Natasha Purai

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Currarino syndrome is a rare autosomal dominant disorder. Mutations in the human homeobox gene, HLXB9, have been associated with this disorder. Affected individuals are at risk for serious complications leading to significant morbidity and mortality. All families of index patients should be offered genetic counseling. Recognition of at-risk individuals(More)
OBJECTIVE To report our experience with stent supported intracranial recanalization for acute ischemic stroke beyond 8 h of symptoms onset. Background Acute ischemic stroke (AIS) therapy is often limited to an 8 h window using mechanical means. However, recent reports have shown delayed recanalization beyond 8 h might be a viable option in a subset of(More)
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