Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shyam Sunder Mahansaria"'
Autor:
Shyam Sunder Mahansaria, Archana Rastogi, Kishore Gurumoorthy Subramanya Bharathy, Piyush Kumar Sinha, Shridhar Vasantrao Sasturkar, Viniyendra Pamecha
Publikováno v:
Hepatology International. 12:67-74
Selection of appropriate donors after rigorous evaluation is of paramount importance in living-donor liver transplantation. Despite this, donor surgery may not proceed due to unforeseen reasons. The aim of this paper is to study reasons for “no go
Autor:
Murali Appukuttan, Chhagan Bihari, Nikhil Agrawal, Tushar Kanti Chattopadhyay, Asit Arora, Shyam Sunder Mahansaria
Publikováno v:
International Journal of Surgical Pathology. 25:585-591
Introduction. Mixed adenoneuroendocrine carcinoma (MANEC) has recently been defined by the World Health Organization in 2010. These are rare tumors and MANECs of ampullary region are even rarer. Only 19 cases have been reported in literature. We pres
Autor:
Viniyendra Pamecha, Senthil Kumar, Shridhar Vasantrao Sasturkar, Shyam Sunder Mahansaria, Vaibhaw Kumar, Niteen Kumar, Kishore G. S. Bharathy, Piyush Kumar Sinha
Publikováno v:
Transplant International. 29:1126-1135
This study aimed to evaluate the association of postoperative thrombocytopenia with outcome following adult living donor liver transplantation (LDLT) for end-stage liver disease (ESLD). It was a prospective study of 120 consecutive adult LDLT from Se
Autor:
Shyam Sunder Mahansaria, Shiv Kumar Sarin, Kishore G. S. Bharathy, Viniyendra Pamecha, Senthil Kumar, Piyush Kumar Sinha, Shridhar Vasantrao Sasturkar
Publikováno v:
HPB. 18
A thorough donor evaluation in the living donation process is mandatory to ensure a safe outcome in an otherwise healthy individual. The aim of the current study was to evaluate the reasons for not proceeding to donation and the outcome of live liver
Autor:
Shyam Sunder Mahansaria, Viniyendra Pamecha, Kishore G. S. Bharathy, Sachin Kumar, Senthil Kumar
Dyskeratosis congenita is a multisystem genetic disorder. Although hepatic involvement is reported in about 7% of patients with dyskeratosis congenita, it is not well characterized and often attributed to hemochromatosis from frequent blood transfusi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c084d154063fe98b4a5c63a11677f96d
https://europepmc.org/articles/PMC4723656/
https://europepmc.org/articles/PMC4723656/
Autor:
Shyam Sunder Mahansaria, Kishore G. S. Bharathy, Shridhar Vasantrao Sasturkar, Shiv Kumar Sarin, Viniyendra Pamecha, Piyush Kumar Sinha, Sudhir Kumar
Publikováno v:
HPB. 18:e575-e576
Publikováno v:
Journal of Gastroenterology and Hepatology. 28:1587-1587