Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Sally J. Peterson-Falzone"'
Autor:
Sally J. Peterson-Falzone
Publikováno v:
Perspectives on Speech Science and Orofacial Disorders. 25:39-43
Missions to developing countries to provide surgical care for children and adults with cleft lip and palate constitute unique opportunities for speech-language pathologists (SLPs). The SLP helps determine if a patient will actually benefit from a pla
Get quick access to the most up-to-date information on cleft palate speech therapy with The Clinician's Guide to Treating Cleft Palate Speech, 2nd Edition. This textbook features an easy-to-use format — including many bulleted lists, tables, and il
Autor:
Sally J. Peterson-Falzone
Publikováno v:
Seminars in Speech and Language. 32:093-114
Speech-language pathologists (SLPs) in the public schools or other nonmedical settings rarely see infants or small children with unrepaired clefts. When children with repaired clefts appear in their caseloads, it may be difficult to comprehend what t
Publikováno v:
Advances in Speech Language Pathology. 8:34-44
Treacher Collins (TCS) and Nager acrofacial dysostosis (NAFD) are complex disorders affecting the craniofacial region. Both are forms of mandibulofacial dysostosis, yet they are clearly distinct fr...
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 38:227-236
A review of clinical findings in 12 children with Kabuki syndrome revealed a high prevalence of otolaryngologic problems, including dysmorphic pinnae (100%), ear disease (92%), hearing loss (82%) and airway problems (58%). The high prevalence of ear
Autor:
Sally J. Peterson-Falzone
Publikováno v:
Cleft Lip and Palate ISBN: 9783642307690
There is certainly reason to be optimistic that we will come closer to making reasonable decisions about the best timing for palatal surgery, taking into account both maxillofacial growth and speech development. More options are now available in term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c274eedf584880a9189e38fead435f9f
https://doi.org/10.1007/978-3-642-30770-6_37
https://doi.org/10.1007/978-3-642-30770-6_37
Autor:
Sally J, Peterson-Falzone
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 49(6)
Autor:
Michael L. McManus, Paul S. Tiwana, Gary F. Rogers, Matthew L. Speltz, Herbert E. Fuchs, Mark R. Proctor, Kevin J. Kelly, Katrina M. Dipple, Joseph Bernstein, Anne Boekelheide, Kirt E. Simmons, Robert J. Havlik, John A. Jane, Sven Kreiborg, Jeffrey A. Fearon, Marilyn T. Miller, Sven Olrik Streubel, Chin-To Fong, Stephen M. Warren, Whitney Burnett, Jeffrey P. Blount, Karin M. Muraszko, Dennis Sklenar, Michael L. Cunningham, Jane C. Edmond, Michelle Gittlen, Scott P. Bartlett, Alvaro A. Figueroa, Mary Michaeleen Cradock, Raymond W. Sze, Patricia Terrell, Terrance A. Yemen, Kathleen A. Kapp-Simon, Steven R. Buchman, Robert F. Keating, Mutaz M. Habal, Joseph G. McCarthy, Douglas G. Ririe, Eric Arnaud, John A. Nackashi, Ann Marie Flannery, J. C. Shirley, Marcie S. Rubin, Karin Vargervik, Sally J. Peterson-Falzone, Patricia D. Chibbaro, Arshad R. Muzaffar, Barry H. Grayson, David A. Plager, John E. Riski, Laura Posada, Lynda Honberg, Brian I. Labow, Isaac L. Wornom
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
Background A multidisciplinary meeting was held from March 4 to 6, 2010, in Atlanta, Georgia, entitled “Craniosynostosis: Developing Parameters for Diagnosis, Treatment, and Management.” The goal of this meeting was to create parameters of care f
Publikováno v:
The Cleft Palate-Craniofacial Journal. 30:369-375
An abnormal cranial base could exert a negative influence on neurocranial development. Because patients with mandibulofacial dysostosis (MFD) present an abnormal cranial base (basilar kyphosis), a retrospective mixed longitudinal cephalometric study
Publikováno v:
Journal of Speech and Hearing Disorders. 55:132-139
Phoneme-specific nasal emission was identified in 36 children ranging in age from 3 years, 3 months to 16 years, 5 months; 19 children had no physical anomalies of the orofacial mechanism, whereas 17 had findings ranging from minor to severe. Five pa