Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Raymond J Harshbarger"'
Autor:
Paola Nicoletti, Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai, John Erol Evangelista, Giacomo B. Marino, Avi Ma’ayan, Anshuman Sewda, Greg Holmes, Sierra R. Britton, Won Jun Lee, Meng Wu, Ying Ru, Eric Arnaud, Lorenzo Botto, Lawrence C. Brody, Jo C. Byren, Michele Caggana, Suzan L. Carmichael, Deirdre Cilliers, Kristin Conway, Karen Crawford, Araceli Cuellar, Federico Di Rocco, Michael Engel, Jeffrey Fearon, Marcia L. Feldkamp, Richard Finnell, Sarah Fisher, Christian Freudlsperger, Gemma Garcia-Fructuoso, Rhinda Hagge, Yann Heuzé, Raymond J. Harshbarger, Charlotte Hobbs, Meredith Howley, Mary M. Jenkins, David Johnson, Cristina M. Justice, Alex Kane, Denise Kay, Arun Kumar Gosain, Peter Langlois, Laurence Legal-Mallet, Angela E. Lin, James L. Mills, Jenny E.V. Morton, Peter Noons, Andrew Olshan, John Persing, Julie M. Phipps, Richard Redett, Jennita Reefhuis, Elias Rizk, Thomas D. Samson, Gary M. Shaw, Robert Sicko, Nataliya Smith, David Staffenberg, Joan Stoler, Elizabeth Sweeney, Peter J. Taub, Andrew T. Timberlake, Jolanta Topczewska, Steven A. Wall, Alexander F. Wilson, Louise C. Wilson, Simeon A. Boyadjiev, Andrew O.M. Wilkie, Joan T. Richtsmeier, Ethylin Wang Jabs, Paul A. Romitti, David Karasik, Ramon Y. Birnbaum, Inga Peter
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101851- (2024)
Purpose: The etiopathogenesis of coronal nonsyndromic craniosynostosis (cNCS), a congenital condition defined by premature fusion of 1 or both coronal sutures, remains largely unknown. Methods: We conducted the largest genome-wide association study o
Externí odkaz:
https://doaj.org/article/7b6e059bb8a041158140daf3599c8d99
Publikováno v:
AIMS Genetics, Vol 3, Iss 1, Pp 99-129 (2016)
Cranial bones articulate in areas called sutures that must remain patent until skull growth is complete. Craniosynostosis is the condition that results from premature closure of one or more of the cranial vault sutures, generating facial deformities
Externí odkaz:
https://doaj.org/article/0323f1666b4942349fd1eb20fad8a002
Autor:
Pravin K. Patel, Derek M Steinbacher, Amir H Dorafshar, Anand R Kumar, Jamie P. Levine, Raymond J Harshbarger, Patrick K Kelley, Patrick D. Combs, Kristopher M. Day
Publikováno v:
Plastic & Reconstructive Surgery. 148:94e-108e
After studying this article, the participant should be able to: 1. Describe the evolution of three-dimensional computer-aided reconstruction and its current applications in craniofacial surgery. 2. Recapitulate virtual surgical planning, or computer-
Autor:
Kristopher M. Day, Pablo L. Padilla, Patrick K. Kelley, Ian X. Collier, Sean A. Knudson, Raymond J. Harshbarger, Patrick D. Combs, Steven L. Henry
Publikováno v:
Craniomaxillofacial Trauma & Reconstruction. 15:206-218
Study Design: Retrospective case series; systematic review. Objective: It is unknown whether the use of virtual surgical planning (VSP) to facilitate same-admission microsurgical reconstruction of the mandible following acute maxillofacial ballistic
Autor:
Sarah A. Frommer, MD, PhD, Sean M. Hill, MD, Tuan A. Truong, MD, René P. Myers, MD, Timothy George, MD, Patrick K. Kelley, MD, Raymond J. Harshbarger, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 5, Iss 9S, Pp 160-161 (2017)
Externí odkaz:
https://doaj.org/article/7967bc6ccc744fb4bf4f47a2623f243f
Publikováno v:
Journal of Craniofacial Surgery. 30:e175-e178
BACKGROUND Proper evaluation and analysis of speech surgery outcomes for cleft-related velopharyngeal incompetence in children and young adults performed on humanitarian missions is poorly characterized. The aim of this study is to examine the effect
Autor:
Raymond J. Harshbarger, Timothy M. George, M.E. Zurita-Jimenez, Yunping Lei, Richard H. Finnell, C.S. Fonteles, A.J. Monteiro
Publikováno v:
Brazilian Journal of Medical and Biological Research v.54 n.11 2021
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Vol 54, Iss 11 (2021)
Brazilian Journal of Medical and Biological Research, Volume: 54, Issue: 11, Article number: e11396, Published: 24 SEP 2021
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Vol 54, Iss 11 (2021)
Brazilian Journal of Medical and Biological Research, Volume: 54, Issue: 11, Article number: e11396, Published: 24 SEP 2021
Current understanding of the genetic factors contributing to the etiology of non-syndromic craniosynostosis (NSC) remains scarce. The present work investigated the presence of variants in ALX4, EFNA4, and TWIST1 genes in children with NSC to verify i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b73e494a00b9ca61f4b29d971c9d4f
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2021001100616
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2021001100616
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 56(8)
An 11-year-old male presented with right proptosis, bulbar conjunctivitis, and diplopia. Computerized tomography (CT) and magnetic resonance imaging revealed an enhancing mass involving the superio-medial orbit, ethmoids, frontal sinus, and anterior
Autor:
Raymond J. Harshbarger, Rafael A. Vega, Jeffrey A. Fearon, Charles F. Opalak, Jennifer L. Rhodes, John J Collins, Ann M. Ritter
Publikováno v:
Journal of Neurosurgery: Pediatrics. 17:694-700
OBJECTIVE This study examines a series of patients with hypophosphatemic rickets and craniosynostosis to characterize the clinical course and associated craniofacial anomalies. METHODS A 20-year retrospective review identified patients with hypophosp
Publikováno v:
AIMS Genetics, Vol 3, Iss 1, Pp 99-129 (2016)
Cranial bones articulate in areas called sutures that must remain patent until skull growth is complete. Craniosynostosis is the condition that results from premature closure of one or more of the cranial vault sutures, generating facial deformities