Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Akhilesh Pujar"'
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 60, Iss 1, Pp 1-5 (2024)
Abstract Background CDKL5 (Cyclin‐Dependent Kinase Like-5) deficiency disorder (CDD; Online Mendelian Inheritance in Man database 300203, 300672) is a rare neurologic disorder, which is caused by mutation in CDKL5 gene, situated on the X chromosome
Externí odkaz:
https://doaj.org/article/493b14136f504e05960849dcb849f712
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 59:344-349
Purpose: To identify and describe the clinical profile at presentation in patients diagnosed as having Leber's hereditary optic neuropathy with primary and secondary mutations and correlate with treatment. Methods: A review of electronic medical reco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec6206d8c6cb8c7900557dc4c9fb76f5
https://doi.org/10.3928/01913913-20220124-02
https://doi.org/10.3928/01913913-20220124-02
Publikováno v:
Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology. 30:169-174
Objective We investigated the null polymorphism in GSTM1 and GSTT1 genes and the antioxidant levels in oral submucous fibrosis (OSMF), leukoplakia and oral cancer patients along with healthy controls in a South Indian cohort. Methods Genotyping was d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f455e95bdbc11387afa8c25fbd5cfbd9
https://doi.org/10.1016/j.ajoms.2017.11.008
https://doi.org/10.1016/j.ajoms.2017.11.008