Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sangeeta H Ravat"'
Autor:
Urvashi Shah, Shivani Rajeshree, Parthvi Ravat, Mayuri Kalika, Saloni Mehta, Antara Sapre, Sangeeta H. Ravat
Publikováno v:
Epilepsia Open, Vol 7, Iss 4, Pp 665-673 (2022)
Abstract Objective The COVID‐19 pandemic impacted the care of people with epilepsy (PWE). Several online surveys were conducted but there is limited data regarding the impact on low‐income PWE from lower‐middle income countries (LMICs) who have
Externí odkaz:
https://doaj.org/article/c071063749464b448f657be3bd1adb78
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
Autor:
Pankaj A. Agarwal, Demy J.S. Kuipers, Christina Fevga, Shruti Agrawal, Sangeeta H. Ravat, Guido J. Breedveld, Kapil Sethi, Vincenzo Bonifati
Publikováno v:
Movement Disorders, 37(10), 2166-2167. John Wiley & Sons Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374d7fe430928d13df8d55d92fcf9d64
https://pure.eur.nl/en/publications/f907bc72-c645-4f74-9c46-58625b935bd7
https://pure.eur.nl/en/publications/f907bc72-c645-4f74-9c46-58625b935bd7
Publikováno v:
Mov Disord Clin Pract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9331691316a758657ccb39aabb91716f
https://doi.org/10.1002/mdc3.13282
https://doi.org/10.1002/mdc3.13282
Publikováno v:
Journal of Pediatric Neurosciences. 13:358
Glut-1 transporter deficiency syndrome (GLUT1-DS) is a rare disorder caused by the mutation in SLC2A1 gene, which results in impaired glucose transport into the brain. It has a broad spectrum of phenotypic presentation ranging from cognitive decline,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::572d080fdcbbad9b261bd46b86114697
https://doi.org/10.4103/jpn.jpn_146_17
https://doi.org/10.4103/jpn.jpn_146_17
Autor:
Sangeeta H, Ravat, Vivek, Jain
Publikováno v:
Journal of the Indian Medical Association. 108(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::925b178b50d51ed56008319c01dc18a3
https://pubmed.ncbi.nlm.nih.gov/21192500
https://pubmed.ncbi.nlm.nih.gov/21192500
Autor:
Sangeeta H Ravat, Rohit Gupta
Publikováno v:
Journal of Pediatric Neurosciences. 3:7
The epilepsies are socially handicapping disorders and even a single seizure occurring in certain circumstances may have disastrous effect. The impact of epilepsy on every aspect of both the lives of the child and family is significant. Issues such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5719f69f08919f7954bffcb4c0dbb9c3
https://doi.org/10.4103/1817-1745.40585
https://doi.org/10.4103/1817-1745.40585