Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pungky Ardani Kusuma"'
Publikováno v:
Paediatrica Indonesiana, Vol 56, Iss 4, Pp 226-9 (2016)
Background Wilms tumor is the most common renal malignancy in children (95%) and one of the leading causes of death in children, with high mortality rates in developing countries. Identifying risk factors for mortality is important in order to provid
Externí odkaz:
https://doaj.org/article/26bb4c11e1564894948a1fb195ed492e
Publikováno v:
Paediatrica Indonesiana, Vol 55, Iss 1, Pp 59-64 (2015)
Congenital obstructive posterior urethral membranes (COPUM) is a complex disease closely related to several pathological changes in kidney development and function, as a result of urinary reflux since in utero. This congenital anomaly of urinary trac
Externí odkaz:
https://doaj.org/article/0c35e8d7141841a39e4a6ffc95f1e5ea
Publikováno v:
Paediatrica Indonesiana, Vol 49, Iss 6, Pp 355-8 (2009)
Background Measurement of protein excretion is not only used for diagnostic purpose but also to monitor disease severity and prognosis in children with nephrotic syndrome (NS). The common method to measure proteinuria is 24-hour urine collection. How
Externí odkaz:
https://doaj.org/article/69d0d6e2758e4f978b05db38dca2f004
Publikováno v:
Paediatrica Indonesiana, Vol 49, Iss 6, Pp 355-8 (2009)
Background Measurement of protein excretion is not only used for diagnostic purpose but also to monitor disease severity and prognosis in children with nephrotic syndrome (NS). The common method to measure proteinuria is 24-hour urine collection. How
Publikováno v:
Paediatrica Indonesiana, Vol 56, Iss 4, Pp 226-9 (2016)
Background Wilms tumor is the most common renal malignancy in children (95%) and one of the leading causes of death in children, with high mortality rates in developing countries. Identifying risk factors for mortality is important in order to provid
Publikováno v:
Paediatrica Indonesiana, Vol 55, Iss 1, Pp 59-64 (2015)
Congenital obstructive posterior urethral membranes (COPUM) is a complex disease closely related to several pathological changes in kidney development and function, as a result of urinary reflux since in utero. This congenital anomaly of urinary trac
Autor:
Teguh Haryo, Sasongko, Ahmad Hamim, Sadewa, Pungky Ardani, Kusuma, Martua Parlindungan, Damanik, Myeong Jin, Lee, Hitoshi, Ayaki, Kandai, Nozu, Akinobu, Goto, Masafumi, Matsuo, Hisahide, Nishio
Publikováno v:
The Kobe journal of medical sciences. 51(3-4)
The angiotensin converting enzyme (ACE) gene carries insertion (I) and deletion (D) polymorphism within its intron 16. The presence of D-allele in the ACE gene has been reported as a probable genetic risk factor for idiopathic nephrotic syndrome (INS
Publikováno v:
Paediatrica Indonesiana, Vol 51, Iss 2, Pp 61-5 (2011)
Background Disturbances in bone mineral metabolism and side effects of corticosteroid treatment may cause decreased bone density in patients v.ith nephrotic syndrome (NS).Objectives To compare the prevalence oflow bone mineral density (BMD) in childr