-
1
-
-
67349189092
-
Craniofacial syndromes
-
Mathes SJ, ed. Philadelphia, PA: Saunders Elsevier
-
Vander Kolk C.A., Menezes J. Craniofacial syndromes. In: Mathes SJ, ed. Plastic Surgery. Philadelphia, PA: Saunders Elsevier, 2006:91-111
-
(2006)
Plastic Surgery
, pp. 91-111
-
-
Vander Kolk, C.A.1
Menezes, J.2
-
2
-
-
0029927959
-
Skull base and calvarial deformities: Association with intracranial changes in craniofacial syndromes
-
Tokumaru AM, Barkovich AJ, Ciricillo SF Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes. ANJR Am J Neuroradiol 1996;17:619-630
-
(1996)
ANJR Am J Neuroradiol
, vol.17
, pp. 619-630
-
-
Tokumaru, A.M.1
Barkovich, A.J.2
Ciricillo, S.F.3
-
3
-
-
0036143730
-
A child with saethre-chotzen syndrome, sensorineural hearing loss, and a TWIST mutation
-
Lee S, Seto M, Sie K., et al. A child with Saethre-Chotzen syndrome, sensorineural hearing loss, and a TWIST mutation. Cleft Palate Craniofac J 2002;39:110-114
-
(2002)
Cleft Palate Craniofac J
, vol.39
, pp. 110-114
-
-
Lee, S.1
Seto, M.2
Sie, K.3
-
5
-
-
33846657232
-
Neurodevelopment of children with single suture craniosynostosis: A review
-
Kapp-Simon K.A., Speltz ML, Cunningham M.L., et al. Neurodevelopment of children with single suture craniosynostosis: a review. Childs Nerv Syst 2007;23:269-281
-
(2007)
Childs Nerv Syst
, vol.23
, pp. 269-281
-
-
Kapp-Simon, K.A.1
Speltz, M.L.2
Cunningham, M.L.3
-
8
-
-
1642359042
-
Apert syndrome: Analysis of associated brain malformations and conformational changes determined by surgical treatment
-
Yacubian-Fernandes A., Palhares A, Giglio A., et al. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. J Neuroradiol 2004;31:116-122
-
(2004)
J Neuroradiol
, vol.31
, pp. 116-122
-
-
Yacubian-Fernandes, A.1
Palhares, A.2
Giglio, A.3
-
9
-
-
0036316559
-
Central nervous system phenotypes in craniosynostosis
-
Aldridge K, Marsh JL, Govier D, et al. Central nervous system phenotypes in craniosynostosis. J Anat 2002;201:31-39
-
(2002)
J Anat
, vol.201
, pp. 31-39
-
-
Aldridge, K.1
Marsh, J.L.2
Govier, D.3
-
10
-
-
34547135679
-
Diagnostic imaging in the management of craniosynostoses
-
Kotrikova B, Krempien R, Freier K., et al. Diagnostic imaging in the management of craniosynostoses. Eur Radiol 2007;17:1968-1978
-
(2007)
Eur Radiol
, vol.17
, pp. 1968-1978
-
-
Kotrikova, B.1
Krempien, R.2
Freier, K.3
-
13
-
-
0029101376
-
Chronic tonsillar herniation in crouzon and Aperts syndromes: The role of premature synostosis of the lambdoid suture
-
Cinalli G, Renier D, Sebag G., et al. Chronic tonsillar herniation in Crouzon and Aperts syndromes: the role of premature synostosis of the lambdoid suture. J Neurosurg 1995;83:575-582
-
(1995)
J Neurosurg
, vol.83
, pp. 575-582
-
-
Cinalli, G.1
Renier, D.2
Sebag, G.3
-
14
-
-
36349033602
-
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
-
15
-
-
0018730202
-
Aperts syndrome with central nervous system anomalies
-
Maksem JA, Roessmann U. Aperts syndrome with central nervous system anomalies. Acta Neuropathol 1979;48:59-61
-
(1979)
Acta Neuropathol
, vol.48
, pp. 59-61
-
-
Maksem, J.A.1
Roessmann, U.2
-
17
-
-
0025159354
-
The central nervous system in the Apert syndrome
-
Cohen MM Jr, Kreiborg S. The central nervous system in the Apert syndrome. Am J Med Genet 1990;35:36-45
-
(1990)
Am J Med Genet
, vol.35
, pp. 36-45
-
-
Cohen Jr., M.M.1
Kreiborg, S.2
-
18
-
-
0017124007
-
Clinical conference: I. Calvarium and cranial base in Apert's syndrome: An autopsy report
-
Kreiborg S, Prydsoe U, Dahl E., et al. Clinical conference: I. Calvarium and cranial base in Apert's syndrome: an autopsy report. Cleft Palate J 1976;13:296-303
-
(1976)
Cleft Palate J
, vol.13
, pp. 296-303
-
-
Kreiborg, S.1
Prydsoe, U.2
Dahl, E.3
-
20
-
-
15444339542
-
Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: A report of six cases
-
Lees MM, Hodgkins P, Reardon W., et al. Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases. Clin Dysmorphol 1998;7:157-162
-
(1998)
Clin Dysmorphol
, vol.7
, pp. 157-162
-
-
Lees, M.M.1
Hodgkins, P.2
Reardon, W.3
-
21
-
-
0033607473
-
Frontonasal dysostosis in two successive generations
-
Nevin NC, Leonard AG, Jones B. Frontonasal dysostosis in two successive generations. Am J Med Genet 1999;87:251-253
-
(1999)
Am J Med Genet
, vol.87
, pp. 251-253
-
-
Nevin, N.C.1
Leonard, A.G.2
Jones, B.3
-
22
-
-
0035079674
-
Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: Defining the phenotype
-
Guion-Almeida M.L., Richieri-Costa A. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype. Clin Dysmorphol 2001;10:81-86
-
(2001)
Clin Dysmorphol
, vol.10
, pp. 81-86
-
-
Guion-Almeida, M.L.1
Richieri-Costa, A.2
-
23
-
-
2442690674
-
Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs
-
Lopes VL, Guion-Almeida ML, Giffoni SD Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs. Clin Dysmorphol 2004;13:35-37
-
(2004)
Clin Dysmorphol
, vol.13
, pp. 35-37
-
-
Lopes, V.L.1
Guion-Almeida, M.L.2
Giffoni, S.D.3
-
25
-
-
0027394497
-
Visceral anomalies in the Apert syndrome
-
Cohen MM Jr, Kreiborg S. Visceral anomalies in the Apert syndrome. Am J Med Genet 1993;45:758-760
-
(1993)
Am J Med Genet
, vol.45
, pp. 758-760
-
-
Cohen Jr., M.M.1
Kreiborg, S.2
-
26
-
-
24044541715
-
Pfeiffer syndrome: Systemic and ocular implications
-
Harb E, Kran B. Pfeiffer syndrome: systemic and ocular implications. Optometry 2005;76:352-362
-
(2005)
Optometry
, vol.76
, pp. 352-362
-
-
Harb, E.1
Kran, B.2
-
28
-
-
0029828621
-
Audiologic and otologic characteristics of Pfeiffer syndrome
-
Vallino-Napoli L. Audiologic and otologic characteristics of Pfeiffer syndrome. Cleft Palate Craniofac J 1996;33:524-549
-
(1996)
Cleft Palate Craniofac J
, vol.33
, pp. 524-549
-
-
Vallino-Napoli, L.1
-
29
-
-
0023143520
-
Frontonasal dysplasia associated with tetralogy of fallot
-
De Moor M.M., Baruch R, Human DG Frontonasal dysplasia associated with tetralogy of Fallot. J Med Genet 1987;24:107-109
-
(1987)
J Med Genet
, vol.24
, pp. 107-109
-
-
De Moor, M.M.1
Baruch, R.2
Human, D.G.3
-
30
-
-
85026147820
-
Ophthalmologic findings in patients with nonsyndromic plagiocephaly
-
Gupta PC, Foster J, Crowe S., et al. Ophthalmologic findings in patients with nonsyndromic plagiocephaly. J Craniofac Surg 2003;14:529-532
-
(2003)
J Craniofac Surg
, vol.14
, pp. 529-532
-
-
Gupta, P.C.1
Foster, J.2
Crowe, S.3
-
31
-
-
0042706626
-
Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: A review of 141 cases
-
Khan SH, Nischal KK, Dean F, et al. Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases. Br J Ophthalmol 2003;87:999-1003
-
(2003)
Br J Ophthalmol
, vol.87
, pp. 999-1003
-
-
Khan, S.H.1
Nischal, K.K.2
Dean, F.3
|