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Hemoglobin: International Journal for Hemoglobin Research

Hemoglobin: International Journal for Hemoglobin Research

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中文名称：血红蛋白：国际血红蛋白研究杂志

ISSN：0363-0269
出版周期：-

发文量：681

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1.Patient Involvement as Experts in the Development and Assessment of a Smartphone App as a Patient Education Tool for the Management of Thalassemia and Iron Overload Syndromes

机译：患者参与作为智能手机应用程序的发展和评估作为患者教育工具的专家，以管理中西血症和铁过载综合征
- 作者：Ward Richard;Taha Karim M.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- Adherence;
- chelation;
- self-management;
- smartphone;
- thalassemia;
2.Analysis of Gene Mutation Types of alpha-and beta-Thalassemia in Fuzhou, Fujian Province in China

机译：福建省福州福州福州和β-地中海贫血基因突变类型分析
- 作者：Chengbo Xu;Bin Liao;Yan Qi;Zhenping Huangfu;Jiawei Chen Yining Chen
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- alpha-Thalassemia (alpha-thal);
- beta-thalassemia (beta-thal);
- gene mutation type;
3.A Novel 31.1kb alpha-Thalassemia Deletion (--(MEX3)) Found in a Mexican Family

机译：在墨西哥家庭中发现的新型31.1KBα-Thalassemia删除（ - （MEX3））
- 作者：Renteria-Lopez Victor M.;Perea-Diaz Francisco J.;Rizo-delaTorre Lourdes C.;Sanchez-Lopez Josefina Y.;Ibarra-Cortes Bertha
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Alu sequences;
- alpha-thalassemia (alpha-thal);
- Mexico;
- novel deletion;
4.The Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in (3-Thalassemia Major

机译：运动应激超声心动图的作用，测定亚临床心脏受累（3-Thalassemia专业
- 作者：Mozhgan Parsaee
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
5.Molecular Characterization of -Thalassemia Mutations in Central Vietnam

机译：越南中央血栓溶膜突变的分子特征
- 作者：Doro Maria G.;Casu Giuseppina;Frogheri Laura;Persico Ivana;Le Phan Minh Triet;Phan Thi Thuy Hoa;Nguyen Huy Hoang;Pirastru Monica;Mereu Paolo;Cucca Francesco;Masala Bruno
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Allele frequency;
- beta-globin gene;
- beta-thalassemia (beta-thal);
- Central Vietnam;
- mutation;
6.Identification of Three Types of alpha-thalassemia Deletion,-alpha21.9,-alpha2.4, and--THAI, and Their Frequencies, in One Family in the Population of Southern Guangxi Zhuang Autonomous Region, People’s Republic of China

机译：中华民国广西壮族自治区南部人口的一个家庭中，鉴定三种类型的α-丘脑血症缺失， - alpha21.9，-alpha2.4和 - 泰国及其频率
- 作者：Wanrong Pang;Ju Long;Xunjin Weng;Qiongying Fan;Lei Sun;Zhijian Pan Zuqian Fan
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Guangxi Zhuang Autonomous Region;
- Thalassemia;
- --THAI;
- -a21.9;
- -alpha2.4;
7.Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [44(CE2)ProSer (1), CCG > TCG; HBA1: c.133C > T], a New -Globin Variant Found in a Pregnant Thai Woman

机译：HB Wiangpapao的血液学特征及分子诊断方面[44（CE2）较胜利（1），CCG> TCG; HBA1：C.133C> T]，在怀孕的泰国女子中发现了一种新的葡萄酒变体
- 作者：Panyasai Sitthichai;Pornprasert Sakorn
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
8.A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as (3-Thalassemia Intermedia Due to a KLF1 Gene Mutation

机译：由SPTB基因的新型纯合突变引起的遗传球致胞致症的情况误诊为（由于KLF1基因突变引起的3-丘脑血症患者
- 作者：Kun Yang
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
9.Prevalence of alpha-Thalassemia in the Egyptian Population

机译：埃及人口中α-地中海贫血的患病率
- 作者：Ilham Youssry;Ayman El Badawy;Rania M. Samy;Niveen Salama;Dalia Abd Elaziz Samia Rizk
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- alpha-Thalassemia (alpha-thal);
- Egypt;
- deletional genotypes;
- polymerase chain reaction (PCR) analysis;
10.MS-275 Chemical Analogues Promote Hemoglobin Production and Erythroid Differentiation of K562 Cells

机译：MS-275化学类似物促进K562细胞的血红蛋白产生和红细胞分化
- 作者：Stella Voskou
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
11.Evaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate -Thalassemia Trait from Iron Deficiency Anemia in the Thai Population

机译：施用红细胞指标和配方组合在泰国人群中施用铁缺血性贫血分析的施用
- 作者：Pornprasert Sakorn;Thongsat Choosak;Panyachadporn Uraiporn
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-Thalassemia (-thal);
- formulas;
- iron deficiency anemia;
- microcytic anemia;
- 11T score;
12.Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newboms and Adults at the Ramathibodi Hospital, Bangkok, Thailand

机译：曼谷，曼谷，泰国曼谷医院幼稚与成人血糖和葡萄糖-6-磷酸脱氢酶缺乏的患病率
- 作者：Wansa Banyatsuppasin;Sumalee Jindadamrongwech;Anchalee Limrungsikul Punnee Butthep
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
13.Hb Moscva [beta24(B6)Gly->Asp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient

机译：Hb moscva [beta24（b6）gly-> asp（ggt> gat），hbb：c.74g> a]：新发现的不稳定血红蛋白作为毛里塔尼亚患者的de novo突变
- 作者：Sidi M. Ghaber;Nawel Trabelsi;Mohamed L. Salem;Faten Haddad;Aminetou Abba;Imen Darragi Salem Abbes
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- De novo mutation;
- Hb Moscva;
- unstable hemoglobin;
14.Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia

机译：突尼斯镰状细胞疾病患者的因子V leiden G1691A，凝血酶原G20210A和MTHFR C677T和A1298C突变
- 作者：Rim Belhaj Nefissi;Radhouene Doggui;Faida Ouali;Taieb Messaoud Nasreddine Gritli
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Hemoglobinopathy;
- polymorphisms;
- sickle cell disease;
- thrombophilic mutations;
- thrombosis;
15.Hb Oslo [beta42(CD1)Phe!Ile; HBB: c.127T>A]: A Novel Unstable Hemoglobin Variant Found in a Norwegian Patient

机译：HB Oslo [Beta42（CD1）PHE！ILE; HBB：C.127T> A]：在挪威患者中发现了一种新的不稳定血红蛋白变体
- 作者：Runa M. Grimholt;Anne Vestli;Petter Urdal;Anne Grete Bechensteen;Bente Fjeld;Bjorn Dalhus Olav Klingenberg
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-Globin gene;
- hemoglobinopathy;
- hemolysis;
- hemolytic anemia;
- unstable hemoglobin (Hb);
16.Left Ventricular Diastolic Dysfunction in b-Thalassemia Major with Heart Failure

机译：B-Thalassemia左心室舒张功能障碍，心力衰竭
- 作者：Luigi Mancuso;Angela Vitrano;Andrea Mancuso;Massimiliano Saccoa;Antonietta Ledda Aurelio Maggio
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
17.Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with beta-Thalassemia/Hb E (HBB: c.79G>A) Disease

机译：Hb Q-Thailand（HBA1：C.223g> C）的复杂相互作用与β-秋季血症/ HB E（HBB：C.79g> A）疾病
- 作者：Sitthichai Panyasai;Surada Satthakarn Sakorn Pornprasert
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
18.Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C(HBB: c.19G>A)

机译：Hb D-Ibadan（HBB：C.263C> A）和Hb C（HBB：C.19G> A）复合杂合性
- 作者：Sirisha Kundrapu;Nafiseh Janaki Howard J. Meyerson
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Hb C;
- Hb D-Ibadan;
- hemoglobinopathy;
19.The Hb E (HBB: c.79G A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- -(SEA) -Thalassemia-1 Carriers are Dependent on Hemoglobin Levels

机译：Hb E（HBB：C.79g＆GT; a），平均碎石体积，平均血小杂小血红蛋白截止点，双杂合HB E / - （海） - 邻血症-1载体依赖于血红蛋白水平
- 作者：Leckngam Prapapun;Limweeraprajak Ektong;Kiewkarnkha Tiemjan;Tatu Thanusak
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Anemia;
- double heterozygosity for Hb E;
- --(SEA) -thal-1;
- Hb E level;
- heterozygous Hb E;
- total Hb levels;
20.Preliminary Evaluation of a Point-of-Care Testing Device (SickleSCAN) in Screening for Sickle Cell Disease

机译：对镰状细胞疾病筛查筛查点的护理点测试装置（SickleScan）的初步评估
- 作者：Nwegbu Maxwell M.;Isa Hezekiah A.;Nwankwo Biyaya B.;Okeke Chinedu C.;Edet-Offong Uduak J.;Akinola Norah O.;Adekile Adekunle D.;Aneke John C.;Okocha Emmanuel C.;Ulasi Thomas;Abjah Usman;Ugwu Ngozi I.;Okolo Angela A.;Madu Anazoeze;Emodi Ifeoma;Girei Ahmed;Balogun Taiwo M.;Diaku-Akinwumi Ijeoma N.;Ohiaeri Chinatu;Brown Biobele J.;Olaniyi John A.;Hassan Abdulaziz;Awwalu Sani;Okoh Dorothy A.;Nnodu Obiageli E.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Point-of-care;
- screening;
- sensitivity;
- sickle cell disease;
- specificity;
21.Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India

机译：在印度奥迪沙州镰状细胞病变患者急性疼痛发作频率的红细胞阵营
- 作者：Bimal P. Jit
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
22.Congenital Nonspherocytic Hemolytic Anemia Caused by Kruppel-Like Factor 7 Gene Variants: Another Case Report

机译：先天性非蕨类植物溶血性贫血引起的Kruppel样因子7基因变体：另一种案例报告
- 作者：Hua Jiang
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
23.A Novel Human beta-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with beta-Thalassemia Trait

机译：一种新型人β-珠蛋白基因变体[Hb London-Ontario，HBB：C.332T> G]与患者中的输血依赖性贫血有关，血红蛋白电泳模式与β-地中海血症特征一致
- 作者：Marc N. Bienz
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
24.Quantitative Trait Loci Influencing Hb F Levels in Southern Thai Hb E (HBB:c.79G>A) Heterozygotes

机译：影响南部HB E水平的定量特质基因座（HBB：C.79G> A）杂合子
- 作者：Aumpika Kesornsit;Nutjaree Jeenduang;Dararat Horpet;Thunyaluk Plyduang Manit Nuinoon
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- BCL11A polymorphism;
- HBS1L polymorphism;
- Hb F levels;
- heterozygous Hb E;
- Thai population;
- XmnI polymorphism;
25.Relationship Between Social Determinants of Health and the Thalassemia Prenatal Diagnosis Test in Zahedan, South Eastern Iran

机译：伊朗Zahedan Zahedan社会决定因素与地中海贫血产前诊断试验的关系
- 作者：Narjes Sargolzaie;Mostafa Montazer Zohour;Erfan Ayubi Fahimeh Shahraki
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-Thalassemia (beta-thal);
- prenatal diagnosis (PND);
- social determinants of health (SDH);
26.Polymorphisms of a-Globin Genes Compromise Poiymerase Chain Reaction-Based alpha-Thalassemia Genotyping in Three Chinese Families

机译：A-球蛋白基因的多态性危及三个中国家庭的基于Poiymerase链反应的α-Thalassemia基因分型
- 作者：Manna Sun;Jiwu Lou;Ying Zhag;Youqing Fu;Yunshi Dai Yanhui Liu
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
27.beta-Thalassemia Mutations in Jamaica: Geographic Variation in Small Communities

机译：牙买加的β-地中海贫血突变：小社区的地理变异
- 作者：Serjeant Graham R.;Serjeant Beryl E.;Mason Karlene P.;Happich Margit;Kulozik Andreas E.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-Thalassemia (beta-thal) mutation;
- Jamaica;
- sickle cell disease;
28.Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China

机译：浙江省湖州地区血红蛋白的流行病学，中国东南
- 作者：Ding Zhong-Ying;Shen Guo-Song;Zhang Su;He Ping-Ya
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- Capillary electrophoresis (CE);
- hemoglobin (Hb);
- variant;
- high resolution melting analysis (HRM);
- iron deficiency;
- thalassemia;
29.Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough {HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del)

机译：HB Peterborough复合杂合子的患者患者患者溶血（HBB：C.334g> T）和HB Lepore-Boston-Washington（NG_000007.3：G.63632_71046DEL）
- 作者：Charles Agbuduwe
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
30.New Insights on -Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G > A) Patients with High Levels of Hb F

机译：对加沙巴勒斯坦人口的新见解：高水平HB F患者纯合子IVS-I-1（HBB：C.92 + 1G> A）高频和较高较高的表型
- 作者：Ghoti Hussam;Fibach Eitan;Rachmilewitz Eliezer A.;Jeadi Hisham;Filon Dvora
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-Thalassemia (-thal);
- Hb F;
- mutations;
31.Rare Association of Hb D-Los Angeles (HBB: c.364GC) with Hb H Disease: Diagnosis and Clinical Implications

机译：HB D-LOS Angeles（HBB：C.364G＆GT; C）罕见的联合协会，具有HB H病：诊断和临床意义
- 作者：Zioga Aikaterini;Thanopoulou Eleni;Hatzi Elissavet;Chaliasos Nikolaos;Georgiou Ioannis;Makis Alexandros
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- alpha-Thalassemia (alpha-thal);
- Hb D-Los Angeles (HBB: c.364Gamp;
- gt;
- C);
32.Complex Interaction of Hb Q-Thailand with (0)- and (0)-Thalassemia in a Chinese Family

机译：Hb Q-Thailand与（0） - 和（0） - 在中国家庭中的复杂相互作用
- 作者：He Sheng;Qin Qian;Lin Li;Chen Qiuli;Yi Shang;Wei Honhwei;Du Juan;Zheng Chenguang;Qiu Xiaoxia;Chen Biyan
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- (0)-Thalassemia ((0)-thal);
- (0)-thalassemia ((0)-thal);
- genetic counseling;
- hemoglobinopathies;
- Hb Q-Thailand;
33.Double Heterozygosity for Hb Durham-N.C. (HBB: c.344T>C) [p114(G16)Leu->Pro] and the IVS-l-110 {HBB: c.93-21G>A) Causing a Severe beta-Thalassemia Phenotype

机译：HB Durham-N.C的双重杂合性。（HBB：C.344T> C）[P114（G16）Leu-> Pro]和IVS-L-110 {HBB：C.93-21G> A），导致严重的β-脑血症表型
- 作者：Monica Cannata
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
34.Hematological and Molecular Characterization of a Novel Hb A(2) Variant with Homozygous alpha-Thalassemia-2 in a Southern Thai Individual

机译：在泰国南部个体中具有纯合的HB A（2）变种的新型HB A（2）变种的血液学和分子表征
- 作者：Nuinoon Manit;Jeenduang Nutjaree;Kesornsit Aumpika;Horpet Dararat;Plyduang Thunyaluk
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Hb A(2) variant;
- novel delta-globin gene mutation;
- Southern Thai population;
35.Quality of Life of Pakistani Children with beta-Thalassemia Major

机译：巴基斯坦儿童的生活质量β-地中海贫民主义者
- 作者：Yasmeen Humaira;Hasnain Shahida
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-Thalassemia major (beta-TM);
- Pakistan;
- quality of life (QoL);
- transfusion-dependent QoL (TranQol);
36.Utility of Transient Elastography in Estimating Hepatic Iron Concentration in Comparison to Magnetic Resonance Imaging in Patients Who are Transfusion-Dependent: A Canadian Center Experience

机译：瞬态弹性成像估算肝脏铁浓度与输血依赖的患者的磁共振成像相比：加拿大中心经验
- 作者：Ou George;Ko Hin Hin;Tiwari Pari;Sandhu Navdeep;Galorport Cherry;Lee Terry;Ezzat Hatoon
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Iron overload;
- magnetic resonance imaging (MRI);
- thalassemia;
- transfusion;
- transient elastography (TE);
37.Insights into the Progression of Labile Hb A1c to Stable Hb A1c via a Mechanistic Assessment of 2,3-Bisphosphoglycerate Facilitation of the Slow Nonenzymatic Glycation Process

机译：通过对慢性非酶促糖化过程的2,3-双次磷酸盐促进的机制评估，在稳定HB A1C进展中探讨了稳定的HB A1C
- 作者：Christina R. Mottishaw
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
38.Hb Hornchurch [beta43(CD2)Glu->Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of beta-Thalassemia in a Chinese Family

机译：HB Hornchurch [Beta43（CD2）Glu-> Lys; HBB：C.130G> A]损害了中国家庭的β-地中海贫血的分子诊断
- 作者：Yuan Zhao;Lv-Yin Huang;Fan Jiang;Jian-Ying Zhou;Xing-Mei Xie Dong-Zhi Li
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-thalassemia (beta-thal);
- Hb Hornchurch;
- double heterozygote;
- reverse dot-blot hybridization;
39.Association of the CCR5A32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients

机译：埃及患者中CCR5A32突变基因型与镰状细胞疾病的关联
- 作者：Maha H. El Sissy
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
40.A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin

机译：在未解释的起源的慢性溶血性贫血的患者中，一种新的稳定变体（HB Hachioji或HbB：C.187C> T）的巧合发现
- 作者：Ferania Mella;Yasuhiro Yamashiro;Chris Adhiyanto;Tatehiko Tanaka;Takenori Nitta;Yuki Amao Masafumi Kimoto
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Abnormal hemoglobin (Hb);
- beta-globin gene variant;
- Hb Hachioji;
41.Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in beta-Thalassemia Intermedia: A Validation Cohort Study

机译：基因组生物标志物在羟基脲疗法和β-地中海贫血血症中胎儿血红蛋白水平增加的作用：验证队列研究
- 作者：Alexra Kolliopoulou;Stavroula Siamoglou
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
42.Genetic Background of p-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new (3°-Thalassemia Frameshift Mutation {HBB: c.374dup; p.Pro126Thrfs*15)

机译：p-thalassemia遗传背景在东北阿尔及利亚的评估剧本和新的评分和新的（3°-thalassemia frameshift突变{hbb：c.374dup; p.pro126thrfs * 15）
- 作者：Wissem Abdaoui
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
43.Hb Milano [alpha109(G16)Leu->Pro (CTOCCG); HBA1: c.329T>C]: A Novel Variant on the alpha.1-Globin Gene in an Italian Family

机译：HB Milano [alpha109（g16）leu-> pro（ctoccg）; HBA1：C.329T> C]：意大利家庭α-珠蛋白基因的一种新型变体
- 作者：Cristina Curcio
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
44.Clinical Course of Two Children with Unstable Hemoglobins: The Effect of Hydroxyurea Therapy

机译：两个血红蛋白的两个儿童临床进程：羟基脲疗法的影响
- 作者：Loovers Harriet M.;Tamminga Nienke;Mulder Andre B.;Tamminga Rienk Y. J.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- Hemoglobinopathy;
- Hb Koln;
- Hb Volga;
- hydroxyurea (HU);
- pediatric;
- unstable hemoglobin;
45.Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [alpha52(E1)Ser->Cys (TCT>TGT); HBA1: C.158OG], and the - -SEA (Southeast Asian) alpha-Thalassemia Deletion

机译：用于不稳定新型血红蛋白变体的复方杂合子，HB Dongguan [α52（E1）Ser-> Cys（TCT> TGT）; HBA1：C.1580OG]， - -SEA（东南亚）α-地中海贫血删除
- 作者：Wei-Dong Chen
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
46.Comparison of Quality of Life in Patients with beta-Thalassemia Intermedia and beta-Thalassemia Major in Southern Iran

机译：伊朗南部β-地中血症患者患者生活质量比较
- 作者：Haghpanah Sezaneh;Vahdati Sara;Karimi Mehran
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-Thalassemia (beta-thal);
- health;
- Quality of life (QoL);
- Short Form-36 (SF36);
47.Hb Alcorn County: A p-Globin Variant [(340(C6)Arg-+Thr; HBB: c.122G>C (p.Arg41Thr)] with Increased Oxygen Affinity

机译：HB Alcorn County：P-球蛋白变体[（340（C6）ARG- + THR; HBB：C.122G> C（P.ARG41THR），随着氧亲和力增加
- 作者：Hung S. Luu
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
48.A De Novo Heterozygous Variant {HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild p-Thalassemia Intermedia Phenotype in a Turkish Child

机译：DE Novo杂合型{HBB：C.379delg，p.val127cysfs * 32）与土耳其儿童中的温和p-thalassemia介质表型相关联
- 作者：Dilek Gurlek-Gokcebay
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
49.Mutation in a Highly Conserved COOH-Terminal Residue of Kruppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous -Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype

机译：高度保守的COOH-末端残留在kruppel样系数1中的突变，其与复合杂合 - 邻脑血症患者中升高的Hb f相关，其具有非传输依赖性的脑血症表型
- 作者：Gallagher Patrick G.;Maksimova Yelena;Schulz Vincent P.;Forget Bernard G.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- Fetal hemoglobin;
- Kruppel-like factor 1;
- thalassemia;
- zinc finger;
50.A Case Report of Compound Heterozygosity for p°/p+-Thalassemia Resulting from under Diagnosed p-Thalassemia Found in a Hb A'2 Sample

机译：由诊断为P-Thalassemia的P°/ P + -Thalassemia复方杂合子的案例报告，其在HB A'2样品中发现
- 作者：Nutjeera lntasai
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
51.Compound Heterozygote for a Novel Elongated C-Terminal beta-Globin Variant (HBB: c.364delG) and Hb E {HBB: c.79G>A) with Heterozygous alpha-Thalassemia-2

机译：复方杂合子用于新颖的细长C-末端β-珠蛋白变体（HBB：C.364DelG）和HB E {HBB：C.79g> A），其具有杂合性α-Thalassemia-2
- 作者：Manit Nuinoon
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
52.Hb Mozhaisk [beta92(F8)His->Arg; HBB: c.278A>G] as a De Novo Mutation in a Child of Mixed Ethnic Origins

机译：HB Mozhaisk [Beta92（F8）他 - > arg; HBB：C.278A> G]作为一个混合族裔的小孩突变
- 作者：Elena Benzoni;Valentina Giannone;Laura Michetti;Manuela Seia;Laura Cavalleri Cristina Curcio
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-Globin variant;
- genetic counseling;
- Hb Mozhaisk;
- hemolytic anemia;
- unstable hemoglobin (Hb);
53.Gene Therapy of the beta Hemoglobinopathies: Success and Challenges

机译：β血管病毒缺失的基因治疗：成功和挑战
- 作者：Emmanuel Payen
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
54.Rivaroxaban Use in Patients with Hemoglobinopathies

机译：Rivaroxaban用于血吸虫病患者
- 作者：Apostolou Chrysoula;Klonizakis Philippos;Mainou Maria;Kapsali Eleni;Kafantari Katerina;Kotsiafti Aggeliki;Vetsiou Evaggelia;Vakalopoulou Sofia;Vlachaki Efthymia
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Rivaroxaban;
- sickle cell disease;
- thalassemia;
55.Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt

机译：埃及儿科中西莫亚洲人口生活质量
- 作者：Adam Soheir;Afifi Hanan;Thomas Manal;Magdy Phoebe;El-Kamah Ghada
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Chronic transfusion;
- quality of life (QoL) outcomes;
- thalassemia;
56.IVS-II-648/649 (-T) (HBB: c.316-202del) Triggers a Novel -Thalassemia Phenotype

机译：IVS-II-648/649（-T）（HBB：C.316-202DEL）触发了一种新型-Thalassemia表型
- 作者：Azimi Azam;Alibakhshi Reza;Hayati Hasibeh;Tahmasebi Soosan;Alimoradi Sasan
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- -Globin gene;
- -thalassemia (-thal);
- in silico analysis;
- novel mutation;
57.A Clinical Update of the Hb Siirt [27(B9)AlaGly; HBB: c.83C G] Hemoglobin Variant

机译：HB Siirt的临床更新[27（b9）alagly; HBB：C.83C＆GT; G]血红蛋白变体
- 作者：Cappabianca Maria Pia;Colosimo Alessia;Sabatucci Annalaura;Dainese Enrico;Di Biagio Paola;Piscitelli Roberta;Sarra Ofelia;Zei Daniela;Amato Antonio
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-Thalassemia intermedia (beta-TI);
- codon 27;
- hemoglobin (Hb) variant;
- Kurdish;
58.Description of a rare p-globin gene mutation, IVS-ll-848 (C>A) (HBB: c.316-3C>A) in association with IVS-l-1 (G>A) {HBB: c.92 + 1G>A), observed in a Syrian family: a case report

机译：罕见的p聚蛋白基因突变，IVS-L1-848（C> A）与IVS-1-1（G> A）相关联的IVS-L1-848（C> A）（HBB：C.316-3C> A）{HBB：C.92 + 1g> a），在叙利亚家庭观察到：案例报告
- 作者：Ahmad Shoujaa
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
59.Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family

机译：用于Hb Alperton（HBB：C.407C> T）和IVS-I-5（G> C）（HBB：C.92 + 5g> C）突变的复合杂合性，呈现为印度家庭中的中度贫血
- 作者：Koumudi G. Godbole;Angalena Ramachran;Ashwini S. Karkamkar Ashwin B. Dalal
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-thalassemia (beta-thal);
- compound heterozygote;
- Hb Alperton;
60.Insulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell Disease

机译：胰岛素分泌和抗性患者镰状细胞疾病患者的分泌和抗性
- 作者：Yavropoulou Maria P.;Pikilidou Maria;Pantelidou Despoina;Tsalikakis Dimitrios G.;Mousiolis Athanasios;Chalkia Panagiota;Yovos John G.;Zebekakis Pantelis
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- -Cell index;
- insulin resistance;
- insulin sensitivity;
- oral glucose load;
- sickle cell disease;
- vitamin D deficiency;
61.First Report of a Coincidental Discovery of Hb Shimonoseki [alpha54(E3)Gln->Arg, HBA2: c.164A>G (or HBA1)] in a Greek Family

机译：HB Shimonoseki的巧合发现的第一报告[alpha54（e3）gln-> arg，hba2：c.164a> g（或hba1）]在希腊家庭中
- 作者：Stamatia Theodoridou;Evangelia Delaki;Evangelia Skatharoudi;Olga Karakasidoua
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Genetic counseling;
- Hb Shimonoseki;
- pre pregnancy counseling;
- pregnancy;
- thalassemia;
62.Successful Use of Veno-Venous Extracorporeal Membrane Oxygenation in an Adult Patient with Sickle Cell Anemia and Severe Acute Chest Syndrome

机译：用镰状细胞贫血和严重急性胸部综合征的成人患者成功使用静脉体外膜氧合
- 作者：Sarah S. Sewaralthahab;Jay Menaker Jennie Y. Law
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Acute chest syndrome (ACS);
- extracorporeal membrane oxygenation (ECMO);
- sickle cell disease;
63.Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the 1-Globin Chain Leads to Increased Oxygen Affinity

机译：HB Bakersfield（HBA1：C.151_152INSGGCC）：在1-珠蛋白链的密码子49和50之间插入ARG-HI之间导致氧亲和力增加
- 作者：Brunner-Agten Saskia;von Kanel Thomas;Rothlisberger Benno;Broquet Charles;Huber Andreas R.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Erythrocytosis;
- Hb Bakersfield;
- HBA1;
- insertion;
- oxygen affinity;
- p50;
64.First Report of Hb Kent [beta37(C3)Trp->Cys (TGG>TGC) HBB: c.114GC] in a Chinese Family

机译：第一报告HB Kent [Beta37（C3）TRP-> CYS（TGG> TGC）HBB：C.114GC]在中国家庭
- 作者：Nelson C.N. Chan;King-Ho Chow;Rico F.Y. Leung;Sequence S.H. Tang;Michelle F.W. Chiu;Rosalind Lie;Kelvin C.K. Cheng;Kin-Mang Lau;Natalie P.H. Chan Margaret H.L. Ng
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- alpha1beta2 Contact;
- alpha-thalassemia (alpha-thal);
- hemoglobin (Hb) variant;
- Hb Kent;
- posttranslational modification;
65.Hb Midnapore [53(D4)AlaVal; HBB: c.161C > T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G > C) (HBB: c.92+5G > C) Found in a Bengali Indian Family

机译：HB Midnapore [53（D4）Alaval; HBB：C.161C> T]：一种新的血红蛋白变体，其结构异常与孟加拉印度家庭中发现的IVS-I-5（G> C）（HBB：C.92 + 5g> C）相关
- 作者：Panja Amrita;Chowdhury Prosanto;Basu Anupam
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- HBB;
- c;
- 161C gt;
- T;
- hemoglobin (Hb) variant;
- Hb Midnapore;
- thalassemia;
66.Life-Threatening Drug-Induced Liver Injury in a Patient with beta-Thalassemia Major and Severe Iron Overload on Polypharmacy

机译：危及生命的药物诱导的患者患者患者患者，β-地中海贫血症，严重铁过载对多酚疾病
- 作者：Maddalena Casale;Stefania Picariello;Felice Corvino;Giuseppe Cerasari;Saverio Scianguettaa
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Chelation therapy;
- druginduced liver injury (DILI);
- iron overload;
- thalassemia;
- warfarin;
67.A Patient with -Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the -Globin Gene

机译：具有-ThalAssemia介药的患者仲成纯度为聚腺苷酸化信号突变（AataAA> AATAGA）（HBB：C. * 112a> g） - Globin基因
- 作者：Lim Yen-Chian;Tan Karen M. L.;Chong Samuel S.;Rajendran Joseph;Sampath Venkatasreekanth
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- -Globin gene;
- paravertebral;
- polyadenylation (polyA) signal mutation (AATAAA gt;
- AATAGA);
- thalassemia;
68.The Spectrum of beta-Thalassemia Mutations in Hamadan Province, West Iran

机译：伊朗哈马德省β-地中海贫血突变的谱
- 作者：Reza Alibakhshi
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
69.Frequency of alpha-Globin Gene Triplications and Coinheritance with beta-Globin Gene Mutations in the Iranian Population

机译：伊朗人口β-珠蛋白基因突变的α-珠蛋白基因三倍次突变的频率
- 作者：Seyedeh Sedigheh Abedini;Fatemeh Forouzesh Pour;Keyvan Karimi;Zhila Ghaderi;Samaneh Farashi
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
70.Efficacy of the National Thalassaemia and Sickle Cell Disease Prevention Programme in Northern Greece: 15-Year Experience, Practice and Policy Gaps for Natives and Migrants

机译：北京北部国家地区和镰状细胞疾病预防方案的疗效：19年的自然和移民的15年经验，实践和政策差距
- 作者：Stamatia Theodoridou;Nikolaos Prapas;Angeliki Balassopoulou;Effrossyni Boutou;Timoleon-Achilleas Vyzantiadis
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Carrier screening;
- gene mutations;
- genetic counseling;
- hemoglobinopathy;
- prenatal diagnosis (PND);
- thalassemia;
71.Detection of a Large Novel alpha-Thalassemia Deletion in an Autochthonous Belgian Family

机译：在自动的比利时家庭中检测大型新型α-丘脑血症缺失
- 作者：Laura Heireman
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
72.Mutational Profile of Homozygous -Thalassemia in Rio de Janeiro, Brazil

机译：巴西里约热内卢的纯合 - 邻苯甲血症的突变概况
- 作者：Carrocini Gisele C. S.;Venancio Larissa P. R.;Pessoa Viviani L. R.;Lobo Clarisse L. C.;Bonini-Domingos Claudia R.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- -Thalassemia (-thal);
- hemoglobin (Hb);
- hemolytic anemia;
- molecular genetics;
- mutations;
73.Analysis of Common beta-Thalassemia Mutations in North Vietnam

机译：北越南常见的β-地中海贫血突变分析
- 作者：Lan Thi Thuong Vo;Trang Thu Nguyen;Hai Xuan Le Ha Thi Thu Le
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
74.Detection of Hb A(2) and Hb Constant Spring (HBA2: c.427TC) by Capillary Electrophoresis in a Patient with Hb H-Hb CS Disease

机译：通过HB H-HB CS疾病的患者毛细管电泳检测Hb A（2）和Hb恒星（HBA2：C.427T＆GT.C）
- 作者：Li You-qiong;Wei Jin-hua;Liang Liang
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Hb A(2);
- high performance liquid chromatography (HPLC);
- capillary electrophoresis (CE);
75.Prevalence and Characteristics of Priapism in Sickle Cell Disease

机译：镰状细胞疾病中PRIAP主义的患病率与特征
- 作者：Giovanna A.O. Arduini Alessra B. Trovo de Marqui
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Complications;
- prevalence;
- priapism;
- sickle cell anemia;
- sickle cell disease;
76.Effect of Assorted Globin Haplotypes and alphalpha-thalassemia on the Clinical Heterogeneity of Hb S-betalpha-thalassemia

机译：各种珠蛋白单倍型和甲状腺血症对Hb S-Betalpha-thalassemia临床异质性的影响
- 作者：Preetina M. Dash;Praveen K. Sahu;Siris Patel;Ranjeet S. Mashon;Kiran R. Kharat Malay B. Mukherjeee
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
77.Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program

机译：中国大陆的预妊娠地中海贫血筛查：预防计划的前两年
- 作者：Fan Jiang;Gui-Lan Chen;Jian Li;Xing-Mei Xie;Jian-Ying Zhou;Can Liao Dong-Zhi Li
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Mainland China;
- pre gestational screening;
- prenatal diagnosis (PND);
78.Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo beta-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual

机译：下一代测序的临床基因分型揭示了一种新颖的denovoβ-珠蛋白基因突变，导致中国个体中的溶血性贫血
- 作者：Jiajie Pu;Li Zhang;Xiaofeng Wei Xiangmin Xu
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Abnormal hemoglobin (Hb);
- beta-globin gene;
- frameshift mutation;
- next generation sequencing (NGS);
79.First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the alpha 2-Globin Gene

机译：由α-I-116（A> G）α2-珠蛋白基因的IVS-I-116（A> G）引起的内膜HB H病的第一报告
- 作者：He Xiao-Hong;Zhang Rui;Mai Guang-Xing;Ren Li-Rong;Li Dong-Zhi
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- alpha-Thalassemia (alpha-thal);
- fetal anemia;
- nondeletional Hb H disease;
80.The Spectrum of alpha-Thalassemia Mutations in the Lak Population of Iran

机译：伊朗的LAK人口中α-丘脑血症突变的谱
- 作者：Keivan Moradi
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
81.Evaluation of the Effect of Support-Training System of Peer Group on Promotion of Self-Care in p-Thalassemia Major Patients in Southern Iran

机译：对伊朗南部P-Thalassemia主要患者自我保健促进促进对同龄人群促进培训体系的评价
- 作者：Sanaz Safaei
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
82.Hemoglobin Variant Profiles among Brazilian Quilombola Communities

机译：巴西奎里奥巴拉社区中的血红蛋白变体概况
- 作者：Santiago Rayra P.;Oliveira Rodrigo M.;Soares Leonardo F.;Figueiredo Camylla V. B.;Silva Denise Oliveira;Hurtado-Guerrero Ana F.;Fiuza Luciana M.;Guarda Caroline C.;Adorno Elisangela V.;Barbosa Cynara G.;Goncalves Marilda S.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Africans;
- hemoglobinopathy;
- hemoglobin (Hb) variant;
- Quilombola;
83.A Novel Mutation of the 2-Globin Gene Causing (+)-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA)

机译：2-珠蛋白基因的新突变导致（+） - 地中海贫血：HB南宁（HBA2：C.369_370Delinsga）
- 作者：Chen Biyan;Lin Li;Yi Shang;Chen Qiuli;Wei Hongwei;Li Guojian;Zheng Chenguang;He Sheng;Qiu XiaoXia
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- alpha-Globin;
- alpha-thalassemia (-thal);
- Hb Nanning;
- nondeletional mutation;
84.Hb Gibbon [p124(H2)Pro->Thr {HBB: c.373C>A, p.P125T)], an Asymptomatic Novel Hemoglobin Variant Detected by Newborn Screening

机译：Hb长臂猿[p124（h2）pro-> thr {hbb：c.373c> a，p.p125t）]，新生儿筛选检测到的无症状新型血红蛋白变体
- 作者：Alejro Wolf
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
85.Severe Thalassemia Caused by Hb Zunyi [p147(HC3)Stop->Gln; HBB: c.442T>Q] on the p-Globin Gene

机译：Hb Zunyi引起的严重性血症[P147（HC3）停止 - > GLN; HBB：C.442t> Q]在p聚蛋白基因上
- 作者：Qiong Su
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
86.Molecular Study of Deletional and Nondeletional Mutations on the -Globin Locus in the Azeri Population of Northwestern Iran

机译：西北伊朗阿塞里人群血液遗迹缺失和紊乱的分子研究
- 作者：Derakhshan Sima M.;Khaniani Mahmoud S.;Afkhami Fateme;Pourfeizi Abbasali H.
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2016年第6期
- -Thalassemia (-thal);
- Azeri population;
- Iran;
- multiplex gap-polymerase chain reaction (gap-PCR);
87.Identification of a Novel 9.7 kb Deletion Causing alpha0-Thalassemia in Two Pregnant Women in Southern China

机译：鉴定新型9.7 kB缺失，导致中国两名孕妇中的α0-inthalsemia
- 作者：Li Lin;Qi Yang;Shujie Zhang;Yangjng Zuo;Sheng He;Xiangmin Xu;Biyan Chen Xiaoxia Qiu
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- alpha-globin;
- alpha-thalassemia (alpha-thal);
- molecular diagnosis;
- novel mutation;
88.First Report of a Novel Deletion Due to epsilon gamma delta beta -Thalassemia in a Chinese Family

机译：由于中国家庭的epsilonγδβ代表epsilonγδβ引起的第一次删除报告
- 作者：Hui Annie S. Y.;Au Patrick K. C.;Ting Yuen-Ha;Kan Anita S. Y.;Cheng Yvonne K. Y.;Leung Alex W. K.;Chan Kelvin Y. K.;Li Chi-Kong;Tang Mary H. Y.;Leung Tak-Yeung
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- Chinese;
- lt;
- boldgt;
- epsilon gamma delta betalt;
- /boldgt;
- -thalassemia (lt;
- boldgt;
- epsilon gamma delta betalt;
- /boldgt;
- -thal);
- fetal anemia;
- neonatal anemia;
- transfusion;
89.Genetic Polymorphisms of Glucose-6-Phosphate Dehydrogenase in Lagos, Nigeria

机译：尼日利亚拉各斯葡萄糖-6磷酸脱氢酶的遗传多态性
- 作者：Musa O. Babalola;Ngozi A. Imaga;Titilola A. Samuel;Iyanu P. Diriwari;Olajumoke Kolade;Irene Ezeamalu
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Genetic polymorphism;
- glucose-6-phosphate dehydrogenase (G6PD);
- Nigeria;
- sickle cell anemia;
90.A Novel Variant with Positive Natural Selection Influenced Hb A(2) Levels in Chinese Individuals with beta-Thalassemia

机译：具有阳性自然选择的新型变体影响了β-地中海贫血的中药中的HB A（2）水平
- 作者：Yu Shanjuan;Chen Yang;Lai Ketong;Dewan Roma Kajal;He Yunyan
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- beta-Thalassemia (beta-thal);
- Hb A(2);
- positive natural selection;
- rs231841 polymorphism;
91.Assessment of Peripheral Neuropathy in Patients with beta-Thalassemia viaElectrophysiological Study: Reevaluation in the Era of Iron Chelators

机译：β-地中海贫血患者外周神经病变的评估 - 铁螯合剂时代重新评估
- 作者：Turan Bayhan;Sule Unal;Bahad?r Konuskan;Onur Erdem;Erdem Karabulut Fatma Gumruk
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-Thalassemia (beta-thal);
- Deferasirox (DFX);
- electrophysiological study;
- peripheral neuropathy;
92.Compound Heterozygosity of beta-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India

机译：β-地中海贫血的复合杂合性和镰状细胞血红蛋白在印度牧师州的各种群体中
- 作者：Aditya N. Jha;Hrishikesh Mishra;Henu K. Verma;Isha Pey Bhaskar V.K.S. Lakkakula
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
93.Compound Heterozygosity for Silent Cap 11570 (T>C) (HBB: c*96T>C), Codon 39 (C>T) (HBB: c.118C>T) and the Presence of alphaalphaalphaanti–3.7/aa in Greece. A Case Presentation

机译：沉默帽11570（T> C）（HBB：C * 96t> C），密码子39（C> T）（HBB：C.118C> T）和αAlphaalphaanti-3.7 / Aa的存在，以及在希腊的存在。案例介绍
- 作者：Stamatia Theodoridou;Timoleon-Achilleas Vyzantiadis Efthymia Vlachaki
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- beta-Thalassemia intermedia (beta-TI);
- genetic counseling;
- silent mutation;
94.Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart's on Capillary Electrophoresis

机译：用Hb A2-Hb H和Hb A2-Hb Bart对毛细管电泳的样品中删除HB H疾病的分析
- 作者：Kunyakan Khongthai
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
95.Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias

机译：网状细胞血红蛋白当量（RET-HE）与红细胞分布宽度相结合，具有差异诊断的Thalassemias
- 作者：Yu Lian;Jun Shi;Neng Nie;Zhendong Huang;Yingqi Shao;Jing Zhang;Jinbo Huang;Xingxin Li;Meili Ge
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
96.Hb Penang [beta78(EF2)Leu->Pro, HBB: c.236T>C]: a Novel beta-Globin Variant

机译：HB Penang [Beta78（EF2）Leu-> Pro，HBB：C.236T> C]：一种新的β-珠蛋白变体
- 作者：Catherine H-W. Hsu;Jonathan Langdown;Roderick Lynn;Chris Fisher;Anna Rose;Melanie Proven
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Hemoglobin (Hb) b chain;
- hemoglobinopathy trait;
- unstable Hb;
- variant;
97.alpha(+)-Thalassemia Caused by an 811bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases

机译：阿尔法（+） - 南宁，广西南宁缺失造成的地中海贫血：两种情况的报告
- 作者：Zhang Qiang;Xu Mingli;Zhou Wanjun;Fan Xin
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2017年第6期
- alpha(+)-Thalassemia (alpha(+)-thal);
- novel deletion;
- thalassemia;
98.Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition

机译：多种治疗型镰状细胞疾病的超热溶解的成功结果：补体抑制的作用
- 作者：Vlachaki Efthymia;Gavriilaki Eleni;Kafantari Katerina;Adamidou Despoina;Tsitsikas Dimitris;Chasapopoulou Eleni;Anagnostopoulos Achilles;Tsapas Apostolos
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2018年第6期
- Complement;
- delayed hemolytic transfusion reaction (DHTR);
- eculizumab;
99.A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with (3-Thalassemia Trait Results in Severe Hemolytic Anemia

机译：在HB Charlieu（HBA1：C.320T> C）的HBA1基因上的纯合突变与（3-Thalassemia特征在重症溶血性贫血中
- 作者：Thomas R. L. Klei
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期
100.The Sub-Phenotypes of Sickle Cell Disease in Kuwait

机译：科威特镰状细胞病的亚表型
- 作者：Adekunle D. Adekile
- 期刊名称：《Hemoglobin: International Journal for Hemoglobin Research》 | 2019年第6期

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