Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kristia Hermawan"'
Autor:
Retno Palupi-Baroto, Kristia Hermawan, Indah Kartika Murni, Tiara Nurlita, Yuli Prihastuti, Ira Puspitawati, Chika Carnation Tandri, Cahyani Gita Ambarsari
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Carotid intima-media thickness (cIMT) is a measure of atherosclerotic vascular disease and a surrogate biomarker for cardiovascular risk in patients with chronic kidney disease (CKD). Mineral and bone disorders (MBD) are complicat
Externí odkaz:
https://doaj.org/article/d020f13003b044e7a9a9ebfddb921119
Publikováno v:
Sari Pediatri, Vol 25, Iss 6, Pp 363-70 (2024)
Latar belakang. Anemia merupakan salah satu komplikasi tersering pada penyakit ginjal kronis serta dapat meningkatkan risiko mortalitas hingga 52%. Terapi anemia dengan recombinant human erythropoietin mampu meningkatkan kadar hemoglobin dengan sifat
Externí odkaz:
https://doaj.org/article/4289989928114b9ab1f6a39fdd880012
Autor:
Indah K Murni, Taichi Kato, Muhammad Taufik Wirawan, Nadya Arafuri, Kristia Hermawan, Anggoro Budi Hartopo, Dyah Wulan Anggrahini, Sasmito Nugroho, Noormanto Noormanto, Noriaki Emoto, Lucia Kris Dinarti
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background In limited resource settings, identification of factors that predict the occurrence of pulmonary hypertension(PH) in children with atrial septal defect(ASD) is important to decide which patients should be prioritized for defect cl
Externí odkaz:
https://doaj.org/article/6e27a5eaea97493691842f68069f1191
Publikováno v:
Paediatrica Indonesiana, Vol 63, Iss 2, Pp 73-9 (2023)
Background Neuroblastoma is an extracranial solid tumor originating from neural crest cells which failed to properly migrate. Neuroblastoma is commonly found in children under 12 months of age. The survival rate of these patients is still relatively
Externí odkaz:
https://doaj.org/article/57f2fb3b6e354bb0a5b1a3e0afd25811
Publikováno v:
Paediatrica Indonesiana, Vol 63, Iss 2, Pp 96-101 (2023)
Background Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease (CKD) in children. Delayed diagnosis of CAKUT due to lack of universal screening (such as prenatal ultrasound screening or pos
Externí odkaz:
https://doaj.org/article/fbb099984a9a4c58bae8834e386cad6d
Autor:
Retno Palupi-Baroto, Braghmandita W. Indraswari, Asal Wahyuni Erlin Mulyadi, Siti N. Rusdhy, Kharisma N. Prabowo, Kristia Hermawan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 34, Iss Suppl 1, Pp S66-S78 (2023)
Health-related quality of life (HRQOL) is an important patient-reported outcome. However, HRQOL research in pediatric patients with chronic kidney disease (CKD) in developing countries is limited. This cross-sectional study involved children with CKD
Externí odkaz:
https://doaj.org/article/efd5231b542c4c558c2e53e409bf17a3
Publikováno v:
JKKI (Jurnal Kedokteran dan Kesehatan Indonesia), Pp 191-197 (2021)
Child with left renal agenesis fulfill the diagnostic criteria for chronic kidney disease due to its structural abnormalities that lasted for more than three months. It is important to monitored the disease progression and also growth, development an
Externí odkaz:
https://doaj.org/article/b5ed63a0dbff4a65aa97ce5123d4a475
Publikováno v:
Sari Pediatri, Vol 18, Iss 3, Pp 214-9 (2017)
Latar belakang. Pneumonia merupakan penyebab utama kematian pada anak usia di bawah lima tahun di negara berkembang. Pengembangan sistem skor yang sederhana untuk memprediksi kematian pada pneumonia dapat meningkatkan kualitas pelayanan dan menurunka
Externí odkaz:
https://doaj.org/article/c42fc17d32114cbcbdb2b57f2d74ac11
Publikováno v:
Sari Pediatri, Vol 18, Iss 1, Pp 17-20 (2016)
Latar belakang. Gejala klinis infeksi saluran kemih (ISK) pada anak yang tidak spesifik dapat menyebabkan keterlambatan diagnosis. Keterlambatan penanganan berkaitan dengan risiko terbentuknya parut ginjal. Tahun 2011 American Academy of Pediatrics (
Externí odkaz:
https://doaj.org/article/72325df173a94082abfcbbe0aafa983f
Publikováno v:
Paediatrica Indonesiana. 63:96-101
Background Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease (CKD) in children. Delayed diagnosis of CAKUT due to lack of universal screening (such as prenatal ultrasound screening or pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::826931fcc5d2a23d61fb5feef603d0be
https://doi.org/10.14238/pi63.2.2023.96-101
https://doi.org/10.14238/pi63.2.2023.96-101