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UnknownTh1/Th2 polarization of peripheral immune response in atherothrombotic and cardioembolic stroke: a prospective study.
Not available
S-EPMC9525580 | biostudies-literature
UnknownA novel stroke mimic prediction score during in-hospital triage for suspected stroke patients: The Stroke Mimics Score (SMS).
Not available
S-EPMC12084216 | biostudies-literature
UnknownAutomated pupillometry is a predictor of outcome of stroke patients: an observational, prospective, cohort study.
Not available
S-EPMC11878543 | biostudies-literature
UnknownHemichorea as a Manifestation of Isolated Insular Infarction Successfully Treated with Mechanical Thrombectomy.
Not available
S-EPMC12697618 | biostudies-literature
UnknownFunctional Outcomes and Symptomatic Intracranial Hemorrhage After Endovascular Treatment in Acute Vertebrobasilar Artery Occlusions: External Validation of Prediction Models.
Not available
S-EPMC12778509 | biostudies-literature
UnknownHereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle.
Not available
S-EPMC3235839 | biostudies-literature
TranscriptomicsTranscription profiling of human acute quadriplegic myopathy patients
AQM shows acute muscle wasting and weakness. Key aspects of AQM include muscle atrophy and myofilament loss. Gene expression profiling, using muscle biopsies from AQM, neurogenic atrophy and normal controls, showed that both myogenic and neurogenic atrophy share induction of myofiber-specific ubiqui...
ORGANISM(S): Homo sapiens 
2007-07-21 | E-GEOD-1017 | biostudies-arrayexpress
UnknownSafety of emergent carotid stenting after thrombolysis: a multicenter retrospective matched analysis.
Not available
S-EPMC12041103 | biostudies-literature
UnknownMyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle.
Not available
S-EPMC1636567 | biostudies-literature
TranscriptomicsTranscription profiling of human quadriceps muscle of young Duchenne muscular dystrophy patients and age matched controls
Albeit increased serum CK level and abnormal muscle histology are always present, boys with DMD are phenotipically indistinguishable from the normal ones at birth and, in their first years of life, acquire early motor milestones at normal times. A clear defect in muscle function becomes generally ap...
ORGANISM(S): Homo sapiens 
2008-06-14 | E-GEOD-6011 | biostudies-arrayexpress
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