Works matching DE "ALPHA-Thalassemia"

Results: 284

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

Molecular profile of tumors with oligodendroglial morphology: Clinical relevance.

Published in:

2018

By:

Geevar, Tulasi;
Pai, Rekha;
Chacko, Geeta;
Malepathi, Karthik;
Patel, Bimal;
John, Jacob;
Chacko, Ari G;
Balakrishnan, Rajesh;
John, Subashini

Publication type:

journal article

Preimplantation genetic diagnosis of alpha-thalassemia using novel multiplex fluorescent PCR.

Published in:

Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 1, p. 95, doi. 10.1007/s10815-011-9641-6

By:

Piyamongkol, Wirawit;
Vutyavanich, Teraporn;
Sanguansermsri, Torpong

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

A holistic overview of hemoglobinopathies interactions with glycated hemoglobin.

Published in:

Medical Laboratory Observer (MLO), 2022, v. 54, n. 9, p. 1

By:

Flamini, Marco

Publication type:

Article

Too much A<sub>2</sub> -- 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

Increased levels of circulating platelet microparticles as a risk of hypercoagulable state in β-thalassemia intermedia patients.

Published in:

Egyptian Journal of Haematology, 2022, v. 47, n. 3, p. 187, doi. 10.4103/ejh.ejh_14_20

By:

Abdel Aziz, Hanan;
El-Beih, Esam;
Sayed, Douaa;
Afifi, Ola;
Thabet, Ahmad;
Elgammal, Sahar;
Mansor, Shima;
Moeen, Sawsan

Publication type:

Article

Molecular characterization and frequency of transforming growth factor beta 1 gene polymorphism and its relation to bone complications in Egyptian patients with β-thalassemia.

Published in:

Egyptian Journal of Haematology, 2022, v. 47, n. 3, p. 174, doi. 10.4103/ejh.ejh_13_22

By:

Elgawhary, Somaya;
Mohammed, Manal;
Ahmed, Heba;
Elamir, Ahmed;
Abdelaziz, Hossam

Publication type:

Article

Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis.

Published in:

Yemeni Journal for Medical Sciences, 2020, v. 14, n. 1, p. 7, doi. 10.20428/yjms.v14i1.1703

By:

Abdulrahman, Thaker A. A.;
Alhaj, Ali;
Saif, Mokhtar E. M.

Publication type:

Article

HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia.

Published in:

Clinical Hemorheology & Microcirculation, 2021, v. 77, n. 3, p. 267, doi. 10.3233/CH-200951

By:

Joly, Philippe;
Bonello-Palot, Nathalie;
Badens, Catherine;
Pissard, Serge;
Chamouine, Abdourahim;
Bernaudin, Françoise;
Bertrand, Yves;
Connes, Philippe;
Renoux, Céline

Publication type:

Article

Hematologic Parameters Cut-off Assessment of Adult Alpha-Thalassemia Patients in Iran.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2024, v. 18, n. 4, p. 323

By:

Keikhaei, Bijan;
Bitaraf, Saeid;
Mafakher, Ladan;
Galehdari, Hamid;
Saki-Malehi, Amal;
Bahadoram, Mohammad

Publication type:

Article

Spectrum of alpha-globin gene mutations among premarital Baluch couples in southeastern Iran.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2015, v. 9, n. 3, p. 138

By:

Miri-Moghaddam, Ebrahim;
Nikravesh, Abass;
Gasemzadeh, Negin;
Badaksh, Mahin;
Rakhshi, Nahid

Publication type:

Article

Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4-year-old boy.

Published in:

2002

By:

Valenzise, Mariella;
Ferrero, Battista;
Tosi, Teresa;
Ferraris, Silvio;
Silengo, Margherita;
Ferrero, Giovanni Battista;
Tosi, Maria Teresa

Publication type:

journal article

Pregnancies Complicated by Hemoglobin H disease.

Published in:

2016

By:

Joob, Beuy;
Wiwanitkit, Viroj

Publication type:

Letter to the Editor

Can Trimodal Distribution of HbS Levels in Sickle Cell Traits Be Used To Predict the Associated Alpha-Thalassemia For Screening Cases in Central India?

Published in:

Iranian Journal of Pathology, 2016, v. 11, n. 2, p. 133

By:

B. M., WARPE;
A. V., SHRIKHANDE;
S. V., POFLEE

Publication type:

Article

The Adverse Effects of Pregnancies Complicated by Hemoglobin H (HBH) Disease.

Published in:

2015

By:

Rabiee, Maryam;
Shams, Jalal-Aldin;
Zafargandie, Nafiseh

Publication type:

Case Study

Association between alpha-thalassaemia trait, Plasmodium falciparum asexual parasites and gametocyte carriage in a malaria endemic area in Southern Ghana.

Published in:

BMC Research Notes, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13104-019-4181-8

By:

Lamptey, Helena;
Ofori, Michael Fokuo;
Adu, Bright;
Kusi, Kwadwo Asamoah;
Dickson, Emmanuel Kakra;
Quakyi, Isabella;
Alifrangis, Michael

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

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

Diagnosis and prevention of thalassemia.

Published in:

Critical Reviews in Clinical Laboratory Sciences, 2013, v. 50, n. 6, p. 125, doi. 10.3109/10408363.2013.847236

By:

Ip, Ho-Wan;
So, Chi-Chiu

Publication type:

Article

Prenatal Diagnosis and Pregnancy Outcome Analysis of Polyhydramnios.

Published in:

Fetal & Pediatric Pathology, 2016, v. 35, n. 1, p. 21, doi. 10.3109/15513815.2015.1122127

By:

Liu, Li-Ling;
Pang, Li-Hong;
Deng, Bi-Ye

Publication type:

Article

Novel ATRX gene damaging missense mutation c.6740A>C segregates with profound to severe intellectual deficiency without alpha thalassaemia.

Published in:

Indian Journal of Medical Research, 2016, v. 143, n. 1, p. 43, doi. 10.4103/0971-5916.178589

By:

Bouazzi, Habib;
Thakur, Seema;
Trujillo, Carlos;
Alwasiyah, Mohammad Khalid;
Munnich, Arnold

Publication type:

Article

Sickle cell disease in tribal populations in India.

Published in:

Indian Journal of Medical Research, 2015, v. 141, n. 5, p. 509, doi. 10.4103/0971-5916.159492

By:

Colah, Roshan B.;
Mukherjee, Malay B.;
Martin, Snehal;
Ghosh, Kanjaksha

Publication type:

Article

Alpha thalassaemia in tribal communities of coastal Maharashtra, India.

Published in:

Indian Journal of Medical Research, 2014, v. 140, n. 2, p. 231

By:

Deo, Madhav G.;
Pawar, Prakash V.

Publication type:

Article

ATRX loss refines the classification of anaplastic gliomas and identifies a subgroup of IDH mutant astrocytic tumors with better prognosis.

Published in:

Acta Neuropathologica, 2013, v. 126, n. 3, p. 443, doi. 10.1007/s00401-013-1156-z

By:

Wiestler, Benedikt;
Capper, David;
Holland-Letz, Tim;
Korshunov, Andrey;
Deimling, Andreas;
Pfister, Stefan;
Platten, Michael;
Weller, Michael;
Wick, Wolfgang

Publication type:

Article

Prenatal Two- and Three-Dimensional Ultrasound Diagnosis of Limb Reduction Defects Associated with Homozygous α-Thalassemia.

Published in:

Fetal Diagnosis & Therapy, 2006, v. 21, n. 4, p. 374, doi. 10.1159/000092468

By:

Chih-Ping Chen;
Tung-Yao Chang;
Yi-Ning Su;
Chin-Yuan Hsu;
Wayseen Wang

Publication type:

Article

Microchimerism and tolerance following intrauterine transplantation and transfusion for alpha-thalassemia-1.

Published in:

1998

By:

Hayward, A.;
Ambruso, D.;
Battaglia, F.;
Donlon, T.;
Eddelman, K.;
Giller, R.;
Hobbins, J.;
Hsia, Y.E.;
Quinones, R.;
Shpall, E.;
Trachtenberg, E.;
Giardina, P.

Publication type:

journal article

Diagnostik von Hämoglobinopathien: Integrierter Befund für mehr Klarheit.

Published in:

Trillium-Diagnostik, 2024, v. 22, n. 4, p. 246, doi. 10.47184/td.2024.04.02

By:

Piehler, Armin;
Hörmann, Gregor

Publication type:

Article

Management of haemoglobin Barts hydrops fetalis syndrome with exchange transfusions.

Published in:

Internal Medicine Journal, 2020, v. 50, n. 5, p. 638, doi. 10.1111/imj.14823

By:

Ong, Jeremy;
Bowden, Donald;
Kaplan, Zane

Publication type:

Article

Detection of α-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.

Published in:

Malaysian Journal of Pathology, 2017, v. 39, n. 1, p. 17

By:

ALAUDDIN, Hafiza;
LANGA, Mustafa;
MOHD YUSOFF, Malisa;
RAJA SABUDIN, Raja Zahratul Azma;
ITHNIN, Azlin;
ABDUL RAZAK, Noor Farisah;
SARDI, Nor Hidayati;
HUSSIN, Noor Hamidah

Publication type:

Article

The need to perform α‐thalassemia genetic testing in Italian patients with β‐thalassemia trait: A case report.

Published in:

2022

By:

Santoro, Graziano;
Cro, Fabiana;
Poma, Federica;
Kullmann, Cristina;
Lapucci, Cristina;
Ferrari, Maurizio

Publication type:

Case Study

Alpha‐thalassemia. Case report alpha‐thalassemia in a Costa Rican family, A case report.

Published in:

Clinical Case Reports, 2021, v. 9, n. 1, p. 291, doi. 10.1002/ccr3.3518

By:

Solano‐Vargas, Mariela;
Chui, David H. K.;
Rodriguez‐Romero, Walter

Publication type:

Article

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

Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-08986-4

By:

Hamid, Mohammad;
keikhaei, Bijan;
Galehdari, Hamid;
Saberi, Alihossein;
Sedaghat, Alireza;
Shariati, Gholamreza;
Mohammadi-Anaei, Marziye

Publication type:

Article

Pregnancy outcomes in women affected by fetal alpha-thalassemia: a case control study.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-95998-1

By:

Li, Jiangheng;
Yan, Jingli;
Huang, Yongquan;
Wei, Jinlu;
Xie, Bingyan;
Zhu, Maoling;
Jiang, Wu

Publication type:

Article

Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China.

Published in:

Journal of Medical Screening, 2014, v. 21, n. 4, p. 167, doi. 10.1177/0969141314548203

By:

Li, Jian;
Xie, Xing-Mei;
Liao, Can;
Li, Dong-Zhi

Publication type:

Article

Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's.

Published in:

Journal of Medical Screening, 2014, v. 21, n. 3, p. 120, doi. 10.1177/0969141314538611

By:

Prayalaw, Patcharawadee;
Fucharoen, Goonnapa;
Fucharoen, Supan

Publication type:

Article

Relationship between neonatal screening results by HPLC and the number of α-thalassaemia gene mutations; consequences for the cut-off value.

Published in:

Journal of Medical Screening, 2011, v. 18, n. 4, p. 182, doi. 10.1258/jms.2011.011043

By:

Bouva, M. J.;
Sollaino, C.;
Perseu, L.;
Galanello, R.;
Giordano, P. C.;
Harteveld, C. L.;
Cnossen, M. H.;
Schielen, P. C. J. I.;
Elvers, L. H.;
Peters, M.

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

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

The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improve Their Survival.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100516

By:

Rumaney, Maryam Bibi;
Ngo Bitoungui, Valentina Josiane;
Vorster, Anna Alvera;
Ramesar, Raj;
Kengne, Andre Pascal;
Ngogang, Jeanne;
Wonkam, Ambroise

Publication type:

Article

A clinical update of compound heterozygosity for hemoglobin Hekinan II [a27(B8)Glu–Asp; HBA1: c.84G>T] variant in China.

Published in:

Laboratory Medicine, 2024, v. 5, n. 5, p. 615, doi. 10.1093/labmed/lmae023

By:

Pan, Liqiu;
Qiu, Yuling;
Ye, Lihua;
Li, Linlin;
Huang, Yuanyuan;
Mo, Wuning;
Lin, Faquan

Publication type:

Article

Stability of Hemoglobin Constant Spring Identified by Capillary Electrophoresis.

Published in:

Laboratory Medicine, 2023, v. 54, n. 3, p. e91, doi. 10.1093/labmed/lmac130

By:

Jaitheang, Jidapa;
Suksusut, Amornchai;
Settapiboon, Rung;
Amornsiriwat, Supaporn;
Sutcharitchan, Pranee;
Uaprasert, Noppacharn;
Rojnuckarin, Ponlapat

Publication type:

Article

Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele.

Published in:

Laboratory Medicine, 2023, v. 54, n. 1, p. 65, doi. 10.1093/labmed/lmac065

By:

Zhang, Min;
Lin, Zhaodong;
Chen, Meihuan;
Pan, Yali;
Zhang, Yanhong;
Chen, Lingji;
Lin, Na;
Ren, Yuanyuan;
Jia, Hongjin;
Cai, Meiying;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Validation of Microarray for the Simultaneous Detection of Common α- and β-Thalassemia Gene Mutations.

Published in:

Laboratory Medicine, 2019, v. 50, n. 3, p. 306, doi. 10.1093/labmed/lmy087

By:

Pornprasert, Sakorn;
Anurak, Rinradee;
Ruengdit, Chedtapak;
Pienthai, Nattasit;
Tookjai, Monthathip;
Punyamung, Manoo;
Pongpunyayuen, Panida

Publication type:

Article

Clinical Features and Genotypes of Patients with Hemoglobin H Disease in Taiwan.

Published in:

Laboratory Medicine, 2019, v. 50, n. 2, p. 168, doi. 10.1093/labmed/lmy043

By:

Lin, Pei-Chin;
Chang, Tai-Tsung;
Liao, Yu-Mei;
Tsai, Shih-Pien;
Chen, Yen-Chu;
Hsu, Wan-Yi;
Su, Hsiu-Lan;
Zeng, Yu-Sheng;
Tseng, Yu-Hsin;
Chiou, Shyh-Shin

Publication type:

Article

Hematological Analysis in Thai Samples With Deletional and Nondeletional HbH Diseases.

Published in:

Laboratory Medicine, 2018, v. 49, n. 2, p. 154, doi. 10.1093/labmed/lmx068

By:

Pornprasert, Sakorn;
Salaeh, Nur-afsan;
Tookjai, Monthathip;
Punyamung, Manoo;
Pongpunyayuen, Panida;
Treesuwan, Kallayanee

Publication type:

Article