Yazar "0000-0001-7335-1985" için Tıp Fakültesi listeleme
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Acute necrotizing encephalopathy of childhood: a single-center experience
Aksoy, Erhan; Öztoprak, Ülkü; Çelik, Halil; Özdemir, Fatih Mehmet Akif; Özkan, Mehpare; Kayalıoğlu, Hülya; Danış, Ayşegül (TUBITAK SCIENTIFIC & TECHNICAL RESEARCH COUNCIL TURKEY, 2021)Background/aim: Acute necrotizing encephalopathy is a rare type of acute encephalopathy characterized by multi-ocal brain lesions and associated severe neurological findings and various organ dysfunctions may accompany ... -
Expanding the genotype-phenotype spectrum of autosomal recessive Charcot-Marie-Tooth disease: A novel PLEKHG5 gene mutation
Yayıcı Köken, Özlem; Öztoprak, Ülkühan; Topçu, Vehap; Kayılıoğlu, Hülya (ASEAN NEUROLOGICAL ASSOC, 2021)Autosomal recessive intermediate Charcot Marie Tooth (CMT) disease type C is a very rarely-seen neurogenetic disorder. Homozygous or compound heterozygous mutation in the Pleckstrin homology domain-containing family G ... -
Treatment of Permanent Junctional Reciprocating Tachycardia in a Preterm Neonate: Case Report
İlhan, Özkan; Hakan, Nilay; Kayılıoğlu, Hülya; Karacan, Mehmet; Olgun, Haşim; Kırlı, Ulviye (GEORG THIEME VERLAG KG, 2021)Permanent junctional reciprocating tachycardia (PJRT) is most often observed in infants and children and can lead to incessant tachycardia. PJRT is usually refractory to medical treatment. Tachycardia may infrequently occur ...