Results 61 to 70 of about 22,111 (213)

Botulinum toxin chemodenervation for childhood strabismus in England: National and local patterns of practice. [PDF]

PLoS ONE, 2018
BackgroundBotulinum toxin injection chemodenervation is a well-established intervention for adult strabismus, and has also been recognised as an effective alternative to routine incisional surgery for paediatric disease.
Ameenat Lola Solebo, Anne-Marie Austin, Maria Theodorou, Chris Timms, Joanne Hancox, Gillian G W Adams   +5 more
doaj   +1 more source

Vision and Reading Difficulties Part 2: Optometric correlates of reading difficulties [PDF]

, 2009
In this second article of the series on vision and reading difficulties, the optometric factors (for example refractive error and orthoptic function) that may be associated with reading problems are discussed in detail.
Allen, Peter M, Evans, Bruce J W, Wilkins, Arnold   +2 more
core  

Robinson's Computerized Strabismus Model Comes of Age [PDF]

, 1996
In this article we review our further development of D.A. Robinson's computerized strabismus model. First, an extensive literature study has been carried out to get more accurate data on the anatomy of the average eye and the eye muscles, and about how ...
Simonsz, H.J. (Huib), Spekreijse, H. (Henk)   +1 more
core   +2 more sources

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li, Deziree L. Coleman, Kelsey Hogan, Danielle Luz, Lindsay Bhandari, Newell Belnap, Tiffany Busa, Charles Coutton, Klaus Dieterich, Svetlana Gorokhova, Clara Hildebrandt, Rachel Logan, Milena Mariani, Manuela Morleo, Vincenzo Nigro, John Pappas, Rachel Rabin, Kelly Schoch, Angelo Selicorni, Vandana Shashi, Rebecca Spillmann, Jennifer Sullivan, Charlotte Tardy, Samantha A. Schrier Vergano, Brock Grill, Kristin Baranano   +25 more
wiley   +1 more source

Long-Term Quality of Life in Adult Patients with Strabismus after Corrective Surgery Compared to the General Population. [PDF]

PLoS ONE, 2016
To evaluate the status of and factors associated with long-term health-related quality of life (HRQOL) in adult patients with strabismus following corrective surgery.Prospective cross-sectional study.
Meiping Xu, Huanyun Yu, Yuanyuan Chen, Jinling Xu, Jingwei Zheng, Xinping Yu   +5 more
doaj   +1 more source

Supplemental peri-operative intravenous crystalloids for postoperative nausea and vomiting: an abridged Cochrane systematic review. [PDF]

, 2020
We conducted a Cochrane systematic review on the effectiveness of supplemental intravenous crystalloid administration in preventing postoperative nausea and vomiting.
Bird, SJ, George, RB, Habib, AS, Jewer, JK, Parker, R, Wong, MJ   +5 more
core  

Factors associated with quality of life and mood in adults with strabismus [PDF]

, 2014
Background/Aims To explore the factors associated with the mood and quality of life (QoL) of patients with strabismus due to undergo realignment surgery. Methods A cross-sectional study was undertaken with adult patients. Along with demographic, clinical
Beauchamp, Carr, Charis Au, Collins, Covic, Crawford, Daniel G Ezra, Durnian, Fichman, Fu, Gillian G W Adams, Hagger, Hatt, Hatt, Hatt, Hayley B McBain, Hirani, Jackson, Jackson, James, Joanne Hancox, Kelly A MacKenzie, Leary, Leske, Martin, Mojon-Azzi, Mojon-Azzi, Moss-Morris, Rosser, Rumsey, Scharloo, Stanton P Newman, Wilkinson, Zigmond, Zimet   +34 more
core   +1 more source

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi, Michael Kutsche, Helena Lichtenfeld, Fanny Kortüm, Angela Abicht, Laura Herrmann, Theresia Herget   +6 more
wiley   +1 more source

Does strabismus surgery improve quality and mood, and what factors influence this? [PDF]

, 2016
Aims To establish the impact of adult strabismus surgery on clinical and psychosocial well-being and determine who experiences the greatest benefit from surgery and how one could intervene to improve quality of life post-surgery.
A Bessell, A Bessell, BA Nelson, D G Ezra, DA Leske, DB Rubin, G G W Adams, GR Beauchamp, H B McBain, H McBain, HB McBain, J Hancox, JP Burke, K A MacKenzie, KB Gunton, L Liebermann, P Glasman, S Jackson, S Jackson, S P Newman, SA Larson, SR Eliason, SR Hatt, SR Hatt, SR Hatt, SR Hatt, SR Hatt, ZI Currie   +27 more
core   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source