Filters

Mallika Fernando, Prasanna Fernando, Thakshila Vipulaguna, Lakshman Perera, Rexan Rodrigo, Marius Suranjan, Roshale Fernando, Sanjaya Paranamana, Sachith Mettananda, B K T P Dayanath, Anuja Premawardhena, Yasintha Costa

Pediatric hematology and oncology 2021;37(4):326-336

Full Text

Abstract

Case series of HbQ-India, a rare alpha globin variant in a referral laboratory setting in South India.

Manu Goyal, Anurag Gupta, Vijay Kumawat, Sreeja T Thekkelakayil, Ayeesha Shaik

Indian journal of pathology & microbiology 2021;63(3):481-484

Full Text

Abstract

Rare hemoglobin variants in Tunisian population.

A Zorai, I Moumni, I Mosbahi, S Abbes, F Guemira, D Chaouachi, K Douzi

International journal of laboratory hematology 2015;37(2):148-54

Full Text

Abstract

Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.

Shirley J Henderson, Adele T Timbs, Janice McCarthy, Alice E Gallienne, Melanie Proven, Michelle J Rugless, Herminio Lopez, Jennifer Eglinton, Dariusz Dziedzic, Matthew Beardsall, Mohamed S M Khalil, John M Old

Hemoglobin 2016;40(2):75-84

Full Text

Abstract

Diagnosis of Hemoglobinopathy and β-Thalassemia by 21 Tesla Fourier Transform Ion Cyclotron Resonance Mass Spectrometry and Tandem Mass Spectrometry of Hemoglobin from Blood.

Christopher L Hendrickson, Alan G Marshall, Chad R Weisbrod, Lissa C Anderson, Archana M Agarwal, Alan L Rockwood, Lidong He

Clinical chemistry 2020;65(8):986-994

Full Text

Abstract

Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity.

Andreas R Huber, Charles Broquet, Benno Röthlisberger, Thomas von Känel, Saskia Brunner-Agten

Hemoglobin 2017;41(1):1-5

Full Text

Abstract

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

Jin Li, Joseph T Glessner, Haitao Zhang, Cuiping Hou, Zhi Wei, Jonathan P Bradfield, Frank D Mentch, Yiran Guo, Cecilia Kim, Qianghua Xia, Rosetta M Chiavacci, Kelly A Thomas, Haijun Qiu, Struan F A Grant, Susan L Furth, Hakon Hakonarson, Patrick M A Sleiman

Human molecular genetics 2013;22(7):1457-64

Free Full Text

Abstract

Results: 1 – 14 / 14

Filters

Expert Opinion

Text Availability

Publication Types

Publication Year

Results for ""alpha-Globins""[mesh_terms]

α-Globin gene mutations in Isfahan Province, Iran.

Characterization and Confirmation of Mildly Unstable Hb Pontoise or α1 63(E12) Ala > Asp and Literature Review.

Hb H disease: clinical course and disease modifiers.

The roles of free iron, heme, haemoglobin, and the scavenger proteins haemopexin and alpha-1-microglobulin in preeclampsia and fetal growth restriction.

2021 update on clinical trials in β-thalassemia.

Diagnosis and Treatment of Alpha Thalassemia Major.

Fetal globin gene inducers: novel agents and new potential.

Microcytic anemia in children: parallel screening for iron deficiency and thalassemia provides a useful opportunity for thalassemia prevention in low- and middle-income countries.

Case series of HbQ-India, a rare alpha globin variant in a referral laboratory setting in South India.

Rare hemoglobin variants in Tunisian population.

Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.

Diagnosis of Hemoglobinopathy and β-Thalassemia by 21 Tesla Fourier Transform Ion Cyclotron Resonance Mass Spectrometry and Tandem Mass Spectrometry of Hemoglobin from Blood.

Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity.

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

Results for
""alpha-Globins""[mesh_terms]