Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine

S Fucharoen, P Winichagoon - Hemoglobin, 1997 - Taylor & Francis
Thalassemia (thal) and hemoglobinopathies are widespread, recessive inherited diseases.
Approximately 250 million people (4.5% of the world population) carry abnormal …

Iron status and oxidative stress in β‐thalassemia patients in Jakarta

DR Laksmitawati, S Handayani… - Biofactors, 2003 - Wiley Online Library
A study on thalassemia intermedia and major patients in Jakarta was initiated to obtain a
comprehensive picture of metabolic dysregulation, iron overload, oxidative stress, and cell …

Molecular scanning of β-thalassemia in the southern region of Central Java, Indonesia; a step towards a local prevention program

L Rujito, M Basalamah, S Mulatsih, ASM Sofro - Hemoglobin, 2015 - Taylor & Francis
Thalassemia is the most prevalent genetic blood disorder worldwide, and particularly
prevalent in Indonesia. The purpose of this study was to determine the spectrum of β …

Kelainan pada Sintesis Hemoglobin: Thalassemia dan Epidemiologi Thalassemia

RD Wulandari - Jurnal Ilmiah Kedokteran Wijaya Kusuma, 2018 - journal.uwks.ac.id
Hemoglobinopati meliputi kelainan pada struktur dan gangguan sintesis hemoglobin
(thalassemia). Kelainan pada Hb ini merupakan kelainan gen tunggal yang pada awalnya …

[HTML][HTML] Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia

S Susanah, NM Sari, D Prihatni, P Sinaga… - Journal of Community …, 2022 - Springer
The thalassemia screening program in Indonesia mostly conducted sporadically. Ideal
prospective screening is still limited. This study aimed to compare thalassemia screening …

The correlation between iron overload and endocrine function in adult transfusion-dependent beta-thalassemia patients with growth retardation

TD Atmakusuma, FD Hasibuan… - Journal of Blood …, 2021 - Taylor & Francis
Background Iron overload is a major problem in patients with transfusion-dependent beta-
thalassemia (TDT). Reports on the correlation between iron overload and endocrine function …

[PDF][PDF] Genetic problems at present and their challenges in the future: Thalassemia as a model

I Wahidiyat, PA Wahidiyat - Paediatrica Indonesiana, 2006 - paediatricaindonesiana.org
Compared to the infectious diseases, genetic disorders are not so frequently encountered in
the clinic, so that there has been a trend that they are neglected by people or even by the …

[HTML][HTML] Homozygous deletion of six olfactory receptor genes in a subset of individuals with Beta-thalassemia

J Van Ziffle, W Yang, FF Chehab - PLoS One, 2011 - journals.plos.org
Progress in the functional studies of human olfactory receptors has been largely hampered
by the lack of a reliable experimental model system. Although transgenic approaches in …

Uji Diagnostik Indeks Darah dan Identifikasi Molekuler Karier Talasemia β pada Pendonor Darah di Banyumas

AT Hapsari, L Rujito - Jurnal Kedokteran Brawijaya, 2015 - jkb.ub.ac.id
Talasemia menempati kelainan genetik yang paling umum di seluruh dunia dengan
prevalensi karier talasemia di Indonesia adalah sekitar 3-10%. Banyumas merupakan salah …

[HTML][HTML] β Thalassemia Mutation Flow in Indonesia: A Migration Perspective

L Rujito, Z Maritska, AS Sofro - Thalassemia Reports, 2023 - mdpi.com
Indonesia is a large island country with a wide variety of ethnic groups. As part of the
thalassemia country belt, Indonesia has alleles that are as distinctive as those found in other …