Works matching Thalassemia

Results: 5000

Béta-thalassaemia, B12-vitamin-hiány és társuló komplementmediált hemolízis.

Published in:

Hungarian Medical Journal / Orvosi Hetilap, 2023, v. 164, n. 24, p. 954, doi. 10.1556/650.2023.32769

By:

Pethő, Ákos Géza;
Nagy, Zsófia Flóra;
Mezei, Zoltán András;
Takács, István;
Demeter, Judit

Publication type:

Article

妊娠合并地中海贫血的产科管理.

Published in:

Journal of International Obstetrics & Gynecology, 2022, v. 49, n. 3, p. 330, doi. 10.12280/gjfckx.20211170

By:

李洋;
杨海澜

Publication type:

Article

LA STORIA DELLA BETA TALASSEMIA IN SARDEGNA: IL CONTRIBUTO DELLE SCUOLE ITALIANE DI PEDIATRIA.

Published in:

Acta Medico-Historica Adriatica, 2019, v. 17, n. 1, p. 65, doi. 10.31952/amha.17.1.4

By:

Martini, Mariano;
Tornali, Cristina;
Bragazzi, Nicola Luigi;
Paluan, Filippo;
Vardeu, Maria Francesca

Publication type:

Article

Thalassaemiás betegen észlelt anaemia perniciosa - a diagnózis nehézségei.

Published in:

Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 33, p. 1368, doi. 10.1556/650.2018.31097

By:

Kurdi, Barnabás;
Mezei, Zoltán András;
Kellner, Ádám;
Egyed, Miklós

Publication type:

Article

DETERMINANT FACTORS OF DEPRESSION IN BETA MAJOR THALASSEMIA CHILDREN.

Published in:

Folia Medica Indonesiana (2355-8393), 2021, v. 57, n. 1, p. 46, doi. 10.20473/fmi.v57i1.24662

By:

Ningtiar, Hapsari Widya;
Suryawan, Ahmad;
Irwanto;
Ugrasena, I. D. G.

Publication type:

Article

ANALYSIS OF DEFERASIROX AND DEFERIPRON USE IN CHILDREN WITH PEDIATRIC β-THALASSEMIA MAJOR.

Published in:

Folia Medica Indonesiana (2355-8393), 2016, v. 52, n. 1, p. 42

By:

Sutrisnaningsih, Evy Sari;
Suharjono;
Sudarmanto, Bambang

Publication type:

Article

RESTLESS LEG SYNDROME IN ADULT PATIENTS WITH β-THALASSEMIA MAJOR .

Published in:

Clinical Neuroscience / Ideggyógyászati Szemle, 2021, v. 74, n. 7/8, p. 266, doi. 10.18071/isz.74.0266

By:

ERDEM, Ramazan;
ERDEM, Nazan Şimşek;
KURTOĞLU, Erdal

Publication type:

Article

Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15).

Published in:

Hemoglobin, 2019, v. 43, n. 4/5, p. 223, doi. 10.1080/03630269.2019.1675689

By:

Abdaoui, Wissem;
Benouareth, Djamel Eddine;
Djenouni, Amel;
Renoux, Celine;
Grifi, Fatiha;
Gouri, Adel;
Athamnia, Fateh;
Benalioua, Manel;
Joly, Philippe

Publication type:

Article

First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.

Published in:

Hemoglobin, 2019, v. 43, n. 1, p. 66, doi. 10.1080/03630269.2019.1577254

By:

Murad, Hossam;
Moassas, Faten

Publication type:

Article

Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia.

Published in:

Hemoglobin, 2019, v. 43, n. 1, p. 12, doi. 10.1080/03630269.2019.1567528

By:

Tamaddoni, Ahmad;
Khabaz Astaneh, Sahar;
Tabaripour, Reza;
Akhavan-Niaki, Haleh

Publication type:

Article

Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia.

Published in:

Hemoglobin, 2018, v. 42, n. 4, p. 236, doi. 10.1080/03630269.2018.1536666

By:

Dash, Preetinanda M.;
Sahu, Praveen K.;
Patel, Siris;
Mashon, Ranjeet S.;
Kharat, Kiran R.;
Mukherjee, Malay B.

Publication type:

Article

Comparison of Quality of Life in Patients with β-Thalassemia Intermedia and β-Thalassemia Major in Southern Iran.

Published in:

Hemoglobin, 2017, v. 41, n. 3, p. 169, doi. 10.1080/03630269.2017.1340307

By:

Haghpanah, Sezaneh;
Vahdati, Sara;
Karimi, Mehran

Publication type:

Article

β -Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β -Thalassemia is Rare in the Indian Population.

Published in:

2015

By:

Sreedharanunni, Sreejesh;
Chhabra, Sanjeev;
Hira, Jasbir Kaur;
Bansal, Deepak;
Sharma, Prashant;
Das, Reena

Publication type:

Case Study

Molecular Characterization of a β-Thalassemia Intermedia Patient Presenting Inferior Vena Cava Thrombosis: Interaction of the β-Globin Erythroid Krüppel-Like Factor Binding Site Mutation with Hb E and α+-Thalassemia.

Published in:

Hemoglobin, 2014, v. 38, n. 6, p. 451, doi. 10.3109/03630269.2014.974608

By:

Prajantasen, Thanet;
Teawtrakul, Nattiya;
Fucharoen, Goonnapa;
Fucharoen, Supan

Publication type:

Article

Report on Patients with Non Transfusion-Dependent β-Thalassemia Major Being Treated with Hydroxyurea Attending the Thalassemia Research Center, Sari, Mazandaran Province, Islamic Republic of Iran in 2013.

Published in:

Hemoglobin, 2014, v. 38, n. 2, p. 115, doi. 10.3109/03630269.2013.869229

By:

Kosaryan, Mehrnoush;
Karami, Hossein;
Zafari, Mandana;
Yaghobi, Negar

Publication type:

Article

Optimizing the Dose of Hydroxyurea Therapy for Patients with β-Thalassemia Intermedia (Hb E-β-thalassemia): A Single Center Study from Eastern India.

Published in:

Hemoglobin, 2014, v. 38, n. 1, p. 44, doi. 10.3109/03630269.2013.845844

By:

Bohara, Vinaykumar V.;
Ray, Sudeshna;
Chakrabarti, Prantar;
Ray, Siddhartha Sankar;
Nath, Uttam Kumar;
Chaudhuri, Utpal

Publication type:

Article

Homozygosity for the Severe β+-Thalassemia Mutation [IVS-I-5 (G>C)] Causes the Phenotype of Thalassemia Trait: An Extremely Rare Presentation.

Published in:

Hemoglobin, 2013, v. 37, n. 1, p. 101, doi. 10.3109/03630269.2012.751395

By:

Bohara, Vinaykumar;
Raut, Lalit;
Badarkhe, Girish;
Roy, Siddartha S.;
Chaudhuri, Utpal

Publication type:

Article

Clinicopathological and Radiological Study of Egyptian ββ-Thalassemia Intermedia and ββ-Thalassemia Major Patients: Relation to Complications and Response to Therapy.

Published in:

Hemoglobin, 2011, v. 35, n. 4, p. 382, doi. 10.3109/03630269.2011.598985

By:

Mokhtar, Galila M.;
Tantawy, Azza A.G.;
Adly, Amira A.M.;
Ismail, Eman A.R.

Publication type:

Article

Severe β-Thalassemia Intermedia in a Compound Heterozygous Patient for the −30 (T>A) β+-Thalassemia Mutation and the δ0β+-Senegalese Deletion.

Published in:

Hemoglobin, 2010, v. 34, n. 5, p. 505, doi. 10.3109/03630269.2010.509230

By:

Griffon, Céline;
Joly, Philippe;
Sénéchal, Agathe;
Philit, François;
Francina, Alain

Publication type:

Article

Molecular Heterogeneity of β-Thalassemia Alleles in Spain and its Importance in the Diagnosis and Prevention of β-Thalassemia Major and Sickle Cell Disorders.

Published in:

Hemoglobin, 2009, v. 33, n. 3/4, p. 226, doi. 10.1080/03630260903089003

By:

Pereira, Maria del Mar Mañú;
Dalmau, Anna Cabot;
Corrons, Joan-Lluis Vives

Publication type:

Article

Standardized T2* Map of a Normal Human Heart to Correct T2* Segmental Artefacts; Myocardial Iron Overload and Fibrosis in Thalassemia Intermedia Versus Thalassemia Major Patients and Electrocardiogram Changes in Thalassemia Major Patients.

Published in:

Hemoglobin, 2008, v. 32, n. 1/2, p. 97, doi. 10.1080/03630260701879514

By:

Ramazzotti, Anna;
Pepe, Alessia;
Positano, Vincenzo;
Scattini, Barbara;
Santarelli, Maria F.;
Landini, Luigi;
De Marchi, Daniele;
Keilberg, Petra;
Derchi, Giorgio;
Formisano, Francesco;
Pili, Marcello;
Lai, Maria E.;
Forni, Gianluca;
Filosa, Aldo;
Prossomariti, Luciano;
Capra, Marcello;
Pitrolo, Lorella;
Borgna-Pignatti, Caterina;
Cianciulli, Paolo;
Maggio, Aurelio

Publication type:

Article

Thalassemia Intermedia Due to Co-inheritance of β0/β+-Thalassemia and (– –SEA) α-Thalassemia/Hb Westmead [α122(H5)His > Gln (α2)] in a Chinese Family.

Published in:

Hemoglobin, 2004, v. 28, n. 2, p. 151, doi. 10.1081/HEM-120035917

By:

Wong, Wai‐Shan;
Chan, Amy Y‐Y.;
Yip, Sze‐Fai;
Shiu‐Kwan Ma, Edmond

Publication type:

Article

Cardiac Involvement in β-Thalassemia Major and β-Thalassemia Intermedia.

Published in:

Hemoglobin, 2004, v. 28, n. 2, p. 123, doi. 10.1081/HEM-120034248

By:

Ferrara, Mara;
Matarese, Sofia M. R.;
Borrelli, Barbara;
Perrotta, Angelo;
Simeone, Gelsomina;
Greco, Natalizia;
Iarussi, Diana;
Esposito, Luigi

Publication type:

Article

Talasemi Konusunda Verilen Eğitimlerin Talasemi Taşıyıcılarının Bilgi Düzeyi Üzerine Etkisinin Belirlenmesi.

Published in:

Ankara Medical Journal, 2015, v. 15, n. 4, p. 184, doi. 10.17098/amj.11897

By:

Keten, Hamit Sırrı;
Çitil, Medine;
Çelik, Yeşim Can;
Işık, Oğuz

Publication type:

Article

Renal function in children with β-thalassemia major and thalassemia intermedia.

Published in:

Pediatric Nephrology, 2008, v. 23, n. 10, p. 1847, doi. 10.1007/s00467-008-0897-8

By:

Smolkin, Vladislav;
Halevy, Raphael;
Levin, Carina;
Mines, Miguel;
Sakran, Waheeb;
Ilia, Katzap;
Koren, Ariel

Publication type:

Article

Assessing Parental Knowledge About Thalassemia in a Thalassemia Center of Karachi, Pakistan.

Published in:

Journal of Genetic Counseling, 2015, v. 24, n. 6, p. 945, doi. 10.1007/s10897-015-9830-z

By:

Maheen, Humaira;
Malik, Farrukh;
Siddique, Barera;
Qidwai, Asim

Publication type:

Article

Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia.

Published in:

International Journal of Laboratory Hematology, 2019, v. 41, n. 4, p. 513, doi. 10.1111/ijlh.13035

By:

Singha, Kritsada;
Taweenan, Wachiraporn;
Fucharoen, Goonnapa;
Fucharoen, Supan

Publication type:

Article

Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study.

Published in:

2019

By:

Mettananda, Sachith;
Pathiraja, Hashan;
Peiris, Ravindu;
Bandara, Dayananda;
de Silva, Udaya;
Mettananda, Chamila;
Premawardhena, Anuja

Publication type:

journal article

Cerebral Artery Velocity Determined by Transcranial Doppler Ultrasonography in Patients With β-Thalassemia Intermedia Compared to β-Thalassemia Major.

Published in:

Clinical & Applied Thrombosis/Hemostasis, 2013, v. 19, n. 4, p. 367, doi. 10.1177/1076029612461068

By:

Karimi, Mehran;
Haghpanah, Sezaneh;
Ashjazadeh, Nahid;
Shariat, Abdolhamid;
Nazeri, Masoume;
Emami, Sajad;
Forough, Amin Abolhasani;
Petramfar, Peyman;
Yaghoubi, Ehsan

Publication type:

Article

Magnetic Resonance Evaluation of Tissue Iron Deposition and Cardiac Function in Adult Regularly Transfused Thalassemia Intermedia Compared with Thalassemia Major Patients.

Published in:

Journal of Clinical Medicine, 2024, v. 13, n. 16, p. 4791, doi. 10.3390/jcm13164791

By:

Meloni, Antonella;
Pistoia, Laura;
Ricchi, Paolo;
Longo, Filomena;
Cecinati, Valerio;
Sorrentino, Francesco;
Borsellino, Zelia;
Bagnato, Sergio;
Rossi, Vincenza;
Fina, Priscilla;
Riva, Ada;
Renne, Stefania;
Peritore, Giuseppe;
Positano, Vincenzo;
Cademartiri, Filippo

Publication type:

Article

Non-transfusion-dependent thalassemia and thalassemia intermedia: epidemiology, complications, and management.

Published in:

2016

By:

Vichinsky, Elliott

Publication type:

journal article

Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.

Published in:

Pediatric Hematology & Oncology, 2015, v. 32, n. 5, p. 349, doi. 10.3109/08880018.2015.1040932

By:

Liu, Sha;
Jiang, Hua;
Wu, Man-Yu;
Zhang, Yong-Ling;
Li, Dong-Zhi

Publication type:

Article

α-Thalassemia Frequency and Mutations in Children with Hypochromic Microcytic Anemias and Relation with β-Thalassemia, Iron Deficiency Anemia.

Published in:

Pediatric Hematology & Oncology, 2012, v. 29, n. 3, p. 241, doi. 10.3109/08880018.2012.661831

By:

Gulen, Huseyin;
Hanimeli, Ozlem;
Karaca, Ozlem;
Taneli, Fatma

Publication type:

Article

Detection of Early Cardiac Dysfunction in Patients with β-Thalassemia Major and Thalassemia Trait by Tissue Doppler Echocardiography.

Published in:

Pediatric Hematology & Oncology, 2011, v. 28, n. 6, p. 486, doi. 10.3109/08880018.2011.568596

By:

Balci, Yasemin Isik;
Gurses, Dolunay

Publication type:

Article

Active spread of β‐thalassemia beyond the thalassemia belt: A study on a Russian population.

Published in:

Clinical Genetics, 2025, v. 107, n. 1, p. 23, doi. 10.1111/cge.14606

By:

Shchemeleva, Ekaterina;
Salomashkina, Valentina V.;
Selivanova, Daria;
Tsvetaeva, Nina;
Melikyan, Anait;
Doronina, Liliya;
Surin, Vadim L.

Publication type:

Article

Comparison Study of Major Thalassemia, Thalassemia Intermedia of Iraqi Patients and Control Groups for Effectiveness of Liver Enzymes.

Published in:

Medico-Legal Update, 2020, v. 20, n. 1, p. 1181, doi. 10.37506/v20/i1/2020/mlu/194462

By:

Jwaid, Shatha H.;
Gata, Abbas Mehsen

Publication type:

Article

Prevalence of Alpha and Beta-Thalassemia Mutations Among Carriers of Thalassemia in Shadegan City, Southwest of Iran.

Published in:

Zahedan Journal of Research in Medical Sciences, 2015, v. 17, n. 8, p. 1, doi. 10.17795/zjrms1032

By:

Irani, Amin Doosti;
Cheraghi, Zahra;
Bitaraf, Saied;
Cheraghi, Parvin;
Safiri, Saeid

Publication type:

Article

β-Thalassemia intermedia Homozygous for Normal Hemoglobin A2 β-Thalassemia.

Published in:

Acta Haematologica, 1982, v. 67, n. 1, p. 57, doi. 10.1159/000207025

By:

Aksoy, Muzaffer;
Bermek, Engin;
Almiş, Gönül;
Kutlar, Abdullah

Publication type:

Article

Interaction between β-Thalassaemia and Hb G Philadelphia Associated with α-Thalassaemia.

Published in:

Acta Haematologica, 1979, v. 62, n. 2, p. 106, doi. 10.1159/000207549

By:

Stathopoulou, Regina;
Sulis, E.;
Lehmann, H.

Publication type:

Article

Utilization of Discriminant Formulas in the Differentiation of Alpha Thalassemia, Beta Thalassemia, and Iron Deficiency in Premarital Setting.

Published in:

Clinical Laboratory, 2021, v. 67, n. 4, p. 922, doi. 10.7754/Clin.Lab.2020.200644

By:

Saboor, Muhammad

Publication type:

Article

干细胞治疗地中海贫血：现状及未来.

Published in:

Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu, 2018, v. 22, n. 21, p. 3431, doi. 10.3969/j.issn.2095-4344.0532

By:

胡俊杰;
陈鑫苹;
符生苗

Publication type:

Article

Evaluation of the Serum Level of Vascular Endothelial Growth Factor in Patients with Beta-Thalassemia Major and Sickle/Beta-Thalassemia, and its Correlation with Clinical and Laboratory Parameters.

Published in:

Journal of Applied Hematology, 2023, v. 14, n. 2, p. 115, doi. 10.4103/joah.joah_98_22

By:

Mohsin, Sara Anmar Abdul;
Al-Bayaa, Israa M.;
Al-Badran, Ihsan Mardan

Publication type:

Article

Combined heterozygosity for hemoglobin Paksé, α-thalassemia and for hemoglobin E, β- thalassemia ̵ first appearance in Europe.

Published in:

Annals of Hematology, 2025, v. 104, n. 3, p. 2059, doi. 10.1007/s00277-025-06286-1

By:

Schnedl, Wolfgang J.;
Leixner, Georg;
Voill-Glaninger, Astrid;
Michaelis, Simon;
Enko, Dietmar;
Mangge, Harald

Publication type:

Article

Optimal Mean Corpuscular Haemoglobin (MCH) Cut-Off Value for Differentiating Alpha Plus and Alpha Zero Thalassaemia in Thalassaemia Screening.

Published in:

Malaysian Journal of Medicine & Health Sciences, 2020, v. 16, n. Supp9, p. 69

By:

Idris, Faridah;
Chiu Yee Liew;
Seman, Zainina;
Mahmud, Noraesah

Publication type:

Article

Mapping of the Beta-Thalassaemia Carrier in Sabah: An Initial Step to Strengthen the Thalassaemia Prevention Program in Malaysia.

Published in:

Malaysian Journal of Medicine & Health Sciences, 2019, v. 15, p. 13

By:

Sena, Asit;
Buang, Saidatul Norbaya;
Soh Chin Li;
Sulaiman, Zaleha;
Daud, Mohd Shahriel Md;
Noor, Kaharnisah Mat;
Mohammed, Don

Publication type:

Article

تنوع ژنتیکی پلی‌مورفیسم HindIIIG در اینترون دوم IVSII-I ژن Gy و ارتباط آن با میزان HbF در بیماران بتا تالاسمی ماژور و اینترمدیا در استان اصفهان

Published in:

Scientific Journal of Iranian Blood Transfusion Organization, 2016, v. 13, n. 2, p. 122

By:

متولی باشی, مجید;
سجادپور, زهرا;
قاسمی, طیبه

Publication type:

Article

Effect of α-Gene Numbers on the Expression of β-Thalassemia intermedia, β-Thalassemia and (δβ)0-Thalassemia Traits.

Published in:

Human Heredity, 1998, v. 48, n. 3, p. 121, doi. 10.1159/000022792

By:

Altay, Ç.;
Öner, C.;
Öner, R.;
Gümrük, F.;
Mergen, H.;
Gürgey, A.

Publication type:

Article

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 11, p. 2115, doi. 10.1515/cclm-2013-0354

By:

Sahli, Chaima Abdelhafidh;
Bibi, Amina;
Ouali, Faida;
Fredj, Sondess Hadj;
Dakhlaoui, Boutheina;
Othmani, Rym;
Laouini, Naouel;
Jouini, Latifa;
Ouenniche, Fekria;
Siala, Hajer;
Touhami, Imed;
Becher, Mariem;
Fattoum, Slaheddine;
Toumi, Nour El Houda;
Messaoud, Taieb

Publication type:

Article

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand.

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1605, doi. 10.1515/cclm-2013-0098

By:

Vip Viprakasit;
Chanin Limwongse;
Sathein Sukpanichnant;
Pornpimol Ruangvutilert;
Chompunut Kanjanakorn;
Waraporn Glomglao;
Monchan Sirikong;
Witayakarn Utto;
Voravarn S. Tanphaichitr

Publication type:

Article

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia.

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1595, doi. 10.1515/cclm-2012-0842

By:

Sahli, Chaima A.;
Bibi, Amina;
Ouali, Faida;
Fredj, Sondess Hadj;
Dakhlaoui, Boutheina;
Othmani, Rym;
Laaouini, Naouel;
Jouini, Latifa;
Ouenniche, Fekria;
Siala, Hajer;
Touhami, Imed;
Becher, Mariem;
Fattoum, Slaheddine;
Toumi, Nour El Houda;
Messaoud, Taieb

Publication type:

Article