Zobrazeno 1 - 10
of 151
pro vyhledávání: '"Aylin, Yaman"'
Autor:
Yasemin Turkan, F. Boray Tek, Fatih Arpaci, Ozan Arslan, Devrim Toslak, Mehmet Bulut, Aylin Yaman
Publikováno v:
IEEE Access, Vol 12, Pp 104031-104051 (2024)
Retinal optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) have emerged as promising, non-invasive, and cost-effective modalities for the early diagnosis of Alzheimer’s disease (AD). However, a comprehensive revi
Externí odkaz:
https://doaj.org/article/0bff1e93dbb54dfa8503d38b216a929d
Autor:
Aylin Yaman, Fatma Kurtuluş Aydın
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionIn this study, we aim to evaluate the treatment responses and prognostic characteristics of Myasthenia Gravis (MG) patients followed in a tertiary neuromuscular diseases center in Turkey.MethodsOne hundred seventy four MG patients (betwee
Externí odkaz:
https://doaj.org/article/d22a6b40d63647ab9e9a88e30d77fad8
Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 1, Pp 264-269 (2021)
A 16-year-old boy with X-linked retinoschisis was examined for the visual decline on his left eye. Upon examination, a vasopermeable elevated mass lesion was determined at the lower temporal retinal periphery associated with surrounding arc-like hard
Externí odkaz:
https://doaj.org/article/bbaa3ad8d0e345b79171754bfe337b59
Publikováno v:
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract Carotid artery dissection should be considered in the differential diagnosis when a clinician faces with a case presenting with a unilateral Purtscher‐like retinopathy.
Externí odkaz:
https://doaj.org/article/d339a5ac77524974a01acca652eea798
Publikováno v:
Ocular Immunology and Inflammation. :1-6
© 2023 Taylor & Francis Group, LLC.Purpose: To elucidate whether wide-field fluorescein angiography (WFFA) can yield additional information in patients with newly diagnosed idiopathic acute anterior uveitis (AAU). Methods: The WFFA was performed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::367626018ebc250b96726c955cc0f58e
https://doi.org/10.1080/09273948.2023.2168697
https://doi.org/10.1080/09273948.2023.2168697
Publikováno v:
Case Reports in Ophthalmology, Vol 9, Iss 2, Pp 375-380 (2018)
A 12-year-old girl with bilateral stage 2B Coats disease was screened meticulously for a possible underlying systemic disease as she was female and the disease was bilateral. Full systemic workout turned out to be unremarkable. However, an ABCA4 gene
Externí odkaz:
https://doaj.org/article/8c5c3291dc3b49318c6de400c0157ea2
Publikováno v:
Beyoglu Eye Journal, Vol 3, Iss 1, Pp 34-37 (2018)
Necrotising fasciitis is a serious soft tissue infection with a significant fatality rate. Although the cause may be polymicrobial, most known microbial agents are Streptococcus pyogenes and Staphyylococcus aureus. Early recognition and aggressive su
Externí odkaz:
https://doaj.org/article/ed65c61bf2a54c6682b39cee10940460
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 48, Iss 1, Pp 42-46 (2018)
Orbital apex syndrome is a rare complication of herpes zoster ophthalmicus. A patient being followed in our clinic for herpes zoster ophthalmicus developed orbital apex syndrome in the second week of treatment. Clinical diagnosis was supported by mag
Externí odkaz:
https://doaj.org/article/7473f2713db44fd89820a16a370fbb19
Autor:
Omer Karti, Saygin Abali, Ziya Ayhan, Eylem Gokmeydan, Serhad Nalcaci, Aylin Yaman, Ali Osman Saatci
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 7, Iss C, Pp 129-133 (2017)
Purpose: CDH3-related hypotrichosis with juvenile macular dystrophy (HJMD) is an autosomal-recessive entity characterized by congenital sparse scalp hair and macular dystrophy, leading to severe central visual loss. We report a family with HJMD cause
Externí odkaz:
https://doaj.org/article/165ded9e3066429aa7dc84c14e1127bb
Autor:
Meral Bilgilisoy Filiz, Naciye Füsun Toraman, Serkan Filiz, Tuncay Cakir, Şebnem Koldaş Doğan, Muhammet Gültekin Kutluk, Aylin Yaman
Publikováno v:
Braz J Phys Ther
Background Increment of lumbar lordosis, a frequent spinal finding in Duchenne Muscular Dystrophy (DMD), is a compensatory mechanism secondary to muscle weakness. However, excessive lumbar lordosis may change the position of the center of mass, and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb4e1446b75833dc8098f5ab84058be2
https://doi.org/10.1016/j.bjpt.2021.05.001
https://doi.org/10.1016/j.bjpt.2021.05.001