{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T08:33:13Z","timestamp":1740126793865,"version":"3.37.3"},"reference-count":15,"publisher":"Georg Thieme Verlag KG","issue":"01","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neuropediatrics"],"published-print":{"date-parts":[[2023,2]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Claude syndrome is a rare midbrain stroke syndrome characterized by ipsilateral third cranial nerve palsy and contralateral hemiataxia. So far, only a few cases have been reported in childhood. We present two children with Claude syndrome at 9 and 15 years of age. The typical clinical picture was consistent with brain magnetic resonance imaging findings. A thorough investigation regarding the underlying etiology revealed no definite diagnosis but clues suggestive of probable neuro-Behcet disease. Awareness of pediatric neurologists on arterial ischemic stroke has been increasing over the past decades, enabling timely diagnosis and appropriate management of rare childhood cases with midbrain stroke.<\/jats:p>","DOI":"10.1055\/s-0042-1759794","type":"journal-article","created":{"date-parts":[[2022,12,24]],"date-time":"2022-12-24T00:37:27Z","timestamp":1671842247000},"page":"082-087","source":"Crossref","is-referenced-by-count":2,"title":["Claude Syndrome in Childhood Associated with Probable Neuro-Behcet Disease"],"prefix":"10.1055","volume":"54","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2475-0004","authenticated-orcid":false,"given":"Pinar","family":"Yavuz","sequence":"additional","affiliation":[{"name":"Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ismail","family":"Solmaz","sequence":"additional","affiliation":[{"name":"Department of Pediatric Neurology, 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