Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Palanisamy, Sivamurukan"'
Autor:
Pediredla Karunakar, Aakash Chandran Chidambaram, Sriram Krishnamurthy, Palanisamy Sivamurukan, Bobbity Deepthi, Mamatha Gowda
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 34, Iss 2, Pp 191-195 (2023)
Information on the genetic profile of congenital nephrotic syndrome (CNS) from India is scarce. The management of CNS is largely supportive of the setting of developing countries, mainly via the administration of intravenous albumin infusions, angiot
Externí odkaz:
https://doaj.org/article/7f916dd1a24e4ce2946d6504e8ea4e8c
Autor:
Jayasurya Suresh, Sriram Krishnamurthy, Jharna Mandal, Nivedita Mondal, Palanisamy Sivamurukan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 32, Iss 3, Pp 703-710 (2021)
Our study aimed to evaluate the diagnostic performance of point-of-care nitrite and leukocyte esterase (LE) dipsticks in the diagnosis of suspected urinary tract infection (UTI) in infants
Externí odkaz:
https://doaj.org/article/9a987d278849434db0bf5191c3635ab2
Autor:
Palanisamy Sivamurukan, Sriram Krishnamurthy, C G Delhikumar, Anbazhagan Jagadeesh, Bheemanathi Hanuman Srinivas, Debdatta Basu
Publikováno v:
Indian Journal of Rheumatology, Vol 15, Iss 1, Pp 49-52 (2020)
Leukocytoclastic vasculitis (LCV) is a complex group of conditions which are characterized by vascular damage and neutrophilic infiltrates. LCV in children is usually considered as a part of connective tissue diseases, autoimmune disorders, and prima
Externí odkaz:
https://doaj.org/article/e62f003646184c8d8b592c3f6d381f41
Autor:
Pediredla Karunakar, Bikash Kumar Naredi, Ramanitharan Manikandan, Sriram Krishnamurthy, Kagnur Ramya, Palanisamy Sivamurukan
Publikováno v:
Indian Journal of Pediatrics. 88:345-350
To study the etiological profile and patterns of clinical presentations of urolithiasis (UL) in children. This observational study included patients
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Publikováno v:
Indian pediatrics. 57(5)
To study the etiological profile and patterns of clinical presentation of nephrocalcinosis.In this observational study, patients 18 years or younger, referred to the pediatric nephrology clinic with nephrocalcinosis were evaluated for etiology. Sympt
An Unusual Presentation of Hemorrhagic Disease in an Infant: A Probable Case of Abetalipoproteinemia
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e429-e430
We report a probable case of abetalipoproteinemia in an infant who presented with unusual symptoms of late-onset vitamin K deficiency. Abetalipoproteinemia is a rare autosomal recessive disease caused by mutation of the microsomal triglyceride transf
Autor:
Barathidasan, Gowri S, Pediredla, Karunakar, Chinnaiah Govindhareddy, Delhikumar, Palanisamy, Sivamurukan
Publikováno v:
Journal of Paediatrics & Child Health; Mar2022, Vol. 58 Issue 3, p512-515, 4p
Autor:
Aravindhan Manoharan, Ramesh Ananthakrishnan, Palanisamy Sivamurukan, Bibekanand Jindal, Sriram Krishnamurthy
Publikováno v:
Indian journal of pediatrics. 87(9)
To estimate the frequency of renal and urinary tract anomalies in first-degree relatives of children with Congenital anomalies of kidney and urinary tract (CAKUT). This descriptive study was conducted on parents and siblings of 138 children with CAKU
Publikováno v:
Indian journal of pediatrics. 87(6)