Works about THALASSEMIA treatment

Results: 249

What are the occupational implications of thalassaemia?

Published in:

Occupational Medicine, 1999, v. 49, n. 2, p. 117, doi. 10.1093/occmed/49.2.117

By:

Evans, G.

Publication type:

Article

commentary.

Published in:

Hastings Center Report, 2002, v. 32, n. 3, p. 12

By:

Terry, Louise M.

Publication type:

Article

Iron chelation therapy in transfusion-dependent thalassemia patients: current strategies and future directions.

Published in:

Journal of Blood Medicine, 2015, v. 6, p. 197, doi. 10.2147/JBM.S72463

By:

Saliba, Antoine N.;
Harb, Afif R.;
Taher, Ali T.

Publication type:

Article

Treating thalassemia major-related iron overload: the role of deferiprone.

Published in:

Journal of Blood Medicine, 2012, v. 3, p. 119, doi. 10.2147/JBM.S27400

By:

Berdoukas, Vasilios;
Farmaki, Kallistheni;
Carson, Susan;
Wood, John;
Coates, Thomas

Publication type:

Article

Health-Related Quality of Life, Treatment Satisfaction, Adherence and Persistence in β-Thalassemia and Myelodysplastic Syndrome Patients with Iron Overload Receiving Deferasirox: Results fromthe EPIC Clinical Trial.

Published in:

Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/297641

By:

Porter, John;
Bowden, Donald K.;
Economou, Marina;
Troncy, Jacques;
Ganser, Arnold;
Habr, Dany;
Martin, Nicolas;
Gater, Adam;
Rofail, Diana;
Abetz-Webb, Linda;
Lau, Helen;
Cappellini, Maria Domenica

Publication type:

Article

Plasma microRNA-451 as a novel hemolytic marker for β0-thalassemia/HbE disease.

Published in:

Molecular Medicine Reports, 2017, v. 15, n. 5, p. 2495, doi. 10.3892/mmr.2017.6326

By:

KAMONLAK LEECHAROENKIAT;
YUKA TANAKA;
YASUKO HARADA;
PORNTIP CHAICHOMPOO;
SARAKUL, ORAWAN;
YASUNOBU ABE;
SMITH, DUNCAN RICHARD;
SUTHAT FUCHAROEN;
SAOVAROS SVASTI;
TSUKURU UMEMURA

Publication type:

Article

Importance of optimal dosing ≥30 mg/kg/d during deferasirox treatment: 2.7-yr follow-up from the ESCALATOR study in patients with β-thalassaemia.

Published in:

European Journal of Haematology, 2011, v. 87, n. 4, p. 355, doi. 10.1111/j.1600-0609.2011.01662.x

By:

Taher, Ali;
Elalfy, Mohsen S.;
Al Zir, Kusai;
Daar, Shahina;
Al Jefri, Abdullah;
Habr, Dany;
Kriemler-Krahn, Ulrike;
El-Ali, Ali;
Roubert, Bernard;
El-Beshlawy, Amal

Publication type:

Article

Reduction of body iron stores to normal range levels in thalassaemia by using a deferiprone/deferoxamine combination and their maintenance thereafter by deferiprone monotherapy Kolnagou et al. Normal body iron stores in thalassaemia.

Published in:

European Journal of Haematology, 2010, v. 85, n. 5, p. 430, doi. 10.1111/j.1600-0609.2010.01499.x

By:

Kolnagou, Annita;
Kleanthous, Marios;
Kontoghiorghes, George J.

Publication type:

Article

Long-term hydroxyurea therapy in beta-thalassaemia patients.

Published in:

European Journal of Haematology, 2003, v. 70, n. 3, p. 151, doi. 10.1034/j.1600-0609.2003.00037.x

By:

de Paula, Erich Vinicius;
Lima, Carmen Silvia Passos;
Arruda, Valder Roberval;
Alberto, Fernando Lopes;
Saad, Sara Teresinha Ollala;
Costa, Fernando Ferreira

Publication type:

Article

Long-term administration of high-dose deferoxamine 2 days per week in thalassemic patients.

Published in:

European Journal of Haematology, 2001, v. 67, n. 4, p. 230, doi. 10.1034/j.1600-0609.2001.00386.x

By:

Hagège, Isabelle;
Becker, Annie;
Kerdaffrec, Thierry;
Kanfer, Alain;
Girot, Robert

Publication type:

Article

Case Report: Hydroxyurea therapy in paraparesis and cauda equina syndrome due to extramedullary haematopoiesis in thalassaemia: improvement of clinical and haematological parameters.

Published in:

European Journal of Haematology, 2000, v. 64, n. 6, p. 426

By:

Cianciuli, P.;
Caravita di Toritto, T.;
Sorrentino, F.;
Sergiacomi, L.;
Massa, A.;
Amadori, A.

Publication type:

Article

Psychosocial Disorders in Childhood, Adolescence and Young Adult Life of Patients with Thalassaemia.

Published in:

Nosileftiki, 2016, v. 55, n. 2, p. 132

By:

Koutelekos, Ioannis;
Haliasos, Nikolaos

Publication type:

Article

Management of Transfusion-Dependent Thalassaemia Patients in Emergency Situations.

Published in:

2022

By:

Aoki, Yoshihiro;
Smith, Chris;
Ariyoshi, Koya

Publication type:

Letter

Safety and Efficacy of Direct-Acting Antivirals in Transfusion-Dependent Thalassemic Patients with Chronic Hepatitis C.

Published in:

Hepatitis Monthly, 2018, v. 18, n. 1, p. 1, doi. 10.5812/hepatmon.61453

By:

Onali, Simona;
Maida, Ivana;
Balestrieri, Cinzia;
Arcadu, Francesco;
Urru, Enrico;
Porcu, Davide;
Serra, Giancarlo;
Flore, Giacomo;
Dore, Elena;
Satta, Caterina;
Bitti, Pier Paolo;
Sanna, Maria Grazia;
Serusi, Loredana;
Casale, Michele;
Conti, Maria;
Loi, Martina;
Figorilli, Francesco;
Pasetto, Maria Cristina;
Babudieri, Sergio;
Chessa, Luchino

Publication type:

Article

Intrathoracic extramedullary hematopoiesis related spontaneous hemothorax.

Published in:

QJM: An International Journal of Medicine, 2015, v. 108, n. 12, p. 989, doi. 10.1093/qjmed/hcv143

By:

Ma, S.-H.;
Hu, S.-Y.;
Hsieh, M.-S.

Publication type:

Article

Non-transfusion Dependent Thalassemias: A Developing Country Perspective.

Published in:

Current Pediatric Reviews, 2015, v. 11, n. 2, p. 87

By:

Mukherjee, Somnath;
Das, Rashmi R.;
Raghuwanshi, Babita

Publication type:

Article

The experience of thalassemic adults with their treatment.

Published in:

Revista Latino-Americana de Enfermagem (RLAE), 2011, v. 19, n. 4, p. 968, doi. 10.1590/S0104-11692011000400016

By:

Ganzella, Marcela;
Zago, Márcia Maria Fontão

Publication type:

Article

Emodin can induce K562 cells to erythroid differentiation and improve the expression of globin genes.

Published in:

Molecular & Cellular Biochemistry, 2013, v. 382, n. 1/2, p. 127, doi. 10.1007/s11010-013-1726-3

By:

Ma, Yan-Ni;
Chen, Ming-Tai;
Wu, Zhi-Kui;
Zhao, Hua-Lu;
Yu, Hai-Chuan;
Yu, Jia;
Zhang, Jun-Wu

Publication type:

Article

Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey.

Published in:

Turkish Journal of Medical Sciences, 2017, v. 47, n. 3, p. 973, doi. 10.3906/sag-1606-49

By:

KAN KARAER, Derya;
ERGÜN, Mehmet Ali;
ILGIN RUHİ, Hatice;
ÖZTÜRK, Jale;
KARA, Halil;
REİSOĞLU ÇAKMAK, Deniz;
AYDOĞMUŞ, Talihanur;
PERÇİN, Emriye Ferda

Publication type:

Article

Cost Structure and Clinical Outcome of a Stem Cell Transplantation Program in a Developing Country: The Experience in Northeast Mexico.

Published in:

Oncologist, 2015, v. 20, n. 4, p. 386, doi. 10.1634/theoncologist.2014-0218

By:

Jaime‐Pérez, José Carlos;
Heredia‐Salazar, Alberto Carlos;
Cantú‐Rodríguez, Olga G.;
Gutiérrez‐Aguirre, Homero;
Villarreal‐Villarreal, César Daniel;
Mancías‐Guerra, Consuelo;
Herrera‐Garza, José Luís;
Gómez‐Almaguer, David

Publication type:

Article

Blood rheology in children with the S/<italic>β</italic>+-thalassemia syndrome.

Published in:

Clinical Hemorheology & Microcirculation, 2018, v. 69, n. 1-2, p. 207, doi. 10.3233/CH-189119

By:

Renoux, Céline;
Joly, Philippe;
Gauthier, Alexandra;
Pialoux, Vincent;
Romanet-Faes, Camille;
Bertrand, Yves;
Garnier, Nathalie;
Cuzzubbo, Daniela;
Cannas, Giovanna;
Connes, Philippe

Publication type:

Article

Efficacy of Deferasirox for the treatment of iron overload in Chinese thalassaemia major patients: results from a prospective, open-label, multicentre clinical trial.

Published in:

Transfusion Medicine, 2013, v. 23, n. 6, p. 389, doi. 10.1111/tme.12077

By:

Lai, Y.‐R.;
Liu, R.‐R.;
Li, C.‐F.;
Huang, S.‐L.;
Li, Q.;
Habr, D.;
Martin, N.;
Shen, Z.‐X.

Publication type:

Article

Randomised clinical trial: sofosbuvir and ledipasvir in patients with transfusion-dependent thalassaemia and HCV genotype 1 or 4 infection.

Published in:

Alimentary Pharmacology & Therapeutics, 2017, v. 46, n. 4, p. 424, doi. 10.1111/apt.14197

By:

Mangia, A.;
Sarli, R.;
Gamberini, R.;
Piga, A.;
Cenderello, G.;
Piazzolla, V.;
Santoro, R.;
Caruso, V.;
Quarta, A.;
Ganga, R.;
Copetti, M.;
Forni, G.

Publication type:

Article

Simeprevir and Sofosbuvir Combination Treatment in a Patient with HCV Cirrhosis and HbS Beta 0-Thalassemia: Efficacy and Safety despite Baseline Hyperbilirubinemia.

Published in:

Case Reports in Hematology, 2016, p. 1, doi. 10.1155/2016/7635128

By:

Papadopoulos, Nikolaos;
Deutsch, Melanie;
Georgalas, Athanasios;
Poulakidas, Helias;
Karnesis, Lazaros

Publication type:

Article

Coexisting Iron Deficiency Anemia and Beta Thalassemia Trait: Effect of Iron Therapy on Red Cell Parameters and Hemoglobin Subtypes.

Published in:

ISRN Otolaryngology, 2014, p. 1, doi. 10.1155/2014/293216

By:

Verma, Sarika;
Gupta, Ruchika;
Kudesia, Madhur;
Mathur, Alka;
Krishan, Gopal;
Singh, Sompal

Publication type:

Article

Preparation of Deferasirox in nano-scale by ultrasonic irradiation and optimization the amount and reaction time parameters.

Published in:

International Journal of Nano Dimension, 2015, v. 6, n. 4, p. 363

By:

Khatamifar, M.;
Ranjbar, Z. Rashidi;
Fatemi, S. J.

Publication type:

Article

A portable volumetric infusion pump controller for treatment of thallassemia disease.

Published in:

Journal of Medical Engineering & Technology, 1999, v. 23, n. 6, p. 225, doi. 10.1080/030919099294087

By:

Vasilakopoulou, E. P.;
Karastergios, G. E.;
Efstathiou, K. A.;
Papadopoulos, G. D.

Publication type:

Article

Cyclosporine therapy during pregnancy in a patient with β–thalassemia major and autoimmune haemolytic anemia: a case report and review of the literature.

Published in:

2013

By:

Agapidou, A.;
Vlachaki, E.;
Theodoridis, T.;
Economou, M.;
Perifanis, V.

Publication type:

Case Study

Efficacy of Oral Acetaminophen and Intravenous Chlorpheniramine Maleate versus Placebo to Prevent Red Cell Transfusion Reactions in Children and Adolescent with Thalassemia: A Prospective, Randomized, Double-Blind Controlled Trial.

Published in:

Anemia (20901267), 2018, p. 1, doi. 10.1155/2018/9492303

By:

Rujkijyanont, Piya;
Monsereenusorn, Chalinee;
Manoonphol, Pimpat;
Traivaree, Chanchai

Publication type:

Article

Lyophilized hemoglobin E control material for the dichlorophenol-indophenol (DCIP) test.

Published in:

Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 6, p. e108, doi. 10.1515/cclm-2016-0652

By:

Pienthai, Nattasit;
Pornprasert, Sakorn

Publication type:

Article

Negative Affect Differentiation and Adherence During Treatment for Thalassemia.

Published in:

International Journal of Behavioral Medicine, 2014, v. 21, n. 1, p. 160, doi. 10.1007/s12529-012-9277-7

By:

Coifman, Karin;
Ross, Gail;
Kleinert, Dorothy;
Giardina, Patricia

Publication type:

Article

Frequency of Red Cell Alloimmunization Among Patients with Transfusion Dependent Beta Thalassemia in Pakistan.

Published in:

UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2011, v. 21, n. 3, p. 166, doi. 10.4999/uhod.09134

By:

USMAN, Muhammad;
MOIN, Saira;
Moinuddun, Moinuddin;
AHMAD, Saeed;
PERVEEN, Rehana;
AZMI, Muhammad A.;
USMAN, Sadia

Publication type:

Article

UPF1 silenced cellular model systems for screening of read-through agents active on β039 thalassemia point mutation.

Published in:

BMC Biotechnology, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12896-018-0435-0

By:

Salvatori, Francesca;
Pappadà, Mariangela;
Breveglieri, Giulia;
D'Aversa, Elisabetta;
Finotti, Alessia;
Lampronti, Ilaria;
Gambari, Roberto;
Borgatti, Monica

Publication type:

Article

Controversial study of thalassemia drug ends early.

Published in:

Canadian Medical Association Journal (CMAJ), 1998, v. 159, n. 7, p. 754

By:

Brown, C.J.;
Sibbald, Barbara

Publication type:

Article

Analysis of CD177 neutrophil expression in β-thalassemia patients.

Published in:

APMIS, 2011, v. 119, n. 10, p. 674, doi. 10.1111/j.1600-0463.2011.02755.x

By:

MONTASER, LAILA MAHMOUD;
EL-RASHIDI, FARIDA HUSSEIN;
ESSA, ENAS SAID;
AZAB, SAMAR MOSTAFA

Publication type:

Article

Erythropoiesis and Iron Homeostasis in Non-Transfusion-Dependent Thalassemia Patients with Extramedullary Hematopoiesis.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/4504302

By:

Huang, Yumei;
Liu, Rongrong;
Wei, Xiaoyun;
Liu, Jiaodi;
Pan, Lingyuan;
Yang, Gaohui;
Lai, Yongrong

Publication type:

Article

Conditioning regimens in allo-SCT for thalassemia major.

Published in:

Bone Marrow Transplantation, 2014, v. 49, n. 5, p. 607, doi. 10.1038/bmt.2013.216

By:

Mathews, V;
Savani, B N

Publication type:

Article

Higher CD3+ and CD34+ cell doses in the graft increase the incidence of acute GVHD in children receiving BMT for thalassemia.

Published in:

Bone Marrow Transplantation, 2012, v. 47, n. 1, p. 107, doi. 10.1038/bmt.2011.3

By:

Gaziev, J;
Isgrò, A;
Marziali, M;
Daniele, N;
Gallucci, C;
Sodani, P;
Simone, M D;
Adorno, G;
Paciaroni, K;
Andreani, M;
Lanti, A;
Del Proposto, G;
Testi, M;
De Angelis, G;
Roveda, A;
Alfieri, C;
Saltarelli, F;
Lucarelli, G

Publication type:

Article

What is the minimum level of donor chimerism necessary to sustain transfusion independence in thalassaemia?

Published in:

2011

By:

Alfred, A.;
Vora, A. J.

Publication type:

Letter

Hematopoietic stem cell transplantation in thalassemia.

Published in:

Bone Marrow Transplantation, 2008, v. 42, p. S41, doi. 10.1038/bmt.2008.112

By:

Gaziev, J.;
Sodani, P.;
Lucarelli, G.

Publication type:

Article

Stem cell transplantation in India.

Published in:

Bone Marrow Transplantation, 2008, v. 42, p. S81, doi. 10.1038/bmt.2008.124

By:

Chandy, M.

Publication type:

Article

Hematopoietic cell transplantation for thalassemia and sickle cell disease: past, present and future.

Published in:

Bone Marrow Transplantation, 2008, v. 41, n. 2, p. 109, doi. 10.1038/sj.bmt.1705943

By:

Bhatia, M.;
Walters, M. C.

Publication type:

Article

Radiographic features of the jaws and teeth in thalassaemia major.

Published in:

British Dental Journal, 2006, v. 201, n. 11, p. 713, doi. 10.1038/sj.bdj.4814308

By:

Watts, Trevor

Publication type:

Article

Mathematical model explaining iron change in patients with thalassemia.

Published in:

Asian Pacific Journal of Tropical Biomedicine, 2015, v. 5, n. 11, p. 974, doi. 10.1016/j.apjtb.2015.07.017

By:

Wiwanitkit, Somsri;
Wiwanitkit, Viroj

Publication type:

Article

α:Non–α and Gγ:Aγ globin chain ratios in thalassemia intermedia patients treated with hydroxyurea.

Published in:

Asian Pacific Journal of Tropical Biomedicine, 2014, v. 4, p. S177, doi. 10.12980/APJTB.4.2014C1161

By:

Najjari, Abbas;
Asouri, Mohsen;
Hosseini Gouhari, Ladan;
Akhavan Niaki, Haleh;
Sasan Mozaffari Nejad, Amir;
Masoumeh Eslami, Seyyedeh;
Abolghasemi, Hassan;
Ataee, Ramin;
Ebrahimi, Abdol Ali;
Moshaei, Masoumeh Rezaei;
Ahmadi, Ali Asghar

Publication type:

Article

Bronze Diabetes.

Published in:

2015

By:

Naik, Akshatha Lalesh;
Shenoy, Mamatha T.;
Yadav, Charu;
Srikantiah, Rukmini Mysore;
Kamath, Nutan

Publication type:

Case Study

Anesthetic management of a patient with sickle β+ thalassemia.

Published in:

2011

By:

Bharati, Saswata;
Das, Subhabrata;
Majee, Prasenjit;
Mandal, Subrata

Publication type:

Case Study

A family empowerment program for families having children with thalassemia, Thailand.

Published in:

2015

By:

Wacharasin, Chintana;
Phaktoop, Maneerat;
Sananreangsak, Siriyupa

Publication type:

Journal Article

In-Silico Computing of the Most Deleterious nsSNPs in HBA1 Gene.

Published in:

PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0147702

By:

AbdulAzeez, Sayed;
Borgio, J. Francis

Publication type:

Article

Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β-Thalassemia Major: A Comprehensive Review in 2015.

Published in:

Advances in Pharmacological Sciences, 2016, p. 1, doi. 10.1155/2016/3046373

By:

Darvishi Khezri, Hadi;
Salehifar, Ebrahim;
Kosaryan, Mehrnoush;
Aliasgharian, Aily;
Jalali, Hossein;
Hadian Amree, Arash

Publication type:

Article