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Cell derived nanovesicles for oral and craniofacial tissue regeneration.
NanoscaleZhong L, Marschall JS, Shin K, Sun H.
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NeuroRehabilitation, 2020 While non-headache, non-oral craniofacial neuralgia is relatively rare in incidence and prevalence, it can result in debilitating pain. Understanding the relevant anatomy of peripheral branches of nerves, natural history, clinical presentation, and management strategies will help the clinician better diagnose and treat craniofacial neuralgias.
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Craniofacial Growth in Premature Craniofacial Synostosis
Scandinavian Journal of Plastic and Reconstructive Surgery, 1981Serial cephalometric radiographs of 55 patients with different types of premature craniofacial synostoses were analysed. The aim of the study was to answer the following four questions in an effort to provide a better rational for classification, treatment, and possibly add insight into the mechanisms controlling craniofacial growth.
S, Kreiborg, S, Pruzansky
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Craniofacial Growth in Unoperated Craniofacial Malformations
The Cleft Palate Craniofacial Journal, 2000Objective and Purpose To review current information on craniofacial growth of unoperated patients with craniofacial malformations and stimulate the study of abnormal craniofacial growth through conventional and newer methods.
A A, Figueroa, H, Friede
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Facial Plastic Surgery Clinics of North America, 2014
Craniosynostosis, in which 1 or more cranial sutures prematurely fuse, is associated with diverse environmental and genetic factors. Whereas isolated single-suture synostosis is usually sporadic and nonfamilial, FGFR mutations account for most cases of syndromic craniosynostosis.
Laszlo, Nagy, Joshua C, Demke
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Craniosynostosis, in which 1 or more cranial sutures prematurely fuse, is associated with diverse environmental and genetic factors. Whereas isolated single-suture synostosis is usually sporadic and nonfamilial, FGFR mutations account for most cases of syndromic craniosynostosis.
Laszlo, Nagy, Joshua C, Demke
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Journal of Pediatric Orthopaedics, 1995
A family with dominant inheritance of a previously unreported syndrome of craniofacial dysplasia and cone-shaped physes of the hands and feet is described. Hydrocephalus and spinal cord compression at the craniocervical junction causes neurological complications and mimics cerebral palsy.
R K, Beals, J H, Piatt, J, Zonana
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A family with dominant inheritance of a previously unreported syndrome of craniofacial dysplasia and cone-shaped physes of the hands and feet is described. Hydrocephalus and spinal cord compression at the craniocervical junction causes neurological complications and mimics cerebral palsy.
R K, Beals, J H, Piatt, J, Zonana
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World Journal of Surgery, 1989
AbstractThe treatment of combined major dislocations of the face and skull requires a craniofacial team consisting of a plastic maxillofacial surgeon, a neurosurgeon, an anesthesiologist, and radiologists. The best results can only be achieved at the primary intervention both from a functional and an esthetic standpoint.
L C, Merville, P A, Diner, I, Blomgren
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AbstractThe treatment of combined major dislocations of the face and skull requires a craniofacial team consisting of a plastic maxillofacial surgeon, a neurosurgeon, an anesthesiologist, and radiologists. The best results can only be achieved at the primary intervention both from a functional and an esthetic standpoint.
L C, Merville, P A, Diner, I, Blomgren
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Medical Journal of Australia, 1979
The historical development of craniofacial surgery for congenital abnormality is reviewed. The work of a second Australian unit of craniofacial surgery which has been formed in Brisbane is described, current indications for surgery are defined, and the preoperative preparation is outlined.
L, Atkinson, A, Emmett, M, Pabari
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The historical development of craniofacial surgery for congenital abnormality is reviewed. The work of a second Australian unit of craniofacial surgery which has been formed in Brisbane is described, current indications for surgery are defined, and the preoperative preparation is outlined.
L, Atkinson, A, Emmett, M, Pabari
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Facial Plastic Surgery Clinics of North America, 2016
Craniofacial microsomia (CFM) encompasses a broad spectrum of phenotypes. It is thought to result from defective development of the first and second pharyngeal arch structures, and generally presents with anomalies of the mandible and other facial bones, ears, and overlying soft tissues. The cause of CFM is thought to involve both extrinsic and genetic
Kathleyn A, Brandstetter +1 more
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Craniofacial microsomia (CFM) encompasses a broad spectrum of phenotypes. It is thought to result from defective development of the first and second pharyngeal arch structures, and generally presents with anomalies of the mandible and other facial bones, ears, and overlying soft tissues. The cause of CFM is thought to involve both extrinsic and genetic
Kathleyn A, Brandstetter +1 more
openaire +2 more sources