Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Pustika Amalia W"'
Autor:
Pustika Amalia W, Djajadiman Gatot, Teny Tjitrasari, Iswari Setianingsih, Nanis Sacharis Marzuki
Publikováno v:
Paediatrica Indonesiana, Vol 46, Iss 1, Pp 41-5 (2016)
Background Hemolytic anemia may result from corpuscular or extracorpuscular abnormalities. One of the types of corpuscular abnormalities is membrane defect. The diagnosis is sometimes difficult and it may need special hematologic investigations. Ther
Externí odkaz:
https://doaj.org/article/6f6584ce702c40da966ecb15bc240d03
Autor:
Reza Fahlevi, Partini Pudjiastuti Trihono, Dina Muktiarti, Pustika Amalia Wahidiyat, Eka Laksmi Hidayati, Cut Nurul Hafifah
Publikováno v:
Sari Pediatri, Vol 26, Iss 3, Pp 189-96 (2024)
Sindrom nefrotik merupakan penyakit ginjal yang sering ditemukan pada anak-anak, dengan insiden 1-3 per 100.000 anak di bawah usia 16 tahun. Sekitar 10-20% anak dengan sindrom nefrotik mengalami sindrom nefrotik resisten steroid (SNRS), dan 10-30% da
Externí odkaz:
https://doaj.org/article/8a09708143664f5caef151827c8c4074
Autor:
William Cheng, Piprim Basarah Yanuarso, Pustika Amalia Wahidiyat, Syarif Rohimi, Partini Pudjiastuti Trihono, Muzal Kadim, Dina Muktiarti
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background In light of prolonged hypoxia, children with cyanotic heart disase (CHD) are at a high risk of developing iron deficiency iron deficiency (ID) and iron deficiency anemia (IDA). Reticulocyte hemoglobin equivalent (Ret-He) is a nove
Externí odkaz:
https://doaj.org/article/385710e287ac4f4db76980647dfa121f
Publikováno v:
Journal Of The Indonesian Medical Association. 70:23-26
Pendahuluan: Thalassemia adalah penyakit anemia hemolitik yang diturunkan. Transfusi berkala pada pasien thalassemia menyebabkan deposit besi di hipofisis yang mengakibatkan hipogonadotropik hipogonadisme. Pemeriksaan MRI mulai digunakan unutuk mengu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa60c317157fcbd1e38222b7c3304f42
https://doi.org/10.47830/jinma-vol.70.2-2020-174
https://doi.org/10.47830/jinma-vol.70.2-2020-174
Autor:
Teny Tjitra Sari, Ludi Dhyani Rahmartani, Angga Wirahmadi, Nathasha Brigitta Selene, Stephen Diah Iskandar, Pustika Amalia Wahidiyat
Publikováno v:
Thalassemia Reports, Vol 14, Iss 2, Pp 33-43 (2024)
Thalassemia a common hereditary blood disorder resulting in anemia. It is an important public health problem, with a high prevalence in Southeast Asia and Mediterranean countries, and preventable through screening programs. However, due to its chroni
Externí odkaz:
https://doaj.org/article/ef6c855ba45041adbb867ba73db80bcc
Publikováno v:
Paediatrica Indonesiana, Vol 63, Iss 4, Pp 245-55 (2023)
Background High protein intake in very preterm neonates (VPN) is important for growth. However, preterm kidneys have fewer functional nephrons and many of the ones present may be immature. Studies have shown that high protein intake induces nephron h
Externí odkaz:
https://doaj.org/article/49bee2a12d3f4454831cba1e72c875e2
Autor:
Teny Tjitrasari, Djajadiman Gatot, Iswari Setianingsih, Pustika Amalia W, Nanis Sacharis Marzuki
Publikováno v:
Paediatrica Indonesiana, Vol 46, Iss 1, Pp 41-5 (2016)
Background Hemolytic anemia may result from corpuscular or extracorpuscular abnormalities. One of the types of corpuscular abnormalities is membrane defect. The diagnosis is sometimes difficult and it may need special hematologic investigations. Ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4510f80f072625c0a6caee77d109848c
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/853
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/853
Autor:
Ludi Dhyani Rahmartani, Micheylla Kusumaning Dewi, Stephen Diah Iskandar, Anastasia Michelle Pratanata, Ganda Ilmana, Teny Tjitra Sari, Anna Mira Lubis, Pustika Amalia Wahidiyat
Publikováno v:
Thalassemia Reports, Vol 13, Iss 1, Pp 1-9 (2022)
Transfusion-dependent thalassemia is the most severe form of thalassemia; patients require regular blood transfusions to maintain their hemoglobin level. The COVID-19 pandemic has disrupted the routine measures for controlling chronic diseases like t
Externí odkaz:
https://doaj.org/article/0b7e1320ff854b31931052c91d191b03
Publikováno v:
International Journal of Technology, Vol 13, Iss 8, Pp 1726-1734 (2022)
Molecular characterization is important prior to clinical management as it can provide additional information for the clinical management of patients. This study aims to characterize the most common mutation and identify genotype-to-phenotype rela
Externí odkaz:
https://doaj.org/article/f7993dda146d4c46ae666beafd20db2b
Publikováno v:
Paediatrica Indonesiana, Vol 62, Iss 2, Pp 91-7 (2022)
Background Iron chelation therapy is used to maintain iron balance in β-thalassemia major patients who undergo repeated blood transfusions. Objective To compare the efficacy, safety, and cost of iron chelation combination regimens [deferiprone (D
Externí odkaz:
https://doaj.org/article/fd8825ada8d34c4cbd4095197f9d3b79