Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Senem Ayç"'
Publikováno v:
Sakarya Tıp Dergisi, Vol 12, Iss 2, Pp 217-222 (2022)
Antiepileptik ilaçların epilepsili çocukların D vitamini düzeylerine etkisi Giriş: Epilepsi çocukluk çağında sık görülebilen bir nörolojik hastalık olup antiepileptik ilaç tedavisini gerektirmektedir. Çeşitli antiepileptik ilaçlar
Externí odkaz:
https://doaj.org/article/5f9322bb092e4a8b86e6b7da1afb5bbc
Autor:
Halil Ural Aksoy, Celil Yılmaz, Senem Ayça, Aslı Kübra Atasever, Muzaffer Polat, Sercan Öztürk
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 11, Iss 3, Pp 295-300 (2021)
Objective: Treatment of childhood refractory epilepsy is a challenge for clinicians. Lacosamide is a new generation antiepileptic drug which is being used for focal onset seizures of adults and children. Efficacy and safety of the drug for adults hav
Externí odkaz:
https://doaj.org/article/93f0a26d208d48ada6c730bf35c2594f
Publikováno v:
İstanbul Medical Journal, Vol 21, Iss 5, Pp 397-400 (2020)
Introduction:Anaemia parameters in children with type- 1 diabetes and their relationship with metabolic control has received little attention in the literature. We aimed to determine the incidence of anaemia and to investigate anaemia parameters and
Externí odkaz:
https://doaj.org/article/a26c7094b6d545c58b583e782bd730a4
Publikováno v:
Haseki Tıp Bülteni, Vol 58, Iss 2, Pp 208-210 (2020)
We present two siblings with elevated serum creatine kinase concentrations, developmental delay, muscle weakness, and contractures of the lower limbs. Cranial magnetic resonance imaging revealed diffuse white matter hyperintensity in both siblings. I
Externí odkaz:
https://doaj.org/article/74a26140879b43348bd0a57088c2afd3
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 3, Pp 213-219 (2019)
Aim:This study aimed to determine the significance of six clinical predictors associated with medically intractable childhood epilepsy.Materials and Methods:A retrospective cohort study was conducted. A total of 241 children with diagnosed epilepsy w
Externí odkaz:
https://doaj.org/article/520906a5218946d2a3ffa3d2db0016ed
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 6, Iss 1, Pp 41-43 (2019)
Pyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive encephalopathy due to mutations in the ALDH7A1 gene. Intractable seizures are the most frequent clinical form in the early infantile period. A case of a 4-month-old female patient pres
Externí odkaz:
https://doaj.org/article/9f79bd76d1594df2be4b1d4d04e8b539
Autor:
Deniz Özalp Kızılay, Asusinem Akyalçın Kırdök, Pelin Ertan, Senem Ayça, Mehmet Murat Demet, Muzaffer Polat
Publikováno v:
Journal of Pediatric Research, Vol 4, Iss 2, Pp 53-58 (2017)
Aim: Febrile seizures (FS) cause great fear and panic in the families. The majority of parents think that they may lose their child during a seizure, and feel anxious about the possibility of seizures recurring in the future. We believe that educatin
Externí odkaz:
https://doaj.org/article/99ad4361dd4d45d2bc53b5274add16d9
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 2, Pp 109-111 (2018)
Patients with Miller Fisher syndrome (MFS) are characterized by acute ophthalmoplegia (AO) and areflexia. MFS is an immune mediated process, triggered by an infection and includes incomplete forms, such as ophthalmoplegia, ataxia and a central nervou
Externí odkaz:
https://doaj.org/article/d88c6e7fc3554a2f8127b09a8356fa3b
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
Publikováno v:
Malang Neurology Journal, Vol 8, Iss 2, Pp 147-149 (2022)
Dyke-Davidoff-Masson Syndrome (DDMS) is a rare syndrome characterized with specific clinical and radiological findings due to involvement of the developing brain with cerebral hemiatrophy of one hemisphere. The syndrome was first described from Dyke,
Externí odkaz:
https://doaj.org/article/bb06d397e9e242abbe848684b4d07329