Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Divya, Nagabushana"'
Publikováno v:
Iranian Journal of Child Neurology; Autumn2024, Vol. 18 Issue 4, p47-60, 14p
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 4, Pp 176-179 (2021)
Externí odkaz:
https://doaj.org/article/c30c49afa0e04df19ef2d81896487c43
Recurrent encephalopathy with metabolic acidosis and hypoglycemia: Do not forget fructose metabolism
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 6, Pp 1250-1252 (2022)
Externí odkaz:
https://doaj.org/article/9a5c1ef0dad74ebe9a02d82ece156ad3
Publikováno v:
Annals of Child Neurology, Vol 30, Iss 1, Pp 42-43 (2022)
Externí odkaz:
https://doaj.org/article/08370fbe7253461287997fda82f9cfa1
Autor:
Divya Nagabushana, Vishal Vishnuram Samaga, Sangeetha Shenoy, Shabari Girishan, Hamsa V. Reddy, Somashekhar AR
Publikováno v:
Journal of Pediatric Neurology.
Mucormycosis is a rare opportunistic fungal infection observed in immunocompromised individuals or in those with uncontrolled diabetes mellitus. During the coronavirus disease 2019 (COVID-19) pandemic, there has been a steep increase in the incidence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f570ed168e935adc69770de11266d8f7
https://doi.org/10.1055/s-0042-1760254
https://doi.org/10.1055/s-0042-1760254
Autor:
Mridula Arabu Manjunath, Divya Nagabushana, Pradeep G. C. M., Sharanabasavesh Mangalgi, Krithika Manne Veerabhadraiah
Publikováno v:
Journal of Pediatric Neurology. 20:407-409
Congenital radial nerve palsy is a rare condition seen in newborns. It is thought to occur due to compression of upper arm against the pelvic rim in the intrauterine period. We report one such case of congenital radial nerve palsy in a preterm neonat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3866b8c0085ef8673f1867308fa674a
https://doi.org/10.1055/s-0041-1742250
https://doi.org/10.1055/s-0041-1742250
Autor:
Veeramani Preethish-Kumar, Atchayaram Nalini, Rita Horvath, Nandeesh Bevinahalli, Ram Murthy Anjanappa, Saraswati Nashi, Mainak Bardhan, Seena Vengalil, Ichizo Nishino, Gautham Arunachal, Divya Nagabushana, Tanushree Chawla, Dhaarini Mohan, Kiran Polavarapu, Leena Shingavi
Publikováno v:
Journal of Human Genetics. 66:813-823
Megaconial congenital muscular dystrophy (CMD)(OMIM #602541), related to CHKB mutation, is a rare autosomal recessive disorder. To date, only 35 confirmed patients are recorded. We present a detailed description of the clinical, histopathological, im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bfb33583b537e41aee934da88ea30bb
https://doi.org/10.1038/s10038-021-00913-1
https://doi.org/10.1038/s10038-021-00913-1
Recurrent encephalopathy with metabolic acidosis and hypoglycemia: Do not forget fructose metabolism
Publikováno v:
Annals of Indian Academy of Neurology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83bb909df5d77c485c87a7a24dbf3398
https://doi.org/10.4103/aian.aian_768_22
https://doi.org/10.4103/aian.aian_768_22
Publikováno v:
Epilepsy & Behavior. 93:43-48
Background and objectives Epilepsy affects the physical, cognitive, emotional, social wellbeing, and thereby the overall quality of life (QOL). Epilepsy is the most prevalent neurological disorder in the pediatric age group with a prevalence of 3.13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d0f1e7d3102723397217228393bac2
https://doi.org/10.1016/j.yebeh.2019.01.021
https://doi.org/10.1016/j.yebeh.2019.01.021
Autor:
Mainak, Bardhan, Kiran, Polavarapu, Nandeesh N, Bevinahalli, Preethish-Kumar, Veeramani, Ram Murthy, Anjanappa, Gautham, Arunachal, Leena, Shingavi, Seena, Vengalil, Saraswati, Nashi, Tanushree, Chawla, Divya, Nagabushana, Dhaarini, Mohan, Rita, Horvath, Ichizo, Nishino, Nalini, Atchayaram
Publikováno v:
Journal of human genetics. 66(8)
Megaconial congenital muscular dystrophy (CMD)(OMIM #602541), related to CHKB mutation, is a rare autosomal recessive disorder. To date, only 35 confirmed patients are recorded. We present a detailed description of the clinical, histopathological, im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ecdf2aa55cbd532b0efbc6f3ef80975
https://pubmed.ncbi.nlm.nih.gov/33767318
https://pubmed.ncbi.nlm.nih.gov/33767318