Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Spolia A"'
Autor:
Akshi Spolia, Arshia Angural, Varun Sharma, Shipra, Sushil Razdan, Manoj K. Dhar, Ankit Mahajan, Vijeshwar Verma, Kamal K. Pandita, Swarkar Sharma, Ekta Rai
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Neurofibromatosis type 1 (NF1) is a multisystemic hereditary disorder associated with an increased risk of benign and malignant tumor formation predominantly on the skin, bone, and peripheral nervous system. It has been reported that out of
Externí odkaz:
https://doaj.org/article/528a8fdef95841a9bd8d7ce5e86460da
Publikováno v:
European Journal of Cardiovascular Medicine. 2023, Vol. 13 Issue 4, p148-154. 7p.
Autor:
Spolia, Akshi1 (AUTHOR), Angural, Arshia1,2 (AUTHOR), Sharma, Varun1,3 (AUTHOR), Shipra1 (AUTHOR), Razdan, Sushil4 (AUTHOR), Dhar, Manoj K.5 (AUTHOR), Mahajan, Ankit5 (AUTHOR), Verma, Vijeshwar1 (AUTHOR), Pandita, Kamal K.6 (AUTHOR), Sharma, Swarkar1,7 (AUTHOR) swarkar.sharma@smvdu.ac.in, Rai, Ekta1 (AUTHOR) ekta.rai@smvdu.ac.in
Publikováno v:
Scientific Reports. 5/15/2023, Vol. 13 Issue 1, p1-7. 7p.
Publikováno v:
European Journal of Cardiovascular Medicine; 2024, Vol. 14 Issue 3, p1242-1247, 6p
Autor:
Arshia Angural, Akshi Spolia, Ankit Mahajan, Vijeshwar Verma, Ankush Sharma, Parvinder Kumar, Manoj Kumar Dhar, Kamal Kishore Pandita, Ekta Rai, Swarkar Sharma
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Rare diseases (RDs) are the clinical conditions affecting a few percentage of individuals in a general population compared to other diseases. Limited clinical information and a lack of reliable epidemiological data make their timely diagnosis and the
Externí odkaz:
https://doaj.org/article/87bb555b3a464ee0a785138e5058e6f3
Autor:
Hani Nasser Abdelhamid, V.L.N. Balaji Gupta Tiruveedhi, Jigna R. Bhamore, More Bhikhu, Yoon-Young Chang, Theodoros Chatzimitakos, Anila Rose Cherian, Joydeep Chowdhury, Flávia Oliveira Monteiro da Silva Abreu, Deepthi Priyanka Damera, Sobhi Daniel, Mittal L. Desai, Khemchand Dewangan, Rohant S. Dhabbe, Pravin R. Dongare, Gollavelli Ganesh, D. Gangadharan, Shah Gaurav, Gangaraju Gedda, Anil H. Gore, Datta B. Gunjal, Nitin Kumar Jaiswal, Suresh Kumar Kailasa, Tushar Kant, Janardhan Reddy Koduru, Govind B. Kolekar, R. Krishnaveni, Manju Kurian, Urvi M. Lad, Lakshmi Prasanna Lingamdinne, Shweta J. Malode, Mehta Mansi, Vaibhavkumar N. Mehta, Chetan K. Modi, Pranjal D. Modi, Amit Nag, Durgadevi Nagarajan, Vaibhav M. Naik, Omkar S. Nille, Bruno Peixoto de Oliveira, Chandrika Ashwinikumar Pal, Amit B. Patel, Swati Patel, Bhimanagouda S. Patil, Anju Paul, Shweta Pawar, Keerthana Ponmudi, Vimalkumar S. Prajapati, C. Ramalechume, Juhi B. Raval, Ankita G. Ravani, Jigneshkumar V. Rohit, Ashima Sharma, Rajendra V. Shejwal, Nagaraj P. Shetti, Kamlesh Shrivas, T. Sivaramakrishnan, Gourav Spolia, Constantine Stalikas, Joga Suribabu, Caroline Mercy Andrew Swamidoss, Humairah Tabasum, Kavita Tapadia, Le Minh Tu Phan, Anitha Varghese, Swarnalatha Venkatanarasimhan, P. Vijayarohini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f44f042909fdf58edc72cf14204e89d
https://doi.org/10.1016/b978-0-323-98350-1.00030-x
https://doi.org/10.1016/b978-0-323-98350-1.00030-x
Autor:
Rohit, Jigneshkumar V., Mehta, Vaibhavkumar N., Patel, Amit B., Tabasum, Humairah, Spolia, Gourav
Publikováno v:
In Carbon Dots in Analytical Chemistry 2023:97-108
Akademický článek
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Autor:
Diksha Langeh, Swarkar Sharma, Arshia Angural, Kalaiarasan Ponnusamy, Akshi Spolia, Ankush Sharma, Ekta Rai, Mamta Kumari, Kamal Kishore Pandita
We report diagnosis of Neuronal Ceroid Lipofuscinosis Type 2 (CLN2), a rare, hereditary neurodegenerative disease of childhood, in a four and a half year old girl, the first child of non-consanguineous parents with no family history. Despite extensiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e62b42092828f9c1dc891f9347360c6f
https://doi.org/10.20944/preprints202107.0661.v1
https://doi.org/10.20944/preprints202107.0661.v1