Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Cynthia Solot"'
Autor:
Connor S. Wagner, BS, Carlos E. Barrero, BS, Zachary D. Valenzuela, BS, Lauren K. Salinero, BS, Matthew E. Pontell, MD, Susan M. McCormack, MA CCC-SLP, Cynthia Solot, MA CCC-SLP, Marilyn Cohen, BA LSLP, Richard E. Kirschner, MD, David W. Low, MD, Oksana Jackson, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 11, Iss 4S, Pp 2-3 (2023)
Externí odkaz:
https://doaj.org/article/4469ff4ff3314e649a61cc184748130c
Autor:
Inge Zink, Cynthia Solot, T. Blaine Crowley, Ann Swillen, Donna McDonald-McGinn, Jente Verbesselt, Jeroen Breckpot, Ellen Van Den Heuvel, Victoria Giunta
Publikováno v:
Genes; Volume 14; Issue 3; Pages: 679
Although it is known that copy number variants (CNVs) on chromosome 22, such as 22q11.2 deletion (22q11.2DS) and 22q11.2 duplication (22q11.2Dup) syndromes, are associated with higher risk for neurodevelopmental issues, few studies have examined the
Autor:
Daniel E. McGinn, Marsha Gerdes, Beverly S. Emanuel, Sean Gallagher, Terrence B. Crowley, Elaine H. Zackai, Donna M. McDonald-McGinn, Raquel E. Gur, Kosha Ruparel, Cynthia Solot, Ruben C. Gur, Monica E. Calkins, Tyler M. Moore, Edward Moss
Publikováno v:
Am J Med Genet B Neuropsychiatr Genet
The 22q11.2 deletion syndrome (22q11DS) is associated with impaired cognitive functions and increased risk for schizophrenia spectrum disorders. Speech and language deficits are prominent, with evidence of decline anteceding emergence of psychosis. T
Autor:
Marilyn Cohen, Alison E. Kaye, Nancy Minugh-Purvis, Oksana A. Jackson, Cynthia Solot, Donna M. McDonald-McGinn, Abbas F. Jawad, Richard E. Kirschner, Elaine H. Zackai, Alfred Lee
Publikováno v:
Annals of Plastic Surgery. 84:665-671
PURPOSE The purpose of this study was to characterize airway problems, speech outcomes, and facial growth in patients with Stickler syndrome undergoing cleft palate repair. METHODS A retrospective, longitudinal study was performed at the Children's H
Autor:
Oksana Jackson, Debbie Sell, Christina Persson, Cynthia Solot, Adriane L. Baylis, Donna M. McDonald-McGinn, Anne Mayne
Publikováno v:
American Journal of Speech-Language Pathology
Purpose Speech and language disorders are hallmark features of 22q11.2 deletion syndrome (22qDS). Learning disabilities, cognitive deficits, palate abnormalities, velopharyngeal dysfunction, behavioral differences, and various medical and psychiatric
Autor:
Cynthia Solot, Oksana Jackson, Kaitlyn M. Paine, Elaine H. Zackai, Leanne Magee, Susan McCormack, Meg Ann Maguire, Donna M. McDonald-McGinn
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 116:43-48
Objective To determine demographics and practice patterns of surgeons treating velopharyngeal dysfunction (VPD) in patients with 22q11.2 deletion syndrome (22q11.2DS). Methods An anonymous electronic survey study was administered to the surgical memb
Autor:
Meg Ann Maguire, Cynthia Solot, Lisa Elden, Vamsee Vemulapalli, Christopher M. Cielo, Donna M. McDonald-McGinn, Thornton B.A. Mason, Alfred Lee, Oksana Jackson, Terrence B. Crowley, Brian L. Chang
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 57(7)
Objective: To determine pre- and postoperative prevalence of obstructive sleep apnea (OSA) in patients with 22q11.2 deletion syndrome (DS) undergoing wide posterior pharyngeal flap (PPF) surgery for velopharyngeal dysfunction (VPD). Design: Retrospec
Autor:
Elaine H. Zackai, Donna M. McDonald-McGinn, Robert R. Clancy, Cynthia Solot, Thomas B. Flynn, Jesse L Chittams, Therese Sammarco, Jessica L Bean Jaworski, Judy Bernbaum, J. William Gaynor, Nancy Burnham, Marsha Gerdes
Publikováno v:
Congenital Heart Disease. 12:421-429
Objective Atypical development, behavioral difficulties, and academic underachievement are common morbidities in children with a history of congenital heart defects and impact quality of life. Language and social-cognitive deficits have been describe
Autor:
Donna M. McDonald-McGinn, Oksana Jackson, Stephanie Jeong, Robert J. Smith, Robert J. Sharkus, T. Blaine Crowley, Cynthia Solot
Publikováno v:
American Journal of Medical Genetics Part A.
Palatal involvement occurs commonly in patients with 22q11.2 Deletion Syndrome (22qDS), and includes palatal clefting and velopharyngeal dysfunction in the absence of overt or submucous clefts. The reported incidence and distribution of palatal abnor
Autor:
Ellen Van Den Heuvel, Christina Reuterskiöld, Ann Swillen, Cynthia Solot, Eric Manders, Inge Zink
Publikováno v:
International Journal of Speech-Language Pathology. 19:490-502
PURPOSE: This study describes the performance on a perspective- and role-taking task in 27 children, ages 6-13 years, with 22q11.2 deletion syndrome (22q11.2DS). A cross-cultural design comparing Dutch- and English-speaking children with 22q11.2DS ex