Functional, imaging, and histological outcomes demonstrated that treated animals recovered fully, while untreated controls experienced permanent impairment
Symptomatic oHCM is a genetic condition where patients have thickened heart muscles and reduced blood flow from the left side of the heart to the rest of the body causing shortness of breath, fatigue, and potentially life-threatening events
Wheeler 7 , Rob Simister 1,2 , Thomas Gattringer 4 , David Werring 1,2 1 Stroke Research Centre, UCL Queen Square Institute of Neurology, Department of Neuroradiology, University College London Hospitals NHS Foundation Trust, London, United Kingdom, 2 Comprehensive Stroke Service, National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Trust, UCL Queen Square Institute of Neurology, London, United Kingdom, 3 Department of Statistical Science, University College London, London, United Kingdom, 4 Department of Neurology, Medical University of Graz, Graz, Austria, 5 Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, Graz, Austria, 6 Lysholm Department of Neuroradiology and the Neuroradiological Academic Unit, Department of Brain Repair and Rehabilitation, UCL Institute of Neurology, Queen Square, London, United Kingdom, 7 Department of Renal Medicine, University College London, London, United Kingdom Background and Aims: Patients with chronic kidney disease (CKD) have severe cerebral small vessel disease in populations with intracerebral haemorrhage (ICH)
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