Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Baris, Ekici"'
Autor:
Seray Nural Sigan, Tugçe Aksu Uzunhan, Nur Aydinli, Emine Eraslan, Baris Ekici, Mine Çaliskan
Publikováno v:
Annals of Indian Academy of Neurology, Vol 16, Iss 3, Pp 342-346 (2013)
Aim: Oral motor dysfunction is a common issue in children with cerebral palsy (CP). Drooling, difficulties with sucking, swallowing, and chewing are some of the problems often seen. In this study, we aimed to research the effect of oral motor therapy
Externí odkaz:
https://doaj.org/article/ec19e53975cb47d290a084ab175f50a7
Publikováno v:
Annals of Indian Academy of Neurology, Vol 15, Iss 3, Pp 196-199 (2012)
Purpose: The main object of the present study is to assess neuromotor development of high-risk infants by using three tests, and to determine inter-test concordance and the feasibility of these tests. Materials and Methods: One-hundred and nine patie
Externí odkaz:
https://doaj.org/article/7c11457b25964df1bebda5f456ef339d
Publikováno v:
Annals of Indian Academy of Neurology, Vol 14, Iss 3, Pp 178-181 (2011)
Purpose: Mutations of the a-1 subunit sodium channel gene (SCN1A) cause severe myoclonic epilepsy of infancy (SMEI). To date, over 300 mutations related to SMEI have been described. In the present study, we report new SCN1A mutations and the clinical
Externí odkaz:
https://doaj.org/article/0449d2245f704ec2a4be3cc2be9a208a
Autor:
Baris Ekici, Yakup Ergül, Burak Tatli, Feride Bilir, Fatih Binboga, Ayse Süleyman, Zeynep Tamay, Mine Çaliskan, Nermin Güler
Publikováno v:
Annals of Indian Academy of Neurology, Vol 14, Iss 3, Pp 182-184 (2011)
Aim: The aim of this work was to assess the respiratory functions of ambulatory Duchenne patients and to propose an earlier time period for intervention. Materials and Methods: Lung functions and North Star Ambulatory Assessment (NSAA) scores of Duch
Externí odkaz:
https://doaj.org/article/ddfcbf3eec2b430bb76a701c66027575
Publikováno v:
Saudi Journal of Anaesthesia, Vol 5, Iss 1, Pp 93-95 (2011)
Hereditary sensory autonomic neuropathy type IV is a rare disorder with an autosomal recessive transmission and characterized by self-mutilation due to a lack in pain and heat sensation. Recurrent hyperpyrexia and anhydrosis are seen in patients as a
Externí odkaz:
https://doaj.org/article/64b5c4759f91417db621cdc9e5d96ffe
Autor:
Deniz Yüksel, Arzu Yilmaz Okten, Rahsan Gocmen, Mehmet Bastemur, Banu Anlar, Baris Ekici, Akin Iscan, Safak Parlak, Elif Acar Arslan
Aim: To investigate etiology and prognostic significance of pontine tegmentum lesions accompanying a cluster of acute flaccid myelitis. Method: We retrospectively examined patients from 6 centers in Turkey who manifested encephalitis or myelitis asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ed23b327a52e56560c509530c9e39e
http://hdl.handle.net/20.500.12645/18488
http://hdl.handle.net/20.500.12645/18488
Publikováno v:
Annals of Indian Academy of Neurology, Vol 15, Iss 4, Pp 350-351 (2012)
Externí odkaz:
https://doaj.org/article/6ae9606e23634cf0844e69cd6685bb50
Publikováno v:
Tuberculin Skin Test in Children. 12:83-85
Sutcocugu doneminde akut ataksi cogu kez viral infeksiyonlar, ilac intoksikasyonlari ve intrakraniyal tumorlere bagli olarak gelisir. Akut serebellar ataksi ve opsomiyoklonus birlikteligi noroblastomun ilk belirtisi olabilir. On dokuz aylik erkek has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20372e9d9ed4971bf4cefed35aa67a71
https://doi.org/10.5222/j.child.2012.083
https://doi.org/10.5222/j.child.2012.083
Autor:
Yakup, Ergul, Baris, Ekici, Kemal, Nisli, Burak, Tatli, Fatih, Binboga, Gonul, Acar, Meral, Ozmen, Rukiye Eker, Omeroglu
Publikováno v:
Journal of paediatrics and child health. 48(7)
We evaluated ambulatory patients with Duchenne muscular dystrophy from the cardiovascular standpoint and studied the correlation between the results of electrocardiographic (ECG) findings, left ventricular ejection fraction (LVEF), troponin T and N-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c922e6f69669e13c340b162928412b7c
https://pubmed.ncbi.nlm.nih.gov/22404693
https://pubmed.ncbi.nlm.nih.gov/22404693