Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Bhanudeep Singanamalla"'
Publikováno v:
Journal of Pediatric Critical Care, Vol 8, Iss 1, Pp 47-49 (2021)
Acute necrotizing encephalopathy of childhood (ANEC) is an uncommon cause of acute onset febrile encephalopathy, which progresses rapidly and has poor outcomes. We reported a 4-year-old female who presented with acute febrile encephalopathy, raised i
Externí odkaz:
https://doaj.org/article/b939adaf58434d039e7d38f48da67dca
Autor:
Shivan Kesavan, Bhanudeep Singanamalla, Dangudubiyyam Sri Krishna Sahitya, Arushi Gahlot Saini, Sameer Vyas
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 2, Pp 239-241 (2020)
Externí odkaz:
https://doaj.org/article/f8cddd066af24699aae2b2d70e6c6a95
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 5, Pp 789-790 (2021)
Externí odkaz:
https://doaj.org/article/d276346d2a07408fb8b5fa65d7f0b99c
Autor:
Bhanudeep Singanamalla, Arushi Gahlot Saini, Savita Verma Attri, Renu Suthar, Kanya Mukhopadhyay
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 5, Pp 820-821 (2021)
Externí odkaz:
https://doaj.org/article/ff3daf66635f4129a963ca0da0a37824
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 3, Pp 386-387 (2020)
Externí odkaz:
https://doaj.org/article/05df9e016a7745ceadf6c1ce48b928f8
Autor:
Bhanudeep, Singanamalla1 singanamalabhanudeep0@gmail.com, Koneti, Bramhini Bhargavi2
Publikováno v:
Annals of Indian Academy of Neurology. Jul/Aug2024, Vol. 27 Issue 4, p467-469. 3p.
Autor:
Bhanudeep, Singanamalla1 singanamalabhanudeep0@gmail.com, Koneti, Bramhini B2
Publikováno v:
Annals of Indian Academy of Neurology. Nov/Dec2024, Vol. 27 Issue 6, p752-753. 2p.
Autor:
Bhanudeep, Singanamalla a, Madaan, Priyanka a, Sankhyan, Naveen a, Saini, Lokesh a, Malhi, Prahbhjot b, Suthar, Renu a, Saini, Arushi Gahlot a, Ahuja, Chirag Kamal c, Vyas, Sameer c, Singh, Paramjeet c, Kaur, Anupriya d, Singh, Gagandeep e, Sharma, Rajni e, Negi, Sandeep a, Jayashree, Muralidharan f, Attri, Savita Verma g, Singhi, Pratibha h, Sahu, Jitendra Kumar a, *
Publikováno v:
In Epilepsy Research July 2021 173
Akademický článek
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Publikováno v:
J Pediatr Genet
Glutaric aciduria type 1 (GA-1) is a treatable inborn error of metabolism caused by glutaryl-CoA dehydrogenase deficiency. This enzyme deficiency leads to accumulation of glutaric acid, 3-hydroxy glutaric acid, and glutaconic acid which are potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2281c3b0bca6a099183cf0aa647f8abb
https://europepmc.org/articles/PMC10118697/
https://europepmc.org/articles/PMC10118697/
