Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mugil Varman"'
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
Autor:
Sangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, Mugil Varman, Maya Thomas, Sniya V Sudhakar, Samuel P Oommen, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 259-261 (2021)
Externí odkaz:
https://doaj.org/article/36f63e70d4fa4abc887405a33c4e8431
Autor:
Sangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, Mugil Varman, Sniya Valsa Sudhakar, Samuel Philip Oommen, Shikha Jain, Maya Thomas, Manimegalai Babuji
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 3, Pp 419-421 (2020)
Externí odkaz:
https://doaj.org/article/056dee52ef7643cd8d3cb83efe25e910
Autor:
Sumita Danda, Mugil Varman, Sniya Valsa Sudhakar, Lisa E. Kratz, Gautham Arunachal, Samuel Philip Oommen, Sangeetha Yoganathan, Maya Thomas
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 1, Pp 113-117 (2020)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::946ec9f1129d7915ed3a1a8b60b947dd
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
Autor:
Sniya Valsa Sudhakar, Sangeetha Yoganathan, Gautham Arunachal, Mugil Varman, Samuel Philip Oommen, Lisa E. Kratz, Manimegalai Babuji, Shikha Jain, Maya Thomas
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 3, Pp 419-421 (2020)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eb77636d03b706c1a3b75ef498f0049
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
Publikováno v:
Journal of Pediatric Neurosciences
Nutritional deficiencies related neurological manifestations are not uncommon in infants and children. Here, we describe an infant with Vitamin B12 deficiency due to depleted maternal Vitamin B12 status presenting with progressive encephalopathy and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e7cf4115c84854147b7df37e2a20d9
http://europepmc.org/articles/PMC5890558
http://europepmc.org/articles/PMC5890558
Autor:
Mahalakshmi Chandran, Sangeetha Yoganathan, Suvasini Sharma, Gautham Arunachal, Maya Thomas, Mukul Malhotra, Mugil Varman
Publikováno v:
The Indian Journal of Pediatrics. 87:850-851
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77904537dec1bebc8c3d1333a1188967
https://doi.org/10.1007/s12098-020-03225-y
https://doi.org/10.1007/s12098-020-03225-y
Publikováno v:
Neurology. 90:e1271-e1272
A 9-year-old boy presented with a slowly progressive spastic ataxic syndrome. Sensorimotor polyneuropathy was detected on nerve conduction studies. MRI (figure) was highly suggestive of autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSAC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57bf2d37ed693c73fb233e534960f531
https://doi.org/10.1212/wnl.0000000000005252
https://doi.org/10.1212/wnl.0000000000005252
Publikováno v:
Neurology. 90:e177-e178
A 10-month-old infant was brought to the hospital in status epilepticus, preceded by a 2-day history of fever and loose stools. Brain MRI revealed swelling and T2 hyperintensity involving the thalami, white matter, and dorsal brainstem (figure 1). Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918e5527e03b0354214f929d33361c88
https://doi.org/10.1212/wnl.0000000000004800
https://doi.org/10.1212/wnl.0000000000004800
A well-built 31-year-old man presented with deformity and restricted movements of the left wrist joint. He gave a history of injury due to a fall 8 months earlier, for which he was initially treated with a wrist slab for 3 months. Clinical examinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15952af9c7f1f5cfcceb70d4e64ef524
https://europepmc.org/articles/PMC4330453/
https://europepmc.org/articles/PMC4330453/
