Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Dhananjay Y Shrikhande"'
Autor:
Santosh Yadav, Prashant Nigwekar, Dhananjay Y Shrikhande, Amit Patil, Amit Yadav,Nilesh Maniya
Publikováno v:
International Journal of Medical Research and Health Sciences, Vol 2, Iss 4, Pp 1009-1012 (2013)
Ketotic hypoglycemia is the most common form of childhood hypoglycemia. Periods of Hypoglycemic episodes typically occur during early morning, especially during intercurrent illness when food intake is limited. The symptoms and signs of hypoglycemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::6e67d3f2e41c6895534febb308e23c72
http://ijmrhs.com/vol-2-issue-4/
http://ijmrhs.com/vol-2-issue-4/
Publikováno v:
Pediatric Infectious Disease. 4:107-111
Aim Sonographic findings can be used as early diagnostic modality even before serological results (IgM/IgG antibodies) become positive in Dengue. Materials & methods DESIGN : Prospective cross-sectional study in a paediatric teaching hospital in rura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfe89c35c854b0d7d3f0719c8e4aaea8
https://doi.org/10.1016/j.pid.2012.07.006
https://doi.org/10.1016/j.pid.2012.07.006
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
Autor:
Rajib Chatterjee, Anuj Kumar, Inderdeep Kochar, Dhananjay Y Shrikhande, Krishna Mandade, Mukesh vasoya
Publikováno v:
IOSR Journal of Dental and Medical Sciences. 13:85-87
The term collodion baby is used for newborns in whom all the body surface is covered by thick skin s heets, so called "collodion membrane". Ichthyosis is an infrequent clinical entity worldwide (1:300,000 births). When diagnosed in a newborn, two for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19d69eba98e40867fe1a5fe38647b022
https://doi.org/10.9790/0853-13228587
https://doi.org/10.9790/0853-13228587
Autor:
Dhananjay Y Shrikhande
Publikováno v:
Journal of Pediatric Critical Care. 5:98
Background : It is an acquired autoimmune mediated postsynaptic disorder that is rare in childhood with prevalence of 5 in 1,00,000. First case was reported in the year 1644 in USA of an Indian chief Opechankanough. The disease is due to circulating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::392be23e74261c75cfb7893feb7234d2
https://doi.org/10.21304/2018.0501.00317
https://doi.org/10.21304/2018.0501.00317
Publikováno v:
Medical Journal Armed Forces India. 68:176-178
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::077c3eb1b50591270d8614c62d424e9e
https://doi.org/10.1016/s0377-1237(12)60026-4
https://doi.org/10.1016/s0377-1237(12)60026-4
Autor:
Jagjit Singh, Gurmit Singh, Dhananjay Y Shrikhande, Rajesh Nandal, Monika Dalal, Harsh Vardhan Gupta, Pankaj Abrol, Shubhangi Nigvekar
Publikováno v:
International Journal of Students' Research. 1:64-66
Wilson's disease, also known as hepatolenticular degeneration, is a rare familial disorder inherited as an autosomal recessive trait with inborn error of copper metabolism leading to toxic accumulation of copper in the body particularly the liver, br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e7fce04d7360a5652cabf02d660147a
https://doi.org/10.5549/ijsr.1.2.64-66
https://doi.org/10.5549/ijsr.1.2.64-66
Autor:
Suhas Patil, Dhananjay Y Shrikhande, Gurmit Singh, Kunal Ahya, Niranjan Bommisetti Kurukuti, Rajiv Girdhar, Apurva Desai, Sankalp Yadav
Publikováno v:
International Journal of Students' Research. 1:29-31
Waardenburg syndrome (WS) is an inherited autosomal dominant disorder characterized by varying degrees of hearing loss and pigmentary anomalies affecting the eye, hair, skin. It is a rare syndrome affecting about 1 in 42,000 individuals. We herein re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b941b2e6653b212aa3782d185813162d
https://doi.org/10.5549/ijsr.1.1.29-31
https://doi.org/10.5549/ijsr.1.1.29-31
Publikováno v:
Italian Journal of Pediatrics, Vol 36, Iss 1, p 62 (2010)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
Leigh syndrome is a rare progressive neurodegenerative, mitochondrial disorder of childhood with only a few cases documented from India. The clinical presentation of Leigh syndrome is highly variable. However, in most cases it presents as a progressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::098e17ac647d0d1d347a013dbf0d350a
http://www.ijponline.net/content/36/1/62
http://www.ijponline.net/content/36/1/62