Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sheela Bharani"'
Autor:
Sheela Bharani, Sejal Thakkar
Publikováno v:
Indian Dermatology Online Journal, Vol 4, Iss 3, Pp 241-243 (2013)
Goltz syndrome is a rare multisystem disorder with cutaneous, ocular, dental and skeletal abnormalities. Other mesoectodermal abnormalities are also present. Its hallmark is thinning of the dermis resulting subcutaneous fat herniation. The present ca
Externí odkaz:
https://doaj.org/article/8db0728bb1874bb79afae6ba4ea7139b
Publikováno v:
National Journal of Community Medicine, Vol 3, Iss 02 (2012)
Background: IMNCI is an integrated approach to decrease morbidity and mortality amongst children between 0-5 years. Training to pre-service level during medical, nursing-education and anganwadi worker (AWW) is the first fundamental stage of IMNCI.
Externí odkaz:
https://doaj.org/article/75ed9f6db7db4cdab3f109ca8b61e3eb
Publikováno v:
Journal of Nepal Paediatric Society. 41:29-34
Introduction: Mechanical ventilation is an important factor contributing to the reduced neonatal mortality in NICU. However, many ventilated babies are left with detrimental sequelae. This study was undertaken to know the prognostic predictors and su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::079e98321334c0bdc52a5997057645d5
https://doi.org/10.3126/jnps.v41i1.30630
https://doi.org/10.3126/jnps.v41i1.30630
Publikováno v:
International Journal of Contemporary Pediatrics. 9:116
Non-compaction of left ventricular (NCLV) is a rare cardiomyopathy of unknown origin characterized by prominent ventricular trabeculations and deep intertrabecular sinusoids, in communication with the left ventricular cavity. The NCLV results due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d20e8e3a102a1aae24cfba6f1fbfc4d0
https://doi.org/10.18203/2349-3291.ijcp20214948
https://doi.org/10.18203/2349-3291.ijcp20214948
Publikováno v:
Journal of Pediatric Neurosciences
Garcia-Hafner-Happle syndrome, also known as Fibroblast growth factor receptor 3 epidermal nevus syndrome, is a new neurocutaneous phenotype, which has been identified in 2008 by Garci'a-Vargas et al. The disorder is caused by a mosaic R248C mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcda4428217dccd625d36d35fa38ae37
http://europepmc.org/articles/PMC4040040
http://europepmc.org/articles/PMC4040040
Autor:
Sejal Thakkar, Sheela Bharani
Publikováno v:
Indian Dermatology Online Journal
Indian Dermatology Online Journal, Vol 4, Iss 3, Pp 241-243 (2013)
Indian Dermatology Online Journal, Vol 4, Iss 3, Pp 241-243 (2013)
Goltz syndrome is a rare multisystem disorder with cutaneous, ocular, dental and skeletal abnormalities. Other mesoectodermal abnormalities are also present. Its hallmark is thinning of the dermis resulting subcutaneous fat herniation. The present ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eb1bf5788647119e07e312cd8511464
http://europepmc.org/articles/PMC3752490
http://europepmc.org/articles/PMC3752490
Autor:
Ritesh Nandlal Parmar, Sheela Bharani
Publikováno v:
International Journal of Contemporary Pediatrics. 4:1585
Background: Infantile tremor syndrome (ITS) is a very common clinical entity. The etiology of ITS remains obscure. Various hypothesis has been proposed including vitamin B12 deficiency. But it remains to be seen whether there are other contributory f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::360c973f6f61a5ddf0987f2a7d63fa46
https://doi.org/10.18203/2349-3291.ijcp20173085
https://doi.org/10.18203/2349-3291.ijcp20173085
Publikováno v:
Indian pediatrics. 50(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27f7b10eba6dd770b3b1d7aca4f1bc40
https://pubmed.ncbi.nlm.nih.gov/23942413
https://pubmed.ncbi.nlm.nih.gov/23942413
Autor:
Sheela, Bharani
Publikováno v:
Indian pediatrics. 40(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b21204cd3edb9e933eb972ce44b99c4
https://pubmed.ncbi.nlm.nih.gov/12768050
https://pubmed.ncbi.nlm.nih.gov/12768050
Publikováno v:
Indian journal of pediatrics. 68(6)
An eight-year-old male child presenting with history of generalized convulsions, gradual loss of speech and generalized EEG (electroencephalography) abnormalities was diagnosed as Landau Kleffner Syndrome. He initially developed generalized convulsio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ebe722618bc17e03afa3d2fa0dd8187
https://pubmed.ncbi.nlm.nih.gov/11450391
https://pubmed.ncbi.nlm.nih.gov/11450391