Zobrazeno 1 - 10
of 48
pro vyhledávání: '"P Saravanapandian"'
Autor:
Vidya Saravanapandian, Melika Madani, India Nichols, Scott Vincent, Mary Dover, Dante Dikeman, Benjamin D. Philpot, Toru Takumi, Christopher S. Colwell, Shafali Jeste, Ketema N. Paul, Peyman Golshani
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-16 (2024)
Abstract Background Sleep disturbances are a prevalent and complex comorbidity in neurodevelopmental disorders (NDDs). Dup15q syndrome (duplications of 15q11.2-13.1) is a genetic disorder highly penetrant for NDDs such as autism and intellectual disa
Externí odkaz:
https://doaj.org/article/7a9ff40a16224580afd1c0543e8114e0
Autor:
Joel Frohlich, Jeffrey N. Chiang, Pedro A. M. Mediano, Mark Nespeca, Vidya Saravanapandian, Daniel Toker, John Dell’Italia, Joerg F. Hipp, Shafali S. Jeste, Catherine J. Chu, Lynne M. Bird, Martin M. Monti
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-17 (2022)
EEG measurements in children with Angelman or duplication 15q11.2-13.1 syndrome reveal a dissociation between consciousness and sleep-like spectral content, with complexity-based measures superseding other markers of consciousness.
Externí odkaz:
https://doaj.org/article/416f5e50dfef4a4c81cd405d0b7ce41e
Akademický článek
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Autor:
Juliana Simon, Carly Hyde, Vidya Saravanapandian, Rujuta Wilson, Charlotte Distefano, Aaron Besterman, Shafali Jeste
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-10 (2022)
Abstract Background The development of advanced genetic technologies has resulted in rapid identification of genetic etiologies of neurodevelopmental disorders (NDDs) and has transformed the classification and diagnosis of various NDDs. However, diag
Externí odkaz:
https://doaj.org/article/11991ecafe5e41e08270f4aa7185ed47
Autor:
Juliana Simon, Carly Hyde, Vidya Saravanapandian, Rujuta Wilson, Benjamin Schneider, Charlotte Distefano, Aaron Besterman, Shafali Jeste
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/db1589af49d444e8ba6444b86b7b6f3f
Autor:
Vidya Saravanapandian, Divya Nadkarni, Sheng-Hsiou Hsu, Shaun A. Hussain, Kiran Maski, Peyman Golshani, Christopher S. Colwell, Saravanavel Balasubramanian, Amos Dixon, Daniel H. Geschwind, Shafali S. Jeste
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-14 (2021)
Abstract Background Sleep disturbances in autism spectrum disorder (ASD) represent a common and vexing comorbidity. Clinical heterogeneity amongst these warrants studies of the mechanisms associated with specific genetic etiologies. Duplications of 1
Externí odkaz:
https://doaj.org/article/5f3b114f4fb34c64b3861c3193773ec2
Publikováno v:
Journal of Ayurveda and Integrative Medicine, Vol 13, Iss 2, Pp 100553- (2022)
Gold, sulfur and mercurial formulations in Indian alchemy are consumed in conjunction with suitable adjuvant for their synergistic action, reduced toxicity and boosting their bioavailability resulting in improved effectiveness. Poorna chandrodaya che
Externí odkaz:
https://doaj.org/article/3b316a91456642b8abb1b0f32322a9de
Autor:
Vidya Saravanapandian, Joel Frohlich, Joerg F. Hipp, Carly Hyde, Aaron W. Scheffler, Peyman Golshani, Edwin H. Cook, Lawrence T. Reiter, Damla Senturk, Shafali S. Jeste
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-15 (2020)
Abstract Background Duplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism, intellectual disability, hypotonia, and epilepsy. The 15q region harbors genes critical for brain development, particularly UBE3A and a cluster of ga
Externí odkaz:
https://doaj.org/article/e15855b4fa354cdb8f21be5a7ddd9caf
Autor:
Joel Frohlich, Jeffrey N. Chiang, Pedro A. M. Mediano, Mark Nespeca, Vidya Saravanapandian, Daniel Toker, John Dell’Italia, Joerg F. Hipp, Shafali S. Jeste, Catherine J. Chu, Lynne M. Bird, Martin M. Monti
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/081a3cb0eb6546d49cb88c42ce6c1866
Autor:
Joel Frohlich, Lawrence T. Reiter, Vidya Saravanapandian, Charlotte DiStefano, Scott Huberty, Carly Hyde, Stormy Chamberlain, Carrie E. Bearden, Peyman Golshani, Andrei Irimia, Richard W. Olsen, Joerg F. Hipp, Shafali S. Jeste
Publikováno v:
Molecular Autism, Vol 10, Iss 1, Pp 1-15 (2019)
Abstract Background Duplications of 15q11.2-q13.1 (Dup15q syndrome), including the paternally imprinted gene UBE3A and three nonimprinted gamma-aminobutyric acid type-A (GABAA) receptor genes, are highly penetrant for neurodevelopmental disorders suc
Externí odkaz:
https://doaj.org/article/7663de861abe46c8bab5e459db26cd65