Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shagun Mehta"'
Autor:
Abhishek Katyal, M.Ch, Aparna Katyal, M.D, Shagun Mehta, M.D, Anita Jagetia, M.Ch, Jawahar Lal Goyal, M.S, Ashok Sharma, M.D, Arvind Kumar Srivastava, M.Ch, Daljit Singh, M.Ch
Publikováno v:
Interdisciplinary Neurosurgery, Vol 31, Iss , Pp 101685- (2023)
Background and objectives: The occipital transtentorial approach (OT) is a useful surgical approach for the treatment of lesions of the pineal region. Because the approach provides wide operative views of superior cerebellar, splenium, quadrigeminal
Externí odkaz:
https://doaj.org/article/5c82734038174bd2829b7674d6a5bf18
Autor:
Emily Machiela, Ritika Jeloka, Nicholas S. Caron, Shagun Mehta, Mandi E. Schmidt, Helen J. E. Baddeley, Colton M. Tom, Nalini Polturi, Yuanyun Xie, Virginia B. Mattis, Michael R. Hayden, Amber L. Southwell
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Huntington disease (HD) is a fatal, inherited neurodegenerative disorder caused by a mutation in the huntingtin (HTT) gene. While mutant HTT is present ubiquitously throughout life, HD onset typically occurs in mid-life. Oxidative damage accumulates
Externí odkaz:
https://doaj.org/article/927e14de01344da3b997cbcf2b24e178
Autor:
Helen J E Baddeley, Nalini Polturi, Mandi E. Schmidt, Yuanyun Xie, Nicholas S. Caron, Colton M Tom, Ritika Jeloka, Emily Machiela, Shagun Mehta, Amber L. Southwell, Virginia B. Mattis, Michael R. Hayden
Publikováno v:
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience, Vol 12 (2020)
Frontiers in Aging Neuroscience, Vol 12 (2020)
Huntington disease (HD) is a fatal, inherited neurodegenerative disorder caused by a mutation in the huntingtin (HTT) gene. While mutant HTT is present ubiquitously throughout life, HD onset typically occurs in mid-life. Oxidative damage accumulates
Autor:
Mandi E. Schmidt, Nalini Potluri, Virginia B. Mattis, Colton M Tom, Shagun Mehta, Ritika Jeloka, Nicholas S. Caron, Emily Machiela, Michael R. Hayden, Yuanyun Xie, Amber L. Southwell
Huntington disease (HD) is a fatal, inherited neurodegenerative disorder caused by a mutation in huntingtin (HTT). While mutant HTT is present ubiquitously throughout life, HD onset typically occurs in mid-life. Oxidative damage accumulates in the ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a793f01a3ebe1b8a8e40aebcbe4492ce
Autor:
Catherine Bresee, Jie Tang, Yizhou Wang, Colton M Tom, Pranav Mathkar, Virginia B. Mattis, Shagun Mehta, David Rushton
Publikováno v:
Cell Reports, Vol 25, Iss 4, Pp 1081-1096.e6 (2018)
Summary: Huntington’s disease (HD) is a neurodegenerative disease caused by an expanded CAG repeat in the Huntingtin (HTT) gene. Induced pluripotent stem cell (iPSC) models of HD provide an opportunity to study the mechanisms underlying disease pat