Hemoglobin

Keyphrases

Publications

volume 48, number 1, 2024

John S Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]. Hemoglobin 48 (1) (2024)
M Mamata, G Padma, T Pragna Laxmi, K Saroja, Dalal Ashwin, Jain Suman
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia. Hemoglobin 48 (1) (2024)
Shao-Min Wu, Chan Li, Su-Ran Huang, Fan Jiang, Dong-Zhi Li
A 6-Year Follow-up of a Chinese Child with Homozygous β 0 -Thalaasemia and a Heterozygous KLF1 Mutation. Hemoglobin 48 (1) (2024)
Adama Isah Ladu, Mairo Usman Kadaura, Mohammed Dauda, Abubakar Sadiq Baba, Nasir Garba Zango, Caroline Jeffery, Abubakar Farate, Adekunle Adekile, Imelda Bates
Malaria Infection in Patients with Sickle Cell Disease in Nigeria: Association with Markers of Hyposplenism. Hemoglobin 48 (1) (2024)
Najmaddin S H Khoshnaw, Jawhar J Omar, Zahir S Hussein, Rebar N Mohammed
Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq. Hemoglobin 48 (1) (2024)
Dan Xie, Yuanyuan Han, Wenyi Zhang, Jiangfen Wu, Banquan An, Shengwen Huang, Fa Sun
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation. Hemoglobin 48 (1) (2024)
Wei-Bin Li, Li-Hong Zheng, You-Qiong Li
Hb Hebei [α20 (B1) His→Leu; HBA2 :C.62A > T]: A Novel Hemoglobin Variant Found during Measurement of Glycated Hemoglobin. Hemoglobin 48 (1) (2024)
Meihuan Chen, Aixiang Lv, Siwen Zhang, Junhao Zheng, Min Zhang, Lingji Chen, Qianqian He, Jianlong Zhuang, Na Lin, Liangpu Xu, Hailong Huang
First Report of Filipino β 0 -Thalassemia/β-Thalassemia in a Chinese Family. Hemoglobin 48 (1) (2024)
Wolney de Oliveira Taques, Gabriele Curvo Bett, Bárbara Lucia Barbosa de Moraes, Iasmin Medeiros, Cor Jesus Fernandes Fontes, Ruberlei Godinho de Oliveira
Factors Associated with Overt Stroke in Children and Adolescents with Sickle Cell Disease: A Retrospective Cohort Study. Hemoglobin 48 (1) (2024)
Li-Hong Zheng, Liang Liang, Jin-Ping Bai, Han-Xian Liao, You-Qiong Li
Misdiagnosis of β-Thalassemia Major Due to Chinese G γ+( A γδβ) 0 -Thalassemia Combined with β 0 -Thalassemia. Hemoglobin 48 (1) (2024)
M Mamata, G Padma, T Pragna Laxmi, K Saroja, Dalal Ashwin, Jain Suman
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia. Hemoglobin 48 (1) (2024)
Shao-Min Wu, Chan Li, Su-Ran Huang, Fan Jiang, Dong-Zhi Li
A 6-Year Follow-up of a Chinese Child with Homozygous β 0 -Thalaasemia and a Heterozygous KLF1 Mutation. Hemoglobin 48 (1) (2024)
Ampaiwan Chuansumrit, Duantida Songdej, Nongnuch Sirachainan, Praguywan Kadegasem, Pawaree Saisawat, Witaya Sungkarat, Ketsuda Kempka, Noppawan Tangbubpha
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload. Hemoglobin 48 (1) (2024)
Olivia Elieff, Lesley Rawlings, Cuong Pham, Samantha Mihalopoulos, Denae Henry, Keryn Simons, Heather Tapp
Hb Mizuho Case Report; Early Genomic Testing Facilitates a Life Changing Diagnosis. Hemoglobin 48 (1) (2024)
Gayatri Desai, Kapilkumar Dave, Sumeet Devare, Shrey Desai
Ethical and Clinical Considerations in the Use of Hydroxyurea in Pregnant Women with Sickle Cell Disease. Hemoglobin 48 (1) (2024)
John S Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]. Hemoglobin 48 (1) (2024)
Wei-Bin Li, Li-Hong Zheng, You-Qiong Li
Hb Hebei [α20 (B1) His→Leu; HBA2 :C.62A > T]: A Novel Hemoglobin Variant Found during Measurement of Glycated Hemoglobin. Hemoglobin 48 (1) (2024)
Shao-Min Wu, Chan Li, Su-Ran Huang, Fan Jiang, Dong-Zhi Li
A 6-Year Follow-up of a Chinese Child with Homozygous β 0 -Thalaasemia and a Heterozygous KLF1 Mutation. Hemoglobin 48 (1) (2024)
Najmaddin S H Khoshnaw, Jawhar J Omar, Zahir S Hussein, Rebar N Mohammed
Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq. Hemoglobin 48 (1) (2024)
Wolney de Oliveira Taques, Gabriele Curvo Bett, Bárbara Lucia Barbosa de Moraes, Iasmin Medeiros, Cor Jesus Fernandes Fontes, Ruberlei Godinho de Oliveira
Factors Associated with Overt Stroke in Children and Adolescents with Sickle Cell Disease: A Retrospective Cohort Study. Hemoglobin 48 (1) (2024)
Li-Hong Zheng, Liang Liang, Jin-Ping Bai, Han-Xian Liao, You-Qiong Li
Misdiagnosis of β-Thalassemia Major Due to Chinese G γ+( A γδβ) 0 -Thalassemia Combined with β 0 -Thalassemia. Hemoglobin 48 (1) (2024)
Ampaiwan Chuansumrit, Duantida Songdej, Nongnuch Sirachainan, Praguywan Kadegasem, Pawaree Saisawat, Witaya Sungkarat, Ketsuda Kempka, Noppawan Tangbubpha
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload. Hemoglobin 48 (1) (2024)
Dan Xie, Yuanyuan Han, Wenyi Zhang, Jiangfen Wu, Banquan An, Shengwen Huang, Fa Sun
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation. Hemoglobin 48 (1) (2024)
Adama Isah Ladu, Mairo Usman Kadaura, Mohammed Dauda, Abubakar Sadiq Baba, Nasir Garba Zango, Caroline Jeffery, Abubakar Farate, Adekunle Adekile, Imelda Bates
Malaria Infection in Patients with Sickle Cell Disease in Nigeria: Association with Markers of Hyposplenism. Hemoglobin 48 (1) (2024)
Olivia Elieff, Lesley Rawlings, Cuong Pham, Samantha Mihalopoulos, Denae Henry, Keryn Simons, Heather Tapp
Hb Mizuho Case Report; Early Genomic Testing Facilitates a Life Changing Diagnosis. Hemoglobin 48 (1) (2024)
Gayatri Desai, Kapilkumar Dave, Sumeet Devare, Shrey Desai
Ethical and Clinical Considerations in the Use of Hydroxyurea in Pregnant Women with Sickle Cell Disease. Hemoglobin 48 (1) (2024)
John S Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]. Hemoglobin 48 (1) (2024)
M Mamata, G Padma, T Pragna Laxmi, K Saroja, Dalal Ashwin, Jain Suman
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia. Hemoglobin 48 (1) (2024)
Meihuan Chen, Aixiang Lv, Siwen Zhang, Junhao Zheng, Min Zhang, Lingji Chen, Qianqian He, Jianlong Zhuang, Na Lin, Liangpu Xu, Hailong Huang
First Report of Filipino β 0 -Thalassemia/β-Thalassemia in a Chinese Family. Hemoglobin 48 (1) (2024)

volume 48, number 2, 2024

John S Waye, Meredith Hanna, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia. Hemoglobin 48 (2) (2024)
Johanne Kodal Breinholt, Andreas Glenthoej, Mustafa Vakur Bor
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature Review. Hemoglobin 48 (2) (2024)
Maria Vousvouki, Evangelia-Eleni Delaki, Effrosyni Boutou, Eleni Yfanti, Genovefa Mantzou, Christina Karipidou, Athanasios Vyzantiadis, Athina Efstathiou, Maria Dimopoulou, Efthymia Vlachaki, Stamatia Theodoridou
A New α1-Globin Variant, Hb Ormylia [ HBA1 :c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece. Hemoglobin 48 (2) (2024)
John S Waye, Meredith Hanna, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia. Hemoglobin 48 (2) (2024)
Maria Vousvouki, Evangelia-Eleni Delaki, Effrosyni Boutou, Eleni Yfanti, Genovefa Mantzou, Christina Karipidou, Athanasios Vyzantiadis, Athina Efstathiou, Maria Dimopoulou, Efthymia Vlachaki, Stamatia Theodoridou
A New α1-Globin Variant, Hb Ormylia [ HBA1 :c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece. Hemoglobin 48 (2) (2024)
Hua Jiang, Dong-Zhi Li
Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report. Hemoglobin 48 (2) (2024)
Nada Assaf, Roba El Zibaoui, Carla Monsef, Tania Abi Nassif, Miguel Abboud, Soha Yazbek
Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and HBA2 : C.*94A > G Mutation. Hemoglobin 48 (2) (2024)
Dewen Liu, Xuejuan Nong, Fengming Lai, Chen Nong, Taizhong Wang, Yulian Tang
Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage. Hemoglobin 48 (2) (2024)
Samin Alavi, Soha Mohammadimoghaddam, Hossein Najmabadi, Sina Maghsoudlou
The First Iranian Case of Unstable Hemoglobin Santa Ana. Hemoglobin 48 (2) (2024)
John S Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup). Hemoglobin 48 (2) (2024)
Samin Alavi, Soha Mohammadimoghaddam, Hossein Najmabadi, Sina Maghsoudlou
The First Iranian Case of Unstable Hemoglobin Santa Ana. Hemoglobin 48 (2) (2024)
Nada Assaf, Roba El Zibaoui, Carla Monsef, Tania Abi Nassif, Miguel Abboud, Soha Yazbek
Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and HBA2 : C.*94A > G Mutation. Hemoglobin 48 (2) (2024)
Hui-Ming Lin, Liang Liang, Yi-Jiao Cai, Li-Hong Zheng, Qing-Peng Qin, You-Qiong Li
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A]. Hemoglobin 48 (2) (2024)
Hua Jiang, Dong-Zhi Li
Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report. Hemoglobin 48 (2) (2024)
Hui-Ming Lin, Liang Liang, Yi-Jiao Cai, Li-Hong Zheng, Qing-Peng Qin, You-Qiong Li
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A]. Hemoglobin 48 (2) (2024)
Nasir A S Al-Allawi, Sulav D Atroshi, Regir K Sadullah, Adil Abozaid Eissa, Gernot Kriegshäuser, Shaima Al-Zebari, Shatha Qadir, Dilan Khalil, Christian Oberkanins
A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia. Hemoglobin 48 (2) (2024)
Nicki Chin, Monika Rani Asnani
Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life. Hemoglobin 48 (2) (2024)
Johanne Kodal Breinholt, Andreas Glenthoej, Mustafa Vakur Bor
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature Review. Hemoglobin 48 (2) (2024)
John S Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfonsam
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup). Hemoglobin 48 (2) (2024)
Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Prasad
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis. Hemoglobin 48 (2) (2024)
Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Prasad
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis. Hemoglobin 48 (2) (2024)