Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Divyank Pathak"'
Publikováno v:
Journal of Pediatric Critical Care, Vol 4, Iss 2, Pp 101-105 (2017)
Externí odkaz:
https://doaj.org/article/be78c5a2b3c545ec9a65aab284849253
Autor:
Divyank Pathak, Dhiren Gupta, Anil Sachdev, Parul Chugh, Neeraj Gupta, A. K. Simalti, Suresh Gupta
Publikováno v:
Pediatric Infectious Disease Journal. 40:797-801
Objective The aim of the study was to identify early predictors of mortality in children with severe dengue fever admitted to pediatric intensive care unit (PICU). Materials and methods All consecutive children with laboratory-confirmed severe dengue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::109d8f8cb6e2a43d122760d8c5d9c60f
https://doi.org/10.1097/inf.0000000000003179
https://doi.org/10.1097/inf.0000000000003179
Publikováno v:
IOSR Journal of Dental and Medical Sciences. 13:92-94
The term Hypoplastic left heart is used to describe a related group of anomalies that include under development of the left side of the heart (atresia of the aortic or mitral orifice) and hypoplasia of the ascending aorta. the left ventricle may be m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d89dd51bd1ce84cf2e9a111ba275e0cf
https://doi.org/10.9790/0853-13329294
https://doi.org/10.9790/0853-13329294
Publikováno v:
IOSR Journal of Dental and Medical Sciences. 13:39-41
Sturge-Weber syndrome is a rare disorder that occurs sporadically with a frequency of1:50,000. It is characterized by facial nevus, seizures, hemiparesis, intracranial calcificationand mental retardation. We report here a case of Sturge-Weber syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebcde33e597946e4b659cd776679cb72
https://doi.org/10.9790/0853-13553941
https://doi.org/10.9790/0853-13553941
Autor:
Jayshree Jadhav, D Y Shrikhande, Amol Pokharkar, Vivek Dholakiya, Amit Narkhede, Divyank Pathak
Publikováno v:
International Journal of Medical Research and Health Sciences, Vol 2, Iss 4, Pp 967-969 (2013)
Severe Peter plus Syndrome is a rare autosomal recessive condition that is characterized by ocular anomaly and associated with other systemic major or minor anomalies. Mutations of B3GALTL gene encoding beta 1,3 glucosyltransferase have been seen in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e78c7db65767176e9031fe483b2cdcc
http://ijmrhs.com/vol-2-issue-4/
http://ijmrhs.com/vol-2-issue-4/
Publikováno v:
JOURNAL OF PEDIATRIC CRITICAL CARE. 4:101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68ef6aa3325d4f45875ba94410889e2e
https://doi.org/10.21304/2017.0402.00186
https://doi.org/10.21304/2017.0402.00186