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Publikováno v:
International Journal of Contemporary Educational Research; Sep2024, Vol. 11 Issue 3, p337-353, 17p
Autor:
Gülay, Alper
Bu araştırmanın amacı, Ankara ilinde özel eğitim ve rehabilitasyon merkezlerinde okul öncesi dönemdeki otizm spektrum bozukluğu (OSB) olan öğrencilerle çalışan öğretmenlerin, öğrencilerinin dil gelişimlerini desteklemek amacıyla h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10208::6e96e82a11f5b9bd02f5599c588675a2
https://acikbilim.yok.gov.tr/handle/20.500.12812/84354
https://acikbilim.yok.gov.tr/handle/20.500.12812/84354
Publikováno v:
Journal of Child Neurology. 14:678-682
Benign macrocephaly of infancy is a common problem in the child neurology practice. The radiologic features of this entity are not well defined. In most of the previous studies, macrocephalic patients were evaluated by computed tomography. To define
Publikováno v:
Pediatric Neurology. 15:60-62
Castleman syndrome (giant lymph node hyperplasia) is a rare, heterogeneous lymphoproliferative disorder of unknown etiology and pathogenesis. Most cases occur as mediastinal masses, although extrathoracic involvement including nodal and extranodal lo
Publikováno v:
Pediatric neurology. 25(4)
Behcet's disease is a chronic, relapsing multisystem disorder, and nervous system involvement is one of the serious manifestations. Neuro-Behcet is rarely reported in children and may present with a wide variety of symptoms because the entire neuraxi
Autor:
Serpil Yilmaz-Degirmenci, Gamze Kilicoglu, Levent Çelik, Gülay Alper, Leyla Karadeniz, Yüksel Yilmaz
Publikováno v:
Journal of child neurology. 16(6)
The aim of this study was to document the magnetic resonance imaging (MRI) findings of cases with a history of severe neonatal indirect hyperbilirubinemia. Ten cases (eight cases with neurologic findings, two normal cases) with a history of severe ne
Publikováno v:
Pediatric neurology. 21(2)
Reported are two patients presenting with both thrombocytopenia and sagittal sinus thrombosis. The first patient is a 42-month-old male with no identified thrombophilic risk factors who developed acute neurologic symptoms after an acute infection. Th
Autor:
Yüksel Yilmaz, Gülay Alper, Gamze Kiliçoglu, Levent Çelik, Leyla Karadeniz, Serpil Yilmaz-Deg*irmenci
Publikováno v:
Journal Of Child Neurology. 16:452