Works matching Hemochromatosis

Results: 2986

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

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

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

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

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

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

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

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

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

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

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

Panhypopituitarism Due to Hemochromatosis.

Published in:

2013

By:

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

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:

NICHOLL, Michael C.

Publication type:

Case Study

Analysis of Hand Joint Space Morphology in Women and Men with Hereditary Hemochromatosis.

Published in:

Calcified Tissue International, 2023, v. 112, n. 4, p. 440, doi. 10.1007/s00223-022-01050-3

By:

Heilmeier, Ursula;
Burghardt, Andrew J.;
Tse, Justin J.;
Kapoor, Puneet;
Stok, Kathryn S.;
Manske, Sarah;
Voll, Reinhard E.;
Schett, Georg;
Finzel, Stephanie

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

By:

Indolfi, Giuseppe;
Bèrczes, Rita;
Pelliccioli, Isabella;
Bosisio, Michela;
Agostinis, Cristina;
Resti, Massimo;
Zambelli, Marco;
Lucianetti, Alessandro;
Colledan, Michele;
D'Antiga, Lorenzo

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

Hepatocellular carcinoma associated with secondary haemochromatosis in non-cirrhotic liver: a case report

Published in:

Hepatology Research, 2003, v. 26, n. 3, p. 254, doi. 10.1016/S1386-6346(03)00109-8

By:

Chung, Hobyung;
Kudo, Masatoshi;
Kawasaki, Toshihiko;
Kitano, Masayuki;
Minami, Yasunori;
Suetomi, Youichirou;
Onda, Hirokazu

Publication type:

Article

Hemochromatosis Presenting with Ascites in a Newborn Infant.

Published in:

2022

By:

Benli, Samet;
Aydin, Mustafa;
Taşkin, Erdal;
Çağlar, Atika;
Poyraz, Ahmet Kürşad;
Özercan, Ibrahim Hanifi

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

By:

Zhang, Wei;
Wang, Xiaoming;
Duan, Weijia;
Xu, Anjian;
Zhao, Xinyan;
Huang, Jian;
You, Hong;
Brissot, Pierre;
Ou, Xiaojuan;
Jia, Jidong

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.

Published in:

American Journal of Undergraduate Research, 2020, v. 16, n. 4, p. 51, doi. 10.33697/ajur.2020.006

By:

Ferqueron, Tyler R.;
Anderson, Angela S.;
Good, Deborah J.

Publication type:

Article

Twenty-Five Years of Contemplating Genotype-Based Hereditary Hemochromatosis Population Screening.

Published in:

Genes, 2022, v. 13, n. 9, p. 1622, doi. 10.3390/genes13091622

By:

Schmidtke, Jörg

Publication type:

Article

Mixed-Etiology Restrictive Cardiomyopathy (Desminopathy and Hemochromatosis) with Complex Liver Lesions.

Published in:

Genes, 2022, v. 13, n. 4, p. 577, doi. 10.3390/genes13040577

By:

Lutokhina, Yulia;
Blagova, Olga;
Panferov, Alexander;
Sedov, Vsevolod;
Kogan, Evgeniya;
Nekrasova, Tatiana;
Nedostup, Alexander;
Zaklyazminskaya, Elena

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

By:

Acevedo, Luis Alfredo Utria;
Alvarenga, Aline Morgan;
Fonseca, Paula Fernanda Silva;
da Silva, Nathália Kozikas;
Cançado, Rodolfo Delfini;
Naoum, Flavio Augusto;
Dinardo, Carla Luana;
Pereira, Alexandre Costa;
Brissot, Pierre;
Santos, Paulo Caleb Junior Lima

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

By:

Sandnes, Miriam;
Vorland, Marta;
Ulvik, Rune J.;
Reikvam, Håkon

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:

Hamada, Yuki;
Hirano, Eiichi;
Sugimoto, Koji;
Hanada, Keizo;
Kaku, Taiichi;
Manda, Naoki;
Tsuchida, Kenichi

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:

Hamada, Yuki;
Hirano, Eiichi;
Sugimoto, Koji;
Hanada, Keizo;
Kaku, Taiichi;
Manda, Naoki;
Tsuchida, Kenichi

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:

Çelik, Vesile Deniz;
Kiliç, Betul Orhan;
Akis±in, Yasemin Ardiçoğlu;
Akar, Nejat;
Tükün, Fatma Ajlan

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

By:

Ouyang, Qin;
Li, Yanmeng;
Xu, Anjian;
Zhang, Ning;
Chen, Sisi;
Zhou, Donghu;
Zhang, Bei;
Ou, Xiaojuan;
Jia, Jidong;
Huang, Jian;
Zhang, Wei

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

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

By:

O'Sullivan, Eoin P.;
Walsh, C. Howel

Publication type:

Article

Hemochromatosis: Ferroptosis, ROS, Gut Microbiome, and Clinical Challenges with Alcohol as Confounding Variable.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 5, p. 2668, doi. 10.3390/ijms25052668

By:

Teschke, Rolf

Publication type:

Article

PATHOLOGY TEACH AND TELL: NEONATAL HEMOCHROMATOSIS WITH MASSIVE HEPATIC NECROSIS.

Published in:

Fetal & Pediatric Pathology, 2004, v. 23, n. 5/6, p. 345, doi. 10.1080/15227950490952406

By:

Goyal, Richa;
Pattari, Sanjib Kumar;
Kakkar, Nandita;
Radotra, BD;
Narang, Anil

Publication type:

Article

Hereditary haemochromatosis and diabetes.

Published in:

Journal of Diabetes Nursing, 2018, v. 22, n. 4, p. 1

By:

Jennison, Erica;
Wainwright, Patrick

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

By:

COLLARDEAU-FRACHON, SOPHIE;
HEISSAT, SOPHIE;
BOUVIER, RAYMONDE;
FABRE, MONIQUE;
BARUTEAU, ULIEN;
BROUE, PIERRE;
CORDIER, MARIE-PIERRE;
DEBRAY, DOMINIQUE;
DEBIEC, HANNA;
RONCO, PIERRE;
GUIGONIS, VINCENT

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

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

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

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

By:

Phatak, Pradyumna D.;
Barton, James C.

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

By:

McCullen, M. A.;
Fletcher, L. M.;
Dimeski, G.;
Pink, A.;
Powell, L. W.;
Crawford, D. H. G.;
Hickman, P. E.

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

By:

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

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

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

By:

Forsberg, Mark;
Galan, Mark;
Kra, Joshua

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

By:

Al-Tikrity, Mustafa A.;
Yassin, Mohamed A.

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

Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report.

Published in:

2018

By:

Cooray, Shamil D.;
Heerasing, Neel M.;
Selkrig, Laura A.;
Subramaniam, V. Nathan;
Hamblin, P. Shane;
McDonald, Cameron J.;
McLean, Catriona A.;
McNamara, Elissa;
Leet, Angeline S.;
Roberts, Stuart K.

Publication type:

journal article

Periodontal status and serum biomarker levels in HFE haemochromatosis patients. A case-series study.

Published in:

2017

By:

Meuric, Vincent;
Lainé, Fabrice;
Boyer, Emile;
Le Gall‐David, Sandrine;
Oger, Emmanuel;
Bourgeois, Denis;
Bouchard, Philippe;
Bardou‐Jacquet, Edouard;
Turmel, Valérie;
Bonnaure‐Mallet, Martine;
Deugnier, Yves

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

By:

Sharma, Soumya;
Sethi, Sean Kumar;
Reese, David;
Gharabaghi, Sara;
Yerramsetty, Kiran Kumar;
Palutla, Vinay Kumar;
Chen, Yongsheng;
Haacke, E. Mark;
Jog, Mandar S.

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

By:

ALADIO, J. MARTÍN;
YAMASATO, FLORENCIA;
SAAD, ARIEL K.;
SORDÁ, JUAN;
GROSSO, OSCAR;
GONZÁLEZ BALLERGA, ESTEBAN;
DARUICH, JORGE;
BERENSZTEIN, SARA

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

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

By:

Kucinskas, Laimutis;
Juzenas, Simonas;
Sventoraityte, Jurgita;
Cedaviciute, Ruta;
Vitkauskiene, Astra;
Kalibatas, Vytenis;
Kondrackiene, Jurate;
Kupcinskas, Limas

Publication type:

Article