Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Anirudh Upmanyu"'
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 33, Iss 1, Pp 95-98 (2021)
Mc Cune Albright Syndrome (MAS) is a rare, sporadic disorder characterized by a triad of symptoms: fibrous dysplasia, cafe-au-lait spots, and endocrinopathy. It is thought to be caused by the mutation of the GNAS1 gene and is predominantly a disease
Externí odkaz:
https://doaj.org/article/c7a7f555bbd842c6aa0568bd2f084671
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-3 (2020)
Abstract Background Parafunctional oral habits are known to cause deleterious effects on maxillofacial structures. One such effect is traumatic injuries secondary to chewing inanimate objects like pencils. Following trauma, the lead of the pencil has
Externí odkaz:
https://doaj.org/article/0132174b62b54364980e71ac913fc8bc
Autor:
Anka Sharma, Subhash P. Kumbhare, Ashita R. Kalaskar, Pawan Motghare, Shailesh Gondivkar, Anirudh Upmanyu
Publikováno v:
Forensic Science International: Reports, Vol 2, Iss , Pp 100085- (2020)
Age estimation has been an ever-evolving aspect of forensic science. There is no dearth of markers in estimating age around 14–15 years; however, there is paucity for adolescent- adult transition markers. Various studies have cited the late closure
Externí odkaz:
https://doaj.org/article/865989b7da934f5ab7710cb191f44235
Publikováno v:
J Oral Biol Craniofac Res
Pycnodysostosis is a rare autosomal recessive condition caused by the mutation of CTSK gene. CTSK regulates the activity of Cathepsin K which is responsible for osteoclast-mediated bone resorption. This mutation causes the bones to become dense, scle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::876c2830ec71559d90280c75cdb09d13
https://doi.org/10.1016/j.jobcr.2021.07.006
https://doi.org/10.1016/j.jobcr.2021.07.006
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 33, Iss 1, Pp 95-98 (2021)
Mc Cune Albright Syndrome (MAS) is a rare, sporadic disorder characterized by a triad of symptoms: fibrous dysplasia, cafe-au-lait spots, and endocrinopathy. It is thought to be caused by the mutation of the GNAS1 gene and is predominantly a disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f90caa8214e679b4b460ef8800ff71b8
http://www.jiaomr.in/article.asp?issn=0972-1363
http://www.jiaomr.in/article.asp?issn=0972-1363
Autor:
Anirudh Upmanyu, Shailesh Gondivkar, Anka Sharma, Subhash P Kumbhare, Pawan Motghare, Ashita R Kalaskar
Publikováno v:
Forensic Science International: Reports, Vol 2, Iss, Pp 100085-(2020)
Age estimation has been an ever-evolving aspect of forensic science. There is no dearth of markers in estimating age around 14–15 years; however, there is paucity for adolescent- adult transition markers. Various studies have cited the late closure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d96a83496c16b7ab452fad7e35ec17bb
http://www.sciencedirect.com/science/article/pii/S2665910720300347
http://www.sciencedirect.com/science/article/pii/S2665910720300347
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 20, Iss 1, Pp 1-3 (2020)
BMC Pediatrics, Vol 20, Iss 1, Pp 1-3 (2020)
Background Parafunctional oral habits are known to cause deleterious effects on maxillofacial structures. One such effect is traumatic injuries secondary to chewing inanimate objects like pencils. Following trauma, the lead of the pencil has been rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa61e1b6c9a5e0dd831636f0ce4b7a33
https://doi.org/10.1186/s12887-020-02428-8
https://doi.org/10.1186/s12887-020-02428-8
Publikováno v:
Journal of Oral Research and Review. 13:139
Congenital midline labial sinus is a rare condition known to affect both the upper and the lower lip. This anomaly has been reported in both genders, but with a slightly increased predilection in females. It can occur either in isolation or in associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f11079f4df320d0ac5ea266e0ec37b2
https://doi.org/10.4103/jorr.jorr_10_20
https://doi.org/10.4103/jorr.jorr_10_20
Publikováno v:
BMC Pediatrics; 11/20/2020, Vol. 20 Issue 1, pN.PAG-N.PAG, 1p