 2021, v. 55, n. 4, p. 565, doi. 10.14744/SEMB.2021.03443

By:

Von Bodelschwingh, Bade;
Ozkurt, Huseyin

Publication type:

Article

Survival Outcomes Among Patients With Hepatocellular Carcinoma in a Large Integrated US Health System.

Published in:

JAMA Network Open, 2024, v. 7, n. 9, p. e2435066, doi. 10.1001/jamanetworkopen.2024.35066

By:

Yilma, Mignote;
Houhong Xu, Richie;
Saxena, Varun;
Muzzin, Monica;
Tucker, Lue-Yen;
Lee, Jeffrey;
Mehta, Neil;
Mukhtar, Nizar

Publication type:

Article

The Definition of Iron Deficiency—An Issue of Health Equity.

Published in:

2024

By:

Tang, Grace H.;
Sholzberg, Michelle

Publication type:

Opinion

Prevalence of Iron Deficiency Using 3 Definitions Among Women in the US and Canada.

Published in:

JAMA Network Open, 2024, v. 7, n. 6, p. e2413967, doi. 10.1001/jamanetworkopen.2024.13967

By:

Barton, James C.;
Wiener, Howard W.;
Barton, Jackson C.;
Acton, Ronald T.

Publication type:

Article

Heart failure of very rare aetiology—haemochromatosis Type 3: a case report.

Published in:

European Heart Journal Case Reports, 2024, v. 8, n. 12, p. 1, doi. 10.1093/ehjcr/ytae637

By:

Montvilaitė-Laurinavičienė, Aistė;
Dirsienė, Rūta;
Neverauskaitė-Piliponienė, Gintarė;
Banišauskaitė, Audra;
Šukys, Marius;
Šakalytė, Gintarė;
Ereminienė, Eglė

Publication type:

Article

HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity.

Published in:

Hereditas, 2022, v. 159, n. 1, p. 1, doi. 10.1186/s41065-022-00237-w

By:

Barton, James C.;
Barton, J. Clayborn;
Acton, Ronald T.

Publication type:

Article

A RARE CASE OF GASTROINTESTINAL BLEEDING: NEONATAL HEMOCHROMATOSIS.

Published in:

2018

By:

Zaharie, Gabriela;
Muresan, D.;
Andreica, S.;
Hosu, Anamaria;
Boitor, D.;
Staicu, Adelina;
Hasmasanu, Monica;
Ighian, Ioana;
Botan, E. C.;
Trif, Andrada R.;
Matyas, Melinda

Publication type:

Case Study

Homeopathy and Hemochromatosis: A Classic Case of Hypochondriasis or a Modern Case for Bloodletting?

Published in:

American Journal of Homeopathic Medicine, 2005, v. 98, n. 4, p. 243

By:

Peck, Kathryn

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

By:

Gebril, Ola H.;
Kirby, Janine;
Savva, George;
Brayne, Carol;
Ince, Paul G.

Publication type:

Article

Frequency of hereditary hemochromatosis gene mutations and their effects on iron overload among beta thalassemia patients of Chennai residents.

Published in:

AIMS Molecular Science, 2021, v. 8, n. 4, p. 233, doi. 10.3934/molsci.2021018

By:

Selvaraj, Bhuvana;
Soundararajan, Sangeetha;
Narayanasamy, Shettu;
Subramanian, Ganesan;
Ramanathan, Senthil Kumar

Publication type:

Article

Hemingway and Hemochromatosis.

Published in:

1990

By:

Beegel, Susan

Publication type:

Literary Criticism

Catheter Ablation of Atrial Fibrillation in Infiltrative Cardiomyopathies: A Narrative Review.

Published in:

Journal of Cardiovascular Electrophysiology, 2025, v. 36, n. 1, p. 276, doi. 10.1111/jce.16487

By:

Satish, Vikyath;
Maliha, Maisha;
Chi, Kuan‐Yu;
Kharawala, Amrin;
Seo, Jiyoung;
Apple, Samuel;
Alhuarrat, Majd Al Deen;
Palaiodimos, Leonidas;
Di Biase, Luigi;
Krumerman, Andrew;
Ferrick, Kevin

Publication type:

Article

Stroke volume monitored by modeling flow from finger arterial pressure waves mirrors blood volume withdrawn by phlebotomy.

Published in:

Clinical Autonomic Research, 2004, v. 14, n. 3, p. 176, doi. 10.1007/s10286-004-0191-1

By:

Leonetti, Pascal;
Audat, Françoise;
Girard, Arlette;
Laude, Dominique;
Lefrère, François;
Elghozi, Jean-Luc

Publication type:

Article

Eryptosis in Haemochromatosis: Implications for rheology.

Published in:

Clinical Hemorheology & Microcirculation, 2018, v. 69, n. 4, p. 457, doi. 10.3233/CH-170325

By:

du Plooy, Jeanette N.;
Bester, Janette;
Pretorius, Etheresia

Publication type:

Article

Haemochromatosis: Pathophysiology and the red blood cell<sup>1</sup>.

Published in:

Clinical Hemorheology & Microcirculation, 2018, v. 69, n. 1-2, p. 295, doi. 10.3233/CH-189128

By:

Richardson, Kieran J.;
McNamee, Antony P.;
Simmonds, Michael J.

Publication type:

Article

Modification of the association between lead exposure and amyotrophic lateral sclerosis by iron and oxidative stress related gene polymorphisms.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2015, v. 16, n. 1/2, p. 72, doi. 10.3109/21678421.2014.964259

By:

Eum, Ki-Do;
Seals, Ryan M.;
Taylor, Kathryn M.;
Grespin, Matthew;
Umbach, David M.;
Hu, Howard;
Sandler, Dale P.;
Kamel, Freya;
Weisskopf, Marc G.

Publication type:

Article

Hemochromatosis and osteoporosis, in reference to 4 cases.

Published in:

Journal of Osteoporosis & Mineral Metabolism / Revista de Osteoporosis y Metabolismo Mineral (English edition), 2016, v. 8, n. 4, p. 134, doi. 10.4321/s1889-836x2016000400006

By:

Jaramillo, D. Montaño;
Curiel, M. Díaz

Publication type:

Article

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

By:

Bhattacharjee, D.;
Vracar, S.;
Round, R. A.;
Nightingale, P. G.;
Williams, J. A.;
Gkoutos, G. V.;
Stratton, I. M.;
Parker, R.;
Luzio, S. D.;
Webber, J.;
Manley, S. E.;
Roberts, G. A.;
Ghosh, S.

Publication type:

Article

THE CLINICAL SIGNIFICANCE OF PIGMENTATION OF THE SKIN.

Published in:

British Journal of Dermatology, 1957, v. 69, n. 6, p. 235

By:

H. R. V.

Publication type:

Article

CLINICAL FEATURES, PATHOLOGY, AND THERAPY OF HAEMOCHROMATOSIS.

Published in:

British Journal of Dermatology, 1955, v. 67, n. 12, p. 461

By:

A. J. R.

Publication type:

Article

A REVIEW OF SOME CASES WITH HAEMOSIDEROSIS.

Published in:

British Journal of Dermatology, 1954, v. 66, n. 2, p. 71

By:

G. W. B.

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

By:

A. J. R.;
J. K.

Publication type:

Article

Iron metabolism and hepcidin concentration in teenagers before and after exercise in relation to the HFE gene status.

Published in:

Baltic Journal of Health & Physical Activity, 2019, v. 11, n. 2, p. 26, doi. 10.29359/BJHPA.11.2.03

By:

Kaczorowska-Hać, Barbara;
Łuszczyk, Marcin;
Antosiewicz, Jędrzej;
Kaczor, Jan Jacek

Publication type:

Article

A novel monoclonal antibody immunoassay for the detection of human serum hepcidin.

Published in:

Journal of Gastroenterology, 2011, v. 46, n. 5, p. 648, doi. 10.1007/s00535-010-0344-z

By:

Schwarz, Peggy;
Strnad, Pavel;
Figura, Guido;
Janetzko, Alfred;
Krayenbühl, Pierre;
Adler, Guido;
Kulaksiz, Hasan

Publication type:

Article

Phlebotomy: a promising treatment for chronic hepatitis C.

Published in:

Journal of Gastroenterology, 2004, v. 39, n. 6, p. 601, doi. 10.1007/s00535-004-1372-3

By:

Tanaka, Naoki;
Kiyosawa, Kendo

Publication type:

Article

Hemochromatosis: Genetics, Pathophysiology, Diagnosis and Treatment Edited by James C. Barton and Corwin Q. Edwards. 600 pp. £110.00 (US$ 215.00) Cambridge University Press, Cambridge, UK, 2000. ISBN 0-521-59380-8.

Published in:

2001

By:

Kohgo, Yutaka

Publication type:

Book Review

A Rare Presentation of Transfusional Hemochromatosis: Hypogonadotropic Hypogonadism.

Published in:

Case Reports in Endocrinology, 2015, v. 2015, p. 1, doi. 10.1155/2015/493091

By:

Ucler, Rifki;
Kara, Erdal;
Atmaca, Murat;
Olmez, Sehmus;
Alay, Murat;
Dirik, Yaren;
Bora, Aydin

Publication type:

Article

The effect of therapeutic phlebotomy for hemochromatosis on non-suicidal self-injury: A case report.

Published in:

International Journal of Psychiatry in Medicine, 2019, v. 54, n. 1, p. 74, doi. 10.1177/0091217418791451

By:

Newham, Benjamin J. C.;
Khanna, Rahul

Publication type:

Article

The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.

Published in:

Bone Marrow Transplantation, 2005, v. 35, n. 12, p. 1155, doi. 10.1038/sj.bmt.1704943

By:

Kallianpur, A. R.;
Hall, L. D.;
Yadav, M.;
Byrne, D. W.;
Speroff, T.;
Dittus, R. S.;
Haines, J. L.;
Christman, B. W.;
Summar, M. L.

Publication type:

Article

A Review on Iron Chelators in Treatment of Iron Overload Syndromes.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2016, v. 10, n. 4, p. 239

By:

Mobarra, Naser;
Shanaki, Mehrnoosh;
Ehteram, Hassan;
Nasiri, Hajar;
Sahmani, Mehdi;
Saeidi, Mohsen;
Goudarzi, Mehdi;
Pourkarim, Hoda;
Azad, Mehdi

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

By:

Rogowski, Wolf H.

Publication type:

Article

Neonatal liver failure: aetiologies and management--state of the art.

Published in:

2011

By:

Shanmugam, Naresh P.;
Bansal, Sanjay;
Greenough, Anne;
Verma, Anita;
Dhawan, Anil

Publication type:

journal article

Diagnosis of juvenile hemochromatosis in an 11-year-old child combining genetic analysis and non-invasive liver iron quantitation.

Published in:

2003

By:

De Gobbi, M.;
Caruso, R.;
Daraio, F.;
Chianale, F.;
Pinto, R. M.;
Longo, F.;
Piga, A.;
Camaschella, C.

Publication type:

journal article

Mutation screening for prenatal and presymptomatic diagnosis: cystic fibrosis and haemochromatosis.

Published in:

European Journal of Pediatrics, 2000, v. 159, n. 15, p. S186, doi. 10.1007/PL00014400

By:

Stuhrmann, Manfred;
Graf, Notker;
Dörk, Thilo;
Schmidtke, Jörg

Publication type:

Article

Iron storage disease (ISD) in a captive toco toucan (Ramphastos toco): a case report.

Published in:

Thai Journal of Veterinary Medicine, 2022, v. 52, n. 4, p. 807, doi. 10.14456/tjvm.2022.95

By:

Ratchanon Kusolsongkhrokul;
Pitchakorn Petcharat;
Watcharin Hin-on;
Pumipuntu, Frank S.;
Tarid Purisotayo;
Natapol Pumipuntu

Publication type:

Article

All that glitters is not gold! Neonatal acute liver failure and liver transplantation.

Published in:

Transplant Journal of Australasia, 2016, v. 25, n. 3, p. 6

By:

Jermyn, Vicki

Publication type:

Article