Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Mia Ratwita Andarsini"'
Publikováno v:
Paediatrica Indonesiana, Vol 63, Iss 6, Pp 464-71 (2023)
Background Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. Emergency complications such as hyperleukocytosis can arise as the disease develops. Exchange transfusion is one of many cytoreductive modalities to resolve the condit
Externí odkaz:
https://doaj.org/article/5cd0df3566854b5aa1e4136b3f8d0924
Autor:
Siti Arifah, Renu Pookboonmee, Autchareeya Patoomwan, Prasong Kittidumrongsuk, Mia Ratwita Andarsini
Publikováno v:
Paediatrica Indonesiana, Vol 63, Iss 5, Pp 405-10 (2023)
Background Acute lymphoblastic leukemia (ALL) is the most common cancer in children worldwide, which requires long treatment. This condition and its subsequent treatment change the body's physiology, reducing children’s quality of life. Objective T
Externí odkaz:
https://doaj.org/article/6ca81083a81f4c6c90cbb0a96403dc37
Relationship between serum ferritin and growth status of pediatric transfusion dependent thalassemia
Autor:
Andi Cahyadi, I Dewa Gede Ugrasena, Mia Ratwita Andarsini, Maria Christina Shanty Larasati, Raden Muhammad Zulfan Jauhari, Diah Kusuma Arumsari
Publikováno v:
Caspian Journal of Internal Medicine, Vol 14, Iss 3, Pp 425-432 (2023)
Background: Growth retardation is a long-term complication in pediatric transfusion-dependent thalassemias (TDTs), presented as short-stature and upper body segment shortening. The cause of this condition was chronic hypoxia, iron overload, endocrino
Externí odkaz:
https://doaj.org/article/632f13e861624fca841429dea7ac4e71
Publikováno v:
Majalah Biomorfologi, Vol 33, Iss 1, Pp 7-13 (2023)
Highlights 1. Diabetes mellitus type 1 (DM) is a chronic autoimmune illness characterized by insulin insufficiency and hyperglycemia as a consequence. 2. Stable HbA1c levels may be indicative of improved growth rates. Abstract Background: Type-1 di
Externí odkaz:
https://doaj.org/article/9f2ced74a5354307bb833569188228d9
Publikováno v:
Indonesian Journal of Anesthesiology and Reanimation (IJAR), Vol 4, Iss 2, Pp 80-86 (2022)
Introduction: Anemia often occurs in critically ill children and is associated with increased morbidity and mortality in women and children and impaired cognitive and behavioral development in children. Objective: This study aims to understand the pr
Externí odkaz:
https://doaj.org/article/8d4cffa1ffd545f4baf846004304d393
Publikováno v:
Jurnal Pengabdian Kepada Masyarakat (Indonesian Journal of Community Engagement), Vol 7, Iss 4, Pp 228-233 (2021)
Thalassemia, the fifth-most catastrophic disease with 10,555 patients, causes physical, emotional, and economic burden for the patient, their family, and the country. Annually, IDR 500 billion are needed to cover the treatment of thalassemia. This pr
Externí odkaz:
https://doaj.org/article/cfc6a51a122043ecad23e5dd0f365d60
Autor:
Yetti Hernaningsih, Yuli Syafitri, Yulia Nadar Indrasari, Prafa Alif Rahmawan, Mia Ratwita Andarsini, Indra Lesmana, Emmanuel Jairaj Moses, Nur Arzuar Abdul Rahim, Narazah Mohd Yusoff
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundThe frequency of the beta-thalassemia (β-thalassemia) gene in Indonesia ranges from 3 to 10%. However, in the East Java province, there is still limited information on the prevalence of β-thalassemia mutations in clinically diagnosed beta
Externí odkaz:
https://doaj.org/article/933675f06f5847ee9a65f4627dbf2f9d
Autor:
Anitha Marllyin Mairuhu, Mia Ratwita Andarsini, Retno Asih Setyoningrum, Andi Cahyadi, Maria Christina Shanty Larasati, I.Dewa Gede Ugrasena, Bambang Permono, Satrio Budiman
Publikováno v:
Heliyon, Vol 7, Iss 6, Pp e07209- (2021)
Background: Over the past 10 years, infection has remained as the main cause of illness and mortality among children with Acute Lymphoblastic Leukemia on chemotherapy. The high incidence of Hospital-Acquired Pneumonia in children with Acute Lymphobla
Externí odkaz:
https://doaj.org/article/50b1d0f4a48149e8a91d2824dcab5133
Publikováno v:
Folia Medica Indonesiana, Vol 53, Iss 1, Pp 49-55 (2017)
Thalassemia is a hereditary form of anemia that affects the synthesis of hemoglobin. The management of therapy in patients with b-thalassemia major which patients should receive continuous blood transfusions and increased iron absorption from the dig
Externí odkaz:
https://doaj.org/article/7e4f32ba5c5840efa81578c77c2ad6a3
Autor:
Maria Christina Shanty, Sherly Yuniarchan, Mia Ratwita Andarsini, I Dewa Gede Ugrasena, Bambang Permono, Risky Vitria Prasetyo
Publikováno v:
Jurnal Urologi Indonesia, Vol 26, Iss 2 (2019)
Objective: Wilms’ tumor is the most common childhood renal tumor for about 6% of pediatric malignant disease. The 5-year survival rate in United States increased from approximately from 70% (1970-1973) to 92% (1989-1996). This study was aim to anal
Externí odkaz:
https://doaj.org/article/81f23351a1c0496fb0e99e904f0d838d