Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Öznur Tunca Yılmaz"'
Publikováno v:
Journal of Rehabilitation Medicine, Vol 50, Iss 1, Pp 80-85 (2017)
Background: Various studies have shown the efficacy of conventional isometric, Pilates and yoga exercises. However, data on the effects and comparison of these specific exercises on the cervical muscle morphology are insufficient or lacking. Objecti
Externí odkaz:
https://doaj.org/article/2004d3b78c4f4421b48e5dd1bac6b439
Autor:
Bilge Koçer, Çağrı Gülşen, Fatih Söke, Elvan Özcan Gülşen, Nursena Ersoy, Öznur Tunca Yılmaz, Selim Selçuk Çomoğlu
Publikováno v:
Acta Neurologica Belgica.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8939c77790eed88195338a92991348cf
https://doi.org/10.1007/s13760-023-02271-5
https://doi.org/10.1007/s13760-023-02271-5
Publikováno v:
Irish Journal of Medical Science (1971 -). 192:285-290
Kinesiophobia can be a barrier for physical activity in patients with multiple sclerosis (PwMS) and it can develop as a result of fear and avoidance reactions due to fatigue. However, there is no valid and reliable scale available to assess kinesioph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f008635250f1bfd51c617d227d43d4b
https://doi.org/10.1007/s11845-021-02902-x
https://doi.org/10.1007/s11845-021-02902-x
Autor:
Aynur Ayşe Karaduman, Ayşe Yeşbek-Kaymaz, Gamze Bora, Hayat Erdem-Yurter, Haluk Topaloglu, I. Alemdaroglu, Şulenur Subaşı-Yıldız, Öznur Tunca-Yılmaz, Numan Bulut
Publikováno v:
Journal of Child Neurology. 33:209-215
Exercise studies in neuromuscular diseases like spinal muscular atrophy (SMA), a devastating disease caused by survival of motor neuron 1 ( SMN1) gene mutations, are drawing attention due to its beneficial effects. In this study, we presented a const
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03e33a22c7954e17d9063e4eb4a6407e
https://doi.org/10.1177/0883073817750500
https://doi.org/10.1177/0883073817750500
Autor:
İpek, Alemdaroğlu, Ayşe, Karaduman, Gözde, İyigün-Yatar, Öznur, Tunca-Yılmaz, Haluk, Topaloğlu
Publikováno v:
The Turkish journal of pediatrics. 56(6)
The Egen Klassifikation Scale version 2 (EK2) is an important functional ability assessment scale for nonambulant neuromuscular patients. We investigated the validity and reliability of the EK2 scale in Turkish Duchenne muscular dystrophy (DMD) and s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b27a1774d90cbbf6ad93179cdcaf46d0
https://pubmed.ncbi.nlm.nih.gov/26388596
https://pubmed.ncbi.nlm.nih.gov/26388596
Publikováno v:
Medicine Science, Vol 8, Iss 4, Pp 1036-40 (2019)
Facioscapulohumeral muscular dystrophy is an uncommon and rarely seen progressive myopathic disorder. It is usually seen during periods of rapid growth (4-5 years). Proximal and distal upper extremities characteristically show weakness and atrophy. F
Externí odkaz:
https://doaj.org/article/3b2805237d844c7e852cbfa3fdf206f2