Early-onset stroke and vasculopathy associated with mutations in ADA2.
New England Journal of Medicine.
Times cited: 251
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
Times cited: 26
Markers of increased risk of intracerebral hemorrhage after intravenous recombinant tissue plasminogen activator therapy for acute ischemic stroke in clinical practice: The multicenter rt-PA acute stroke survey.
Times cited: 332