Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nihal Olgaç Dundar"'
Autor:
Yiğithan Güzin, Ayşe Özbay Yıldız, Bakiye Tunçay, Pınar Gençpınar, Figen Baydan, Nihal Olgaç Dündar
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 14, Iss 2, Pp 97-102 (2024)
Objective: Spinal muscular atrophy (SMA) is a hereditary disorder with progressive muscle weakness and atrophy. Nusinersen is an antisense oligonucleotide directed against SMN2 and has been shown in studies to improve the motor skills of patients. Th
Externí odkaz:
https://doaj.org/article/b7dfeb4b6e834c58a534665eac32a750
Autor:
Dilek Cavusoglu, Melis Kose, Esra Er, Muhsin Elmas, Pinar Gencpinar, Nihal Olgaç Dundar, Kursad Aydin
Background: Folate metabolism disorders can affect various organ systems, including the nervous system. 5,10-methenyltetrahydrofolate synthetase deficiency is a rare cerebral folate deficiency in which MTHFS activity is disrupted with low-normal cere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae22078db792de13bea46d864bd010a
https://hdl.handle.net/20.500.12511/9688
https://hdl.handle.net/20.500.12511/9688
Autor:
Osman BÜYÜKŞEN, Nihal Olgaç DÜNDAR
Publikováno v:
Forbes Tıp Dergisi, Vol 4, Iss 2, Pp 109-115 (2023)
During the pandemic process announced by the World Health Organization on March 11, 2020, some neurological outcomes were observed in pediatric cases with Severe acute respiratory syndrome- Coronavirus-2 infection. It is thought that this new virus i
Externí odkaz:
https://doaj.org/article/2ee04690be0a4f3c819b073da0207415
Autor:
Hakan SALMAN, Nihal OLGAÇ DÜNDAR
Publikováno v:
Forbes Tıp Dergisi, Vol 3, Iss 1, Pp 18-23 (2022)
Objective: Since management of different seizure types are different, it was deemed necessary to classify the cases presenting with seizures. Patients who admitted to our hospital for the first time with seizures were evaluated. Methods: The study wa
Externí odkaz:
https://doaj.org/article/68951d2cf44043be8bae0055744fa35f
Autor:
Semra Gursoy, Esra Ataman, Bahar Toklu Baysal, Berk Özyılmaz, Pınar Gençpınar, Ayşe Semra Hız, Uluç Yiş, Aycan Ünalp, Nihal Olgaç Dündar, Ayfer Ülgenalp, Derya Erçal
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 2, Pp 206-210 (2020)
Background and Aims:PCDH19 gene, which encodes protocadherin 19, is associated with epilepsy and intellectual disability, mainly in affected females. The clinical manifestations are heterogeneous and the main features include early onset seizure, gen
Externí odkaz:
https://doaj.org/article/c09e579b34b3452381f5265ddeb77d7b
Autor:
Sinem Akbay, Esra Ozer, Ozkan Ilhan, Berat Kanar, Seyma Memur, Gulden Diniz, Dilek Cavusoglu, Nihal Olgaç Dündar
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 3, Pp 259-262 (2019)
The diagnosis of the hypotonia at the neonatal period is difficult. In the neonatal period, the differential must include acute illnesses and systemic diseases such as sepsis, congestive heart failure and inborn errors of metabolism. Congenital disor
Externí odkaz:
https://doaj.org/article/c1f949a4ec994c5782f9b232300a6a9a
Autor:
Dilek Çavusoglu, Melike Ataseven Kulali, Nihal Olgaç Dündar, Cigdem Ozer Gokaslan, Kurşad Aydin
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 1, Pp 133-134 (2022)
Externí odkaz:
https://doaj.org/article/6843db3b655645deb69a2a198e568b32
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2014 (2014)
To the best of our knowledge this is the first case report describing exposure to varenicline, an α4β2 nicotinic acetylcholine partial receptor agonist used for smoking cessation therapy in pregnancy. A 29-year-old multiparous woman with an unplann
Externí odkaz:
https://doaj.org/article/80481b820a7649fab86d39e0b4d69f8d
Autor:
Nihal Olgac Dundar, Berrin Aktekin, Nilufer Cicek Ekinci, Duygu Sahinturk, Ugur Yavuzer, Olcay Yegin, Senay Haspolat
Publikováno v:
Neurology International, Vol 5, Iss 3, Pp e17-e17 (2013)
Mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS) is a common medically intractable epilepsy syndrome. Although pathogenesis of HS still remains highly controversial, genetics may play a role as a predisposing factor. Previous eviden
Externí odkaz:
https://doaj.org/article/851d016a4aea446ca695e4fa5fdc7c08