Results 21 to 30 of about 130,655 (306)
Spatial contextual effects in primary visual cortex limit feature representation under crowding
Nature Communications, 2020 Visual crowding can strongly limit perceptual discriminability, yet its neural basis remains unclear. Here, the authors show that perceptual crowding is similar in monkeys and humans, and that feature encoding in neuronal populations in primary visual ...
Christopher A. Henry, Adam Kohn
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Alteration of transcriptomic networks in adoptive-transfer experimental autoimmune encephalomyelitis
Frontiers in Integrative Neuroscience, 2007 Adoptive transfer experimental autoimmune encephalomyelitis (AT-EAE) is an inflammatory demyelination that recapitulates in mouse spinal cord (SC) the human multiple sclerosis disease.
Dumitru A Iacobas +4 more
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Caplacizumab for Acquired Thrombotic Thrombocytopenic Purpura.
New England Journal of Medicine, 2016 BACKGROUND Acquired thrombotic thrombocytopenic purpura (TTP) is caused by aggregation of platelets on ultralarge von Willebrand factor multimers. This microvascular thrombosis causes multiorgan ischemia with potentially life-threatening complications ...
F. Peyvandi +13 more
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Coordination between Translation and Degradation Regulates Inducibility of mGluR-LTD
Cell Reports, 2015 Dendritic protein homeostasis is crucial for most forms of long-term synaptic plasticity, and its dysregulation is linked to a wide range of brain disorders.
Matthew E. Klein +2 more
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Childhood IgA Vasculitis (Henoch Schonlein Purpura)—Advances and Knowledge Gaps
Frontiers in Pediatrics, 2019 Immunoglobulin A vasculitis (IgAV; formerly Henoch Schonlein Purpura) is the most common form of childhood vasculitis. It can occur in any age and peaks around 4–6 years old.
L. Oni, S. Sampath
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Idiopathic Thrombocytopenic Purpura
Definitions, 2020 Five patients with idiopathic thrombocytopenic purpura (ITP) associated with malignant lymphoma are presented, and twelve other cases reported in the literature are reviewed. Thirteen patients (76%) had Hodgkin's disease; two had diffuse histiocytic, one,
K. Fink
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A role for cerebellum in the hereditary dystonia DYT1
eLife, 2017 DYT1 is a debilitating movement disorder caused by loss-of-function mutations in torsinA. How these mutations cause dystonia remains unknown. Mouse models which have embryonically targeted torsinA have failed to recapitulate the dystonia seen in patients,
Rachel Fremont +3 more
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Henoch–Schonlein purpura due to sodium valproate: A case report
Clinical Case Reports, 2022 We report a 5‐year‐old girl with a generalized seizure treated with sodium valproate syrup. She returned to the clinic with Henoch–Schonlein purpura after 20 days due to the consumption of sodium valproate.
Firozeh Hosseini, Mojgan Safari
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Skin manifestations of COVID-19
RUDN Journal of Medicine, 2021 The infection caused by the recently identified SARS-CoV-2, dubbed coronavirus disease-19 (COVID-19), has become a pandemic. With exponential growth of morbidity among the people around the world, the clinical characteristics of COVID-19 are becoming ...
E. V. Dvoryankova +2 more
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Characterization and treatment of congenital thrombotic thrombocytopenic purpura.
Blood, 2019 Congenital thrombotic thrombocytopenic purpura (cTTP) is an ultra-rare thrombomicroangiopathy caused by an inherited deficiency of a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13).
F. Alwan +27 more
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