Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Sumanth, Shivaram"'
Autor:
Sumanth Shivaram, Manisha Gupta, A V R. Taallapalli, Saraswati Nashi, Anita Mahadevan, P R Srijithesh
Publikováno v:
Annals of Indian Academy of Neurology, Vol 26, Iss 2, Pp 197-199 (2023)
Externí odkaz:
https://doaj.org/article/14a12808e3df40438d3bf073d52b1778
Autor:
Sumanth Shivaram, Madhu Nagappa, Doniparthi V Seshagiri, Anita Mahadevan, Yashwanth Gangadhar, T N Sathyaprabha, Vijay Kumavat, Rose D Bharath, Sanjib Sinha, Arun B Taly
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 178-185 (2021)
Background: The clinical spectrum of contactin-associated protein-like 2 (CASPR2) antibody-associated disease is wide and includes Morvan syndrome. Studies describing treatment and long-term outcome are limited. Aims: We report the clinical profile a
Externí odkaz:
https://doaj.org/article/1a32bb1b94f7475c987ff366b86bea16
Autor:
Sumanth Shivaram, Madhu Nagappa, Doniparthi V Seshagiri, Jayanth Shimoga Shanthakumar, Swayang Sudha Panda, Ravi Anadure, B N Nandeesh, Yasha T Chickabasaviah, Rose D Bharath, Joy Vijayan, Bakula Kashyap, Sanjib Sinha, Arun B Taly
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 3, Pp 405-409 (2021)
Vogt-Koyanagi-Harada (VKH) syndrome is an immune-mediated granulomatous disease which affects melanin-rich organs like eyes, skin, nervous system, and ears. Neurological and auditory manifestations usually precede the involvement of other sites. Pati
Externí odkaz:
https://doaj.org/article/d2f72c93ca914e779d06262c0f0c161d
Clinico-pathological features in köhlmeier–degos disease with cutaneous and neurological involvement
Autor:
Dodmallur Mallikarjuna Sindhu, Sumanth Shivaram, Shilpa Rao, Madhu Nagappa, Doniparthi V Seshagiri, Vani Santosh, J Madhukara, A S Shreedhara, Maya D Bhat, Rose D Bharath, Sanjib Sinha
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 6, Pp 1005-1009 (2021)
Externí odkaz:
https://doaj.org/article/cd198070a9c94f8193f040824ad5e856
Autor:
Sumanth Shivaram, Ashok V. Reddy Tallapalli, Manisha Gupta, Saraswati Nashi, Girish B. Kulkarni, Suvarna Alladi
Publikováno v:
Journal of Neurosciences in Rural Practice. 13:546-549
Spontaneous downbeat nystagmus and ocular flutter are rare clinical signs. Such findings are commonly related to cerebellar pathology, predominantly ischemia. In a significant percentage of patients, the cause may not be found. If these signs are ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c46aefa24acc259308457a6ad1c40ab
https://doi.org/10.1055/s-0042-1749404
https://doi.org/10.1055/s-0042-1749404
Autor:
Praveen P. Sharma, Doniparthi V. Seshagiri, Madhu Nagappa, Thrinath Mullapudi, Nikhitha Sreenivas, Saikat Dey, Sumanth Shivaram, Rahul Wahatule, Vijay Kumawat, Binu V. Sreekumaran Nair, Sriganesh Kamath, Sanjib Sinha, Arun B. Taly, Monojit Debnath
Publikováno v:
European Journal of Neurology. 29:2074-2083
The IL-33/ST2 immune axis plays crucial roles in infection and immunity. A dysregulated IL-33/ST2 axis can induce autoimmune reaction and inflammatory responses. Guillain-Barré syndrome (GBS) is an acute peripheral neuropathy, mostly caused by post-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2da2b25a2f5b8ee1d30614eecd2178c6
https://doi.org/10.1111/ene.15334
https://doi.org/10.1111/ene.15334
Autor:
Parayil Sankaran Bindu, Periyasamy Govindaraj, Doniparthi V. Seshagiri, Madhu Nagappa, Sumanth Shivaram, Sanjib Sinha, Arun B Taly, Jitender Saini
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49:708-712
Vanishing white matter disease (VWMD) due to eIF2B mutations is a common leukodystrophy characterised by childhood onset, autosomal recessive inheritance, and progressive clinical course with episodic worsening. There are no reports of genetically co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cf62e4cc7b1469b85410b8c89eaca2d
https://doi.org/10.1017/cjn.2021.202
https://doi.org/10.1017/cjn.2021.202
Publikováno v:
Indian Journal of Psychological Medicine, Vol 37, Iss 4, Pp 413-418 (2015)
Background: The term catatonia was first introduced in 1874 and several etiologies, both organic and psychiatric have been attributed to the clinical phenotype of catatonia. The interesting feature is their response to lorazepam irrespective of their
Externí odkaz:
https://doaj.org/article/a4d8a0a4c4be43668f98e01bd8f29a3c
Publikováno v:
The Neurohospitalist. :194187442311793
Spinal dural tears are being increasingly recongnized to cause superficial siderosis and intracranial hypotension. We report a patient with chronic headache who was detected to have cerebellar superficial siderosis and subtle signs of intracranial hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::432720a135ff1893d05c7e5c77bd47ff
https://doi.org/10.1177/19418744231179346
https://doi.org/10.1177/19418744231179346
Autor:
Anita Mahadevan, Yashwanth Gangadhar, Talakad N. Sathyaprabha, Arun B Taly, Madhu Nagappa, Rose Dawn Bharath, Doniparthi V. Seshagiri, Sanjib Sinha, Vijay Kumavat, Sumanth Shivaram
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 178-185 (2021)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Background: The clinical spectrum of contactin-associated protein-like 2 (CASPR2) antibody-associated disease is wide and includes Morvan syndrome. Studies describing treatment and long-term outcome are limited. Aims: We report the clinical profile a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3ddab372e48cc33a7a6c603473eb000
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327