Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Devon Barrett"'
Autor:
Pankaj B. Agrawal, Thomas E. Mullen, Monica H. Wojcik, Margaret A. Kenna, Rachel Stadelmaier, Olaf Bodamer, Caroline D. Robson, Devon Barrett
Publikováno v:
Am J Med Genet A
Recognition of distinct phenotypic features is an important component of genetic diagnosis. Although CHARGE syndrome, Kabuki syndrome, and a recently delineated KMT2D Ex 38/39 allelic disorder exhibit significant overlap, differences on neuroimaging
Autor:
Ronald M. Hansen, Lucia Ambrosio, Andrea M. Oza, Genevieve Medina, Kosuke Kawai, Anne Moskowitz, Anne B. Fulton, Margaret A. Kenna, Juliana Manganella, Devon Barrett
Publikováno v:
Documenta Ophthalmologica. 143:39-51
Purpose: To determine the utility of ophthalmology evaluation, dark-adapted threshold, and full-field electroretinogram for early detection of Usher syndrome in young patients with bilateral sensorineural hearing loss. Methods: We identified 39 patie
Publikováno v:
Journal of the American Academy of Dermatology. 87:AB158
Autor:
Ramoncito L. Caleon, Krittin J. Supapannachart, Devon Barrett, Patrick E. McCleskey, Laura Ragmanauskaite, Howa Yeung
Publikováno v:
MedEdPORTAL, Vol 17 (2021)
MedEdPORTAL : the Journal of Teaching and Learning Resources
MedEdPORTAL : the Journal of Teaching and Learning Resources
Introduction Despite increasing emphasis on LGBTQ health in medical education, evidence-based training on LGBTQ patient care in dermatology is lacking. We designed an interactive online didactic session on dermatologic care of LGBTQ patients for medi
Publikováno v:
The Ultrasound Journal
The Ultrasound Journal, Vol 13, Iss 1, Pp 1-12 (2021)
The Ultrasound Journal, Vol 13, Iss 1, Pp 1-12 (2021)
Background Ultrasound was first introduced in clinical dermatology in 1979. Since that time, ultrasound technology has continued to develop along with its popularity and utility. Main text summary Today, high-frequency ultrasound (HFUS), or ultrasoun
Autor:
Lucia, Ambrosio, Ronald M, Hansen, Anne, Moskowitz, Andrea, Oza, Devon, Barrett, Juliana, Manganella, Genevieve, Medina, Kosuke, Kawai, Anne B, Fulton, Margaret, Kenna
Publikováno v:
Documenta ophthalmologica. Advances in ophthalmology. 143(1)
To determine the utility of ophthalmology evaluation, dark-adapted threshold, and full-field electroretinogram for early detection of Usher syndrome in young patients with bilateral sensorineural hearing loss.We identified 39 patients with secure gen
Autor:
Daniel J. Lee, Esther X. Vivas, Mallory Raymond, Nikhila Raol, Shenita R. Peterson, Devon Barrett
Publikováno v:
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery. 164(1)
To systematically review the evidence for the use of cognitive screening tools for adults with postlingual hearing loss.PubMed, Embase, Scopus, PsycINFO (EBSCO), CINAHL (EBSCO), and CENTRAL (Cochrane Library) electronic databases were searched from i
Autor:
Devon Barrett, Juliana Manganella, Derek J. Stiles, Kosuke Kawai, Laura B. O'Brien, Margaret A. Kenna
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 113:94-98
Objectives To examine if the tablet-based Agilis Health Mobile Audiogram (Agilis Audiogram) is an effective and valid measure of hearing thresholds compared to a pure-tone audiogram in an adult and pediatric population. Methods Participants underwent
Autor:
Laura Ragmanauskaite, Devon Barrett, Howa Yeung, Krittin J. Supapannachart, Ramoncito L. Caleon, Patrick E. McCleskey
Publikováno v:
Journal of the American Academy of Dermatology. 85:AB3
Autor:
Jacob R. Brodsky, Talia N. Shoshany, Karampreet Kaur, Kosuke Kawai, Makenzie Murray, Greg R. Licameli, Amanda Stolzer, Victoria Albano, Juliana Manganella, Devon Barrett, Margaret A. Kenna
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 131:109862
To evaluate the association between torticollis and enlarged vestibular aqueduct (EVA).An online/phone survey was administered to parents of 133 children diagnosed with the following disorders: EVA, GJB2 (Connexin 26) mutations associated congenital