Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mitesh Chandarana"'
Autor:
Jayesh Sheth, Aadhira Nair, Frenny Sheth, Manali Ajagekar, Tejasvi Dhondekar, Inusha Panigrahi, Ashish Bavdekar, Sheela Nampoothiri, Chaitanya Datar, Ajit Gandhi, Mamta Muranjan, Anupriya Kaur, Manisha Desai, Mehul Mistri, Chitra Patel, Premal Naik, Maulin Shah, Koumudi Godbole, Seema Kapoor, Neerja Gupta, Sunita Bijarnia-Mahay, Sandeep Kadam, Dhaval Solanki, Soham Desai, Anand Iyer, Ketan Patel, Harsh Patel, Raju C. Shah, Shalmi Mehta, Ruchi Shah, Riddhi Bhavsar, Jhanvi Shah, Mili Pandya, Bhagyadhan Patel, Sudhir Shah, Heli Shah, Shalin Shah, Shruti Bajaj, Siddharth Shah, Nilam Thaker, Umesh Kalane, Mahesh Kamate, Vykunta Raju KN, Naresh Tayade, Sujatha Jagadeesan, Deepika Jain, Mitesh Chandarana, Jitendra Singh, Sanjiv Mehta, Beena Suresh, Harsh Sheth
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-17 (2024)
Abstract Background Rare disorders comprise of ~ 7500 different conditions affecting multiple systems. Diagnosis of rare diseases is complex due to dearth of specialized medical professionals, testing labs and limited therapeutic options. There is sc
Externí odkaz:
https://doaj.org/article/2e11021daa8849e989ed195e21ef0b00
Publikováno v:
Annals of Movement Disorders, Vol 5, Iss 1, Pp 23-37 (2022)
Movement disorders are relatively sparse amongst COVID-19 patients. However, in the setting of large number of COVID-19 cases, relatively rare acute to subacute onset, para-infectious or post-infectious movement disorders such as myoclonus and myoclo
Externí odkaz:
https://doaj.org/article/4a2f73683d784a718dc18e87ee719f2c
Publikováno v:
Annals of Movement Disorders, Vol 5, Iss 1, Pp 12-22 (2022)
The novel coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been associated with a myriad of potential neurological manifestations, with de novo movement disorders still being reported.
Externí odkaz:
https://doaj.org/article/86c6aeca0dd741b587ad30fdd5354f4a
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 1, Pp 26-34 (2022)
Oromandibular dystonia (OMD) is a clinical problem which is commonly encountered in the practice of movement disorders. OMD results from a variety of genetic and acquired etiologies and can occur as an isolated manifestation, or as part of an isolate
Externí odkaz:
https://doaj.org/article/306bd036796245c0b0317dec3c40f43f
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 3, Pp 327-338 (2021)
Myoclonus is a hyperkinetic movement disorder characterized by a sudden, brief, involuntary jerk. Positive myoclonus is caused by abrupt muscle contractions, while negative myoclonus by sudden cessation of ongoing muscular contractions. Myoclonus can
Externí odkaz:
https://doaj.org/article/bb15e9b470c54dbcbda42adc33877483
Publikováno v:
Annals of Movement Disorders, Vol 4, Iss 2, Pp 86-88 (2021)
ADCY5-related dyskinesia is a childhood-onset autosomal dominant disorder that is caused by gain-of-function mutations in the ADCY5 gene. The core clinical features include a varying combination of hyperkinetic movement disorders (chorea, athetosis,
Externí odkaz:
https://doaj.org/article/d2247fc09e944323a7178598b402507b
Autor:
Ajith Cherian, Mitesh Chandarana, Ashish Anand Susvirkar, K P Divya, Udit U Saraf, Syam Krishnan
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 4, Pp 630-632 (2021)
Externí odkaz:
https://doaj.org/article/d6667ea731c54e0698fcea16005895ff
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 3, Pp 327-338 (2021)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Myoclonus is a hyperkinetic movement disorder characterized by a sudden, brief, involuntary jerk. Positive myoclonus is caused by abrupt muscle contractions, while negative myoclonus by sudden cessation of ongoing muscular contractions. Myoclonus can
Autor:
Syam Krishnan, Divya Kalikavil Puthenveedu, Asha Kishore, Mitesh Chandarana, Krishnakumar Kesavapisharady, Udit Saraf
Publikováno v:
Mov Disord Clin Pract
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 49(5)