Laporan Riset Iptekkes 2020 Studi Kelayakan Model Extended Family Sebagai Met…

Edition

-

ISBN/ISSN

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Collation

69 hlm.; bibl. : ilus.; 29 cm

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Call Number

UMU 2020 19

Laporan Riset Iptekkes 2020 Uji Diagnostik Perangkat Lunak Pengklasifikasi Se…

Edition

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ISBN/ISSN

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Collation

107 hlm.; bibl. : ilus.; 29 cm

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UMU 2020 22

Thalasemia : Mengenal, Mendampingi, & Merawat

Edition

Cet-1.

ISBN/ISSN

978-602-9473-92-6

Collation

vi, 88 hlm. : ilus.; 21 cm

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-

Call Number

WH 170 ROH 2016

Karakterisasi Genotipe dan Pengamatan Membran Sel Darah Merah pada Pasien Tha…

Edition

-

ISBN/ISSN

-

Collation

43p.; bibl.; ilus.; 30 cm.

Series Title

-

Call Number

1856 UMU

Studi Karakterisasi Aktivitas Sel Imun Bawaan pada Pasien Talasemia dengan da…

Edition

-

ISBN/ISSN

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Collation

18p.; bibl.; ilus.; 30 cm.

Series Title

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Call Number

1823 UMU

Correlation Between T2* Cardiovascular Magnetic Resonance with Left Ventricul…

Aim: to assess for a correlation between T2 *CMR with LV function and mass in thalassemic patients with iron overload. Methods: a cross-sectional study on thalassemic patients was conducted between July and September 2010 at Cipto Mangunkusumo and Premier Hospitals, Jakarta, Indonesia. Clinical examinations, review of medical charts, electrocardiography, echocardiography, and T2 *CMR were perfo…

Kualitas Hidup Anak Yang Menderita Thalassemia (Quality of Life Child with T…

ABSTRACT Thallassemia is a hemathology disorder and chronic disease. The numbers of thalassemia in Indonesia has been increased every year about 2500 patients. The objective of this research is to describe factors related to quality of life of school age children with thalassemia. It used Cross Sectional study design, which aimed to get description of relationship between independent and depen…

Plasma lipid pattern and red cell membrane structure in β-thalassemia patien…

Background: Over the last 10 years, we have investigated thalassemia patients in Jakarta to obtain a comprehensive picture of iron overload, oxidative stress, and cell damage. Methods: In blood samples from 15 transfusion-dependent patients (group T), 5 non-transfused patients (group N) and 10 controls (group C), plasma lipids and lipoproteins, lipid-soluble vitamin E, malondialdehyde (MDA) …

Posterior transverse interarch discrepancy on HbE βThalassemia Patients

Background: One of the symptoms that often arises on thalassemia patients is disharmony dentofacial,class II skeletal malocclusion, as a result of the malrelation of maxilla and mandible. This malrelation can be affected by either maxillary bone position, dentoalveolar maxillary position, mandibular bone position, dentoalveolar mandibular position, or combinations of those components. Purpose:…

Risk Factors to Growth Retardation in Major Thalassemia

The increasing in the life span of patients with major thalassemia should be followed by increased quality of life. There are factors which can affect growth retardation in these patients. The aim of this study was to find out the risk factors for growth retardation in patients with major thalassemia. An analytical study with cross-sectional design was conducted at Pediatric Thalassemia Clinics…