Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Philip Oommen"'
Publikováno v:
Current Medical Issues, Vol 20, Iss 1, Pp 16-21 (2022)
Background and Objectives: The assessment of general movements (GMs), particularly fidgety movements, helps identify preterm infants likely to suffer from Neurodevelopmental deficits; less is known about preterm GMs. This study evaluates the predicti
Externí odkaz:
https://doaj.org/article/39451f01973b4d1ea821825f8ee99053
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, 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:
Deepa John, Samuel Philip Oommen, S Mahasampath Gowri, Sarojini Ramani, Deepa Ravi, Kavitha Nagarajan, Gordon N Dutton
Publikováno v:
Indian Journal of Ophthalmology, Vol 69, Iss 8, Pp 2232-2233 (2021)
Externí odkaz:
https://doaj.org/article/e9244a7e406042c792c0e7914dd7028c
Autor:
Rangan Srinivasaraghavan, Suvasiniz Sharma, Lisa Kratz, Prateek Malik, Sangeetha Yoganathan, Sumita Danda, Samuel Philip Oommen
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 6, Pp 933-934 (2021)
Externí odkaz:
https://doaj.org/article/5e45bdc11d874b8abb668e3b8c409030
Autor:
Monica Juneja, Arpita Gupta, Smitha Sairam, Ridhimaa Jain, Monika Sharma, Anjana Thadani, Roopa Srinivasan, Lokesh Lingappa, Shabina Ahmed, K. S. Multani, Pankaj Buch, Nandita Chatterjee, Samir Dalwai, Madhulika Kabra, Seema Kapoor, Prarthana Kharod Patel, K. M. Girisha, Madhuri Kulkarni, P. A. M. Kunju, Prahbhjot Malhi, Zafar Meenai, Devendra Mishra, Nandini Mundkur, M. K. C. Nair, Samuel Philip Oommen, Chhaya Prasad, Arun Singh, Leena Srivastava, Praveen Suman, Rahul Thakur
Publikováno v:
Indian Pediatrics. 59:401-415
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02b39104e394ce26499c00dd28ba4c98
https://doi.org/10.1007/s13312-022-2522-5
https://doi.org/10.1007/s13312-022-2522-5
Autor:
Vivi M. Srivastava, Samuel Philip Oommen, Vandana Kamath, S Yuvarani, Beena Koshy, Mary Purna Chacko
Publikováno v:
International Journal of Infertility & Fetal Medicine. 12:60-65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3a1b80baafb12b54100b0df3d5ae79b
https://doi.org/10.5005/jp-journals-10016-1228
https://doi.org/10.5005/jp-journals-10016-1228
Autor:
Lydia Mathew, Karthik Muthusamy, Beena Koshy, Sangeetha Yoganathan, Samuel Philip Oommen, Lakshmanan Jeyaseelan, Renu George, Jayaprakash Muliyil, Maya Thomas, Sirisha Varala, Paul Russell
Publikováno v:
Indian Dermatology Online Journal, Vol 12, Iss 1, Pp 84-89 (2021)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e353ef28eb29cee36c068fb5180aa44
http://www.idoj.in/article.asp?issn=2229-5178
http://www.idoj.in/article.asp?issn=2229-5178
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:
Atanu Kumar Jana, Hannah Grace, Rachel Beulah, T O Swathi, Samuel Philip Oommen, Niranjan Thomas, Manish Kumar, Bijesh Yadav, Sridhar Santhanam, Caroline Sanjeev Padankatti, Hima B John, Reeba Roshan
Publikováno v:
Journal of Tropical Pediatrics. 65:552-560
Objective To determine the prevalence and risk factors for poor neurodevelopmental outcome in a cohort of very low birth weight (VLBW) infants. Subjects and methods Four hundred and twenty-two infants of a total of 643 VLBW survivors from a teaching
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::934d3db20f26be6526e1d0c3eebb7f2d
https://doi.org/10.1093/tropej/fmz006
https://doi.org/10.1093/tropej/fmz006