Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Priya T Thomas"'
Autor:
Manu S Girija, Deepak Menon, Kiran Polavarapu, Veeramani Preethish-Kumar, Seena Vengalil, Saraswati Nashi, Madassu Keertipriya, Mainak Bardhan, Priya T Thomas, Valasani R Kiran, Vikas Nishadham, Arun Sadasivan, Akshata Huddar, Gopi K Unnikrishnan, Ganagarajan Inbaraj, Arjun Krishnamurthy, Boris W Kramer, Talakad N Sathyaprabha, Atchayaram Nalini
Publikováno v:
Annals of Indian Academy of Neurology, Vol 27, Iss 1, Pp 53-57 (2024)
Background: Electrocardiography (ECG) remains an excellent screening tool for cardiac assessment in Duchenne muscular dystrophy (DMD), but an accurate interpretation requires comparison with age-matched healthy controls. Objective: We examined variou
Externí odkaz:
https://doaj.org/article/5b87316a68604fec83954623ac4d4310
Autor:
Zacharias Lithin, Priya T Thomas, G Manjusha Warrier, Adhin Bhaskar, Saraswathi Nashi, Seena Vengalil, Kiran Polavarapu, Preethish Kumar, Ravi Yadav, Suvarna Alladi, Nalini Atchayaram, Pramod K Pal
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 3, Pp 313-317 (2020)
Background and Aims: Palliative care is an important area of intervention in neurodegenerative diseases. The aim of this study is to understand the relationship between Palliative Care Needs and Caregiver Burden among persons diagnosed with neurodege
Externí odkaz:
https://doaj.org/article/2ffa1072e2a140bb9479ed9cbd184a77
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 8, Iss 7, Pp 2424-2428 (2019)
Context: The incidence of stroke is evolving to be a major public health issue in recent years. The situation is aggravated by the limited public awareness about its risk factors and treatment procedures. It is important to explore the level of aware
Externí odkaz:
https://doaj.org/article/34439f9fd7854e82a620d2e21fe8135f
Autor:
Priya T. Thomas, Gargi S. Kumar, Priya Baby, Seena Vengalil, P. R. Srijithesh, B. K. Yamini, M Netravathi, Ravi Yadav, R. Dhanasekhara Pandian, Anupam Gupta, Suvarna Alladi, Atchayaram Nalini
Publikováno v:
Annals of Indian Academy of Neurology, Vol 27, Iss 3, Pp 332-334 (2024)
Externí odkaz:
https://doaj.org/article/a788a323496240568e846b5450ab7e8f
Autor:
Valakunja H. Ganaraja, Kiran Polavarapu, Mainak Bardhan, Veeramani Preethish-Kumar, Shingavi Leena, Ram M. Anjanappa, Seena Vengalil, Saraswati Nashi, Gautham Arunachal, Swetha Gunasekaran, Dhaarini Mohan, Sanita Raju, Gopikrishnan Unnikrishnan, Akshata Huddar, Valasani Ravi-Kiran, Priya T. Thomas, Atchayaram Nalini
Publikováno v:
Global Medical Genetics, Vol 09, Iss 01, Pp 034-041 (2022)
Calpainopathy is caused by mutations in the CAPN3. There is only one clinical and genetic study of CAPN3 from India and none from South India. A total of 72 (male[M]:female [F] = 34:38) genetically confirmed probands from 72 independent families are
Externí odkaz:
https://doaj.org/article/75ac141fc6ea457c8322411f21a69471