Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Bhuvaneshwari M. Kandalkar"'
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:
Medical Journal of Dr. D.Y. Patil University, Vol 8, Iss 1, Pp 106-107 (2015)
Teratomas are neoplasms, which are foreign to the anatomic site of occurrence. They occur in children, most commonly in sacrococcygeal region and gonads and less frequently at other sites. Teratomas of gastrointestinal tract are very rare. We report
Externí odkaz:
https://doaj.org/article/d946b0b9a88440f99db510f613a9e446
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 56, Iss 3, Pp 323-324 (2013)
Externí odkaz:
https://doaj.org/article/afcd4d3ed3db4cc69d25f45deb8a4c7d
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 56, Iss 4, Pp 471-472 (2013)
Externí odkaz:
https://doaj.org/article/55159a6285da4f9382db3144a3e2819e
Autor:
Kranti Khadilkar, Anurag R. Lila, Pragati Sathe, Tushar Bandgar, Sweta Budyal, Nalini S. Shah, Sandesh V. Parelkar, Bhuvaneshwari M Kandalkar, Beejal V Sanghvi, Rajeev Kasaliwal
Publikováno v:
Endocrine Practice. 21:770-776
Ovotesticular disorder of sex development (OT DSD) is a rare disorder of sex development characterized by the presence in the same individual of both histologically proven testis and ovary. There are scant data from the Indian subcontinent regarding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fcb5dc14021a59207494eba248c6383
https://doi.org/10.4158/ep15606.or
https://doi.org/10.4158/ep15606.or
Publikováno v:
Congenital Heart Disease. 9:280-285
Objective Nephropathy is a known complication in cyanotic congenital heart disease (CCHD). This study was undertaken for an objective analysis of histopathological changes of cyanotic nephropathy at autopsy. Design Retrospective case records studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f5ec40696356f9daee4fac4264f236b
https://doi.org/10.1111/chd.12121
https://doi.org/10.1111/chd.12121
Publikováno v:
Autopsy Practices
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2817904d52918e44f734ee34db18f1bd
https://doi.org/10.5005/jp/books/13011_7
https://doi.org/10.5005/jp/books/13011_7
Autor:
Sarangarajan Ranganathan, Hardik Shah, Kanchan Kothari, Pragati A. Sathe, Bhuvaneshwari M Kandalkar
Publikováno v:
Pediatric and Developmental Pathology. 15:329-332
Adrenal leiomyomas are rare, bilateral ones being rarer. Literature available on these rare tumors documents only 4 cases in children less than 12 years of age. Each case has been associated with acquired immune deficiency syndrome or some other immu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea1c6cc1bedae4d60c236ab4d741d109
https://doi.org/10.2350/12-01-1135-cr.1
https://doi.org/10.2350/12-01-1135-cr.1
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d78437dbb0a725dffd5ea202d0005c
https://doi.org/10.7860/jcdr/2016/22453.8932
https://doi.org/10.7860/jcdr/2016/22453.8932
Autor:
Pragati Sathe, Vageriya Natasha Laxmilal, Parelkar Sandesh Vinod, Bhuvaneshwari M Kandalkar, Ratnaprabha Kundlikrao Ghodke
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 of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4207f23dd81c4dd3a514fe4b284c0cff
https://europepmc.org/articles/PMC4606243/
https://europepmc.org/articles/PMC4606243/