Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Chandni Shekhawat"'
Autor:
Shikha Saxena, Sankalp Mittal, Sonal Priya, Krishna S Sundaragiri, Chandni Shekhawat, Akshay Bhargava, Bharat Sankhla
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 6, Pp 3326-3329 (2022)
Squamous odontogenic tumor is a rare epithelial odontogenic tumor. Only a few cases have been reported in the literature, out of which central cases occurring within the jawbones are more common, and very rarely peripheral cases have been reported. H
Externí odkaz:
https://doaj.org/article/2f1af909e939429c9e69c7d1c6b819ab
Publikováno v:
RUHS Journal of Health Sciences (2023)
Introduction: Mast cells (MC) are the local residents of the connective tissue and are associated with the release of certain pro-inflammatory and mitogenic cytokines. These substances, when released from the mast cells, may play a significant role i
Externí odkaz:
https://doaj.org/article/933ed049d9be40128236316e907386ca
Autor:
Bharat Sankhla, Chandni Shekhawat, Krishna Sireesha Sundaragiri, Akshay Bhargava, Priyanka Singh, Shikha Saxena
Publikováno v:
RUHS Journal of Health Science. 6
Autor:
Geetika Sobti, Astha Chaudhry, Jaishree Thanvi, Isha Gaurav, Chandni Shekhawat, Debopriya Banerjee, Lalit Kumar Likhyani, Sugandhi Soni
Publikováno v:
The Cleft Palate-Craniofacial Journal. :105566562210891
The present study aimed to assess the co-occurrence of taurodontism in nonsyndromic cleft lip and palate (NSCLP) patients in a subset of Indian population using cone beam computed tomography (CBCT).The study was a retrospective case–control kinds a
Publikováno v:
International Journal of Head and Neck Pathology. 1:48
Oral mucosal melanoma is a rare oral malignancy with well defined clinical presentation of a pigmented brown macular to nodular lesion. The careful histopathological examination along with immunohistochemistry of the biopsy specimen was helpful in id
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology. 28:470
Gardner's syndrome is a hereditary autosomal dominant disorder with complete penetrance and variable expression. The disease is characterized by multiple intestinal polyps, osteomas and supernumerary teeth. Gardner's syndrome is linked to mutations o