Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Sangeetha, Yoganathan"'
Autor:
Balamurugan Nagarajan, Vykuntaraju K. Gowda, Sangeetha Yoganathan, Indar Kumar Sharawat, Kavita Srivastava, Nitish Vora, Rahul Badheka, Sumita Danda, Umesh Kalane, Anupriya Kaur, Priyanka Madaan, Sanjiv Mehta, Sandeep Negi, Prateek Kumar Panda, Surekha Rajadhyaksha, Arushi Gahlot Saini, Lokesh Saini, Siddharth Shah, Varunvenkat M. Srinivasan, Renu Suthar, Maya Thomas, Sameer Vyas, Naveen Sankhyan, Jitendra Kumar Sahu
Publikováno v:
Epilepsia Open, Vol 8, Iss 4, Pp 1383-1404 (2023)
Abstract Objective Literature on the genotypic spectrum of Infantile Epileptic Spasms Syndrome (IESS) in children is scarce in developing countries. This multicentre collaboration evaluated the genotypic and phenotypic landscape of genetic IESS in In
Externí odkaz:
https://doaj.org/article/2042c5f568e642f6a08dd0240ef34435
Autor:
Shridhar P Joshi, Maya Thomas, Sangeetha Yoganathan, Sumita Danda, Mahalakshmi Chandran, Anitha Jasper
Publikováno v:
Annals of Indian Academy of Neurology, Vol 26, Iss 3, Pp 268-274 (2023)
Background: Status dystonicus (SD) is a life-threatening movement disorder emergency characterized by increasingly frequent and severe episodes of generalized dystonia, requiring urgent hospital admission. The diverse clinico-etiological spectrum, hi
Externí odkaz:
https://doaj.org/article/f621727f415047c9a0b57a4888eb296b
Autor:
Narmadham K Bharathi, Maya Mary Thomas, Sangeetha Yoganathan, Mahalakshmi Chandran, Rekha Aaron, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 6, Pp 1104-1108 (2022)
Background: Arginase deficiency is considered a masquerader of diplegic cerebral palsy. The rarity of hyperammonemic crisis and the slowly progressive course has made it a unique entity among the urea cycle defects. Objectives: The aim of our study i
Externí odkaz:
https://doaj.org/article/5c5a27a0cc2948cbb8803788bd55e170
Autor:
Madhan Kumar, Sangeetha Yoganathan, Siddarth Todari, Parvathy Suresh, Mahalakshmi Chandran, Sumita Danda, Leni Grace Mathew, Beena Koshy, Maya Thomas
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 6, Pp 1238-1241 (2022)
Externí odkaz:
https://doaj.org/article/fb69ae2593db4bfa8232318cfe76a35d
Autor:
Madhan Kumar, T P Murugan, Arul P Lionel, Maya M Thomas, Pavithra Mannam, Sangeetha Yoganathan
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 4, Pp 698-702 (2022)
Background: Most centers in developing countries prefer chelation therapy with D-penicillamine for the management of Wilson's disease (WD) because of its easy availability and affordability. Neurological worsening following treatment with D-penicilla
Externí odkaz:
https://doaj.org/article/4314355f68d34e12bb6989a289d6ab98
Autor:
Sophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, Mahalakshmi Chandran, Chrithunesa S Christudass, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 5, Pp 983-985 (2022)
Externí odkaz:
https://doaj.org/article/96a9566f1f484fe682834e2542d3054f
Autor:
Sangeetha Yoganathan, Rangan Srinivasaraghavan, Madhan Kumar, Lisa Kratz, Shraddha Mular, Sniya V Sudhakar, Prateek Malik, Mahalakshmi Chandran, Maya Thomas, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 4, Pp 738-740 (2022)
Externí odkaz:
https://doaj.org/article/8463256bec224d26918595e532a7202a
Autor:
Sirisha Varala, Renu George, Lydia Mathew, Paul Russell, Beena Koshy, Samuel P Oommen, Maya Thomas, Karthik Muthusamy, Sangeetha Yoganathan, L Jeyaseelan, Jayaprakash Muliyil
Publikováno v:
Indian Dermatology Online Journal, Vol 12, Iss 1, Pp 84-89 (2021)
Background and Aims: Cutaneous lesions are the defining features of several neurocutaneous syndromes like neurofibromatosis1(NF1), tuberous sclerosis complex (TSC), and Sturge Weber syndrome to name a few. With this background, we explored the possib
Externí odkaz:
https://doaj.org/article/8d7457be741549cf965f67aa1c183625
Autor:
Sangeetha Yoganathan, Rangan Srinivasaraghavan, Mahalakshmi Chandran, Lisa Kratz, Beena Koshy, Sniya Valsa Sudhakar, Gautham Arunachal, Maya Thomas, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 261-264 (2021)
Externí odkaz:
https://doaj.org/article/f1197676d3a146ca9b35a519160c60c4
Autor:
Sangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, Mugil Varman, Maya Thomas, Sniya Valsa Sudhakar, Samuel Philip Oommen, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 1, Pp 113-117 (2020)
Succinic semialdehyde dehydrogenase (SSADH) deficiency is an autosomal recessive disorder of gamma-aminobutyric acid metabolism. Children with SSADH deficiency usually manifest with developmental delay, behavioral symptoms, language dysfunction, seiz
Externí odkaz:
https://doaj.org/article/4b12d668aa3648e6bd2ea4ba1dd4dbb3