Yazar "İnce, Hülya" için listeleme
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Are diagnostic magnetic resonance patterns life-saving in children with biotin-thiamine-responsive basal ganglia disease?
Kamaşak, Tülay; Havalı, Cengiz; İnce, Hülya; Eyüboğlu, İlker; Çebi, Alper Han; Şahin, Sevim; Cansu, Ali; Aydın, Kürşad (Elsevier Sci Ltd, 2018)Background: Biotin-thiamine responsive basal ganglia disease (BTBGD) is an autosomal recessive disorder caused by mutations in the SLC19A3 gene and characterized by recurrent sub-acute episodes of encephalopathy that ... -
Evaluation of immunization status in patients with cerebral palsy: A multicenter CP-VACC study
Bozkaya Yılmaz, Sema; Karadağ Öncel, Eda; Olgaç Dündar, Nihal; Gençpınar, Pınar; Sarıoğlu, Berrak; Arıcan, Pınar; Ersen, Atilla; Yılmaz Çiftdoğan, Dilek; Yüksel, Merve Feyza; Bektaş, Ömer; Teber, Serap; Kılıç, Betül; Çalık, Mustafa; Karaca, Meryem; Canpolat, Mehmet; Kumandaş, Sefer; Per, Hüseyin; Gümüş, Hakan; Öztürk, Selcan; Okuyaz, Çetin; Kömür, Mustafa; İpek, Rojan; Özbudak, Pınar; Arhan, Ebru; İnce, Hülya; Gürbüz, Gürkan; Mert, Gülen Gül; Özcan, Neslihan; Ölmez Türker, Akgün; Gazeteci Tekin, Hande; Kırık, Serkan; Günbey, Ceren; Çarman, Kürşat Bora; Yarar, Coşkun; Çavuşoğlu, Dilek (Springer, 2022)Children with chronic neurological diseases, including cerebral palsy (CP), are especially susceptible to vaccine-preventable infections and face an increased risk of severe respiratory infections and decompensation of ... -
Vanishing white matter disease with different faces
Güngör, Gülay; Güngör, Olcay; Çakmaklı, Seda; Maraş Genç, Hülya; İnce, Hülya; Yeşil, Gözde; Dilber, Cengiz; Aydın, Kürşad (Springer, 2020)Purpose: The goal of this study was to better understand vanishing white matter (VWM) disease, which is one of the most common hereditary white matter disorders, and its relationship to radiologic features, genetic analyses, ...