Works matching DE "ALPHA-Thalassemia"

Results: 272

Invasive prenatal diagnosis of α-thalassemia to control Hb Bart's hydrops fetalis syndrome: 15 years of experience.

Published in:

2018

By:

Lai, Ketong;
Li, Shuquan;
Lin, Weixiong;
Yang, Dezhai;
Chen, Wenqiang;
Li, Minqing;
Pang, Lihong;
Chen, Ping

Publication type:

journal 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

False HbA<sub>1c</sub> 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

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

Prevalence of Deletional Alpha Thalassemia and Sickle Gene in a Tribal Dominated Malaria Endemic Area of Eastern India.

Published in:

ISRN Hematology, 2014, p. 1, doi. 10.1155/2014/745245

By:

Purohit, Prasanta;
Dehury, Snehadhini;
Patel, Siris;
Patel, Dilip Kumar

Publication type:

Article

Hemoglobin A<sub>2</sub> Lowered by Iron Deficiency and α-Thalassemia: Should Screening Recommendation for β-Thalassemia Change?

Published in:

ISRN Hematology, 2013, p. 1, doi. 10.1155/2013/858294

By:

Denic, Srdjan;
Agarwal, Mukesh M.;
Dabbagh, Bayan Al;
Essa, Awad El;
Takala, Mohamed;
Showqi, Saad;
Yassin, Javed

Publication type:

Article

Detection of Common Deletional Alpha-Thalassemia Spectrum by Molecular Technique in Kelantan, Northeastern Malaysia.

Published in:

ISRN Hematology, 2012, p. 1, doi. 10.5402/2012/462969

By:

Rosnah, B.;
Rosline, H.;
Zaidah, A. Wan;
Haslina, M. N. Noor;
Marini, R.;
Shafini, M. Y.;
Ain, F. A. Nurul

Publication type:

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

Subgroup stratification of adult diffuse gliomas and outcomes: an adaptation of the updated WHO classification in a resource-constrained environment.

Published in:

Journal of Radiotherapy in Practice, 2021, v. 20, n. 1, p. 55, doi. 10.1017/S1460396919000918

By:

Naveen, T.;
Uday Krishna, A. S.;
Santosh, Vani;
Arivazhagan, A.;
Lokesh, V.

Publication type:

Article

Deletional Alpha-Thalassemia Alleles in Amazon Blood Donors.

Published in:

Advances in Hematology, 2020, p. 1, doi. 10.1155/2020/4170259

By:

Anselmo, Fernanda Cozendey;
Ferreira, Natália Santos;
Mota, Adolfo José da;
Gonçalves, Marilda de Souza;
Albuquerque, Sérgio Roberto Lopes;
Fraiji, Nelson Abrahim;
Ferreira, Ana Carla Dantas;
Moura Neto, José Pereira de

Publication type:

Article

Screening for hemoglobin E trait in pregnant women

Published in:

2004

By:

Sirichotiyakul, S.;
Tongprasert, F.;
Tongsong, T.

Publication type:

journal article

Erythrocyte osmotic fragility test for screening of alpha-thalassemia-1 and beta-thalassemia trait in pregnancy

Published in:

2004

By:

Sirichotiyakul, S.;
Tantipalakorn, C.;
Sanguansermsri, T.;
Wanapirak, C.;
Tongsong, T.

Publication type:

journal article

Molecular prenatal diagnosis of thalassemia in Taiwan.

Published in:

2000

By:

Chern, Schu-Rern;
Chen, Chih-Ping;
Chern, S R;
Chen, C P

Publication type:

journal article

Prenatal strategies for reducing severe thalassemia in pregnancy.

Published in:

1998

By:

Wanapirak, C;
Tongsong, T;
Sirivatanapa, P;
Sa-nguansermsri, T;
Sekararithi, R;
Tuggapichitti, A

Publication type:

journal 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

The Prevalence and Role of Hemoglobin Variants in Biometric Screening of a Multiethnic Population: One Large Health System's Experience.

Published in:

2017

By:

Wilburn, Clayton R.;
Bernard, David W.;
Zieske, Arthur W.;
Andrieni, Julia;
Miller, Tara;
Ping Wang;
Wang, Ping

Publication type:

journal article

Identification of One or Two α-Globin Gene Deletions by Isoelectric Focusing Electrophoresis.

Published in:

American Journal of Clinical Pathology, 2013, v. 140, n. 3, p. 301, doi. 10.1309/AJCPF4UIJKH3EOBY

By:

Agarwal, Archana M.;
Nussenzveig, Roberto H.;
Hoke, Carolyn;
Lorey, Thomas S.;
Greene, Dina N.

Publication type:

Article

Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2577, doi. 10.3390/ijms24032577

By:

Cardiero, Giovanna;
Musollino, Gennaro;
Prezioso, Romeo;
Nigro, Vincenzo;
Lacerra, Giuseppina

Publication type:

Article

SA4503, A Potent Sigma-1 Receptor Ligand, Ameliorates Synaptic Abnormalities and Cognitive Dysfunction in a Mouse Model of ATR-X Syndrome.

Published in:

International Journal of Molecular Sciences, 2018, v. 19, n. 9, p. 2811, doi. 10.3390/ijms19092811

By:

Yamaguchi, Kouya;
Shioda, Norifumi;
Yabuki, Yasushi;
Zhang, Chen;
Han, Feng;
Fukunaga, Kohji

Publication type:

Article

Cut-Off Values of Hematologic Parameters to Predict the Number of Alpha Genes Deleted in Subjects with Deletional Alpha Thalassemia.

Published in:

International Journal of Molecular Sciences, 2017, v. 18, n. 12, p. 2707, doi. 10.3390/ijms18122707

By:

Velasco-Rodríguez, Diego;
Blas, Carlos;
Alonso-Domínguez, Juan-Manuel;
Vega, Gala;
Soto, Carlos;
García-Raso, Aránzazu;
Llamas-Sillero, Pilar

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

Bone microarchitecture deteriorations and a fragility fracture in a patient with beta and alpha heterozygous thalassemia: a case report.

Published in:

Wiener Klinische Wochenschrift, 2017, v. 129, n. 5/6, p. 212, doi. 10.1007/s00508-016-1032-7

By:

Feichtinger, Xaver;
Kocijan, Roland;
Resch, Heinrich;
Muschitz, Christian

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

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

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

The First Asian, Single-Center Experience of Blastocyst Preimplantation Genetic Diagnosis with HLA Matching in Thailand for the Prevention of Thalassemia and Subsequent Curative Hematopoietic Stem Cell Transplantation of Twelve Affected Siblings.

Published in:

BioMed Research International, 2020, p. 1, doi. 10.1155/2020/5292090

By:

Tiewsiri, Kasorn;
Manipalviratn, Somjate;
Sutheesophon, Warachaya;
Vanichsetakul, Preeda;
Thaijaroen, Piyarat;
Ketcharoon, Pagawadee;
Bradley, Cara K.;
McArthur, Steven J.;
Krutsawad, Weena;
Marshall, James T. A.;
Papadopoulos, Konstantinos I.

Publication type:

Article

A novel high-throughput molecular counting method with single base-pair resolution enables accurate single-gene NIPT.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50378-8

By:

Tsao, David S.;
Silas, Sukrit;
Landry, Brian P.;
Itzep, Nelda P.;
Nguyen, Amy B.;
Greenberg, Samuel;
Kanne, Celeste K.;
Sheehan, Vivien A.;
Sharma, Rani;
Shukla, Rahul;
Arora, Prem N.;
Atay, Oguzhan

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

Role of Fetal Blood Sampling in the Prenatal Diagnosis of Thalassemia.

Published in:

Balkan Medical Journal, 2023, v. 40, n. 5, p. 380, doi. 10.4274/balkanmedj.galenos.2023.2023-5-92

By:

Xing-Mei Xie;
Dong-Zhi Li;
Yenilmez, Ebru Dündar

Publication type:

Article

Cord Blood Hematological Parameters of Fetuses Detected Different Thalassemia Genotypes in the Second Trimester of Pregnancy.

Published in:

Balkan Medical Journal, 2023, v. 40, n. 4, p. 279, doi. 10.4274/balkanmedj.galenos.2023.2023-1-86

By:

Yenilmez, Ebru Dündar;
Tuli, Abdullah

Publication type:

Article

The Applicability of Haarlem Integrated Diagnostic System in Diffuse Glial Tumors and Molecular Methods Affecting Prognosis.

Published in:

Balkan Medical Journal, 2019, v. 36, n. 4, p. 222, doi. 10.4274/balkanmedj.galenos.2018.2018.1221

By:

Terzi, Neslihan Kaya;
Yılmaz, İsmail;
Öz, Ayşim Büge

Publication type:

Article

Prevalence of microcytosis in cord blood samples and admitted neonates in Tehran, Iran.

Published in:

Iranian Journal of Pediatric Hematology & Oncology, 2016, v. 6, n. 3, p. 166

By:

Goudarzipour, Kourosh;
PeymanEshghi;
Tara, Zahra;
Afjeh, Abolfazl;
FaridSolat;
Shiravi, Masoumeh

Publication type:

Article

Demographic data of patients with β-thalassemia major recorded in the electronic system in the north of Iran, 2016.

Published in:

Tanzania Journal of Health Research, 2018, v. 20, n. 3, p. 1, doi. 10.4314/thrb.v20i3.3

By:

KOSARYAN, MEHRNOUSH;
KARAMI, HOSSEIN;
DARVISHI-KHEZRI, HADI;
AKBARZADEH, ROSSETA;
ALIASGHARIAN, AILY;
BROMAND, KHADIJEH

Publication type:

Article

Prevalence and molecular characterization of alpha-thalassemia among newborns in Ardabil Province.

Published in:

Electronic Physician, 2020, v. 12, n. 2, p. 7703, doi. 10.19082/7703

By:

Fathi, Afshin;
Damandan, Mahshid;
Valizadeh, Mehdi;
Farshi, Yadolah;
Moradpour, Rouhallah

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

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

Three Different Co-existing α-Thalassemia Mutations and Sickle Cell Disease in a Pregnant Woman.

Published in:

Laboratory Medicine, 2013, v. 44, n. 1, p. e72, doi. 10.1309/LMKQEVYZFO7MV6RZ

By:

Fakher Rahim;
Fateme Hamid;
Hamid Galedari;
Gholamreza Khamisipour;
Bijan Keikhaei;
Kaveh Jaseb;
Najmaldin Saki

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

Molecular patterns of alpha-thalassemia in the kingdom of Saudi Arabia: identification of prevalent genotypes and regions with high incidence.

Published in:

Thrombosis Journal, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12959-023-00560-w

By:

Alhuthali, Hayaa M.;
Ataya, Eman F.;
Alsalmi, Alaa;
Elmissbah, Triq E;
Alsharif, Khalaf F;
Alzahrani, Hind A.;
Alsaiari, Ahad Amer;
Allahyani, Mamdouh;
Gharib, Amal F.;
Qanash, Husam;
Elmasry, Heba M.;
Hassanein, Doha Elsayed

Publication type:

Article

Third-generation sequencing identified a novel complex variant in a patient with rare alpha-thalassemia.

Published in:

BMC Pediatrics, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12887-024-04811-1

By:

Zhou, Cong;
Du, Yepei;
Zhang, Haixia;
Wei, Xing;
Li, Rui;
Wang, Jing

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