Hemoglobin, Volume 40, Issue 6 (2016)

Browse this journal
Sample our Medicine, Dentistry, Nursing & Allied Health journals, sign in here to start your FREE access for 14 days

Hemoglobin, Volume 40, Issue 6 (2016)

See all volumes and issues
Vol 48, 2024 Vol 47, 2023 Vol 46, 2022 Vol 45, 2021 Vol 44, 2020 Vol 43, 2019 Vol 42, 2018 Vol 41, 2017 Volume 40, 2016 Vol 39, 2015 Vol 38, 2014 Vol 37, 2013 Vol 36, 2012 Vol 35, 2011 Vol 34, 2010 Vol 33, 2009 Vol 32, 2008 Vol 31, 2007 Vol 30, 2006 Vol 29, 2005 Vol 28, 2004 Vol 27, 2003 Vol 26, 2002 Vol 25, 2001 Vol 24, 2000 Vol 23, 1999 Vol 22, 1998 Vol 21, 1997 Vol 20, 1996 Vol 19, 1995 Vol 18, 1994 Vol 17, 1993 Vol 16, 1992 Vol 15, 1991 Vol 14, 1990 Vol 13, 1989 Vol 12, 1988 Vol 11, 1987 Vol 10, 1986 Vol 9, 1985 Vol 8, 1984 Vol 7, 1983 Vol 6, 1982 Vol 5, 1981 Vol 4, 1980 Vol 3, 1979 Vol 2, 1978 Vol 1, 1976-1977
Download citations Download PDFs Download issue

Original Article

Article
The Molecular Spectrum of β- and α-Thalassemia Mutations in Non-Endemic Umbria, Central Italy
Paolo Gorello, Francesco Arcioni, Antonietta Palmieri, Ylenia Barbanera, Laura Ceccuzzi, Cecilia Adami, Mauro Marchesi, Antonella Angius, Olivia Minelli, Marina Onorato, Antonio Piga, Maurizio Caniglia, Cristina Mecucci & Antonella Roetto
Pages: 371-376
Published online: 31 Mar 2017
AbstractforThe Molecular Spectrum of β- and α-Thalassemia Mutations in Non-Endemic Umbria, Central Italy | Full Text | References | PDF (540.6 KB)
  • 173 Views
  • 8 CrossRef citations
  • 0Altmetric
Article
Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon
Gift D. Pule, Valentina J. Ngo Bitoungui, Bernard Chetcha Chemegni, Andre P. Kengne & Ambroise Wonkam
Pages: 377-380
Published online: 10 Nov 2016
AbstractforStudies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon | Full Text | References | PDF (430.8 KB)
  • 91 Views
  • 4 CrossRef citations
  • 0Altmetric

Review Article

Review Article
Can Neuroimaging Markers of Vascular Pathology Explain Cognitive Performance in Adults With Sickle Cell Anemia? A review of the Literature
Dana R. Jorgensen, Caterina Rosano & Enrico M. Novelli
Pages: 381-387
Published online: 31 Mar 2017
AbstractforCan Neuroimaging Markers of Vascular Pathology Explain Cognitive Performance in Adults With Sickle Cell Anemia? A review of the Literature | Full Text | References | PDF (737.9 KB)
  • 181 Views
  • 12 CrossRef citations
  • 0Altmetric

Original Article

Article
Lactate Dehydrogenase: A Marker of the Severity of Vaso-Occlusive Crisis in Children with Sickle Cell Disease Presenting at the Emergency Department
Marina García-Morin, Carolina López-Sangüos, Paula Vázquez, Teresa Alvárez, Rafael Marañón, Jorge Huerta & Elena Cela
Pages: 388-391
Published online: 31 Mar 2017
AbstractforLactate Dehydrogenase: A Marker of the Severity of Vaso-Occlusive Crisis in Children with Sickle Cell Disease Presenting at the Emergency Department | Full Text | References | PDF (549.7 KB)
  • 228 Views
  • 7 CrossRef citations
  • 0Altmetric
Article
β-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study
Ayşegül Kurtoğlu, Volkan Karakuş, Özgür Erkal & Erdal Kurtoğlu
Pages: 392-395
Published online: 03 Mar 2017
Abstractforβ-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study | Full Text | References | PDF (394.4 KB)
  • 287 Views
  • 6 CrossRef citations
  • 0Altmetric
Article
A comprehensive screening program for β-thalassemia and other hemoglobinopathies in the Hooghly District of West Bengal, India, dealing with 21 137 cases
Kallol Kumar Bhattacharyya, Tridip Chatterjee & Ujjalendu Bikash Mondal
Pages: 396-399
Published online: 03 Mar 2017
AbstractforA comprehensive screening program for β-thalassemia and other hemoglobinopathies in the Hooghly District of West Bengal, India, dealing with 21 137 cases | Full Text | References | PDF (543.1 KB)
  • 131 Views
  • 4 CrossRef citations
  • 0Altmetric
Article
A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers
Nelson C.N. Chan, Kin-Mang Lau, Kelvin C. K. Cheng, Natalie P.H. Chan & Margaret H.L. Ng
Pages: 400-404
Published online: 14 Nov 2016
AbstractforA Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers | Full Text | References | PDF (641.8 KB)
  • 182 Views
  • 3 CrossRef citations
  • 0Altmetric
Article
Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients
Yunli Lai, Yun Chen, Biyan Chen, Haiyang Zheng, Sheng Yi, Guojian Li, Hongwei Wei, Sheng He & Chenguang Zheng
Pages: 405-410
Published online: 31 Mar 2017
AbstractforGenetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients | Full Text | References | PDF (684.1 KB)
  • 171 Views
  • 9 CrossRef citations
  • 0Altmetric
Article
First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients
Awatef Mejri, Marwa Mansri, Sondess Hadj Fredj, Faida Ouali, Amina Bibi, Raouf Hafsia, Taieb Messaoud & Hajer Siala
Pages: 411-416
Published online: 09 Nov 2016
AbstractforFirst description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients | Full Text | References | PDF (772.3 KB)
  • 71 Views
  • 3 CrossRef citations
  • 0Altmetric

Short Communication

Rapid Communication
Detection of the Unstable Hb Köln (HBB: c.295G>A) by a Capillary Electrophoresis Method
You-Qiong Li, Li-Hua Ye & Yun Mo
Pages: 417-419
Published online: 31 Mar 2017
AbstractforDetection of the Unstable Hb Köln (HBB: c.295G>A) by a Capillary Electrophoresis Method | Full Text | References | PDF (668.1 KB)
  • 233 Views
  • 4 CrossRef citations
  • 0Altmetric
Rapid Communication
Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl
Hua Jiang, Jin-Mei Yan, Jian-Ying Zhou & Dong-Zhi Li
Pages: 420-421
Published online: 31 Mar 2017
AbstractforHb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl | Full Text | References | PDF (491.1 KB)
  • 85 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
First Report of Hb Limassol [β8(A5)Lys→Asn; HBB: c.27G>C] from Odisha, India
Satyabrata Meher, Snehadhini Dehury, Arpita Jana, Subhra Bhattacharya, Amrita Patel, Kishalaya Das, Siris Patel, Biswanath Sarkar & Pradeep Kumar Mohanty
Pages: 422-424
Published online: 31 Mar 2017
AbstractforFirst Report of Hb Limassol [β8(A5)Lys→Asn; HBB: c.27G>C] from Odisha, India | Full Text | References | PDF (931.4 KB)
  • 55 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok
Fan Jiang, Jian-Ying Zhou, Jin-Mei Yan, Yue-Cheng Lu & Dong-Zhi Li
Pages: 425-427
Published online: 31 Mar 2017
AbstractforFirst Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok | Full Text | References | PDF (892.8 KB)
  • 122 Views
  • 4 CrossRef citations
  • 0Altmetric
Rapid Communication
A novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C)
Lin Zhao, Jilin Qing, Yue Liang & Zhizhong Chen
Pages: 428-430
Published online: 10 Nov 2016
AbstractforA novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C) | Full Text | References | PDF (703.3 KB)
  • 110 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations
Helena H. L. Lee, Annisa S. L. Mak, K. O. Kou, C. F. Poon, W. S. Wong, K. H. Chiu, Patrick K. C. Au, Kelvin Y. K. Chan, Anita S. Y. Kan, Mary H. Y. Tang & K. Y. Leung
Pages: 431-434
Published online: 31 Mar 2017
AbstractforAn Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations | Full Text | References | PDF (835.9 KB)
  • 216 Views
  • 10 CrossRef citations
  • 0Altmetric
Rapid Communication
A Case of Fatal Agranulocytosis That Developed in a Patient with β-Thalassemia Major Treated with Deferiprone
Maria Mainou, Aggeliki Kotsiafti, Philippos Klonizakis, Vasiliki Soulountsi, Chrysoula Apostolou, Kiriakos Psarras & Efthymia Vlachaki
Pages: 435-437
Published online: 31 Mar 2017
AbstractforA Case of Fatal Agranulocytosis That Developed in a Patient with β-Thalassemia Major Treated with Deferiprone | Full Text | References | PDF (353.5 KB)
  • 118 Views
  • 1 CrossRef citations
  • 0Altmetric

Explore articles

Explore the most recently published articles

A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient
Xiaohong He et al.
Brief Report | Published online: 1 May 2024
Sickle Cell Disease in Brazil: Current Management
Aderson da Silva Araújo et al.
Review Article | Published online: 25 Apr 2024
A Novel Frameshift Mutation(HBA2:C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China
Lei Pan et al.
Brief Report | Published online: 23 Apr 2024
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg,HBD: C.139G > A]
Hui-Ming Lin et al.
Brief Report | Published online: 7 Mar 2024
View all latest articles