Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rajanikanth V. Patcha"'
Autor:
Perumal Karnan, Sathish Kumar Krishnan, Joy Varghese, Selvakumar Malleeswaran, Karattupalayam Sampath Mouleeswaran, Mettu Srinivas Reddy, Somashekara Hosaagrahara Ramakrishna, Prasanna Gopal, Rajanikanth V. Patcha
Publikováno v:
J Clin Exp Hepatol
Liver tumours are uncommon in the paediatric population, constituting 1–2 % of all paediatric tumours and 4% of all paediatric liver tumours. Hepatoblastoma followed by hepatocellular carcinoma is the most common tumours in this age group. Simultan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbdba20859e7e75d35f6730493c21073
https://doi.org/10.1016/j.jceh.2021.05.006
https://doi.org/10.1016/j.jceh.2021.05.006
Autor:
Rajanikanth V. Patcha, Mohan Babu Kasala, Somashekara Hosaagrahara Ramakrishna, Malathy Sathiyasekaran, Selvakumar Malleeswaran, Mettu Srinivas Reddy, Karnan Perumal, Joy Varghese
Publikováno v:
J Clin Exp Hepatol
ABO-incompatible living donor liver transplantation (ABOi-LDLT) is on the rise as a viable option in countries with limited access to deceased donor grafts. While reported outcomes of ABOi-LT in children are similar to ABO- Compatible liver transplan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bff59df33e1bb4385627b0cc0d7b74ee
https://doi.org/10.1016/j.jceh.2021.08.008
https://doi.org/10.1016/j.jceh.2021.08.008
Autor:
Joy Varghese, Sathish Kumar Krishnan, Somashekara Hosaagrahara Ramakrishna, Rajanikanth V. Patcha, Mettu Srinivas Reddy
Publikováno v:
Pediatric Transplantation. 25
BACKGROUND Biliary strictures after living donor liver transplantation (LDLT) are a significant cause of post-transplant morbidity. Endoscopic therapy is usually the first choice of treatment though surgical treatment may provide better biliary drain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee811c43e7914764d1fac0c5c16b66cf
https://doi.org/10.1111/petr.14115
https://doi.org/10.1111/petr.14115
Autor:
Selvakumar Malleeswaran, Mohan Babu Kasala, Karnan Perumal, Joy Varghese, Somashekara Hosaagrahara Ramakrishna, Rajanikanth V. Patcha
Publikováno v:
J Clin Exp Hepatol
Late-onset liposomal acid lipase deficiency (LAL deficiency), previously known as Cholesteryl ester storage disease (CESD) is a rare genetic lysosomal storage disorder caused by deficiency of lysosomal acid lipase (LAL) due to mutations in the LIPA g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f80d44f3211807d1925d5aec3ec5ff2f
https://europepmc.org/articles/PMC9077196/
https://europepmc.org/articles/PMC9077196/
Autor:
Vinayak Nikam, Kota Venugopal, Ravi Mohanka, Selvakumar Malleeswaran, Prashantha S Rao, Ellango Appusamy, Chandhan Kumar Kedarisetty, Raghavendra Babu Yalakanti, Bhaskaran Pillai Venugopal, Sunil D. Shenvi, Perumal Karnan, Anurag Shrimal, Nigel Heaton, Joy Varghese, Dharmesh Kapoor, Rajanikanth V. Patcha, Karan Kumar, Balbir Singh
Publikováno v:
Liver Transplantation
As of August 2020, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has affected more than 213 countries, leading to more than 18 million cases and 690,000 deaths. India is the second most affected country, with the majority of cases in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09dce9e535fcb1371241cfcb211bf542
Autor:
Kasala Mohan Babu, Joy Varghese, Perumal Karnan, Selvakumar Malleswaran, Rajanikanth V. Patcha, Vivek Vij, Ramya Murthy, Dheivamani Nirmala, Karattupalayam Sampath Mouleeswaran, Vijai Williams
Publikováno v:
Gastroenterology, Hepatology and Endoscopy Practice. 1:123
Bile acid synthesis defects (BASDs) are rare inborn errors of metabolism, causing neonatal hepatitis. These disorders are difficult to diagnose, especially in resource-limited settings where extensive laboratory and genetic analysis are not always fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5523cfc1d279a52ec53c914efaeacfa5
https://doi.org/10.4103/ghep.ghep_36_20
https://doi.org/10.4103/ghep.ghep_36_20