Works about ALPHA-Thalassemia

Results: 288

Prenatal diagnosis and management of fetal anemia caused by hemoglobin H‐Adana: A case report.

Published in:

Journal of Obstetrics & Gynaecology Research, 2025, v. 51, n. 5, p. 1, doi. 10.1111/jog.16310

By:

Sirilert, Sirinart;
Srisupundit, Kasemsri;
Charoenkwan, Pimlak;
Phusua, Arunee;
Tongsong, Theera

Publication type:

Article

Optimal cutoff of mean corpuscular volume (MCV) for screening of alpha‐thalassemia 1 trait.

Published in:

Journal of Obstetrics & Gynaecology Research, 2020, v. 46, n. 5, p. 774, doi. 10.1111/jog.14222

By:

Nunchai, Chanhathai;
Sirichotiyakul, Supatra;
Tongsong, Theera

Publication type:

Article

Correlation between dynamic susceptibility contrast perfusion MRI and genomic alterations in glioblastoma.

Published in:

Neuroradiology, 2021, v. 63, n. 11, p. 1801, doi. 10.1007/s00234-021-02674-2

By:

Ozturk, Kerem;
Soylu, Esra;
Cayci, Zuzan

Publication type:

Article

False HbA1c value due to a rare variant of hemoglobin Petie Salpetriere coinherited with alpha thalassemia.

Published in:

Advances in Laboratory Medicine / Avances en Medicina de Laboratorio, 2024, v. 5, n. 4, p. 447, doi. 10.1515/almed-2024-0037

By:

Lepe Balsalobre, Esperanza;
Varo Sánchez, Gema María;
Rico Rodríguez, Marta;
Fuentes Cantero, Sandra

Publication type:

Article

Prevalence of thalassemia in the Vietnamese population and building a clinical decision support system for prenatal screening for thalassemia.

Published in:

Electronic Journal of General Medicine, 2023, v. 20, n. 4, p. 1, doi. 10.29333/ejgm/13206

By:

Danh Cuong Tran;
Anh Linh Dang;
Thi Ngoc Lan Hoang;
Chi Thanh Nguyen;
Thi Minh Phuong Le;
Thi Ngoc Mai Dinh;
Van Anh Tran;
Thi Kim Phuong Doan;
Thi Trang Nguyen

Publication type:

Article

Hereditary Hemochromatosis and Alpha-Thalassemia Presenting with Diabetes Mellitus: A Rare Case Report.

Published in:

Case Reports in Clinical Practice, 2022, v. 7, n. 3, p. 144

By:

Farhangi, Pourya;
Hajmiri, Minoo Sadat;
Shirzad, Nooshin;
Hemmatabadi, Mahboobeh

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

Causes of Death and Mortality Trends in Individuals with Thalassemia in the United States, 1999-2020.

Published in:

Journal of Blood Medicine, 2024, v. 15, p. 331, doi. 10.2147/JBM.S470177

By:

Tan, Jia Yi;
Yeo, Yong Hao;
Chan, Kok Hoe;
Shaaban, Hamid S;
Guron, Gunwant

Publication type:

Article

Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome.

Published in:

Epigenetics & Chromatin, 2017, v. 10, p. 1, doi. 10.1186/s13072-017-0118-4

By:

Schenkel, Laila C.;
Kernohan, Kristin D.;
McBride, Arran;
Reina, Ditta;
Hodge, Amanda;
Ainsworth, Peter J.;
Rodenhiser, David I.;
Pare, Guillaume;
Bérubé, Nathalie G.;
Skinner, Cindy;
Boycott, Kym M.;
Schwartz, Charles;
Sadikovic, Bekim

Publication type:

Article

A stepwise α-thalassemia screening strategy in high-prevalence areas.

Published in:

European Journal of Haematology, 2013, v. 91, n. 2, p. 164, doi. 10.1111/ejh.12136

By:

Alkindi, Salam S.;
AlZadjali, Shoaib;
Daar, Shahina;
Sindhuvi, Eunice;
Wali, Yasser;
Pathare, Anil V.;
Venugopal, Suresh;
Lapoumeroulie, Claudine;
Srivastava, Alok;
Krishnamoorthy, Rajagopal

Publication type:

Article

Evidence of differential selection for the −α3.7 and −α4.2 single-α-globin gene deletions within the same population.

Published in:

European Journal of Haematology, 2013, v. 90, n. 3, p. 210, doi. 10.1111/ejh.12058

By:

Yap, Zhi Min;
Sun, Kar Mun;
Teo, Clara R.L.;
Tan, Arnold S.C.;
Chong, Samuel S.

Publication type:

Article

The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score.

Published in:

European Journal of Haematology, 2012, v. 88, n. 1, p. 61, doi. 10.1111/j.1600-0609.2011.01705.x

By:

Joly, Philippe;
Pondarré, Corinne;
Bardel, Claire;
Francina, Alain;
Martin, Cyril

Publication type:

Article

Facteurs pronostiques de sévérité de la maladie drépanocytaire chez l'enfant.

Published in:

Médecine Thérapeutique: Pédiatrie, 2017, v. 20, n. 4, p. 276, doi. 10.1684/mtp.2018.0654

By:

Brousse, Valentine

Publication type:

Article

Epigenetic Etiology of Intellectual Disability.

Published in:

Journal of Neuroscience, 2017, v. 37, n. 45, p. 10773, doi. 10.1523/JNEUROSCI.1840-17.2017

By:

Iwase, Shigeki;
Bérubé, Nathalie G.;
Zhaolan Zhou;
Kasri, Nael Nadif;
Battaglioli, Elena;
Scandaglia, Marilyn;
Barco, Angel

Publication type:

Article

Homozygous Sickle Cell Disease in Uganda and Jamaica A Comparison of Bantu and Benin Haplotypes.

Published in:

West Indian Medical Journal, 2012, v. 61, n. 7, p. 684

By:

Ndugwa1, C.;
Higgs, D.;
Fisher, C.;
Hambleton, I.;
Mason, K.;
Serjeant, B. E.;
Serjeant, G. R.

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

Renal function in patients with β-thalassaemia major: a long-term follow-up study†.

Published in:

Nephrology Dialysis Transplantation, 2012, v. 27, n. 9, p. 3547, doi. 10.1093/ndt/gfs169

By:

Lai, Maria Eliana;
Spiga, Alessandra;
Vacquer, Stefania;
Carta, Maria Paola;
Corrias, Claudia;
Ponticelli, Claudio

Publication type:

Article

Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Hemoglobinopathies for Confirmation of Alpha-Thalassemia Trait.

Published in:

International Journal of Neonatal Screening (IJNS), 2025, v. 11, n. 1, p. 12, doi. 10.3390/ijns11010012

By:

Shook, Lisa M.;
Haygood, Deidra;
Quinn, Charles T.

Publication type:

Article

Intrauterine Fetal Growth Restriction and Oligohydramnios of Undetermined Etiology.

Published in:

2017

By:

Gallego, Daniel Fernando;
Neufeld-Kaiser, Whitney;
Weiss, Sheila;
Liu, Yajuan J.;
Ma, Kimberly K.;
Fligner, Corinne L.;
Lockwood, Christina M.

Publication type:

Case Study

A novel variant of ATRX gene is potentially associated with alpha-thalassemia X-linked intellectual disability syndrome: Case report and literature review.

Published in:

2024

By:

Sarah, Berrada;
Amal, Tazzite;
Bouchaib, Gazzaz;
Hind, Dehbi

Publication type:

Case Study

Alpha-thallasaemia Zero and Schizophrenia – a Case Report and Discussion.

Published in:

European Psychiatry, 2015, v. 30, p. 278, doi. 10.1016/S0924-9338(15)30226-1

By:

Mandlik, E.C.;
Roy, B.B.

Publication type:

Article

Alpha-thallasaemia Zero and Schizophrenia – a Case Report and Discussion.

Published in:

2015

By:

Mandlik, E.C.;
Roy, B.B.

Publication type:

Case Study

Molecular and Hematological Analysis of Alpha Thalassemia in Middle East Patients; A Cross-Sectional Retrospective Study.

Published in:

Egyptian Academic Journal of Biological Sciences, C Physiology & Molecular Biology, 2024, v. 16, n. 2, p. 455, doi. 10.21608/EAJBSC.2024.397463

By:

Morsi, Maha H.;
Alhuthali, Hayaa M.;
Elmasry, Heba M.;
Alghuraibi, Shmoukh;
Elgaddar, Ola;
Gharib, Amal F.;
Ahmed, Doha E.

Publication type:

Article

Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report.

Published in:

2016

By:

Na Sun;
Peng Cheng;
Dong-Hong Deng;
Rong-Rong Liu;
Yong-Rong Lai

Publication type:

Case Study

Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.

Published in:

Clinical Hemorheology & Microcirculation, 2014, v. 57, n. 1, p. 63, doi. 10.3233/CH-131772

By:

Lamarre, Yann;
Romana, Marc;
Lemonne, Nathalie;
Hardy-Dessources, Marie-Dominique;
Tarer, Vanessa;
Mougenel, Danielle;
Waltz, Xavier;
Tressières, Benoît;
Lalanne-Mistrih, Marie-Laure;
Etienne-Julan, Maryse;
Connes, Philippe

Publication type:

Article

Infective Endocarditis in a β-thalassemia Major Child.

Published in:

2015

By:

Rahayuningsih, Sri Endah;
Kuswiyanto, Rahmat Budi;
Situmorang, Herdiana Elizabeth;
Phangkawira, Evelyn

Publication type:

Case Study

Alpha Thalassemia/Intellectual Disability X-Linked Deficiency Sensitizes Non-Small Cell Lung Cancer to Immune Checkpoint Inhibitors.

Published in:

Frontiers in Oncology, 2020, v. 11, p. N.PAG, doi. 10.3389/fonc.2020.608300

By:

Hou, Tao;
Jiang, Shun;
Wang, Yapeng;
Xie, Yangchun;
Zhang, Haixia;
Feng, Yeqian;
Ma, Fang;
Ma, Jin'an;
Liu, Xianling;
Hu, Chunhong

Publication type:

Article

Cognitive decline in an adult with ATR-16 syndrome due to an unbalanced translocation between 11p15.5 and 16p13.3: a case report.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1595298

By:

Krutish, Angela;
Kukurudz-Gorowski, Rebekah;
Borlot, Felippe;
Frosk, Patrick;
Rockman-Greenberg, Cheryl;
Mhanni, Aizeddin A.

Publication type:

Article

Vitamin B12 Deficiency and Hemoglobin H Disease Early Misdiagnosed as Thrombotic Thrombocytopenic Purpura: A Series of Unfortunate Events.

Published in:

2015

By:

Andreadis, Panagiotis;
Theodoridou, Stamatia;
Pasakiotou, Marily;
Arapoglou, Stergios;
Gigi, Eleni;
Vetsiou, Evaggelia;
Vlachaki, Efthymia

Publication type:

Case Study

Prevalence of common point mutations of alpha globin gene in Babol, Iran (2005-09).

Published in:

Journal of Gorgan University of Medical Sciences, 2012, v. 14, n. 1, p. 75

By:

Akhavan-Niaki, H.;
Pourtaghi, M.;
Firouzjahi, A. R.;
Banihashemi, A.;
Sedaghat, S.

Publication type:

Article

? case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent.

Published in:

Hippokratia, 2020, v. 24, n. 1, p. 43

By:

A., Tampaki;
S., Theodoridou;
Ch., Apostolou;
E. E., Delaki;
E., Vlachaki

Publication type:

Article

Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 7329, doi. 10.2147/IJGM.S338419

By:

Zheng, Lin;
Huang, Hailong;
Wu, Xiaoqing;
Su, Linjuan;
Shen, Qingmei;
Wang, Meiying;
Lin, Na;
Xu, Liangpu

Publication type:

Article

Rapid detection of non-deletional mutations causing α-thalassemia by multicolor melting curve analysis.

Published in:

Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 3, p. 397, doi. 10.1515/cclm-2015-0173

By:

Qiuying Huang;
Xudong Wang;
Ning Tang;
Chunjiang Zhu;
Tizhen Yan;
Ping Chen;
Qingge Li

Publication type:

Article

Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion).

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 6, p. 1199, doi. 10.1515/cclm-2012-0732

By:

Wangmaung, Nantawan;
Promptmas, Chamras;
Chomean, Sirinart;
Sanchomphu, Chularat;
Ittarat, Wanida

Publication type:

Article

Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysis.

Published in:

Clinical Chemistry & Laboratory Medicine, 2012, v. 50, n. 2, p. 273, doi. 10.1515/cclm.2011.759

By:

Liu, Ying-Na;
Li, Ru;
Zhou, Jian-Ying;
Xie, Xing-Mei;
Li, Jian;
Liao, Can;
Li, Dong-Zhi

Publication type:

Article

Changes in hematological parameters in α-thalassemia individuals co-inherited with erythroid Krüppel-like factor mutations.

Published in:

Clinical Genetics, 2015, v. 88, n. 1, p. 56, doi. 10.1111/cge.12443

By:

Yu, L.‐H.;
Liu, D.;
Cai, R.;
Shang, X.;
Zhang, X.‐H.;
Ma, X.‐X.;
Yan, S.‐H.;
Fang, P.;
Zheng, C.‐G.;
Wei, X.‐F.;
Liu, Y.‐H.;
Zhou, T.‐B.;
Xu, X.‐M.

Publication type:

Article

Molecular nature of alpha-globin genes in the Saudi population.

Published in:

Saudi Medical Journal, 2015, v. 36, n. 11, p. 1271, doi. 10.15537/smj.2015.11.12704

By:

Borgio, J. Francis

Publication type:

Article

Extramedullary haematopoiesis presented as intrathoracic tumour in a patient with alpha-thalassaemia.

Published in:

2013

By:

Bobylev, Dmitry;
Zhang, Ruoyu;
Haverich, Axel;
Krueger, Marcus

Publication type:

Case Study

Deferiprone.

Published in:

Hospital Pharmacy, 2012, v. 47, n. 2, p. 129, doi. 10.1310/hpj4702-129

By:

Cada, Dennis J.;
Levien, Terri L.;
Baker, Danial E.

Publication type:

Article

Compromised genomic integrity impedes muscle growth after Atrx inactivation.

Published in:

Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4412, doi. 10.1172/JCI63765

By:

Huh, Michael S.;
O'Dea, Tina Price;
Ouazia, Dahmane;
McKay, Bruce C.;
Parise, Gianni;
Parks, Robin J.;
Rudnicki, Michael A.;
Picketts, David J.

Publication type:

Article

The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of Kenya.

Published in:

2006

By:

Wambua, Sammy;
Mwangi, Tabitha W;
Kortok, Moses;
Uyoga, Sophie M;
Macharia, Alex W;
Mwacharo, Jedidah K;
Weatherall, David J;
Snow, Robert W;
Marsh, Kevin;
Williams, Thomas N

Publication type:

journal article

α-thalassemia-associated hydrops fetalis: A rare cause of thyrotoxic cardiomyopathy.

Published in:

Journal of Obstetrics & Gynaecology Research, 2015, v. 41, n. 6, p. 967, doi. 10.1111/jog.12648

By:

Tumian, Nor Rafeah;
Wong, Ming;
Wong, Chieh Lee

Publication type:

Article

First-trimester combined screening for trisomy 21 in women at risk for α-thalassemia.

Published in:

2016

By:

Zhen, Li;
Pan, Min;
Han, Jin;
Yang, Xin;
Liao, Can;
Li, Dong-Zhi

Publication type:

journal article

Too much A2 -- but does the patient really have beta thalassemia trait?

Published in:

Medical Laboratory Observer (MLO), 2018, v. 50, n. 2, p. 14

By:

Young, Andrew N.;
Burgess, Thomas

Publication type:

Article

New insertions-induced Hb H disease.

Published in:

Genetics & Applications, 2021, v. 5, n. 1, p. 64, doi. 10.31383/ga.vol5iss1pp64-67

By:

Alipour, Marzieh;
Afzali, Sara;
Varnamkhasti, Khalil Khashei

Publication type:

Article

A retrospective comparison of pregnancy outcomes between women with alpha-thalassaemia 1 trait and normal controls.

Published in:

2017

By:

Traisrisilp, Kuntharee;
Jatavan, Phudit;
Tongsong, Theera

Publication type:

journal article

THALASSEMIA: A Centennial Commemoration.

Published in:

Canadian Journal of Medical Laboratory Science, 2024, v. 86, n. 1, p. 11

By:

LITAVEC, TERENCE;
CHOONG, SHAYNA

Publication type:

Article

Alpha-Thalassemia in North Morocco: Prevalence and Molecular Spectrum.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/2080352

By:

Laghmich, Achraf;
Alaoui Ismaili, Fatima Zahra;
Barakat, Amina;
Ghailani Nourouti, Naima;
Khattab, Mohamed;
Bennani Mechita, Mohcine

Publication type:

Article

Hemoglobinopathy gone astray-three novel forms of α-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing.

Published in:

2021

By:

Grimholt, Runa M.;
Fjeld, Bente;
Klingenberg, Olav

Publication type:

journal article

Electrophoresis features and genotypes of Hb bart's hydrops fetalis.

Published in:

2020

By:

Li, Youqiong;
Liang, Liang;
Tian, Mao;
Qing, Ting;
Wu, Xin

Publication type:

journal article