Two siblings with familial idiopathic scoliosis with conjugate gaze palsy
dc.authorscopusid | 8541259900 | |
dc.authorscopusid | 6505874835 | |
dc.authorscopusid | 6602216538 | |
dc.authorscopusid | 7801391179 | |
dc.authorscopusid | 8721933400 | |
dc.authorscopusid | 6701769368 | |
dc.contributor.author | Incecik, Faruk | |
dc.contributor.author | Elkay, Mürüvet | |
dc.contributor.author | Hergüner, M. Özlem | |
dc.contributor.author | Yerdelen, Deniz | |
dc.contributor.author | Özcan, Kenan | |
dc.contributor.author | Altunbasak, Sakir | |
dc.date.accessioned | 2024-09-19T15:49:43Z | |
dc.date.available | 2024-09-19T15:49:43Z | |
dc.date.issued | 2005 | |
dc.department | Hatay Mustafa Kemal Üniversitesi | en_US |
dc.description.abstract | Familial idiopathic scoliosis with conjugate gaze palsy is a rare autosomal recessive disorder characterized by progressive scoliosis and congenital absence of conjugate horizontal eye movement. In this article, two siblings who had scoliosis and conjugate gaze palsy are presented regarding clinical and laboratory findings. | en_US |
dc.identifier.doi | 10.1177/08830738050200011303 | |
dc.identifier.endpage | 83 | en_US |
dc.identifier.issn | 0883-0738 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 15791929 | en_US |
dc.identifier.scopus | 2-s2.0-15544381851 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 81 | en_US |
dc.identifier.uri | https://doi.org/10.1177/08830738050200011303 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12483/15341 | |
dc.identifier.volume | 20 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | BC Decker Inc. | en_US |
dc.relation.ispartof | Journal of Child Neurology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | adolescent | en_US |
dc.subject | article | en_US |
dc.subject | autosomal recessive disorder | en_US |
dc.subject | binocular convergence | en_US |
dc.subject | case report | en_US |
dc.subject | clinical feature | en_US |
dc.subject | consanguineous marriage | en_US |
dc.subject | eye movement disorder | en_US |
dc.subject | familial disease | en_US |
dc.subject | female | en_US |
dc.subject | gaze paralysis | en_US |
dc.subject | human | en_US |
dc.subject | idiopathic scoliosis | en_US |
dc.subject | karyotyping | en_US |
dc.subject | laboratory test | en_US |
dc.subject | male | en_US |
dc.subject | priority journal | en_US |
dc.subject | rare disease | en_US |
dc.subject | sibling | en_US |
dc.title | Two siblings with familial idiopathic scoliosis with conjugate gaze palsy | en_US |
dc.type | Article | en_US |
Dosyalar
Orijinal paket
1 - 1 / 1