Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Sonam, Kothari"'
Autor:
Bindu, Parayil Sankaran, Sonam, Kothari, Chiplunkar, Shwetha, Govindaraj, Periyasamy, Nagappa, Madhu, Vekhande, Chetan Chandrakanth, Aravinda, Hanumanthapura R., Ponmalar, JN Jessiena, Mahadevan, Anita, Gayathri, Narayanappa, Bharath, MM Srinivas, Sinha, Sanjib, Taly, Arun B.
Publikováno v:
In Multiple Sclerosis and Related Disorders February 2018 20:84-92
Autor:
Bindu, Parayil Sankaran, Sonam, Kothari, Govindaraj, Periyasamy, Govindaraju, Chikkanna, Chiplunkar, Shwetha, Nagappa, Madhu, Kumar, Rakesh, Vekhande, Chetan Chandrakanth, Arvinda, Hanumanthapura R., Gayathri, Narayanappa, Srinivas Bharath, M.M., Ponmalar, J.N. Jessiena, Philip, Mariyamma, Vandana, V.P., Khan, Nahid Akhtar, Nunia, Vandana, Paramasivam, Arumugam, Sinha, Sanjib, Thangaraj, Kumarasamy, Taly, Arun B.
Publikováno v:
In Clinical Neurology and Neurosurgery January 2018 164:182-189
Autor:
Vandana, V.P., Bindu, Parayil Sankaran, Sonam, Kothari, Govindaraj, Periyasamy, Taly, Arun B., Gayathri, Narayanappa, Chiplunkar, Shwetha, Govindaraju, Chikkanna, Arvinda, H.R., Nagappa, Madhu, Sinha, Sanjib, Thangaraj, Kumarasamy
Publikováno v:
In Clinical Neurology and Neurosurgery September 2016 148:17-21
Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations
Autor:
Sonam, Kothari, Khan, Nahid Akthar, Bindu, Parayil Sankaran, Taly, Arun B., Gayathri, N., Bharath, M.M. Srinivas, Govindaraju, C., Arvinda, H.R., Nagappa, Madhu, Sinha, Sanjib, Thangaraj, K.
Publikováno v:
In Brain and Development October 2014 36(9):807-812
Autor:
Sanjib Sinha, Arun B. Taly, Shwetha Chiplunkar, Sonam Kothari, Periyasamy Govindaraj, Madhu Nagappa, Bindu Parayil Sankaran
Publikováno v:
Journal of Child Neurology. 35:433-441
The overlapping clinical and neuroimaging phenotypes of leukodystrophies pose a diagnostic challenge to both clinicians and researchers alike. Studies on the application of exome sequencing in the diagnosis of leukodystrophies are emerging. We used t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f8ab813925ce65e1d1f0e0c17ebd7ce
https://doi.org/10.1177/0883073820904294
https://doi.org/10.1177/0883073820904294
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 34, Iss 4, Pp 299-300 (2015)
Externí odkaz:
https://doaj.org/article/75097b2cca1041119ec26b30ae7ed2c8
Autor:
Sankaran, Bindu Parayil, Nagappa, Madhu, Shwetha Chiplunkar, Sonam Kothari, Periyasamy Govindaraj, Sanjib Sinha, Taly, Arun B.
Supplemental Material, Supplementary_file._Case_reports_16.10.19 for Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel by Bindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056df060ba6b4b3ccb15f927741b165f
Autor:
Josef Finsterer, Sonam Kothari
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 235-236 (2014)
Externí odkaz:
https://doaj.org/article/af92b1209cb0426baae1acc025e865c0
Autor:
Vandana, V. P., Bindu, Parayil Sankaran, Sonam, Kothari, Taly, Arun B., Gayathri, N., Madhu, N., Sinha, S.
Publikováno v:
Journal of Pediatric Neurosciences
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare mitochondrial disease. The available studies on MELAS syndrome are limited to evaluation of radiological, audiological, genetic, and neurolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c865dd5ce66ddd35219f2fa54b35b514
http://europepmc.org/articles/PMC4395941
http://europepmc.org/articles/PMC4395941
Autor:
Rita Christopher, Arun B Taly, Madhu Nagappa, Rose Dawn Bharath, Narayanappa Gayathri, Parayil Sankaran Bindu, Sanjib Sinha, Maya P. Bhatt, Sonam Kothari
Publikováno v:
Brain and Development. 35:398-405
Background: Epilepsy is an early and important feature in Menkes disease (MD), an X-linked recessive neurodegenerative disorder of childhood with defect in copper metabolism. There are only few reports on the electro-clinical and magnetic resonance i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e2da66921d68b1cd572c57eb331676
https://doi.org/10.1016/j.braindev.2012.07.016
https://doi.org/10.1016/j.braindev.2012.07.016