Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vinay Kumar Palutla"'
Autor:
Yan Li, Sean K. Sethi, Chunyan Zhang, Yanwei Miao, Kiran Kumar Yerramsetty, Vinay Kumar Palutla, Sara Gharabaghi, Chengyan Wang, Naying He, Jingliang Cheng, Fuhua Yan, Ewart Mark Haacke
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2021)
PurposeTo evaluate the effect of resolution on iron content using quantitative susceptibility mapping (QSM); to verify the consistency of QSM across field strengths and manufacturers in evaluating the iron content of deep gray matter (DGM) of the hum
Externí odkaz:
https://doaj.org/article/33e2fb0f716746f39c64edeec10fe166
Autor:
Zenghui Cheng, Naying He, Pei Huang, Yan Li, Rongbiao Tang, Sean K. Sethi, Kiarash Ghassaban, Kiran Kumar Yerramsetty, Vinay Kumar Palutla, Shengdi Chen, Fuhua Yan, E. Mark Haacke
Publikováno v:
NeuroImage: Clinical, Vol 25, Iss , Pp - (2020)
Parkinson's disease (PD) is a clinically heterogeneous chronic progressive neuro-degenerative disease with loss of dopaminergic neurons in the nigrosome 1 (N1) territory of the substantia nigra pars compacta (SNpc). To date, there has been a major ef
Externí odkaz:
https://doaj.org/article/807f308a0ce546bfa62cdf896c864533
Autor:
Ewart Mark Haacke, Evanthia Bernitsas, Karthik Subramanian, David Utriainen, Vinay Kumar Palutla, Kiran Yerramsetty, Prashanth Kumar, Sean K. Sethi, Yongsheng Chen, Zahid Latif, Pavan Jella, Sara Gharabaghi, Ying Wang, Xiaomeng Zhang, Robert A. Comley, John Beaver, Yanping Luo
Publikováno v:
Diagnostics, Vol 12, Iss 1, p 77 (2021)
Magnetic resonance imaging (MRI) is a sensitive imaging modality for identifying inflammatory and/or demyelinating lesions, which is critical for a clinical diagnosis of MS and evaluating drug responses. There are many unique means of probing brain t
Externí odkaz:
https://doaj.org/article/e731727d80cb486496df63604751f7a5
Autor:
Soumya Sharma, Sean Kumar Sethi, David Reese, Sara Gharabaghi, Kiran Kumar Yerramsetty, Vinay Kumar Palutla, Yongsheng Chen, E. Mark Haacke, Mandar S. Jog
Publikováno v:
European Journal of Neurology. 29:1417-1426
Hereditary haemochromatosis (HH) is the most common inherited disorder of systemic iron excess in Northern Europeans. Emerging evidence indicates that brain iron overload occurs in HH. Despite this observation, there is a paucity of literature regard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052289fdbd1d1faf77b9bd1727c19f8e
https://doi.org/10.1111/ene.15242
https://doi.org/10.1111/ene.15242
Autor:
Rongbiao Tang, Sean K. Sethi, Yan Li, Sheng-Di Chen, Kiran Kumar Yerramsetty, Naying He, Pei Huang, Vinay Kumar Palutla, Fuhua Yan, Zenghui Cheng, E. Mark Haacke, Kiarash Ghassaban
Publikováno v:
NeuroImage: Clinical, Vol 25, Iss, Pp-(2020)
NeuroImage : Clinical
NeuroImage : Clinical
Highlights • To date, there is no standard MR imaging protocol to characterize the nigrosome1 territory of the substantia nigra. • Nigrosome 1 can be consistently visualized using true SWI with a resolution of at least 0.67 × 0.67 × 1.34 mm3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d67086fd4422ddc5adc957dd88e00c78
http://www.sciencedirect.com/science/article/pii/S2213158219304504
http://www.sciencedirect.com/science/article/pii/S2213158219304504