Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Suryono Yudha Patria"'
Autor:
Muhammad Taufik Wirawan, Indah Kartika Murni, Suryono Yudha Patria, Nadya Arafuri, Noormanto Noormanto, Sasmito Nugroho
Publikováno v:
Paediatrica Indonesiana, Vol 64, Iss 5, Pp 454-8 (2024)
Takayasu arteritis (TA) is a rare chronic granulomatous vasculitis mainly affecting the aorta and its main branches. Clinical presentations of TA are non-specific, especially in the initial phase, which likely contributes to delayed diagnosis besides
Externí odkaz:
https://doaj.org/article/5d6aed2bcd5144c4b49cd9e0ece6fde3
Publikováno v:
Paediatrica Indonesiana, Vol 62, Iss 1, Pp 37-43 (2022)
Background The use of long-term oral glucocorticoid therapy, specifically in the treatment of systemic lupus erythematosus (SLE), has increased in the past two decades. Chronic glucocorticoid use may lead to a linear growth disturbances. Objective
Externí odkaz:
https://doaj.org/article/1c73605c1aff45bb808789e82e1f091d
Autor:
Kristy Iskandar, Agung Triono, Sunartini, Ery Kus Dwianingsih, Braghmandita Widya Indraswari, Ignatia Rosalia Kirana, Gabriele Ivana, Retno Sutomo, Suryono Yudha Patria, Elisabeth Siti Herini, Gunadi
Publikováno v:
PLoS ONE, Vol 17, Iss 10 (2022)
Introductions Duchenne muscular dystrophy (DMD) is an X-linked recessive progressive muscular disease marked by developmental delays due to mutations in the DMD gene, which encodes dystrophin. Brain comorbidity adds to the burden of limited mobility
Externí odkaz:
https://doaj.org/article/0ba8b78f4d5241f8bba2c22b516ee009
Publikováno v:
Paediatrica Indonesiana, Vol 59, Iss 4, Pp 169-74 (2019)
Background Diabetic ketoacidosis (DKA) is an acute complication in type 1 diabetes mellitus (DM) and a significant cause of morbidity and mortality in developing countries. Diabetic ketoacidosis can be prevented by good management of the disease. Ris
Externí odkaz:
https://doaj.org/article/f7e97e80f0a24c768145a0d323848529
Publikováno v:
Paediatrica Indonesiana, Vol 58, Iss 4, Pp 186-91 (2018)
Background Hyperleukocytosis in childhood acute lymphoblastic leukemia (ALL) is an emergency in oncology. This condition showed high mortality and relapse rates, as well as low survival rate. The outcomes of this group of patients are not yet well st
Externí odkaz:
https://doaj.org/article/d65e434769724d76a5316b9340bea17d
Autor:
Kristy Iskandar, Suryono Yudha Patria, Emy Huriyati, Harry Freitag Luglio, Madarina Julia, Rina Susilowati
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Objectives FTO rs9939609 variant has been shown to be associated with insulin resistance in Caucasian children. However, studies in Asia show inconsistent findings. We investigated the association between FTO rs9939609 polymorphisms and insu
Externí odkaz:
https://doaj.org/article/47df1e0f2f0c44c7b7cbbae5d9569a18
Publikováno v:
Sari Pediatri, Vol 18, Iss 6, Pp 436-42 (2017)
Latar belakang. Deteksi dan pengobatan dini hipotiroid kongenital dapat mengurangi risiko terjadinya disabilitas intelektual, sehingga ketepatan waktu pelayanan merupakan kunci keberhasilan program skrining hipotiroid kongenital (SHK) pada bayi baru
Externí odkaz:
https://doaj.org/article/dea3273729e7437f84f14bcd85b41322
Publikováno v:
Sari Pediatri, Vol 9, Iss 5, Pp 342-7 (2016)
Latar belakang. Mortalitas akibat meningitis bakterial menurun dengan ditemukan antibotik yang poten dan penanganan yang baik pada saat pasien kritis. Walaupun demikian, sekuele akibat meningitis bakterial masih tinggi, sekitar 50%-65% di negara berk
Externí odkaz:
https://doaj.org/article/d84f187a3a274988a6c109d292d13bbe
Publikováno v:
Paediatrica Indonesiana, Vol 49, Iss 1, Pp 1-6 (2009)
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and other cases of hereditary, unconjugated hyperbilirubinemia in several Asian populations. Currently, DNA sequencing is the only method available to identify
Externí odkaz:
https://doaj.org/article/4840e01b07d943a3a7baa8485349f3aa
Publikováno v:
Indonesia Journal of Biomedical Science. 16:65-69
Background: Down syndrome is the most common congenital chromosomal anomaly and occurs in about 1-10:1.000 live births globally. Various reports stated an increasing survival rate because of advanced medical and surgical care. The highest mortality i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f52c9e76f1ec5c73dbf7f531bd1e19ff
https://doi.org/10.15562/ijbs.v16i2.409
https://doi.org/10.15562/ijbs.v16i2.409