Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Congenital X-linked retinoschisis"'
Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background This case report describes the surgical outcome in a patient with congenital X-linked retinoschisis (CXLRS) and the results of proteomic analysis of surgically extracted samples from both vitreous and intraschisis cavities by mass
Externí odkaz:
https://doaj.org/article/4686c7ae736844b3a29cb678ee672f6e
Akademický článek
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Akademický článek
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Publikováno v:
BMC Ophthalmology
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-6 (2022)
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-6 (2022)
Background This case report describes the surgical outcome in a patient with congenital X-linked retinoschisis (CXLRS) and the results of proteomic analysis of surgically extracted samples from both vitreous and intraschisis cavities by mass spectrom
Autor:
Kimberly A. Drenser
Publikováno v:
A Quick Guide to Pediatric Retina ISBN: 9789811565519
Congenital X-linked Retinoschisis (CXRS) is a vitreoretinopathy that is primarily inherited in an X-linked recessive pattern. It is typically bilateral and is the most common cause of juvenile macular degeneration in males. The primary defect is in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f3b417ced6dcacf9090735f1665a838
https://doi.org/10.1007/978-981-15-6552-6_23
https://doi.org/10.1007/978-981-15-6552-6_23
Publikováno v:
Asia-Pacific Journal of Ophthalmology.
We present an updated clinical review of the pathophysiology, progression, and current treatments in pediatric patients with congenital X-linked retinoschisis (CXLRS). CXLRS is an X-linked inherited retinal degeneration characterized by splitting of
Autor:
Michael T. Trese, Kimberly A. Drenser, Joshua Robinson, Prethy Rao, Yoshihiro Yonekawa, Antonio Capone, Benjamin J. Thomas
Publikováno v:
Retina (Philadelphia, Pa.). 36(6)
PURPOSE To describe wide-field imaging features of patients with congenital X-linked retinoschisis. METHODS This is a retrospective nonconsecutive series of 36 eyes from 18 patients with congenital X-linked retinoschisis from 2008 to 2014. Wide-field
Autor:
Paul A. Sieving, Yuichiro Takada, Michael T. Trese, Jonathan L. Prenner, Stefano Ciaccia, Antonio Capone
Publikováno v:
Retina. 26:S61-S64
To establish a classification system for congenital X-linked retinoschisis (CXLRS) using clinical examination and optical coherence tomography (OCT).Thirty-eight eyes of 19 patients who carried a clinical diagnosis of CXLRS were examined with OCT and
Autor:
Kimberly A. Drenser, Antonio Capone, Wendy A Dailey, Mandar M. Joshi, Michael T. Trese, Michael Hartzer
Publikováno v:
Retina. 26:S57-S60
To describe the intraschisis cavity protein composition in congenital X-linked retinoschisis (CXLRS) from two eyes of one child.The authors present a child with complex, Type 3 CXLRS who underwent bilateral surgical repair with autologous plasmin enz
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