Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Rahil Ansari"'
Autor:
Neeraj Jain, Dnyaneshwar Jadhav, Akash Chheda, Sangeeta Ravat, Rahil Ansari, Mayur Thakkar, Rishikesh Joshi, A. Santosh Sriram, Vrug Durge
Publikováno v:
SciMedicine Journal, Vol 4, Iss 1, Pp 13-24 (2022)
Objective: Covid-19 is a highly infectious viral disease, and our understanding of the impact of this virus on the nervous system is limited. Therefore, we aimed to do a systematic analysis of the neurological manifestations. Methods: We retrospectiv
Externí odkaz:
https://doaj.org/article/4a1e5efb0b35439c885e5f1f3c53bf60
Autor:
Karan M. Desai, Piyush Kumar, Parthvi S. Ravat, Sangeeta H. Ravat, Neeraj Jain, Shruti Agrawal, Rahil Ansari
Publikováno v:
Epilepsy & Behavior Reports, Vol 15, Iss , Pp 100401- (2021)
Cerebrotendinous Xanthomatosis (CTX) is a rare autosomal-recessive inborn disorder of bile acid metabolism due to mutations in the CYP27A1 gene. It presents with a diverse range of neurological and non-neurological symptoms. We present a case of CTX
Externí odkaz:
https://doaj.org/article/fa84c2943f5d4104933b8a51b9b2d6eb
Publikováno v:
Journal of the Neurological Sciences. 429:119141
Autor:
Rahil Ansari, Priyanka Walzade, Piyush Anshu, Neeraj Jain, Sangeeta Ravat, Karan Desai, Gajanan Panandikar
Publikováno v:
Journal of the Neurological Sciences. 429:119191
Autor:
Sangeeta Ravat, Rishikesh Joshi, Santosh Sriram Andugulapati, Rahil Ansari, Neeraj Jain, Parag Maheshkar, Piyush Anshu
Publikováno v:
Journal of the Neurological Sciences. 429:118604
Autor:
Mayur Thakkar, Sangeeta Ravat, Rahil Ansari, Piyush Anshu, Neeraj Jain, Santosh Sriram Andugulapati, Rushikesh Joshi
Publikováno v:
Journal of the Neurological Sciences. 429:118800
Autor:
Sangeeta Ravat, Mayur Thakkar, Karan Desai, Akash Chheda, Neeraj Jain, Dnyaneshwar Jadhav, Rahil Ansari
Publikováno v:
Journal of the Neurological Sciences. 429:118362
Autor:
Priyanka Walzade, Gajanan Panandikar, Piyush Anshu, Rahil Ansari, Sangeeta Ravat, Karan Desai, Neeraj Jain
Publikováno v:
Journal of the Neurological Sciences. 429:118701
Autor:
Rahil Ansari, Karan Desai, Neeraj Jain, Sangeeta Ravat, Piyush Kumar, Parthvi S. Ravat, Shruti Agrawal
Publikováno v:
Epilepsy & Behavior Reports
Epilepsy & Behavior Reports, Vol 15, Iss, Pp 100401-(2021)
Epilepsy & Behavior Reports, Vol 15, Iss, Pp 100401-(2021)
Highlights • Epilepsy is rarely a presenting neurological feature of CTX, but a progressive myoclonic epilepsy. • A 'progressive myoclonic epilepsy'-like presentation of Cerebrotendinous Xanthomatosis (CTX) is novel to the best of our knowledge.<
Autor:
Rajiv Yadav, Rateena Rajbhandari, Ganesh Shah, Pratistha Maskey, Rashmila Maharjan, Biplav Manandhar, Imran Ansari, Shiva Chalise, Rahil Ansari
Publikováno v:
Journal of Patan Academy of Health Sciences. 1:4-7
Introductions: Congenital malformations need to be identified and intervened early to save lives and prevent sufferings. Many birth defects have well known incidence/prevalence rates but these have not been studied thoroughly in the local population