Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fatih Arslanoğlu"'
Publikováno v:
Sakarya Tıp Dergisi, Vol 12, Iss 1, Pp 63-70 (2022)
Objective: AO (Arbeitsgemeinschaft für Osteosynthesefragen) type C distal humerus fractures are difficult fractures to reduce and fix due to the difficulty of the elbow anatomy and small size of the broken bone parts. We hypothesize that although pa
Externí odkaz:
https://doaj.org/article/da65369c4229417ab5cdd1677579606e
Publikováno v:
Case Reports in Orthopedics, Vol 2019 (2019)
Introduction. ACTS secondary to amyloidosis is a very rare situation in the literature, and here, we present a unique case of ACTS secondary to amyloidosis. Case Report. A 61-year-old male patient was admitted to our hospital with complaints of numbn
Externí odkaz:
https://doaj.org/article/197613b8e5e841a9ab860306c8ce704f
Autor:
Fatih Arslanoğlu, Güzelali Özdemir, Nazım Karahan, Serda Duman, Mehmet Serkan Cetin, Duygu Kolukısa
Publikováno v:
Medical Principles and Practice. 29:174-180
Background: The objective of this study was to evaluate the efficacy of subacromial injections of collagenase and corticosteroid in rats with experimentally induced adhesive capsulitis. Method: Thirty adult Wistar albino male rats were distributed in
Autor:
Kadir Buyukdogan, Ömer Serdar Hakyemez, Murat Birinci, Mehmet Akif Çaçan, Musa Uğur Mermerkaya, Fatih Arslanoğlu, Yasin Güler
Background: Haglund syndrom is characterized as a painful posterosuperior deformity of the heel with possible causes as tight Achilles tendon, high-arched foot and tendency to walk on the outside of the heel. Surgical treatment may be recommended in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::967bfe514b207cbe691a324840f6d0bc
https://hdl.handle.net/20.500.12511/7432
https://hdl.handle.net/20.500.12511/7432
Publikováno v:
TOTBID Dergisi. 19
Publikováno v:
Case Reports in Orthopedics
Case Reports in Orthopedics, Vol 2019 (2019)
Case Reports in Orthopedics, Vol 2019 (2019)
Introduction. ACTS secondary to amyloidosis is a very rare situation in the literature, and here, we present a unique case of ACTS secondary to amyloidosis. Case Report. A 61-year-old male patient was admitted to our hospital with complaints of numbn