Works matching DE "HEMOCHROMATOSIS diagnosis"

Results: 88

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders.

Published in:

Journal of Gastroenterology, 2010, v. 45, n. 11, p. 1163, doi. 10.1007/s00535-010-0259-8

By:

Kaneko, Yoshibumi;
Miyajima, Hiroaki;
Piperno, Alberto;
Tomosugi, Naohisa;
Hayashi, Hisao;
Morotomi, Natsuko;
Tsuchida, Ken-ichi;
Ikeda, Takaaki;
Ishikawa, Akihisa;
Ota, Yusuke;
Wakusawa, Shinya;
Yoshioka, Kentaro;
Kono, Satoshi;
Pelucchi, Sara;
Hattori, Ai;
Tatsumi, Yasuaki;
Okada, Toshihide;
Yamagishi, Masakazu

Publication type:

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

An Observational Preliminary Study on the Safety of Long-Term Consumption of Micronutrients for the Treatment of Psychiatric Symptoms.

Published in:

Journal of Alternative & Complementary Medicine, 2019, v. 25, n. 6, p. 613, doi. 10.1089/acm.2018.0352

By:

Rucklidge, Julia J.;
Eggleston, Matthew J. F.;
Ealam, Breanne;
Beaglehole, Ben;
Mulder, Roger T.

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

Hemochromatosis assesment in β thalasemia major.

Published in:

Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2011, v. 60, n. 4, p. 332

By:

Diaconu, Adriana;
Bălăceanu, Alice

Publication type:

Article

A Novel Approach to Improving Utilization of Laboratory Testing.

Published in:

Archives of Pathology & Laboratory Medicine, 2018, v. 142, n. 2, p. 243, doi. 10.5858/arpa.2017-0031-OA

By:

Yaolin Zhou;
Procop, Gary W.;
Riley, Jacquelyn D.

Publication type:

Article

Clinical Perspectives on Hereditary Hemochromatosis.

Published in:

Critical Reviews in Clinical Laboratory Sciences, 2008, v. 45, n. 5, p. 451, doi. 10.1080/10408360802335716

By:

Ayonrinde, Oyekoya T.;
Milward, Elizabeth A.;
Chua, Anita C. G.;
Trinder, Debbie;
Olynyk, John K.

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

Authors' reply.

Published in:

2018

By:

Rambhia, Kinjal D;
Chowdhary, Sushma;
Rao, G Venkateswara;
Khopkar, Uday S

Publication type:

Letter

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

HFE Genotyping in Patients with Elevated Serum Iron Indices and Liver Diseases.

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/164671

By:

Evangelista, Andreia Silva;
Nakhle, Maria Cristina;
de Araújo, Thiago Ferreira;
Abrantes-Lemos, Clarice Pires;
Deguti, Marta Mitiko;
Carrilho, Flair José;
Cançado, Eduardo Luiz Rachid

Publication type:

Article

Isolated focal intrahepatic extramedullary hematopoiesis mimicking hepatocellular carcinoma in a cirrhotic patient with secondary hemochromatosis from thalassemia.

Published in:

Gastroenterology & Hepatology from Bed to Bench, 2023, v. 16, n. 1, p. 527, doi. 10.22037/ghfbb.v15i4.2476

By:

Tatsanai Sattayaraksa;
Cheep Charoenlap;
Keerati Akarapatima;
Attapon Rattanasupar;
Arunchai Chang

Publication type:

Article

The Correlation of Cardiac and Hepatic Hemosiderosis as Measured by T2*MRI Technique with Ferritin Levels and Hemochromatosis Gene Mutations in Iranian Patients with Beta Thalassemia Major.

Published in:

Oman Medical Journal, 2018, v. 33, n. 1, p. 48, doi. 10.5001/omj.2018.09

By:

Soltanpour, Mohammad Soleiman;
Davari, Kambiz

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

Levonorgestrel-Releasing Intrauterine System and Iron Overload Syndrome.

Published in:

Clinical Medicine Insights: Case Reports, 2013, n. 6, p. 93, doi. 10.4137/CCRep.S11888

By:

Vieira da Motta, Marcia;
Vieira da Motta, Eduardo

Publication type:

Article

Genetic knowledge among participants of a German pilot study on hemochromatosis screening.

Published in:

2006

By:

Stihrmann, M.;
Nippert, I.;
Hoy, L.;
Schmidtke, J.

Publication type:

Letter

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

Gastric bypass surgery as an intervention for obese patients with hemochromatosis.

Published in:

QJM: An International Journal of Medicine, 2014, v. 107, n. 12, p. 1023, doi. 10.1093/qjmed/hcs073

By:

Gopaluni, S.;
Martinez-Balzano, C.;
Graziano, S.

Publication type:

Article

A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations.

Published in:

QJM: An International Journal of Medicine, 2008, v. 101, n. 8, p. 631, doi. 10.1093/qjmed/hcn070

By:

K. Cooper;
J. Bryant;
J. Picot;
A. Clegg;
P.R. Roderick;
W.M. Rosenberg;
C. Patch

Publication type:

Article

ROLE OF HEPATIC IRON INDEX IN THE MANAGEMENT OF IRON OVERLOAD SYNDROMES IN 1990'S.

Published in:

1998

By:

Chasalani, Naga;
Gitlin, Norman;
Johnson, David

Publication type:

Abstract

Neonatal hemochromatosis associated with rupture of esophageal varices.

Published in:

2019

By:

Hatayama, Kazuki;
Washio, Yosuke;
Okamura, Tomoka;
Noda, Takuo;
Tsukahara, Hirokazu

Publication type:

Case Study

Genotyping as a diagnostic aid in genetic haemochromatosis.

Published in:

Journal of Gastroenterology & Hepatology, 1999, v. 14, n. 5, p. 427, doi. 10.1046/j.1440-1746.1999.01884.x

By:

Rossi, Enrico;
Henderson, Sandra;
Chin, Christine;
Olynyk, John;
Beilby, John;
Reed, William;
Jeffrey, Gary

Publication type:

Article

Utility of genotyping in diagnosis of genetic haemochromatosis.

Published in:

1999

By:

Crawford, Darrell;
Fletcher, Linda

Publication type:

Editorial

Panhypopituitarism Due to Hemochromatosis.

Published in:

2013

By:

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

Publication type:

Case Study

Case Study: Haemochromatosis: causing metatarsalgia in a patient with type II diabetes?

Published in:

2011

By:

Rooney, Claire

Publication type:

Case Study

"Ferritin Out" a Cause of Acute Hepatitis.

Published in:

2015

By:

Colom Steele, Diego;
Mojtahed, Amirkaveh;
Samedi, Von;
Alcorn, Joseph

Publication type:

journal article

Diagnosis of Hereditary Hemochromatosis in the Era of Genetic Testing.

Published in:

Digestive Diseases & Sciences, 2012, v. 57, n. 11, p. 2988, doi. 10.1007/s10620-012-2243-z

By:

Trieß, Christiane;
von Figura, Guido;
Stuhrmann, Manfred;
Butzeck, Barbara;
Krayenbuehl, Pierre;
Strnad, Pavel;
Kulaksiz, Hasan

Publication type:

Article

Illness representations, knowledge and motivation to perform presymptomatic testing for late-onset genetic diseases.

Published in:

Psychology, Health & Medicine, 2017, v. 22, n. 2, p. 244, doi. 10.1080/13548506.2016.1159704

By:

Leite, Ângela;
Dinis, Maria Alzira P.;
Sequeiros, Jorge;
Paúl, Constança

Publication type:

Article

Testing and Management of Iron Overload After Genetic Screening–Identified Hemochromatosis.

Published in:

JAMA Network Open, 2023, v. 6, n. 10, p. e2338995, doi. 10.1001/jamanetworkopen.2023.38995

By:

Savatt, Juliann M.;
Johns, Alicia;
Schwartz, Marci L. B.;
McDonald, Whitney S.;
Salvati, Zachary M.;
Oritz, Nicole M.;
Masnick, Max;
Hatchell, Kathryn;
Hao, Jing;
Buchanan, Adam H.;
Williams, Marc S.

Publication type:

Article

Simultaneous presentation of hereditary hyperferritinaemia cataract syndrome and hereditary haemochromatosis.

Published in:

2018

By:

Maccora, Katia A;
Souzeau, Emmanuelle;
Ruddle, Jonathan B;
Craig, Jamie E

Publication type:

Case Study

Hepatology Clinical.

Published in:: Journal of Gastroenterology & Hepatology, 2016, v. 31, p. 89, doi. 10.1111/jgh.13520
Publication type:: Article

Screening for Hemochromatosis: Recommendation Statement.

Published in:: Annals of Internal Medicine, 2006, v. 145, n. 3, p. 204, doi. 10.7326/0003-4819-145-3-200608010-00008
Publication type:: Article

Hemochromatosis Presenting with Diabetic Ketoacidosis: A Rare Case Report.

Published in:

Erciyes Medical Journal / Erciyes Tip Dergisi, 2016, v. 38, n. 2, p. 81, doi. 10.5152/etd.2016.150026

By:

Jain, Deepak;
Katyal, V. K.;
Mittal, Ashima;
Jain, Promil

Publication type:

Article

Hereditary hyperferritinaemia-cataract syndrome and differential diagnosis of hereditary haemochromatosis.

Published in:

2003

By:

Sanders S J;
Suri M;
Ross I;
Sanders, S J;
Suri, M;
Ross, I

Publication type:

journal article

Multiorgan involvement in thalassaemia major.

Published in:

2003

By:

Ghai, S.;
Sharma, R.;
Kulshreshtha, B.

Publication type:

journal article

Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.

Published in:

1997

By:

Aslam, S.;
Standen, G. R.

Publication type:

journal article

Genetic haemochromatosis: diagnosis and treatment of an iron overload disorder.

Published in:

Nursing Standard, 2022, v. 37, n. 11, p. 77, doi. 10.7748/ns.2022.e11896

By:

Johnson, Martin;
Mortimore, Gerri

Publication type:

Article

Haemochromatosis: the role of the HCA and the AP in tackling iron overload.

Published in:

British Journal of Healthcare Assistants, 2014, v. 8, n. 7, p. 328, doi. 10.12968/bjha.2014.8.7.328

By:

Peate, Ian

Publication type:

Article

What is HFE haemochromatosis?

Published in:

British Journal of Hospital Medicine (17508460), 2016, v. 77, n. 6, p. C91, doi. 10.12968/hmed.2016.77.6.C91

By:

Marjot, Tom;
Collier, Jane;
Ryan, John D.

Publication type:

Article

- 174 G>C IL-6 polymorphism and primary iron overload in male patients.

Published in:

2018

By:

Tetzlaff, Walter F.;
Meroño, Tomás;
Botta, Eliana E.;
Martín, Maximiliano E.;
Sorroche, Patricia B.;
Boero, Laura E.;
Castro, Marcelo;
Frechtel, Gustavo D.;
Rey, Jorge;
Daruich, Jorge;
Cerrone, Gloria E.;
Brites, Fernando

Publication type:

journal article

SQUID biosusceptometry in the measurement of hepatic iron.

Published in:

2003

By:

Sheth, Sujit

Publication type:

journal article

Bone morphogenetic protein (BMP)-responsive elements located in the proximal and distal hepcidin promoter are critical for its response to HJV/BMP/SMAD.

Published in:

Journal of Molecular Medicine, 2009, v. 87, n. 5, p. 471, doi. 10.1007/s00109-009-0447-2

By:

Casanovas, Guillem;
Mleczko-Sanecka, Katarzyna;
Altamura, Sandro;
Hentze, Matthias W.;
Muckenthaler, Martina U.

Publication type:

Article

Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice.

Published in:

Journal of Genetic Counseling, 2014, v. 23, n. 6, p. 891, doi. 10.1007/s10897-014-9743-2

By:

Prince, Anya;
Roche, Myra

Publication type:

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

Unsaturated iron binding capacity and transferrin saturation are equally reliable in detection of HFE hemochromatosis

Published in:

American Journal of Gastroenterology (Springer Nature), 2002, v. 97, n. 8, p. 2093, doi. 10.1111/j.1572-0241.2002.05927.x

By:

Murtagh, Luke J.;
Whiley, Michael;
Wilson, Susan;
Tran, Huy;
Bassett, Mark L.

Publication type:

Article

Genetic haemochromatosis: diagnosing and treating hereditary iron overload.

Published in:: Gastrointestinal Nursing, 2017, v. 15, p. S16, doi. 10.12968/gasn.2017.15.Sup10.S16
Publication type:: Article

Clinical-Pathological Conference Series from the Medical University of Graz.

Published in:

Wiener Klinische Wochenschrift, 2016, v. 128, n. 21/22, p. 846, doi. 10.1007/s00508-016-1010-0

By:

Fabian, Elisabeth;
Schiller, Dietmar;
Graninger, Winfried;
Langner, Cord;
Frei, Johannes;
Schoellnast, Helmut;
Alibegovic, Vedat;
Stauber, Rudolf;
Schoefl, Rainer;
Krejs, Guenter

Publication type:

Article

Diagnostic testing fails the test.

Published in:

Nature, 2002, v. 415, n. 6872, p. 577, doi. 10.1038/415577a

By:

Merz, Jon F.;
Kriss, Antigone G.;
Leonard, Debra G.B.;
Cho, Mildred K.

Publication type:

Article

Sporadic Porphyria Cutanea Tarda as the Initial Manifestation of Hereditary Hemochromatosis.

Published in:

ACG Case Reports Journal, 2019, v. 6, n. 11, p. 1, doi. 10.14309/crj.0000000000000247

By:

Edwards, Mitchell V.;
Ray, Jennifer Michelle;
Bacon, Bruce R.

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