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pro vyhledávání: '"Parayil Sankaran, Bindu"'
Akademický článek
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Autor:
Huddar, Akshata, Govindaraj, Periyasamy, Chiplunkar, Shwetha, Deepha, Sekar, Jessiena Ponmalar, J.N., Philip, Mariyamma, Nagappa, Madhu, Narayanappa, Gayathri, Mahadevan, Anita, Sinha, Sanjib, Taly, Arun B., Parayil Sankaran, Bindu
Publikováno v:
In Mitochondrion September 2021 60:170-177
Publikováno v:
Epilepsy & Behavior Reports, Vol 14, Iss , Pp 100357- (2020)
A 6-year-old girl presented with history of infantile onset epileptic encephalopathy and developmental delay. She had polymorphic seizures that were refractory to regular anti-seizure medication. Incomplete control of seizures was achieved on startin
Externí odkaz:
https://doaj.org/article/60376f5246214564bd66779747d0a980
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
Autor:
Madhu Nagappa, Arun B Taly, Anita Mahadevan, Mailankody Pooja, Parayil Sankaran Bindu, Yasha T Chickabasaviah, Narayanappa Gayathri, Sanjib Sinha
Publikováno v:
Annals of Indian Academy of Neurology, Vol 18, Iss 4, Pp 445-448 (2015)
Tangier disease is a rare metabolic disorder that causes neuropathy in half of the affected individuals. We present the clinical, electrophysiological, and histopathological findings in a middle-aged gentleman of Tangier disease who was initially dia
Externí odkaz:
https://doaj.org/article/c994c3ca7396439e9652aaf45ef27706
Autor:
Saketh Kapoor, Mohd Hussain Shah, Nivedita Singh, Mohammad Iqbal Rather, Vishwanath Bhat, Sindhura Gopinath, Parayil Sankaran Bindu, Arun B Taly, Sanjib Sinha, Madhu Nagappa, Rose Dawn Bharath, Anita Mahadevan, Gayathri Narayanappa, Yasha T Chickabasaviah, Arun Kumar
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0155605 (2016)
Mutations in PLA2G6 were identified in patients with a spectrum of neurodegenerative conditions, such as infantile neuroaxonal dystrophy (INAD), atypical late-onset neuroaxonal dystrophy (ANAD) and dystonia parkinsonism complex (DPC). However, there
Externí odkaz:
https://doaj.org/article/c9cd827477da49d1ae272b6a360701a5
Autor:
Madhu Nagappa, Manjula Subbanna, Malathi Anil Kumar, Parayil Sankaran Bindu, Arun B Taly, Venkataram Shivakumar, Pinku Mani Talukdar, Rahul Wahatule, Sundar Periyavan, G.S. Umamaheswara Rao, Debprasad Dutta, Sanjib Sinha, Monojit Debnath
Publikováno v:
ORCID
Microsoft Academic Graph
Europe PubMed Central
Microsoft Academic Graph
Europe PubMed Central
Data indexing the contribution of various immuno-inflammatory components in the cerebrospinal fluid (CSF) towards the pathophysiology of Guillain Barre Syndrome (GBS) are limited. Th17 pathway plays crucial role in many immune mediated disorders of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b06f84b7ab27791cbdeec15b863f3248
https://doi.org/10.1016/j.jocn.2020.03.010
https://doi.org/10.1016/j.jocn.2020.03.010
Autor:
Parayil Sankaran Bindu
Publikováno v:
The Application of Clinical Genetics. 13:13-24
Sjogren Larsson syndrome (SLS) is a rare autosomal recessive inborn error of lipid metabolism due to mutations in the ALDH3A2 that result in a deficiency of fatty aldehyde dehydrogenase (FALDH). The syndrome has a high prevalence in Sweden where it w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4e410ed9ad4556169c8430ef22f7d9d
https://doi.org/10.2147/tacg.s193969
https://doi.org/10.2147/tacg.s193969
Autor:
Bevinahalli N Nandeesh, Vani Santosh, Gayathri Narayanappa, Anita Mahadevan, T. Chickabasaviah Yasha, Parayil Sankaran Bindu, Karthik Kulanthaivelu
Publikováno v:
Neuropathology. 40:93-98
Stroke is a major cause of mortality and morbidity with a wide variety of etiological risk factors. Cerebral small vessel disease (SVD) is an important cause of stroke in the young with several hereditary disorders affecting these small blood vessels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b65838a74640b00b22e91747b7a6fff
https://doi.org/10.1111/neup.12607
https://doi.org/10.1111/neup.12607
Autor:
Sumanth, Shivaram, Madhu, Nagappa, Doniparthi Venkata, Seshagiri, Jitender, Saini, Periyasamy, Govindaraj, Sanjib, Sinha, Parayil Sankaran, Bindu, Arun B, Taly
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 49(5)
Vanishing white matter disease (VWMD) due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58edacb448676f451be25e34893cc4f7
https://pubmed.ncbi.nlm.nih.gov/34663487
https://pubmed.ncbi.nlm.nih.gov/34663487