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The NOTCH3 mutation is a common cause of hereditary cerebral small vessel disease (CSVD) and may be a cause of spontaneous intracerebral haemorrhage (ICH). The aim was to investigate the… Click to show full abstract
The NOTCH3 mutation is a common cause of hereditary cerebral small vessel disease (CSVD) and may be a cause of spontaneous intracerebral haemorrhage (ICH). The aim was to investigate the clinical/imaging features for identifying the NOTCH3‐mutation‐related ICH.
Keywords:
comparison clinical;
intracerebral haemorrhage;
neuroimaging features;
spontaneous intracerebral;
clinical neuroimaging
Journal Title: European Journal of Neurology
Year Published: 2022
Link to full text (if available)
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Journal Title: European Journal of Neurology
Year Published: 2022
Link to full text (if available)
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recommendations!