Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Allyson Berent"'
Autor:
Dandan Chen, Christina K. Zigler, Li Lin, Nicole Lucas, Molly McFatrich, Jennifer Panagoulias, Allyson Berent, Bryce B. Reeve
Publikováno v:
Journal of Patient-Reported Outcomes, Vol 8, Iss 1, Pp 1-7 (2024)
Abstract Aims Caregivers rate improved communication ability as one of the most desired outcomes for successful interventions for individuals with Angelman syndrome (AS). When measuring communication ability in clinical trials, the reliability of suc
Externí odkaz:
https://doaj.org/article/7c1ba299b85e4ea292481cd5df58de30
Autor:
Allison Kendall, Julie K. Byron, Jodi L. Westropp, Joan R. Coates, Shelly Vaden, Chris Adin, Garrett Oetelaar, Joe W. Bartges, Jonathan D. Foster, Larry G. Adams, Natasha Olby, Allyson Berent
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 38, Iss 2, Pp 878-903 (2024)
Abstract Urinary incontinence (UI) is a disorder of micturition that can occur in dogs of any age, sex, and breed depending on the underlying cause and time of onset. Diagnosis and treatment for various causes of UI in dogs have been described by mul
Externí odkaz:
https://doaj.org/article/1cd452897cab4610b0482aa6a667fdea
Autor:
Emilie Véran, Catherine Vachon, Julie Byron, James Howard, Allyson Berent, Chick Weisse, Romain Javard, Ashley Spencer, Sarah Gradilla, Carrie Palm, William Culp, Andréanne Cléroux, Marilyn Dunn
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 36, Iss 5, Pp 1677-1685 (2022)
Abstract Background Placement of a subcutaneous ureteral bypass (SUB) device is an effective method to relieve all causes of ureteral obstruction in cats. Complications involving migration within the gastrointestinal tract have been seldomly describe
Externí odkaz:
https://doaj.org/article/769aad6a93bc4c04802386e4948f1600
Autor:
Miranda Rogers, Stéphane Motola, Yacine Bechichi, Céline Cluzeau, Tanguy Terray, Allyson Berent, Jennifer Panagoulias, Jessica Duis, Damien Eggenspieler, Laurent Servais
Publikováno v:
Children, Vol 10, Iss 9, p 1462 (2023)
Previous patient-centered concept models of Angelman syndrome (AS) are integral in developing our understanding of the symptoms and impact of this condition with a holistic perspective and have highlighted the importance of motor function. We aimed t
Externí odkaz:
https://doaj.org/article/4b87d75f4b3148a082904adfde2203f6
Autor:
Jessica Duis, Mark Nespeca, Jane Summers, Lynne Bird, Karen G.C.B. Bindels‐de Heus, M. J. Valstar, Marie‐Claire Y. deWit, C. Navis, Maartje ten Hooven‐Radstaake, Bianca M. vanIperen‐Kolk, Susan Ernst, Melina Dendrinos, Terry Katz, Gloria Diaz‐Medina, Akshat Katyayan, Srishti Nangia, Ronald Thibert, Daniel Glaze, Christopher Keary, Karine Pelc, Nicole Simon, Anjali Sadhwani, Helen Heussler, Anne Wheeler, Caroline Woeber, Margaret DeRamus, Amy Thomas, Emily Kertcher, Lauren DeValk, Kristen Kalemeris, Kara Arps, Carol Baym, Nicole Harris, John P. Gorham, Brenda L. Bohnsack, Reid C. Chambers, Sarah Harris, Henry G. Chambers, Katherine Okoniewski, Elizabeth R. Jalazo, Allyson Berent, Carlos A. Bacino, Charles Williams, Anne Anderson
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Background Angelman syndrome (AS) is a rare neurogenetic disorder present in approximately 1/12,000 individuals and characterized by developmental delay, cognitive impairment, motor dysfunction, seizures, gastrointestinal concerns, and abnor
Externí odkaz:
https://doaj.org/article/eb69721114bc440fbbb670148e293148
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 34, Iss 2, Pp 725-733 (2020)
Abstract Background Dogs with tracheal stents often have positive airway bacterial cultures. The pathogenicity of these organisms and risk factors for infection have not been investigated. Objective Describe bacterial infection in dogs with tracheal
Externí odkaz:
https://doaj.org/article/b5cf422ffc7b496aa2c380b8baa8db18
Autor:
Nicole M. Tate, Katie M. Minor, Jody P. Lulich, James R. Mickelson, Allyson Berent, Jonathan D. Foster, Kasey H. Petersen, Eva Furrow
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100792- (2021)
Hereditary xanthinuria is a rare autosomal recessive disease caused by missense and loss of function variants in the xanthine dehydrogenase (XDH) or molybdenum cofactor sulfurase (MOCOS) genes. The aim of this study was to uncover variants underlying
Externí odkaz:
https://doaj.org/article/d0d68e09b2a84a188ca82aec80814820
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 32, Iss 2, Pp 693-700 (2018)
Background Despite multiple dilatation procedures, benign esophageal strictures (BES) remain a recurring cause of morbidity and mortality in dogs and cats. Objective Investigate the use of an indwelling Balloon Dilatation esophagostomy tube (B‐Tube
Externí odkaz:
https://doaj.org/article/c1a2865695d24100a4569ed635352510
Autor:
Christina K. Zigler, Nicole Lucas, Molly McFatrich, Kelly L. Gordon, Harrison N. Jones, Allyson Berent, Jennifer Panagoulias, Paula Evans, Bryce B. Reeve
Publikováno v:
American Journal on Intellectual and Developmental Disabilities. 128:185-203
Communication deficits have a substantial impact on quality of life for individuals with Angelman syndrome (AS) and their families, but limited qualitative work exists to support the necessary content of measures aiming to assess communication for th
Autor:
Philipp D. Mayhew, Allyson Berent
Publikováno v:
Small Animal Soft Tissue Surgery. :533-547