메뉴 건너뛰기




Volumn 131, Issue 1, 2013, Pages

Craniofacial syndromes and surgery

Author keywords

[No Author keywords available]

Indexed keywords

CHILD; CLINICAL PROTOCOL; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; GENETIC MARKER; GENETICS; HUMAN; INFANT; METHODOLOGY; ORTHOPEDIC SURGERY; PATHOPHYSIOLOGY; PRESCHOOL CHILD; REVIEW; SYNDROME;

EID: 84872059951     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/PRS.0b013e318272c12b     Document Type: Article
Times cited : (72)

References (67)
  • 1
    • 0001248309 scopus 로고    scopus 로고
    • Perspectives on craniofacial anomalies, syndromes and other disorders
    • Lin KY, Ogle RC, Jane JA, eds. Philadelphia: Saunders
    • Cohen MM Jr. Perspectives on craniofacial anomalies, syndromes and other disorders. In: Lin KY, Ogle RC, Jane JA, eds. Craniofacial Surgery: Science and Surgical Techniques. Philadelphia: Saunders; 2002:3-38.
    • (2002) Craniofacial Surgery: Science and Surgical Techniques , pp. 3-38
    • Cohen Jr., M.M.1
  • 3
    • 77649207609 scopus 로고    scopus 로고
    • Genetics of craniosynostosis: Review of the literature
    • Ciurea AV, Toader C. Genetics of craniosynostosis: Review of the literature. J Med Life 2009;2:5-17.
    • (2009) J Med Life , vol.2 , pp. 5-17
    • Ciurea, A.V.1    Toader, C.2
  • 6
    • 0021810807 scopus 로고
    • The incidence of isolated craniosynostosis in the newborn infant
    • Shuper A, Merlob P, Grunebaum M, Reisner SH. The incidence of isolated craniosynostosis in the newborn infant. Am J Dis Child. 1985;139:85-86.
    • (1985) Am J Dis Child , vol.139 , pp. 85-86
    • Shuper, A.1    Merlob, P.2    Grunebaum, M.3    Reisner, S.H.4
  • 8
    • 67349229415 scopus 로고    scopus 로고
    • The changing epidemiologic spectrum of single-suture synostoses
    • Selber J, Reid RR, Chike-Obi CJ, et al. The changing epidemiologic spectrum of single-suture synostoses. Plast Reconstr Surg. 2008;122:527-533.
    • (2008) Plast Reconstr Surg , vol.122 , pp. 527-533
    • Selber, J.1    Reid, R.R.2    Chike-Obi, C.J.3
  • 9
    • 0029940878 scopus 로고    scopus 로고
    • The "back to sleep campaign" and deformational plagiocephaly: Is there cause for concern?
    • Turk AE, McCarthy JG, Thorne CH, Wisoff JH. The "back to sleep campaign" and deformational plagiocephaly: Is there cause for concern? J Craniofac Surg. 1996;7:12-18.
    • (1996) J Craniofac Surg , vol.7 , pp. 12-18
    • Turk, A.E.1    McCarthy, J.G.2    Thorne, C.H.3    Wisoff, J.H.4
  • 10
    • 67749119968 scopus 로고    scopus 로고
    • Regarding true lambdoid synostosis: Long term results of surgical and conservative therapy
    • author reply 673-674
    • Menard RM, David DJ. Regarding true lambdoid synostosis: Long term results of surgical and conservative therapy. Plast Reconstr Surg. 2008;122:673; author reply 673-674.
    • (2008) Plast Reconstr Surg , vol.122 , pp. 673
    • Menard, R.M.1    David, D.J.2
  • 11
    • 45849092258 scopus 로고    scopus 로고
    • Genetics of craniosynostosis: Genes, syndromes, mutations and genotype-phenotype correlations
    • Passos-Beuno MR, Serti Eacute AE, Jehee F, Fanganiello R, Yeh E. Genetics of craniosynostosis: Genes, syndromes, mutations and genotype-phenotype correlations. Front Oral Biol. 2008;12:107-143.
    • (2008) Front Oral Biol , vol.12 , pp. 107-143
    • Passos-Beuno, M.R.1    Serti Eacute, A.E.2    Jehee, F.3    Fanganiello, R.4    Yeh, E.5
  • 13
    • 22844439789 scopus 로고    scopus 로고
    • Twenty-six novel efnb1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)
    • Wieland I, Reardon W, Jakubiczka S, et al. Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS). Hum Mutat. 2005;26:113-118.
    • (2005) Hum Mutat , vol.26 , pp. 113-118
    • Wieland, I.1    Reardon, W.2    Jakubiczka, S.3
  • 14
    • 0036047887 scopus 로고    scopus 로고
    • Clinical features, treatment and genetic background of treacher collins syndrome
    • Marszałek B, Wó jcicki P, Kobus K, Trzeciak WH. Clinical features, treatment and genetic background of Treacher Collins syndrome. J Appl Genet. 2002;43:223-233.
    • (2002) J Appl Genet , vol.43 , pp. 223-233
    • Marszałek, B.1    Wójcicki, P.2    Kobus, K.3    Trzeciak, W.H.4
  • 15
    • 35649021284 scopus 로고    scopus 로고
    • 31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): Clinical, neuroradiologic, audiologic and cytogenetic findings
    • Engiz O, Balci S, Unsal M, Ozer S, Oguz KK, Aktas D. 31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): Clinical, neuroradiologic, audiologic and cytogenetic findings. Genet Couns. 2007;18:277-288.
    • (2007) Genet Couns , vol.18 , pp. 277-288
    • Engiz, O.1    Balci, S.2    Unsal, M.3    Ozer, S.4    Oguz, K.K.5    Aktas, D.6
  • 17
    • 37249002800 scopus 로고    scopus 로고
    • Subtypes of frontonasal dysplasia are useful in determining clinical prognosis
    • Wu E, Vargevik K, Slavotinek AM. Subtypes of frontonasal dysplasia are useful in determining clinical prognosis. Am J Med Genet A 2007;143A:3069-3078.
    • (2007) Am J Med Genet A , vol.143 A , pp. 3069-3078
    • Wu, E.1    Vargevik, K.2    Slavotinek, A.M.3
  • 18
    • 26044452389 scopus 로고    scopus 로고
    • Intracranial pressure monitoring in children with single suture and complex craniosynostosis: A review
    • Tamburrini G, Caldarelli M, Massimi L, Santini P, Di Rocco C. Intracranial pressure monitoring in children with single suture and complex craniosynostosis: A review. Childs Nerv Syst. 2005;21:913-921.
    • (2005) Childs Nerv Syst , vol.21 , pp. 913-921
    • Tamburrini, G.1    Caldarelli, M.2    Massimi, L.3    Santini, P.4    Di Rocco, C.5
  • 20
    • 26044439069 scopus 로고    scopus 로고
    • Venous hypertension and craniosynostosis
    • Hayward R. Venous hypertension and craniosynostosis. Childs Nerv Syst. 2005;21:880-888.
    • (2005) Childs Nerv Syst , vol.21 , pp. 880-888
    • Hayward, R.1
  • 21
    • 36549040580 scopus 로고    scopus 로고
    • Measurement of intracranial pressure in children: A critical review of current methods
    • Wiegand C, Richards P. Measurement of intracranial pressure in children: A critical review of current methods. Dev Med Child Neurol. 2007;49:935-941.
    • (2007) Dev Med Child Neurol , vol.49 , pp. 935-941
    • Wiegand, C.1    Richards, P.2
  • 22
    • 0031059009 scopus 로고    scopus 로고
    • Upper airway obstruction and raised intracranial pressure in children with craniosynostosis
    • Gonsalez S, Hayward R, Jones B, Lane R. Upper airway obstruction and raised intracranial pressure in children with craniosynostosis. Eur Respir J. 1997;10:367-375.
    • (1997) Eur Respir J , vol.10 , pp. 367-375
    • Gonsalez, S.1    Hayward, R.2    Jones, B.3    Lane, R.4
  • 23
    • 77953253237 scopus 로고    scopus 로고
    • Syndromic craniosynostosis: Complicated airway obstruction calls for progressive strategies in surgical management
    • Hardin KA. Syndromic craniosynostosis: Complicated airway obstruction calls for progressive strategies in surgical management. Expert Rev Respir Med. 2010;4:315-319.
    • (2010) Expert Rev Respir Med , vol.4 , pp. 315-319
    • Hardin, K.A.1
  • 24
    • 33745845820 scopus 로고    scopus 로고
    • Prevalence and causes of visual impairment in craniosynostotic syndromes
    • Tay T, Martin F, Rowe N, et al. Prevalence and causes of visual impairment in craniosynostotic syndromes. Clin Experiment Ophthalmol. 2006;34:434-440.
    • (2006) Clin Experiment Ophthalmol , vol.34 , pp. 434-440
    • Tay, T.1    Martin, F.2    Rowe, N.3
  • 25
    • 36349033602 scopus 로고    scopus 로고
    • Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: A review
    • Raybaud C, Di Rocco C. Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: A review. Childs Nerv Syst. 2007;23:1379-1388.
    • (2007) Childs Nerv Syst , vol.23 , pp. 1379-1388
    • Raybaud, C.1    Di Rocco, C.2
  • 26
    • 0032133085 scopus 로고    scopus 로고
    • Psychological aspects of cleft lip and palate
    • Turner SR, Rumsey N, Sandy Jr. Psychological aspects of cleft lip and palate. Eur J Orthod. 1998;20:407-415.
    • (1998) Eur J Orthod , vol.20 , pp. 407-415
    • Turner, S.R.1    Rumsey, N.2    Sandy, J.R.3
  • 27
    • 0030886682 scopus 로고    scopus 로고
    • Research of psychosocial issues of children with craniofacial anomalies: Progress and challenges
    • Pope AW, Speltz ML. Research of psychosocial issues of children with craniofacial anomalies: Progress and challenges. Cleft Palate Craniofac J. 1997;34:371-373.
    • (1997) Cleft Palate Craniofac J , vol.34 , pp. 371-373
    • Pope, A.W.1    Speltz, M.L.2
  • 28
    • 34548593458 scopus 로고    scopus 로고
    • Visible difference amongst children and adolescents: Issues and interventions
    • Rumsey N, Harcourt D. Visible difference amongst children and adolescents: Issues and interventions. Dev Neurorehabil. 2007;10:113-123.
    • (2007) Dev Neurorehabil , vol.10 , pp. 113-123
    • Rumsey, N.1    Harcourt, D.2
  • 29
    • 0025768260 scopus 로고
    • Directions and issues in psychosocial research and methods as applied to cleft lip and palate and craniofacial anomalies
    • Strauss RP, Broder H. Directions and issues in psychosocial research and methods as applied to cleft lip and palate and craniofacial anomalies. Cleft Palate Craniofac J. 1991;28:150- 156.
    • (1991) Cleft Palate Craniofac J , vol.28 , pp. 150-156
    • Strauss, R.P.1    Broder, H.2
  • 30
    • 0033772008 scopus 로고    scopus 로고
    • Prominent basal emissary foramina in syndromic craniosynostosis: Correlation with phenotypic and molecular diagnoses
    • Robson CD, Mulliken JB, Robertson RL, et al. Prominent basal emissary foramina in syndromic craniosynostosis: Correlation with phenotypic and molecular diagnoses. AJNR Am J Neuroradiol. 2000;21:1707-1717.
    • (2000) AJNR Am J Neuroradiol , vol.21 , pp. 1707-1717
    • Robson, C.D.1    Mulliken, J.B.2    Robertson, R.L.3
  • 31
    • 33748290012 scopus 로고    scopus 로고
    • Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: A novel case of P450 oxidoreductase deficiency
    • Williamson L, Arlt W, Shackleton C, Kelley RI, Braddock SR. Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: A novel case of P450 oxidoreductase deficiency. Am J Med Genet A 2006;140A:1797-1803.
    • (2006) Am J Med Genet A , vol.140 A , pp. 1797-1803
    • Williamson, L.1    Arlt, W.2    Shackleton, C.3    Kelley, R.I.4    Braddock, S.R.5
  • 32
    • 38049075709 scopus 로고    scopus 로고
    • P450 oxidoreductase deficiency and Antley-Bixler syndrome
    • Arlt W. P450 oxidoreductase deficiency and Antley-Bixler syndrome. Rev Endocr Metab Disord. 2007;8:301-307.
    • (2007) Rev Endocr Metab Disord , vol.8 , pp. 301-307
    • Arlt, W.1
  • 33
    • 0000003824 scopus 로고
    • De l'acrocephalosyndactylie
    • Apert ME. De l'acrocephalosyndactylie. Bull Soc Med Hop Paris 1906;23:1310-1330.
    • (1906) Bull Soc Med Hop Paris , vol.23 , pp. 1310-1330
    • Apert, M.E.1
  • 34
    • 0027263856 scopus 로고
    • Newly recognized autosomal dominant disorder with craniosynostosis
    • Warman ML, Mulliken JB, Hayward PG, Mu? ller U. Newly recognized autosomal dominant disorder with craniosynostosis. Am J Med Genet. 1993;46:444-449.
    • (1993) Am J Med Genet , vol.46 , pp. 444-449
    • Warman, M.L.1    Mulliken, J.B.2    Hayward, P.G.3    Muller, U.4
  • 35
    • 0034067020 scopus 로고    scopus 로고
    • Craniofacial disorders caused by mutations in homeobox genes msx1 and msx2
    • Cohen MM Jr. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2. J Craniofac Genet Dev Biol. 2000;20:19-25.
    • (2000) J Craniofac Genet Dev Biol , vol.20 , pp. 19-25
    • Cohen Jr., M.M.1
  • 36
    • 0027431005 scopus 로고
    • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
    • Jabs EW, Mu? ller U, Li X, et al. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 1993;75:443-450.
    • (1993) Cell , vol.75 , pp. 443-450
    • Jabs, E.W.1    Muller, U.2    Li, X.3
  • 37
    • 15844388219 scopus 로고    scopus 로고
    • Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
    • Przylepa KA, Paznekas W, Zhang M, et al. Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet. 1996;13:492-494.
    • (1996) Nat Genet , vol.13 , pp. 492-494
    • Przylepa, K.A.1    Paznekas, W.2    Zhang, M.3
  • 38
    • 68249089808 scopus 로고    scopus 로고
    • Perspectives on craniosynostosis: Sutural biology, some well-known syndromes, and some unusual syndromes
    • Cohen MM Jr. Perspectives on craniosynostosis: Sutural biology, some well-known syndromes, and some unusual syndromes. J Craniofac Surg. 2009;20(Suppl 1):646-651.
    • (2009) J Craniofac Surg , vol.20 , Issue.SUPPL. 1 , pp. 646-651
    • Cohen Jr., M.M.1
  • 40
    • 40549123762 scopus 로고    scopus 로고
    • Craniofacial dysmorphology of carpenter syndrome: Lessons from three affected siblings
    • Perlyn CA, Marsh JL. Craniofacial dysmorphology of Carpenter syndrome: Lessons from three affected siblings. Plast Reconstr Surg. 2008;121:971-981.
    • (2008) Plast Reconstr Surg , vol.121 , pp. 971-981
    • Perlyn, C.A.1    Marsh, J.L.2
  • 41
    • 33646879391 scopus 로고    scopus 로고
    • The origin of EFNB1 mutations in craniofrontonasal syndrome: Frequent somatic mosaicism and explanation of the paucity of carrier males
    • Twigg SR, Matsumoto K, Kidd AM, et al. The origin of EFNB1 mutations in craniofrontonasal syndrome: Frequent somatic mosaicism and explanation of the paucity of carrier males. Am J Hum Genet. 2006;78:999-1010.
    • (2006) Am J Hum Genet , vol.78 , pp. 999-1010
    • Twigg, S.R.1    Matsumoto, K.2    Kidd, A.M.3
  • 42
    • 0001326304 scopus 로고
    • Dysostose cranio-faciale hereditaire
    • Crouzon F. Dysostose cranio-faciale hereditaire. Bull Mem Soc Med Hop Paris 1912;33:545-555.
    • (1912) Bull Mem Soc Med Hop Paris , vol.33 , pp. 545-555
    • Crouzon, F.1
  • 43
    • 0035153450 scopus 로고    scopus 로고
    • Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3
    • Schweitzer DN, Graham JM Jr, Lachman RS, et al. Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3. Am J Med Genet. 2001;98: 75-91.
    • (2001) Am J Med Genet , vol.98 , pp. 75-91
    • Schweitzer, D.N.1    Graham Jr., J.M.2    Lachman, R.S.3
  • 44
    • 0029957404 scopus 로고    scopus 로고
    • FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variation
    • Steinberger D, Reinhartz T, Unso?ld R, Mu? ller U. FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variation. Am J Med Genet. 1996;66:81-86.
    • (1996) Am J Med Genet , vol.66 , pp. 81-86
    • Steinberger, D.1    Reinhartz, T.2    Unsold, R.3    Muller, U.4
  • 45
    • 84886621421 scopus 로고
    • Craniosynostosis, midfacial hypoplasia and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred
    • Jackson CE, Weiss L, Reynolds WA, Forman TF, Peterson JA. Craniosynostosis, midfacial hypoplasia and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred. J Pediatr. 1976;88:963-968.
    • (1976) J Pediatr , vol.88 , pp. 963-968
    • Jackson, C.E.1    Weiss, L.2    Reynolds, W.A.3    Forman, T.F.4    Peterson, J.A.5
  • 46
    • 0344487278 scopus 로고
    • The Kleeblattschaedel syndrome: A grotesque form of hydrocephalus
    • Comings DE. The Kleeblattschaedel syndrome: A grotesque form of hydrocephalus. J Pediatr. 1965;67:126-129.
    • (1965) J Pediatr , vol.67 , pp. 126-129
    • Comings, D.E.1
  • 47
    • 16944367030 scopus 로고    scopus 로고
    • A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
    • Muenke M, Gripp KW, McDonald-McGinn DM et al., A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet. 1997;60:555-564.
    • (1997) Am J Hum Genet , vol.60 , pp. 555-564
    • Muenke, M.1    Gripp, K.W.2    McDonald-Mcginn, D.M.3
  • 48
    • 0000008683 scopus 로고
    • Dominant hereditary acrocephalosyndactylia
    • (in German)
    • Pfeiffer RA. Dominant hereditary acrocephalosyndactylia (in German). Z Kinderheilkd. 1964;90:301-320.
    • (1964) Z Kinderheilkd , vol.90 , pp. 301-320
    • Pfeiffer, R.A.1
  • 50
    • 84873796754 scopus 로고
    • The mandibulofacial dysostosis; A new hereditary syndrome
    • Franceschetti A, Klein D. The mandibulofacial dysostosis; a new hereditary syndrome. Acta Ophthalmol (Copenh.) 1949; 27:143-224.
    • (1949) Acta Ophthalmol (Copenh.) , vol.27 , pp. 143-224
    • Franceschetti, A.1    Klein, D.2
  • 52
    • 0002696740 scopus 로고
    • Das Gehorogan bei den angeborenen Kopfmisbildungen
    • Nager FR, de Reynier JP. Das Gehorogan bei den angeborenen Kopfmisbildungen. Pract Otorhinolaryngol. 1948;10:1-7.
    • (1948) Pract Otorhinolaryngol , vol.10 , pp. 1-7
    • Nager, F.R.1    De Reynier, J.P.2
  • 53
    • 0017334556 scopus 로고
    • Nager acrofacial dysostosis: Early intervention and long-term planning
    • Meyerson MD, Jensen KM, Meyers JM, Hall BD. Nager acrofacial dysostosis: Early intervention and long-term planning. Cleft Palate J. 1977;14:35-40.
    • (1977) Cleft Palate J , vol.14 , pp. 35-40
    • Meyerson, M.D.1    Jensen, K.M.2    Meyers, J.M.3    Hall, B.D.4
  • 54
    • 0029088227 scopus 로고
    • OMENS-Plus: Analysis of craniofacial and extracraniofacial anomalies in hemifacial microsomia
    • Horgan JE, Padwa BL, LaBrie RA, Mulliken JB. OMENS-Plus: Analysis of craniofacial and extracraniofacial anomalies in hemifacial microsomia. Cleft Palate Craniofac J. 1995;32:405-412.
    • (1995) Cleft Palate Craniofac J , vol.32 , pp. 405-412
    • Horgan, J.E.1    Padwa, B.L.2    Labrie, R.A.3    Mulliken, J.B.4
  • 56
    • 35248846538 scopus 로고    scopus 로고
    • Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (hemifacial microsomia)
    • Hartsfield JK. Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (hemifacial microsomia). Orthod Craniofac Res. 2007;10:121-128.
    • (2007) Orthod Craniofac Res , vol.10 , pp. 121-128
    • Hartsfield, J.K.1
  • 57
    • 33750578752 scopus 로고    scopus 로고
    • The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: Phenotypic and aetiological considerations
    • Richieri-Costa A, Guion-Almeida ML. The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: Phenotypic and aetiological considerations. Int J Med Sci. 2004;1:34-42.
    • (2004) Int J Med Sci , vol.1 , pp. 34-42
    • Richieri-Costa, A.1    Guion-Almeida, M.L.2
  • 60
    • 0000636066 scopus 로고
    • Dysostosis maxillo-nasalis, ein archinencephaler Missbildungskomplex
    • Binder KH. Dysostosis maxillo-nasalis, ein archinencephaler Missbildungskomplex. Dtsch Zahnarztl Z. 1962;17:438- 444.
    • (1962) Dtsch Zahnarztl Z , vol.17 , pp. 438-444
    • Binder, K.H.1
  • 61
    • 77956708654 scopus 로고    scopus 로고
    • Longterm functional outcome in 167 patients with syndromic craniosynostosis: Defining a syndrome-specific risk profile
    • de Jong T, Bannink N, Bredero-Boelhouwer HH, et al. Longterm functional outcome in 167 patients with syndromic craniosynostosis: Defining a syndrome-specific risk profile. J Plast Reconstr Aesthet Surg. 2009;63:1635-1641.
    • (2009) J Plast Reconstr Aesthet Surg , vol.63 , pp. 1635-1641
    • De Jong, T.1    Bannink, N.2    Bredero-Boelhouwer, H.H.3
  • 62
    • 0034034407 scopus 로고    scopus 로고
    • Analysis of frontoorbital advancement for Apert, Crouzon, Pfeiffer, and Saethre-Chotzen syndromes
    • Wong GB, Kakulis EG, Mulliken JB. Analysis of frontoorbital advancement for Apert, Crouzon, Pfeiffer, and Saethre-Chotzen syndromes. Plast Reconstr Surg. 2000;105: 2314-2323.
    • (2000) Plast Reconstr Surg , vol.105 , pp. 2314-2323
    • Wong, G.B.1    Kakulis, E.G.2    Mulliken, J.B.3
  • 63
    • 67649415219 scopus 로고    scopus 로고
    • Reoperation for intracranial hypertension in TWIST1-confirmed Saethre- Chotzen syndrome: A 15-year review
    • Woods RH, Ul-Haq E, Wilkie AO, et al. Reoperation for intracranial hypertension in TWIST1-confirmed Saethre- Chotzen syndrome: A 15-year review. Plast Reconstr Surg. 2009; 123:1801-1810.
    • (2009) Plast Reconstr Surg , vol.123 , pp. 1801-1810
    • Woods, R.H.1    Ul-Haq, E.2    Wilkie, A.O.3
  • 65
    • 0029120044 scopus 로고
    • Twenty-year experience with early surgery for craniosynostosis: II. The craniofacial synostosis syndromes and pansynostosis-Results and unsolved problems
    • discussion 296-298
    • McCarthy JG, Glasberg SB, Cutting CB, et al. Twenty-year experience with early surgery for craniosynostosis: II. The craniofacial synostosis syndromes and pansynostosis - Results and unsolved problems. Plast Reconstr Surg. 1995;96: 284-295; discussion 296-298.
    • (1995) Plast Reconstr Surg , vol.96 , pp. 284-295
    • McCarthy, J.G.1    Glasberg, S.B.2    Cutting, C.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.