Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pinar Topaloğlu"'
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 39, Iss 1, Pp 53-55 (2022)
Glucose transporter type 1 deficiency syndrome (GLUT-1 DS) is an inborn error of metabolism that results in defective glucose transport and consequently a reduced supply of glucose to the brain. Here, we describe a patient with a molecularly proven G
Externí odkaz:
https://doaj.org/article/5dd6d87fad6f4987975ff864e8acc64e
Autor:
Arife Çimen Atalar, Aynur Özge, Bengi Gül Türk, Esme Ekizoğlu, Duygu Kurt Gök, Betül Baykan, Semih Ayta, Füsun Ferda Erdoğan, Seher Naz Yeni, Bahar Taşdelen, IDEM Study Group, Sibel K. Velioğlu, Zuhal Yapıcı, İpek Midi, Saygı Serap, Çelebi Ulufer, Elif Sarıca Darol, Kadriye Ağan, Senem Ayç, Sibel Gazioğlu, Zeynep Vildan Okudan, Nermin Görkem Şirin, Nerses Bebek, Neşe Dericioğlu, İlknur Güçlü Altun, Ayşe Destina Yalçın, Reyhan Sürmeli, Oğuz Osman Erdinç, Abidin Erdal, Demet İlhan Algın, Gülnihal Kutlu, Semai Bek, Yüksel Erdal, Akçay Övünç Özön, Aylin Reyhani, Babürhan Güldiken, Barış Baklan, Bülent Oğuz Genç, Ebru Aykutlu Altindağ, Gökçen Karahan, Güray Koç, Handan Mısırlı, İbrahim Öztura, Kezban Aslan-Kara, Melodi Çakar Merve, Nur Türkmen, Onur Bulut, Karadaş Ömer, Özlem Kesim Çahin, Sevgi Ferik, Taylan Peköz Mehmet, Pınar Topaloğlu, Sibel Üstün Özek, Ülkühan Düzgün, Vildan Yayla, Yasemin Gömceli, Zeynep Ünlüsoy Acar
Publikováno v:
Frontiers in Neurology, Vol 13 (2023)
BackgroundMigraine without aura (MwoA) is a very frequent and remarkable comorbidity in patients with idiopathic/genetic epilepsy (I/GE). Frequently in clinical practice, diagnosis of MwoA may be challenging despite the guidance of current diagnostic
Externí odkaz:
https://doaj.org/article/63f182df8f6b4bcdb757b52ed7bc79f9
Autor:
Gündüz, Tuncay, Tektürk, Pınar Topaloğlu, Yapıcı, Zuhal, Kürtüncü, Murat, Somer, Ayper, Törün, Selda Hançerli, Eraksoy, Mefkure
Publikováno v:
In Journal of the Neurological Sciences 15 January 2017 372:305-306
Publikováno v:
In Clinical Neurophysiology 2008 119 Supplement 1:S20-S20
Publikováno v:
Türk Nöroloji Dergisi, Vol 12, Iss 1, Pp 59-64 (2006)
The patient who had been treated symptomatically with the diagnosis of Huntington Disease was hospitalized in our clinic, got the diagnosis of neuroacanthocytosis with clinical findings and laboratory investigations was discussed in comparison wit
Externí odkaz:
https://doaj.org/article/49d0f856bcb84d05ba049b05edfda6b2