Works matching DE "ALPHA-Thalassemia"

Results: 273

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
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
EP07.63: Signs of cortical development malformation in homozygous alpha‐thalassemia fetus with vascular‐type disruptive defects.
Published in:
Ultrasound in Obstetrics & Gynecology, 2024, v. 64, p. 179, doi. 10.1002/uog.28311
By:
- Dinh, V. Nguyen;
- Nguyen, L.T.;
- Nguyen, L.;
- Tran, K.;
- Tran, T.
Publication type:
Article
P18.19: Prenatal diagnosis and treatment of alpha-thalassemia major.
Published in:
Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 296, doi. 10.1002/uog.14368
By:
- Debska, M.;
- Kretowicz, P.;
- Turowski, P.;
- Dangel, J.;
- Debski, R.
Publication type:
Article
Erratum.
Published in:
2021
Publication type:
Correction Notice
Alpha-Thalassemia Carrier due to –α3.7 Deletion: Not So Silent.
Published in:
Acta Haematologica, 2020, v. 143, n. 5, p. 432, doi. 10.1159/000503023
By:
- Gilad, Oded;
- Steinberg-Shemer, Orna;
- Dgany, Orly;
- Krasnov, Tanya;
- Noy-Lotan, Sharon;
- Tamary, Hannah;
- Yacobovich, Joanne
Publication type:
Article
A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α0-Thalassemia.
Published in:
2017
By:
- Huang, Lv-Yin;
- Yan, Jin-Mei;
- Zhou, Jian-Ying;
- Li, Jian;
- Xie, Xing-Mei;
- Li, Dong-Zhi
Publication type:
Case Study
Benign Cardiac Effects of Hemoglobin H Disease.
Published in:
Acta Haematologica, 2016, v. 135, n. 4, p. 200, doi. 10.1159/000442193
By:
- Sheeran, Claire;
- Bowden, Donald K.;
- Pasricha, Sant-Rayn;
- Cheng, Ken;
- Romanelli, Giovanni;
- Peverill, Roger E.
Publication type:
Article
Investigating the Alpha1NcoI Mutation.
Published in:
Acta Haematologica, 2015, v. 133, n. 2, p. 145, doi. 10.1159/000363440
By:
- Desogus, Maria Franca;
- Paglietti, Maria Elisabetta;
- Sollaino, Maria Carla;
- Barella, Susanna;
- Origa, Raffaella
Publication type:
Article
A novel α0‐thalassemia deletion in a Brazilian child with Hb H disease: −−Mococa.
Published in:
2024
By:
- Soler, A. M.;
- Pedroso, G. A.;
- Geraldo, A. P. M.;
- Albuquerque, D. M.;
- Costa, F. F.;
- Santos, M. N. N.;
- Knijnenburg, J.;
- Harteveld, C. L.;
- Sonati, M. F.;
- da Luz, J. A.
Publication type:
Letter to the Editor
Hb Bart's immunochromatographic test result and Hb F level in normal cord blood and in selected haemoglobinopathy cases.
Published in:
2024
By:
- Chan, George;
- Wong, Jenna;
- Sami, Viraj
Publication type:
Letter to the Editor
Identification of a novel and rare α0‐thalassemia 27.0 kb deletion with 9 bp insertion (Lamphun deletion; ‐‐LAMPHUN) in a Thai family.
Published in:
International Journal of Laboratory Hematology, 2024, v. 46, n. 1, p. 176, doi. 10.1111/ijlh.14177
By:
- Khamphikham, Pinyaphat;
- Tepakhan, Wanicha;
- Tongjai, Siripong;
- Jan‐ngam, Varit;
- Laonan, Apichaya;
- Thimsin, Woraya;
- Boontha, Siriraj;
- Santiyos, Sasithorn;
- Pornprasert, Sakorn
Publication type:
Article
False positive Hb Bart's immunochromatographic strip test for alpha thalassaemia in delta‐beta thalassaemia carriers.
Published in:
International Journal of Laboratory Hematology, 2023, v. 45, n. 6, p. 984, doi. 10.1111/ijlh.14122
By:
- Chan, George;
- Wong, Jenna;
- Tan, Tina;
- Ghallyan, Nikhil;
- Browett, Peter
Publication type:
Article
Additional value of red blood cell parameters in predicting uncommon α‐thalassemia; experience from 10 years of α‐globin gene sequencing and copy number variation analysis.
Published in:
International Journal of Laboratory Hematology, 2023, v. 45, n. 2, p. 250, doi. 10.1111/ijlh.14010
By:
- Fjeld, Bente;
- Sudmann‐Day, Åshild Amelie;
- Grimholt, Runa Marie;
- Larstorp, Anne Cecilie Kjeldsen;
- Urdal, Petter;
- Klingenberg, Olav
Publication type:
Article
Alectinib‐induced red cell morphological changes in a patient with underlying α‐thalassaemia trait.
Published in:
International Journal of Laboratory Hematology, 2022, v. 44, n. 1, p. 65, doi. 10.1111/ijlh.13730
By:
- Li, Ting Hon Stanford;
- Chik, Yin Kwan Jeannie;
- Wong, Wai Shan
Publication type:
Article
Breakpoint characterization of a rare alpha0‐thalassemia deletion using targeted locus amplification on genomic DNA.
Published in:
International Journal of Laboratory Hematology, 2021, v. 43, n. 6, p. 1628, doi. 10.1111/ijlh.13651
By:
- Hottentot, Quint P.;
- de Meijer, Emile;
- Buermans, Henk P. J.;
- White, Stefan J.;
- Harteveld, Cornelis L.
Publication type:
Article
A novel deletion of the major regulatory element flanking the α‐globin gene cluster as a cause of α0‐thalassemia.
Published in:
International Journal of Laboratory Hematology, 2021, v. 43, n. 4, p. O190, doi. 10.1111/ijlh.13505
By:
- Jiang, Fan;
- Xu, Li‐Li;
- Tang, Xue‐Wei;
- Li, Dong‐Zhi
Publication type:
Article
Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart's disease: A hematological, molecular, and diagnostic aspects.
Published in:
International Journal of Laboratory Hematology, 2020, v. 42, n. 4, p. e173, doi. 10.1111/ijlh.13224
By:
- Singha, Kritsada;
- Wiangnon, Surapon;
- Fucharoen, Goonnapa;
- Jetsrisuparb, Arunee;
- Komwilaisak, Patcharee;
- Fucharoen, Supan
Publication type:
Article
A combination of the (αα)GZ and ‐‐SEA deletions causing a severe form of hemoglobin H disease.
Published in:
2020
By:
- Cheng, Yi;
- Cai, Decheng;
- Shang, Xuan;
- Pang, Dejian;
- Wei, Xiaofeng;
- Zhong, Jianmei;
- Xu, Xiangmin
Publication type:
Case Study
Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic.
Published in:
International Journal of Laboratory Hematology, 2020, v. 42, n. 1, p. 23, doi. 10.1111/ijlh.13118
By:
- Singha, Kritsada;
- Srivorakun, Hataichanok;
- Fucharoen, Goonnapa;
- Fucharoen, Supan
Publication type:
Article
Evaluation of an immunochromatographic test for alpha thalassaemia screening in a multi‐ethnic population.
Published in:
International Journal of Laboratory Hematology, 2019, v. 41, n. 3, p. 397, doi. 10.1111/ijlh.12994
By:
- Nelson, Anna Clare;
- Motum, Penelope Irene;
- Emeto, Theophilus I.
Publication type:
Article
The first report of hemoglobin E in combination with the highly unstable alpha‐globin variant Hb Adana: The importance of molecular confirmation.
Published in:
2019
By:
- Achour, Ahlem;
- Grouw, Elke;
- Erp, Femke;
- Arkesteijn, Sandra;
- Schaap, Rianne;
- Huurne, Jeanet ter;
- Bisoen, Sharda;
- Verschuren, Maaike;
- Harteveld, Cornelis L.
Publication type:
Letter to the Editor
The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center.
Published in:
International Journal of Laboratory Hematology, 2019, v. 41, n. 2, p. 218, doi. 10.1111/ijlh.12948
By:
- Nadkarni, Anita H.;
- Gorakshakar, Ajit C.;
- Sawant, Pratibha M.;
- Italia, Khushnooma Y.;
- Upadhye, Dipti S.;
- Gorivale, Manju S.;
- Mehta, Pallavi R.;
- Hariharan, Priya;
- Ghosh, Kanjaksha;
- Colah, Roshan B.
Publication type:
Article
Evaluation of an immunochromatographic strip test for alpha‐thalassaemia screening.
Published in:
International Journal of Laboratory Hematology, 2018, v. 40, n. 6, p. 691, doi. 10.1111/ijlh.12905
By:
- Bunkall, Carolyn;
- Ghallyan, Nikhil;
- Elliott, Catherine;
- Van de Water, Neil;
- Chan, George
Publication type:
Article
Co-inheritance of α0-thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications.
Published in:
International Journal of Laboratory Hematology, 2017, v. 39, n. 5, p. 508, doi. 10.1111/ijlh.12677
By:
- Singha, K.;
- Srivorakun, H.;
- Fucharoen, G.;
- Fucharoen, S.
Publication type:
Article
Diagnosis and molecular characterization of a novel α0-thalassemia deletion (- Kozani) found in a Greek child with unexplained microcytic hypochromic anemia.
Published in:
International Journal of Laboratory Hematology, 2017, v. 39, n. 5, p. e124, doi. 10.1111/ijlh.12690
By:
- Makis, A.;
- Georgiou, I.;
- Traeger‐Synodinos, J.;
- Chaliasos, N.;
- Grosso, M.;
- Gambale, A.;
- Iolascon, A.
Publication type:
Article
Identification of a novel 44.6-kb deletion causing α0-thalassemia in southern China.
Published in:
International Journal of Laboratory Hematology, 2017, v. 39, n. 4, p. e94, doi. 10.1111/ijlh.12643
By:
- Wang, Y.;
- Liu, C.;
- Zhang, L.;
- Du, L.;
- Zhou, W.;
- Huang, S.;
- Liu, L.;
- Yin, A.
Publication type:
Article
Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain.
Published in:
International Journal of Laboratory Hematology, 2017, v. 39, n. 1, p. 76, doi. 10.1111/ijlh.12577
By:
- Abuamer, S.;
- Shome, D. K.;
- Jaradat, A.;
- Radhi, A.;
- Bapat, J. P.;
- Sharif, K. A.;
- Al‐Touq, J.;
- Al‐Asheeri, A.;
- Al‐Ajami, A.
Publication type:
Article
Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha0-thalassemia deletions - -Mex1 and - -Mex2.
Published in:
International Journal of Laboratory Hematology, 2016, v. 38, n. 5, p. 535, doi. 10.1111/ijlh.12536
By:
- de‐la‐Cruz‐Salcedo, E. I.;
- Ibarra, B.;
- Rizo‐de‐la‐Torre, L. C.;
- Sánchez‐López, J. Y.;
- González‐Mercado, A.;
- Harteveld, C. L.;
- Perea‐Díaz, F. J.
Publication type:
Article
Rapid detection of α-thalassaemia variants using droplet digital PCR.
Published in:
International Journal of Laboratory Hematology, 2016, v. 38, n. 4, p. 435, doi. 10.1111/ijlh.12520
By:
- Lee, T.‐Y.;
- Lai, M.‐I.;
- Ramachandran, V.;
- Tan, J. A. M. A.;
- Teh, L.‐K.;
- Othman, R.;
- Hussein, N. H.;
- George, E.
Publication type:
Article
Hemoglobin H identification by high-performance liquid chromatography in confirmed hemoglobin H disease.
Published in:
International Journal of Laboratory Hematology, 2015, v. 37, n. 5, p. 668, doi. 10.1111/ijlh.12382
By:
- Turley, E.;
- McFarlane, A.;
- Halchuk, L.;
- Verhovsek, M.
Publication type:
Article
Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it?
Published in:
International Journal of Laboratory Hematology, 2015, v. 37, n. 5, p. 649, doi. 10.1111/ijlh.12376
By:
- Wu, M.‐Y.;
- Xie, X.‐M.;
- Li, J.;
- Li, D.‐Z.
Publication type:
Article
Evaluation of the new red cell parameters on Beckman Coulter DxH800 in distinguishing iron deficiency anaemia from thalassaemia trait.
Published in:
International Journal of Laboratory Hematology, 2015, v. 37, n. 2, p. 199, doi. 10.1111/ijlh.12262
By:
- Ng, E. H. Y.;
- Leung, J. H. W.;
- Lau, Y. S.;
- Ma, E. S. K.
Publication type:
Article
Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of Hb SD-Punjab.
Published in:
International Journal of Laboratory Hematology, 2014, v. 36, n. 4, p. 444, doi. 10.1111/ijlh.12165
By:
- Patel, D. K.;
- Purohit, P.;
- Dehury, S.;
- Das, P.;
- Dutta, A.;
- Meher, S.;
- Patel, S.;
- Bag, S.;
- Mashon, R. S.;
- Das, K.
Publication type:
Article
An investigation of the protective effect of alpha+-thalassaemia against severe Plasmodium falciparum amongst children in Kumasi, Ghana.
Published in:
International Journal of Laboratory Hematology, 2014, v. 36, n. 1, p. 62, doi. 10.1111/ijlh.12122
By:
- Opoku‐Okrah, C.;
- Gordge, M.;
- Kweku Nakua, E.;
- Abgenyega, T.;
- Parry, M.;
- Robertson, C.;
- Smith, C. L.
Publication type:
Article
Diagnostic testing for α-globin gene disorders in a heterogeneous North American population.
Published in:
International Journal of Laboratory Hematology, 2013, v. 35, n. 3, p. 306, doi. 10.1111/ijlh.12066
By:
- Waye, J. S.;
- Eng, B.
Publication type:
Article
Hb A2 levels in patients with nondeletional Hb H disease.
Published in:
2012
By:
- Y.-Q. Li;
- D.-Z. Li
Publication type:
Letter
Co-inherited β-thalassemia trait and HbH disease: clinical characteristics and interference in diagnosis of thalassemia by high-performance liquid chromatography.
Published in:
International Journal of Laboratory Hematology, 2012, v. 34, n. 4, p. 427, doi. 10.1111/j.1751-553X.2012.01415.x
By:
- YIN, X.-L.;
- WU, Z.-K.;
- ZHOU, X.Y.;
- ZHOU, T.-H.;
- ZHOU, Y.-L.;
- WANG, L.;
- HUANG, J.;
- ZHANG, X.-H.
Publication type:
Article
Red blood cell disorders in recently arrived African immigrants to Gran Canaria, Spain.
Published in:
Transactions of the Royal Society of Tropical Medicine & Hygiene, 2013, v. 107, n. 2, p. 91, doi. 10.1093/trstmh/trs017
By:
- de-la-Iglesia-Iñigo, Silvia;
- Carranza-Rodriguez, Cristina;
- Ropero-Gradilla, Paloma;
- González-Fernandez, Fernando-Ataulfo;
- Molero-Labarta, Teresa;
- Hemmersbach-Miller, Marion;
- Pérez-Arellano, José-Luis
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
Presentation of two new mutations in the 3'untranslated region of the β-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey.
Published in:
2021
By:
- Arpaci, Abdullah;
- Gul, Bahar Unlu;
- Ozcan, Oguzhan;
- Ilhan, Gul;
- El, Cigdem;
- Dirican, Emre;
- Elmacioglu, Sibel;
- Kaya, Hasan
Publication type:
journal article
Severe hemolytic anemia due to combined α thalassemia and de novo Hemoglobin Sabine.
Published in:
2019
By:
- Chen, XinPing;
- Hu, JunJie;
- Zhu, Juan;
- Xu, WeiHua;
- Yao, HongXia;
- Wu, AiZhu;
- Xiao, MeiFang;
- Lu, Zhe;
- Yin, LiYan;
- Fu, ShengMiao
Publication type:
Letter to the Editor
Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia.
Published in:
2017
By:
- Ferrão, José;
- Silva, Marisa;
- Gonçalves, Lúcia;
- Gomes, Susana;
- Loureiro, Pedro;
- Coelho, Andreia;
- Miranda, Armandina;
- Seuanes, Filomena;
- Reis, Ana;
- Pina, Francisca;
- Maia, Raquel;
- Kjöllerström, Paula;
- Monteiro, Estela;
- Lacerda, João;
- Lavinha, João;
- Gonçalves, João;
- Faustino, Paula;
- Ferrão, José;
- Gonçalves, Lúcia;
- Reis, Ana Batalha
Publication type:
journal article
A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease.
Published in:
2017
By:
- Surapolchai, Pacharapan;
- Chuansumrit, Ampaiwan;
- Sirachainan, Nongnuch;
- Kadegasem, Praguywan;
- Leung, Ka-Chun;
- So, Chi-Chiu
Publication type:
journal article
The epidemiologic transition of thalassemia and associated hemoglobinopathies in southern Taiwan.
Published in:
2017
By:
- Wang, Hui-Ching;
- Hsieh, Li-Ling;
- Liu, Yi-Chang;
- Hsiao, Hui-Hua;
- Lin, Shu-Kai;
- Tsai, Wen-Chan;
- Liu, Ta-Chih
Publication type:
journal article
Evaluation of bone mineral density in patients with hemoglobin H disease.
Published in:
2016
By:
- Zarei, Tahereh;
- Haghpanah, Sezaneh;
- Parand, Shirin;
- Moravej, Hossein;
- Dabbaghmanesh, Mohammad;
- Omrani, Gholamhossein;
- Karimi, Mehran;
- Dabbaghmanesh, Mohammad Hossein;
- Omrani, Gholamhossein Ranjbar
Publication type:
journal article
Screening and Diagnosis of Rare Thalassemia Variants.
Published in:
Archives of Pathology & Laboratory Medicine, 2025, v. 149, n. 1, p. e1, doi. 10.5858/arpa.2023-0382-oa
By:
- Haishen Tang;
- Yi Xiong;
- Jiaqi Tang;
- Xiaohong Wang;
- Ya Wang;
- Liping Huang;
- Runli Wang;
- Degang Wang
Publication type:
Article
Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population.
Published in:
Archives of Pathology & Laboratory Medicine, 2023, v. 147, n. 2, p. 208, doi. 10.5858/arpa.2021-0510-OA
By:
- Jianlong Zhuang;
- Chunnuan Chen;
- Wanyu Fu;
- Yuanbai Wang;
- Qianmei Zhuang;
- Yulin Lu;
- Tiantian Xie;
- Ruofan Xu;
- Shuhong Zeng;
- Yuying Jiang;
- Yingjun Xie;
- Gaoxiong Wang
Publication type:
Article
Performance Evaluation of Automated Impedance and Optical Fluorescence Platelet Counts Compared With International Reference Method in Patients With Thalassemia.
Published in:
Archives of Pathology & Laboratory Medicine, 2017, v. 141, n. 6, p. 830, doi. 10.5858/arpa.2016-0222-OA
By:
- Tantanate, Chaicharoen;
- Khowawisetsut, Ladawan;
- Pattanapanyasat, Kovit
Publication type:
Article
High Prevalence of Alpha- and Beta-Thalassemia in the Kadazandusuns in East Malaysia: Challenges in Providing Effective Health Care for an Indigenous Group.
Published in:
Journal of Biomedicine & Biotechnology, 2010, p. 1, doi. 10.1155/2010/706872
By:
- Tan, Jin-Ai Mary Anne;
- Ping-Chin Lee;
- Yong-Chui Wee;
- Kim-Lian Tan;
- Mahali, Noor Fadzlin;
- George, Elizabeth;
- Kek-Heng Chua
Publication type:
Article