Works matching Hemochromatosis

Results: 3024

Haemochromatosis: a clinical update for the practising physician.

Published in:

Internal Medicine Journal, 2018, v. 48, n. 5, p. 509, doi. 10.1111/imj.13784

By:

Radford‐smith, Daniel E.;
Powell, Elizabeth E.;
Powell, Lawrie W.

Publication type:

Article

Quantitative and qualitative analysis of quality of life in people diagnosed with genetic haemochromatosis in the United Kingdom.

Published in:

Journal of Patient-Reported Outcomes, 2025, v. 9, n. 1, p. 1, doi. 10.1186/s41687-025-00865-6

By:

Craven-Smith, Leah;
McClements, Neil;
Gomes, Diogo;
Pointon, Victoria

Publication type:

Article

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

Juvenile Hemochromatosis in Iran: A Case Report with 5-Year Follow-up after Treatment.

Published in:

Middle East Journal of Digestive Diseases, 2016, v. 8, n. 2, p. 143, doi. 10.15171/mejdd.2016.20

By:

Nobakht, Hossein;
Zolfaghari, Sheida;
Pourazizi, Mohsen;
Malek, Mojtaba

Publication type:

Article

New Mutations in HFE2 and TFR2 Genes Causing Non HFE -Related Hereditary Hemochromatosis.

Published in:

2021

By:

Hernández, Gonzalo;
Ferrer-Cortès, Xenia;
Venturi, Veronica;
Musri, Melina;
Pilquil, Martin Floor;
Torres, Pau Marc Muñoz;
Rodríguez, Ines Hernandez;
Mínguez, Maria Àngels Ruiz;
Kelleher, Nicholas J.;
Pelucchi, Sara;
Piperno, Alberto;
Alberca, Esther Plensa;
Ricós, Georgina Gener;
Giró, Eloi Cañamero;
Pérez-Montero, Santiago;
Tornador, Cristian;
Villà-Freixa, Jordi;
Sánchez, Mayka

Publication type:

Case Study

Novel homozygote variant in the HJV gene leading to juvenile hemochromatosis: a case report.

Published in:

Gastroenterology & Hepatology from Bed to Bench, 2023, v. 16, n. 4, p. 441, doi. 10.22037/ghfbb.v16i4.2721

By:

Ghanadi, Koruosh;
Mahmoudvand, Golnaz;
Rouzbahani, Arian Karimi

Publication type:

Article

Panhypopituitarism Due to Hemochromatosis.

Published in:

2013

By:

zkaya, Mesut;
Gisi, Kadir;
€etinkaya, Ali;
Köröğlu, Sedat

Publication type:

Case Study

An unfortunate case of acquired hemochromatosis: a case report review of the clinical presentation, diagnosis, management, and prognosis.

Published in:

International Medical Case Reports Journal, 2016, v. 9, p. 385, doi. 10.2147/imcrj.s117322

By:

Tariq, Anam;
Westra, Kevin;
Santo, Arben

Publication type:

Article

Juvenile Hemochromatosis Connecting Cardiac Arrest and Hypogonadotropic Hypogonadism in a Young Woman.

Published in:

2024

By:

Zinecker, Kevin Alexander;
Sliwinska, Aleksandra;
Wilson, Leah M;
Zahr, Roula

Publication type:

Case Study

Longer survival associated with HLA-A03, B14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping Longer survival associated with HLA-A03, B14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping Barton et al. Hemochromatosis survival and HLA-A03, B14

Published in:

European Journal of Haematology, 2010, v. 85, n. 5, p. 439, doi. 10.1111/j.1600-0609.2010.01511.x

By:

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

Publication type:

Article

Serum ferritin concentration predicts hepatic fibrosis better than hepatic iron concentration in human HFE-Haemochromatosis.

Published in:

Liver International, 2017, v. 37, n. 9, p. 1382, doi. 10.1111/liv.13395

By:

Wood, Marnie J.;
Crawford, Darrell H. G.;
Wockner, Leesa F.;
Powell, Lawrie W.;
Ramm, Grant A.

Publication type:

Article

Magnetic resonance imaging of neonatal hemochromatosis.

Published in:

Pediatric Radiology, 2022, v. 52, n. 2, p. 334, doi. 10.1007/s00247-021-05008-9

By:

Chavhan, Govind B.;
Kamath, Binita M.;
Siddiqui, Iram;
Tomlinson, Christopher

Publication type:

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.

Published in:

Scandinavian Journal of Gastroenterology, 2000, v. 35, n. 12, p. 1301, doi. 10.1080/003655200453665

By:

Bell, H.;
Berg, J. P.;
Undlien, D. E.;
Distante, S.;
Raknerud, N.;
Heier, H. E.;
Try, K.;
Thomassen, Y.;
Haug, E.;
Raha-Chowdhury, R.;
Thorsby, E.

Publication type:

Article

Idiopathic hand osteoarthritis vs haemochromatosis arthropathy—a clinical, functional and radiographic study.

Published in:

Rheumatology, 2013, v. 52, n. 5, p. 910, doi. 10.1093/rheumatology/kes392

By:

Dallos, Tomáš;
Sahinbegovic, Enijad;
Stamm, Tanja;
Aigner, Elmar;
Axmann, Roland;
Stadlmayr, Andreas;
Englbrecht, Matthias;
Datz, Christian;
Schett, Georg;
Zwerina, Jochen

Publication type:

Article

A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis.

Published in:

2003

By:

Cadet, E.;
Capron, D.;
Perez, A. S.;
Crépin, S. N.;
Arlot, S.;
Ducroix, J.-P.;
Dautréaux, M.;
Fardellone, P.;
Leflon, P.;
Merryweather-Clarke, A. T.;
Livesey, K. J.;
Pointon, J. J.;
Rose, P.;
Harcourt, J.;
Emery, J.;
Sueur, J. M.;
Feyt, R.;
Robson, K. J. H.;
Rochette, J.;
Crépin, S N

Publication type:

journal article

Bloodlettings in Hemochromatosis Result in Increased Blood Lead (Pb) Concentrations.

Published in:

Biological Trace Element Research, 2023, v. 201, n. 7, p. 3193, doi. 10.1007/s12011-022-03424-y

By:

Yazdani, Mazyar;
Distante, Sonia;
Mørkrid, Lars;
Ulvik, Rune J.;
Bolann, Bjørn J.

Publication type:

Article

Successful pregnancy outcome with the use of antenatal high-dose intravenous immunoglobulin following previous neonatal death associated with neonatal haemochromatosis.

Published in:

2010

By:

NICHOLL, Michael C.

Publication type:

Case Study

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

By:

Sigmirean, Victor

Publication type:

Article

The hemochromatosis protein HFE 20 years later: An emerging role in antigen presentation and in the immune system.

Published in:

Immunity, Inflammation & Disease, 2017, v. 5, n. 3, p. 218, doi. 10.1002/iid3.158

By:

Reuben, Alexandre;
Chung, Jacqueline W.;
Lapointe, Réjean;
Santos, Manuela M.

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

Facilitation of blood donation amongst haemochromatosis patients.

Published in:

Transfusion Medicine, 2015, v. 25, n. 4, p. 239, doi. 10.1111/tme.12182

By:

Marrow, B.;
Clarkson, J.;
Chapman, C. E.;
Masson, S.

Publication type:

Article

Risk of Disease in Siblings of Patients with Hereditary Hemochromatosis.

Published in:

Digestion, 2001, v. 64, n. 2, p. 120, doi. 10.1159/000048850

By:

Nelson, Richard L.;
Persky, Victoria;
Davis, Faith;
Becker, Eugene

Publication type:

Article

Effect of hereditary haemochromatosis genotypes and iron overload on other trace elements.

Published in:

European Journal of Nutrition, 2013, v. 52, n. 1, p. 255, doi. 10.1007/s00394-012-0319-3

By:

Beckett, Jeffrey;
Ball, Madeleine

Publication type:

Article

Hereditary Hemochromatosis of a Young Girl: Detection of Early Iron Deposition in Liver Cell Lysosomes Using Transmission Electron Microscopy and Electron Energy Loss Spectroscopy.

Published in:

Ultrastructural Pathology, 2002, v. 26, n. 1, p. 23, doi. 10.1080/01913120252934297

By:

Jonas, Ludwig;
Fulda, Gerhard;
Kyank, Ulrike;
Steiner, Michael;
Sarich, Wolfgang;
Nizze, Horst

Publication type:

Article

Mouse models of hereditary hemochromatosis do not develop early liver fibrosis in response to a high fat diet.

Published in:

PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0221455

By:

Wagner, John;
Fillebeen, Carine;
Haliotis, Tina;
Charlebois, Edouard;
Katsarou, Angeliki;
Mui, Jeannie;
Vali, Hojatollah;
Pantopoulos, Kostas

Publication type:

Article

CR48 Innovative Whole Genome Joint Analysis – case report of early diagnosis and preventive approach to HFE Hemochromatosis.

Published in:

Lijecnicki Vjesnik, 2023, v. 145, p. 70, doi. 10.26800/LV-145-supl2-CR48

By:

Kulaš, Marjan;
Gržan, Dina;
Kukić, Sandro;
Lovrenčić, Luka;
Ćuk, Mario

Publication type:

Article

Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors.

Published in:

Annals of Hepatology: Official Journal of the Mexican Association of Hepatology, 2014, v. 13, n. 5, p. 568, doi. 10.1016/s1665-2681(19)31259-1

By:

Pelusi, Serena;
Rametta, Raffaela;
Corte, Claudia Della;
Congia, Riccardo;
Dongiovanni, Paola;
Pulixi, Edoardo A.;
Fargion, Silvia;
Fracanzani, Anna L.;
Nobili, Valerio;
Valenti, Luca

Publication type:

Article

Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review.

Published in:

2019

By:

Kong, Xiaomu;
Xie, Lingding;
Zhu, Haiqing;
Song, Lulu;
Xing, Xiaoyan;
Yang, Wenying;
Chen, Xiaoping

Publication type:

journal article

Optimizing the management of hereditary haemochromatosis: the value of MRI R2* quantification to predict and monitor body iron stores.

Published in:

British Journal of Haematology, 2018, v. 183, n. 3, p. 491, doi. 10.1111/bjh.14982

By:

França, Manuela;
Martí‐Bonmatí, Luis;
Silva, Sara;
Oliveira, Carla;
Alberich Bayarri, Ángel;
Vilas Boas, Filipa;
Pessegueiro‐Miranda, Helena;
Porto, Graça

Publication type:

Article

How we manage patients with hereditary haemochromatosis.

Published in:

British Journal of Haematology, 2016, v. 175, n. 5, p. 759, doi. 10.1111/bjh.14376

By:

Rombout ‐ Sestrienkova, Eva;
Kraaij, Marian G. J.;
Koek, Ger H.

Publication type:

Article

Compound heterozygous C282Y/Q283P and Q283P/H63D mutations in haemochromatosis.

Published in:

British Journal of Haematology, 2015, v. 171, n. 4, p. 650, doi. 10.1111/bjh.13417

By:

Gammeren, Adriaan;
Baar, Ellen;
Schrauwen, Lianne;
Wijngaarden, Peter

Publication type:

Article

Characterization of the second HFE gross deletion highlights the potential importance of Alu-mediated recombination in haemochromatosis.

Published in:

British Journal of Haematology, 2015, v. 168, n. 5, p. 759, doi. 10.1111/bjh.13145

By:

Ka, Chandran;
Chen, Jian‐Min;
Gourlaouen, Isabelle;
Quemener, Sylvia;
Ronsin, Christophe;
Massonnet, Simone;
Thérond, Jean‐Paul;
Férec, Claude;
Le Gac, Gérald

Publication type:

Article

Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations.

Published in:

British Journal of Haematology, 2013, v. 162, n. 2, p. 278, doi. 10.1111/bjh.12350

By:

Bardou‐Jacquet, Edouard;
Cunat, Severine;
Beaumont‐Epinette, Marie‐Pascale;
Kannengiesser, Caroline;
Causse, Xavier;
Sauvion, Sylvie;
Pouliquen, Bruno;
Deugnier, Yves;
David, Veronique;
Loréal, Olivier;
Aguilar‐Martinez, Patricia;
Brissot, Pierre;
Jouanolle, Anne‐marie

Publication type:

Article

Hereditary haemochromatosis is unlikely to cause movement disorders: A critical review.

Published in:

Journal of Neurology, 2004, v. 251, n. 7, p. 849, doi. 10.1007/s00415-004-0445-9

By:

Russo, Noemi;
Edwards, Mark;
Andrews, Thomasin;
O'Brien, Michael;
Bhatia, Kailash P.

Publication type:

Article

Night sweats: it may be hemochromatosis.

Published in:

2016

By:

Murday, H. K. M.;
Rusli, F. D.;
Blandy, C.;
Vollenhoven, B.

Publication type:

journal article

Pituitary hyposignal characteristic of hemochromatosis on MRI.

Published in:

2023

By:

Yehouenou Tessi, Romeo Thierry;
Oze, Rita Koudouhonon;
Outznit, Mustapha;
Hadj Hsain, Ihssan;
Nassar, Ittimade;
Moatassim Billah, Nabil

Publication type:

Case Study

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

By:

Koura, Uta;
Horikawa, Shinjiro;
Okabe, Mako;
Kawasaki, Yukako;
Makimoto, Masami;
Mizuta, Koichi;
Yoshida, Taketoshi

Publication type:

Article

Juvenile Hemochromatosis: Rheumatic Manifestations of 2 Sisters Responding to Deferasirox Treatment. A Case Series and Literature Review.

Published in:

Open Access Rheumatology: Research & Reviews, 2021, v. 13, p. 15, doi. 10.2147/OARRR.S276112

By:

Alqanatish, Jubran;
Alsowailmi, Banan;
Alfarhan, Haneen;
Alhamzah, Albandari;
Alharbi, Talal

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:

Kowdley, Devan S;
Kowdley, Kris V

Publication type:

Article

HFE hemochromatosis screening in patients with severe hip osteoarthritis: A prospective cross-sectional study.

Published in:

PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0207415

By:

Oppl, Bastian;
Husar-Memmer, Emma;
Pfefferkorn, Svea;
Blank, Martha;
Zenz, Peter;
Gollob, Eva;
Wurnig, Christian;
Engel, Alfred;
Stadlmayr, Andreas;
Uyanik, Gökhan;
Brozek, Wolfgang;
Klaushofer, Klaus;
Zwerina, Jochen;
Datz, Christian

Publication type:

Article

SLC40A1-related hemochromatosis associated with a p.Y333H mutation in mainland China: a pedigree report and literature review.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01929-0

By:

Li, Yue;
Duan, Fangfang;
Yang, Song

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

By:

Rodrigues de Araújo, Cristiane da Silva;
Duro Barp, Anna Laura;
Glimm, Déborah;
Beber Lemanski, Francisco Costa;
Silva Gonçalves Santos, Lara Beatriz;
Bueno de Azeredo, Saulo;
Pasqualotti, Adriano

Publication type:

Article

The role of hereditary hemochromatosis in aseptic loosening following primary total hip arthroplasty

Published in:

Journal of Orthopaedic Research, 2005, v. 23, n. 3, p. 542, doi. 10.1016/j.orthres.2004.11.004

By:

Lunn, J.V.;
Gallagher, P.M.;
Hegarty, S.;
Kaliszer, M.;
Crowe, J.;
Murray, P.;
Bouchier-Hayes, D.

Publication type:

Article

Neonatal hemochromatosis with εγδβ-thalassemia: a case report and analysis of serum iron regulators.

Published in:

2022

By:

Tsuge, Mitsuru;
Kodera, Aya;
Sumitomo, Hiromi;
Araki, Tooru;
Yoshida, Ryuichi;
Yasui, Kazuya;
Sato, Hiroki;
Washio, Yosuke;
Washio, Kana;
Shigehara, Kenji;
Yashiro, Masato;
Yagi, Takahito;
Tsukahara, Hirokazu

Publication type:

journal 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

By:

Sotiropoulos, Georgios C.;
Molmenti, Ernesto P.;
Lang, Hauke;
Beckebaum, Susanne;
Kaiser, Gernot M.;
Brokalaki, Eirini I.;
Frilling, Andrea;
Malagó, Massimo;
Neuhäuser, Markus;
Broelsch, Christoph E.

Publication type:

Article

Hepatocarcinoma with tumor thrombus occupying the right atrium and portal vein in a patient with hereditary hemochromatosis and liver cirrhosis.

Published in:

2018

By:

Orasan, Olga Hilda;
Stefan, Andreea Maria;
Urian, Laura;
Mihailov, Anca;
Fabian, Ovidiu;
Muresan, Flaviu;
Breaban, Iulia;
Secara, Sorina Cezara;
Sarlea, Simina Tarmure;
Negrean, Vasile;
Sampelean, Dorel;
Cozma, Angela

Publication type:

Case Study

Movement Disorders Associated With Hemochromatosis.

Published in:

Canadian Journal of Neurological Sciences, 2016, v. 43, n. 6, p. 801, doi. 10.1017/cjn.2016.286

By:

Kumar, Niraj;
Rizek, Philippe;
Sadikovic, Bekim;
Adams, Paul C.;
Jog, Mandar

Publication type:

Article

Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia.

Published in:

2017

By:

Hyun Jin Kim;
Yoon-Myung Kim;
Eungu Kang;
Beom Hee Lee;
Jin-Ho Choi;
Han-Wook Yoo

Publication type:

Case Study

Allelic Diversity of the Hemochromatosis Gene (HFE) in Malays, Chinese and Indians.

Published in:

Malaysian Journal of Medicine & Health Sciences, 2021, n. 3, p. 49

By:

Norul Hajar, Che Ghazali;
Akhir, Suhaida Md.;
Zefarina, Zulkafli;
Riffin, Nor Suhaila Md.;
Tuan Mohammad, Tuan Hulwani;
Hassan, Mohd Nazri;
Safuan, Sabreena;
Aziz, Mohd Yusmaidie;
Pati, Siddhartha;
Chambers, Geoffrey Keith;
Edinur, Hisham Atan

Publication type:

Article

Secondary Haemochromatosis in a Patient with Thalassemia Intermedia.

Published in:

2014

By:

ROTARU, IONELA;
GAMAN, AMELIA;
GAMAN, G.

Publication type:

Case Study