Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sangeeta Hasmukh Ravat"'
Publikováno v:
Annals of Indian Academy of Neurology, Vol 22, Iss 4, Pp 496-499 (2019)
Isolated hemichorea (HC) in adults has a relatively restricted differential diagnosis including stroke of contralateral basal ganglia nuclei, nonketotic hyperglycemia, and basal ganglia toxoplasmosis in HIV infection. Hypoparathyroidism-related basal
Externí odkaz:
https://doaj.org/article/77ba5a4f737c4fcc811e8814b67ba10a
Autor:
Shreyas Hasmukh Ravat, Amit Ashok Bhatti, Mansi Viraj Shah, Dattatraya P Muzumdar, Sangeeta Hasmukh Ravat
Publikováno v:
Annals of Indian Academy of Neurology, Vol 20, Iss 1, Pp 55-57 (2017)
Seizures are associated with fascinatingly varied cardiac and autonomic manifestations, of which ictal tachycardia is common, and asystole and bradycardia are rare. Ictal asystole (IA), an often unsought autonomic phenomenon, occurs most commonly wit
Externí odkaz:
https://doaj.org/article/c2489b76c7f94d73bb8e8037d6c23920
Publikováno v:
Annals of Indian Academy of Neurology, Vol 22, Iss 4, Pp 496-499 (2019)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Isolated hemichorea (HC) in adults has a relatively restricted differential diagnosis including stroke of contralateral basal ganglia nuclei, nonketotic hyperglycemia, and basal ganglia toxoplasmosis in HIV infection. Hypoparathyroidism-related basal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::451a93445f0f736a4716b094fbc7a72e
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
Autor:
Pankaj Agarwal, Shruti Agrawal, Sangeeta Hasmukh Ravat, Priyanka Walzade, Stephen G. Reich, Karan Desai, Alberto J. Espay
Publikováno v:
Mov Disord Clin Pract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ab60e37f6865d49485ae7aa912848c1
https://pubmed.ncbi.nlm.nih.gov/34514039
https://pubmed.ncbi.nlm.nih.gov/34514039
Publikováno v:
BMJ Case Reports. 15:e249200
Tumour-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is an uncommon paraneoplastic syndrome which poses a diagnostic challenge. The hallmark feature is severe acquired hypophosphataemic osteomalacia due to renal phosphate wasting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ceae3b16218a65cdcd93c1d49f0f625
https://doi.org/10.1136/bcr-2022-249200
https://doi.org/10.1136/bcr-2022-249200
Publikováno v:
Movement Disorders Clinical Practice. 6:74-76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25547b2162f079845fc8a39a1ac44236
https://doi.org/10.1002/mdc3.12686
https://doi.org/10.1002/mdc3.12686