Adaptation to anemia in hemoglobin E-β thalassemia (Blood (2010) 116, 24 (5368-5370))

Adaptation to anemia in hemoglobin E-β thalassemia (Blood (2010) 116, 24 (5368-5370))

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Allen, A, Fisher, C, Premawardhena, A, Peto, T, Allen, S, Arambepola, M, Thayalsutha, V, Olivieri, N, Weatherall, D
التنسيق:	Journal article
اللغة:	English
منشور في:	2011

مواد مشابهة

Adaptation to anemia in hemoglobin E-beta thalassemia (vol 116, pg 5368, 2011)
حسب: Allen, A, وآخرون
منشور في: (2011)

Adaptation to anemia in hemoglobin E-ß thalassemia.
حسب: Allen, A, وآخرون
منشور في: (2010)

Hemoglobin E-beta-thalassemia: Progress report from the International Study Group.
حسب: Premawardhena, A, وآخرون
منشور في: (2005)

Thalassemia in Sri Lanka: a progress report.
حسب: Premawardhena, A, وآخرون
منشور في: (2004)

Age-related changes in adaptation to severe anemia in childhood in developing countries.
حسب: O'Donnell, A, وآخرون
منشور في: (2007)

Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.
حسب: Jones, E, وآخرون
منشور في: (2014)

Interaction of malaria with a common form of severe thalassemia in an Asian population.
حسب: O'Donnell, A, وآخرون
منشور في: (2009)

Genetic influences on bone disease in thalassemia.
حسب: Basran, R, وآخرون
منشور في: (1998)

The population genetics and dynamics of the thalassemias.
حسب: Weatherall, D, وآخرون
منشور في: (2010)

“As we are mocked with art” (5.3.68): The Winter’s Tale comme anatomie de la réception
حسب: Pierre Iselin
منشور في: (2011-12-01)

Association of Endothelin-1 rs5370 G>T gene polymorphism with the risk of nephrotic syndrome in children
حسب: Mohammad Hashemi, وآخرون
منشور في: (2017-07-01)

Polymorphism of the endothelin-1 gene (rs5370) is a potential contributor to sickle cell disease pathophysiology
حسب: Kristen G. Navarro, وآخرون
منشور في: (2016-12-01)

Endothelin-1 RS5370 gene polymorphism in primary nephrotic syndrome: A case-control study
حسب: Hoda Rizk, وآخرون
منشور في: (2021-12-01)

alpha+-Thalassemia protects children against disease caused by other infections as well as malaria.
حسب: Allen, S, وآخرون
منشور في: (1997)

α+-Thalassemia protects children against disease caused by other infections as well as malaria
حسب: Allen, S, وآخرون
منشور في: (1997)

Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia.
حسب: Premawardhena, A, وآخرون
منشور في: (2001)

Haemoglobin E beta thalassaemia in Sri Lanka.
حسب: Premawardhena, A, وآخرون
منشور في: (2005)

The evolutionary and clinical implications of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances.
حسب: Premawardhena, A, وآخرون
منشور في: (2016)

The evolutionay and clilnical impllications of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances
حسب: Premawardhena, A, وآخرون
منشور في: (2016)

Hemoglobin profiles of siblings of thalassemia patients
حسب: Muhammad Riza, وآخرون
منشور في: (2015-04-01)

MOLECULAR ANALYSIS OF NON-TRANSFUSION DEPENDENT THALASSEMIA ASSOCIATED WITH HEMOGLOBIN E-β-THALASSEMIA DISEASE WITHOUT α--THALASSEMIA
حسب: Paramee Phanrahan, وآخرون
منشور في: (2019-06-01)

IRON OVERLOAD IN NON-TRANSFUSED SIDEROBLASTIC ANEMIAS
حسب: Pippard, M, وآخرون
منشور في: (1982)

The α-thalassemias.
حسب: Piel, F, وآخرون
منشور في: (2014)

The evolving spectrum of the epidemiology of thalassemia
حسب: Weatherall, D
منشور في: (2018)

Hemoglobin Interlaken in combination with beta thalassemia trait
حسب: Mara J. Ojeda, وآخرون
منشور في: (2013-01-01)

Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group.
حسب: de Silva, S, وآخرون
منشور في: (2000)

Unresolved laboratory issues of the heterozygous state of β-thalassemia: a literature review
حسب: Shyamali Thilakarathne, وآخرون
منشور في: (2023-06-01)

Multiplex Mutagenically Separated PCR: Diagnosis of β-Thalassemia and Hemoglobin Variants
حسب: J.-G. Chang, وآخرون
منشور في: (1997-03-01)

A “One-Stop” Screening Protocol for Haemoglobinopathy Traits and Iron Deficiency in Sri Lanka
حسب: Angela Allen, وآخرون
منشور في: (2019-08-01)

Low Hemoglobin among Pregnant Women in Midwives Practice of Primary Health Care, Jatinangor, Indonesia: Iron Deficiency Anemia or β-Thalassemia Trait?
حسب: Ari Indra Susanti, وآخرون
منشور في: (2017-01-01)

Molecular identification of Sicilian (dß)º-thalassemia associated with ß-thalassemia and hemoglobin S in Brazil
حسب: Andrade T.G. de, وآخرون
منشور في: (2002-01-01)

Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia
حسب: Xiuqin Bao, وآخرون
منشور في: (2024-03-01)

Iron status and anaemia in Sri Lankan secondary school children: A cross-sectional survey
حسب: Allen, A, وآخرون
منشور في: (2017)

Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis
حسب: Sitthichai Panyasai, وآخرون
منشور في: (2023-08-01)

Thalassemia and Hemoglobin E in Southern Thai Blood Donors
حسب: Manit Nuinoon, وآخرون
منشور في: (2014-01-01)

Reactivation of fetal hemoglobin in thalassemia and sickle cell disease
حسب: Sandro Eridani, وآخرون
منشور في: (2014-09-01)

Endothelin-1 Gene Polymorphisms rs5370, rs1476046, and rs3087459 are not Associated with Diabetic Nephropathy in Caucasians with Type 2 Diabetes Mellitus
حسب: Šeruga Maja, وآخرون
منشور في: (2017-09-01)

Thalassemia intermedia in HbH-CS disease with compound heterozygosity for β-thalassemia: challenges in hemoglobin analysis and clinical diagnosis
حسب: Tan, Mary Anne Jin Ai, وآخرون
منشور في: (2009)

Double heterozygocity for hemoglobin C and beta thalassemia dominant: A rare case of thalassemia intermedia
حسب: Alexandra Agapidou, وآخرون
منشور في: (2018-01-01)

Thalassaemia in Sri Lanka: A molecular basis.
حسب: Fisher, C, وآخرون
منشور في: (1999)