Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ayfer A Akçay"'
Publikováno v:
JGH Open, Vol 8, Iss 6, Pp n/a-n/a (2024)
Abstract Background and Aim The aim of this study is to compare the effects of osteopathic manipulative therapy home program (OMT‐H) versus abdominal massage home program (AMHP) in treating constipation in children with cerebral palsy (CP). Methods
Externí odkaz:
https://doaj.org/article/e32429be38454918ae4277173adf5791
Autor:
Ayfer Arduç Akçay, Serap Uysal
Publikováno v:
Journal of Pediatric Research, Vol 11, Iss 4, Pp 220-224 (2024)
Aim: We evaluated the clinical and electroencephalography (EEG) characteristics, treatments, and outcomes of children with hot-water epilepsy (HWE), a specific type of reflex epilepsy. Materials and Methods: This retrospective study included 11 chil
Externí odkaz:
https://doaj.org/article/aafdbc55f4e2415bbb1534805b8efd1b
Autor:
Gulshan Yunisova, Ayfer Arduç Akçay, Şahin Avci, Serpil Eraslan, Hülya Kayserili, Piraye Oflazer
Publikováno v:
Sunday, April 23.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f16eb3eb7c33fcf76bc8c827a37bad9
https://doi.org/10.1212/wnl.0000000000203759
https://doi.org/10.1212/wnl.0000000000203759
Publikováno v:
Journal of Cardiothoracic Surgery. 18
Introduction Spinal muscular atrophy (SMA) is a severe, inherited neuromuscular disorder characterized by progressive muscle weakness and atrophy. Cardiac pathology co-existence is reported more frequently in the severely affected patient groups. Str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe16e6782761ffecbfa76d8f8b3eb789
https://doi.org/10.1186/s13019-023-02170-z
https://doi.org/10.1186/s13019-023-02170-z
Autor:
Tuğçe Aksu Uzunhan, Biray Ertürk, Kürşad Aydın, Akif Ayaz, Umut Altunoğlu, Murat Hakkı Yarar, Alper Gezdirici, Dilara Füsun İçağasıoğlu, Ezgi Gökpınar İli, Bülent Uyanık, Metin Eser, Yaşar Bekir Kutbay, Yasemin Topçu, Betül Kılıç, Gonca Bektaş, Ayfer Arduç Akçay, Barış Ekici, Amet Chousein, Şahin Avcı, Atıl Yüksel, Hülya Kayserili
Publikováno v:
Clinical Neurology and Neurosurgery. 224:107560
© 2022 Elsevier B.V.Objective: Joubert syndrome is a neurodevelopmental disorder with a distinctive hindbrain malformation called molar tooth sign, causing motor and cognitive impairments. More than 40 genes have been associated with Joubert syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f57581bf06a2db57ba2d0c85721f96c
https://doi.org/10.1016/j.clineuro.2022.107560
https://doi.org/10.1016/j.clineuro.2022.107560