Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Rui‐Juan Lv"'
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 6, Pp 911-923 (2020)
Abstract Objective Type I sialidosis (ST‐1) is a rare autosomal recessive inherited disorder. To date, there has been no study on ST‐1 patients in mainland China. Methods We reported in detail the cases of five Chinese ST‐1 patients from two ce
Externí odkaz:
https://doaj.org/article/7e8f2de99dc64047b1d2822492236af7
Publikováno v:
BMC Neuroscience, Vol 21, Iss 1, Pp 1-11 (2020)
Abstract Background Patients positive for anti-glutamic acid decarboxylase 65 (GAD65) antibodies have attracted increasing attention. Their clinical manifestations are highly heterogeneous and can be comorbid with tumors. Currently, there is no conse
Externí odkaz:
https://doaj.org/article/8f16bfceebfb4541b39e5ed00869f769
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: This study aimed to analyze the clinical characteristics of anti-leucine-rich glioma-inactivated protein 1 (LGI1) encephalitis patients and investigate prognostic factors by using a large-sample and long-term follow-up cohort.Methods: The
Externí odkaz:
https://doaj.org/article/455c97075bfe406ab0c9333a89f0bdf6
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Externí odkaz:
https://doaj.org/article/f4bb0281cc0646e3873b4a0a58918653
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Objective: The purpose of this study is to evaluate the potential diagnostic benefit of SPM-based semi-quantitative FDG-PET analysis in autoimmune encephalitis (AE) compared with visual analysis by experienced neuroradiologists using a larger sample
Externí odkaz:
https://doaj.org/article/b5a9fb5c1eea4d5190f73cfe87df3aa8
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Leigh syndrome (LS) is a mitochondrial disease of infancy and early childhood, that is rarely seen in adults. The high degree of genetic and clinical heterogeneity makes LS a very complex syndrome. The clinical manifestations include neurological sym
Externí odkaz:
https://doaj.org/article/3f09b444b5304a9f8517020697c4a6b7
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 3 (2018)
Increasing evidence indicates that neuroinflammation plays a crucial role in the pathogenesis of temporal lobe epilepsy (TLE). However, it is unclear how the perpetuate inflammation develops. Some recent studies have suggested the possible involvemen
Externí odkaz:
https://doaj.org/article/f642af46e27748c4a22c1ef40abf39dc
Publikováno v:
CNS Neuroscience & Therapeutics
Aims To identify the metabolic pattern and prognostic predictors in anti‐gamma‐aminobutyric‐acid B (GABAB) receptor encephalitis using 18F‐fluorodeoxy‐glucose positron emission tomography (18F‐FDG‐PET). Methods Twenty‐one patients dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b248bc2a30fdca61362e0be1bd35e7
https://doi.org/10.1111/cns.13767
https://doi.org/10.1111/cns.13767
Publikováno v:
CNS Neuroscience & Therapeutics
Aims Anti‐leucine‐rich glioma‐inactivated 1 (LGI1) autoimmune encephalitis (AE) is characterized by complex manifestations of seizures. Here, we report a new seizure semiology, attempt to classify the disease by semiology type, and explore the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d5bca014670602564c0a5722a2dd71
http://europepmc.org/articles/PMC8446218
http://europepmc.org/articles/PMC8446218
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 6, Pp 911-923 (2020)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective Type I sialidosis (ST‐1) is a rare autosomal recessive inherited disorder. To date, there has been no study on ST‐1 patients in mainland China. Methods We reported in detail the cases of five Chinese ST‐1 patients from two centers, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c34368749b011a21b7a33b4c3a840df0
https://doaj.org/article/7e8f2de99dc64047b1d2822492236af7
https://doaj.org/article/7e8f2de99dc64047b1d2822492236af7