Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Pragati A. Sathe"'
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 67, Iss 3 (2024)
Externí odkaz:
https://doaj.org/article/ff3ad56b9378495f846e57febdacb27c
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 67, Iss 1, Pp 156-158 (2024)
Externí odkaz:
https://doaj.org/article/cea160c1fce6407bb75e0db92aa6716a
Akademický článek
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Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 63, Iss 4, Pp 672-674 (2020)
Externí odkaz:
https://doaj.org/article/8c1598b3828049aab363f860a83a47ab
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 2, Pp 337-338 (2019)
Externí odkaz:
https://doaj.org/article/be2f741e675d47d3ba413019380ac80a
Autor:
Pragati A, Sathe, Mona A, Agnihotri
Publikováno v:
Indian journal of pathologymicrobiology. 65(3)
Autor:
Devdas S Samala, Sandesh V Parelkar, Beejal V Sanghvi, Natasha L Vageriya, Bhupesh A Paradkar, Bhuvaneshwari M Kandalkar, Pragati A Sathe
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 19, Iss 1, Pp 5-9 (2014)
Objectives: The aim of this experimental study was to observe the intensity of the inflammatory reaction caused by neonatal urine and meconium on the intestinal wall of rats to better understand etiology of intestinal damage in gastroschisis. Materia
Externí odkaz:
https://doaj.org/article/312e6bb0d41041c5b3869dfc7e77985e
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 12, Pp ED03-ED05 (2016)
Hirschsprung disease (HD) in late childhood is uncommon and often undiagnosed or misdiagnosed. However, in a patient with Hirschsprung disease, of greater significance is the occurrence of life threatening enterocolitis. In its more severe form, thi
Externí odkaz:
https://doaj.org/article/84faf3aa7d034810adda71ddf387c2a6
Autor:
Tejaswini Priyadarshan Waghmare, Pragati Aditya Sathe, Naina Atul Goel, Bhuvaneshwari Mahendra Kandalkar
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 11, Pp ED23-ED24 (2016)
Holoprosencephaly is a rare congenital disorder which results from failure of cleavage or incomplete differentiation of the forebrain structures at various levels or to various degrees. Depending on the degree of involvement, it is classified into 4
Externí odkaz:
https://doaj.org/article/88dafdd1569e40e59915b03a004b6708
Autor:
Pragati Aditya Sathe, Ratnaprabha Kundlikrao Ghodke, Vageriya Natasha Laxmilal, Bhuvaneshwari Mahendra Kandalkar, Parelkar Sandesh Vinod
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 9, Pp ED07-ED08 (2015)
The neurenteric cyst is a rare developmental lesion arising as a result of persistence of the neurenteric canal. It usually presents in the second and third decade. Lesions occurring in children are rare. Majority of the cases presented with signs o
Externí odkaz:
https://doaj.org/article/052db52363244e3fb6ef75ce8b79ac8c