Searched for: Department/Unit:Plastic Surgery
Prophylactic craniofacial surgery. A preliminary report
Epstein, F; McCarthy, J
On the basis of their experience the authors conclude that the pendulum is now swinging to early neonatal surgery, and that in the future stripping of the appropriate sutures of the craniofacial junction will totally correct the deformity making future radical craniofacial surgery unneccessary
SCOPUS:0018149906
ISSN: 1131-3722
CID: 581472
Craniofacial surgery. A new horison
Epstein, F; Wood-Smith, D; McCarthy, J; Converse, J
SCOPUS:0017863791
ISSN: 1131-3722
CID: 581912
Making slides for lecture or teaching
Morello, D C; Barton, F E Jr
Technical details are provided for making slides of several types for lecture or teaching. Advantages are simplicity, versatility, speed, high quality, and low cost.
PMID: 727689
ISSN: 0148-7043
CID: 552332
Laryngopharyngeal closure following supraglottic laryngectomy
Maves, M D; Conley, J; Baker, D C
PMID: 362095
ISSN: 0023-852x
CID: 155832
The surgical treatment of extratemporal facial paralysis: an overview
Conley, J; Baker, D C
At present there is no single surgical approach that is ideally suited to rehabilitation of the paralyzed face. Dynamic reconstruction and neural reconstitution are usually preferred to static methods, except under special circumstances. Experience with over 150 autogenous facial-nerve grafts using epineural suture technique has resulted in return of movement in 95% of properly selected patients. When grafting is not feasible, as in the obliterated central facial nerve, hypoglossal-facial-nerve crossover is a simple and powerful source of reinnervation, usually resulting in minimal intraoral crippling and mild mass movement. A newer procedure, the cross-face nerve graft, is an alternative to hypoglossal crossover, although it results in less axonal input and longer regenerative time. In cases of long-standing facial paralysis with muscle atrophy, temporalis and masseter transfers are dependable and may sometimes be combined with a nerve graft.
PMID: 387668
ISSN: 0148-6403
CID: 155833
Genetic histocompatibility (HLA) associations with congenital craniofacial anomalies amenable to reconstructive surgery
McCarthy JG; Rapaport FT; Bachvaroff RJ; Bach FH; Converse JM
PMID: 401279
ISSN: 0071-8041
CID: 11455
A combined biceps and semitendinosus muscle flap in the repair of ischial sores
Baker DC; Barton FE Jr; Converse JM
PMID: 342026
ISSN: 0007-1226
CID: 51115
Recognition in adult patients of malformations induced by folic-acid antagonists [Case Report]
Reich, E W; Cox, R P; Becker, M H; Genieser, N B; McCarthy, J G; Converse, J M
Three patients are reported, two of whom had mothers who revealed ingestion of abortifacient drugs during pregnancy. All patients resemble one another and those described earlier with malformations that were probably either aminopterin- or methotrexate-induced. It is likely that Patients I and II have abnormalities associated with the teratogenic action of these folic-acid antagonists. The etiology of Patient III's defects remains uncertain
PMID: 728558
ISSN: 0547-6844
CID: 99084
Early skeletal release in the infant with craniofacial dysostosis: the role of the sphenozygomatic suture
McCarthy, J G; Coccaro, P J; Eptstein, F; Converse, J M
We describe our experience with early skeletal release in 10 infants with craniofacial dysostosis. The cranial base is the key to the deformity, and we extend the release toward it as well as resecting strips from the calvarium. Three procedures are described. The early results are encouraging
PMID: 693662
ISSN: 0032-1052
CID: 99083
Replantation of digits
Strauch, B; Terzis, J K
Replanted digital survivals range between 85% to over 90% at established microsurgery centers around the world. The time has come that all surgeons engaged in this activity must utilize the basic principles of reconstructive hand surgery in order to achieve the maximum functional return of the replanted parts. The vascular repair is only one step in the road toward functional restoration of the replanted part
PMID: 688716
ISSN: 0009-921x
CID: 115233