Hemoglobin,volume 37,issue 6  (12-2013)

Period of time： 2013年6期

Publisher： Informa Healthcare

Founded in： 1976

Total resources： 6

ISSN： 0363-0269

Subject： R5 Internal Medicine

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Hemoglobin,volume 37,issue 6

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Perinatal Outcome in Sickle Cell Anemia: A Prospective Study from India

By Daigavane Mayoor M.,Jena Rabindra K.,Kar Tushar J. in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 507-515

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Gene Expression Analysis of the Brazilian Type of Hereditary Persistence of Fetal Hemoglobin: Identification of Genes that Could be Related to γ-Globin Activation

By Roversi Fernanda Marconi,da Cunha Anderson Ferreira,Brugnerotto Ana Flávia,Carazzolle Marcelo Falsarella,de Albuquerque Dulcinéia Martins,Lanaro Carolina,Machado-Neto João Agostinho,Olalla Saad Sara Teresinha,da Costa Fernando Ferreira in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 516-535

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Anemia in Patients with Coinherited Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency

By Pornprasert Sakorn,Phanthong Siratcha in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 536-543

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The Spectrum of β-Thalassemia Mutations in Kermanshah Province in West Iran and its Association with Hematological Parameters

By Mehrabi Masomeh,Alibakhshi Reza,Fathollahi Soheila,Farshchi Mohammad Reza in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 544-552

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β- And α-Thalassemia Intermedia in Basra, Southern Iraq

By Abdulwahid Dhurgham A.,Hassan Mea’ad K. in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 553-563

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Peroxisome Proliferator-Activated Receptor-γ Pro12Ala Polymorphism and Risk of Osteopenia in β-Thalassemia Major Patients

By Sahmani Mehdi,Gholami Abdollah,Azarkeivan Azita,Darabi Masoud,Ahmadi Mohammad Hossein,Sabet Majid Sirati,Najafipour Reza in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 564-573

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Detection of Hb H Disease Genotypes Common in Northern Thailand by Quantitative Real-Time Polymerase Chain Reaction and High Resolution Melting Analyses

By Seeratanachot Teerapat,Sanguansermsri Torpong,Shimbhu Dawan in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 574-583

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A New High Affinity Variant Hb Aurillac (β141Leu→Val)

By Boursier Guilaine,Trouillier Sébastien,Blaizot Muriel Giansily,Igual Hélène,Schved Jean-François,Martinez Patricia Aguilar in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 584-588

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Hb Papanui [α99(G8)Lys→Arg; HBA2: c.299A>G]: A Novel Silent Substitution Interfering in Hb A1c Determination

By Brennan Stephen O.,Chan Tim in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 589-592

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Utility and Importance of Accurate Hb A2 Measurements for Defining a Strategy for β-Thalassemia Screening: Experience in the Balearic Islands, Spain

By López-Escribano Herminio,Parera Maria M.,Guix Pilar,Castro José A.,Ramon Misericòrdia,Picornell Antònia in (2013)

Hemoglobin,volume 37,issue 6 , Vol. 37, Iss. 6, 2013-12 , pp. 593-598

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