-
1
-
-
0029876886
-
An increase in infant cranial deformity with supine sleeping position
-
Argenta L.C., David L.R., Wilson J.A., Bell W.O. An increase in infant cranial deformity with supine sleep positioning. J Craniofac Surg. 1996;7:5-11. (Pubitemid 26153022)
-
(1996)
Journal of Craniofacial Surgery
, vol.7
, Issue.1
, pp. 5-11
-
-
Argenta, L.C.1
David, L.R.2
Wilson, J.A.3
Bell, W.O.4
-
2
-
-
0026598656
-
Frontal plagiocephaly:Synostotic, compensational, or deformational
-
Bruneteau R.J., Mulliken J.B. Frontal plagiocephaly:Synostotic, compensational, or deformational. Plast Reconstr Surg. 1992;89:21-31.
-
(1992)
Plast Reconstr Surg.
, vol.89
, pp. 21-31
-
-
Bruneteau, R.J.1
Mulliken, J.B.2
-
4
-
-
0021792281
-
Premature closure of the frontozygomatic suture:Unusual frontoorbital dysplasia mimicking unilateral coronal synostosis
-
Currarino G. Premature closure of the frontozygomatic suture:Unusual frontoorbital dysplasia mimicking unilateral coronal synostosis. AJNR Am J Neuroradiol. 1985;6:643-646.
-
(1985)
AJNR Am J Neuroradiol
, vol.6
, pp. 643-646
-
-
Currarino, G.1
-
5
-
-
36348942474
-
Frontosphenoidal synostosis:A rare cause of unilateral anterior plagiocephaly
-
de Ribaupierre S, Czorny A, Pittet B, Jacques B, Rilliet B. Frontosphenoidal synostosis:A rare cause of unilateral anterior plagiocephaly. Childs Nerv Syst. 2007;23:1431-1438.
-
(2007)
Childs Nerv Syst.
, vol.23
, pp. 1431-1438
-
-
De Ribaupierre, S.1
Czorny, A.2
Pittet, B.3
Jacques, B.4
Rilliet, B.5
-
6
-
-
0029102262
-
Frontal plagiocephaly secondary to synostosis of the frontosphenoidal suture:Case report
-
Francel P.C., Park T.S., Marsh J.L., Kaufman B.A. Frontal plagiocephaly secondary to synostosis of the frontosphenoidal suture:Case report. J Neurosurg. 1995;83:733-736.
-
(1995)
J Neurosurg.
, vol.83
, pp. 733-736
-
-
Francel, P.C.1
Park, T.S.2
Marsh, J.L.3
Kaufman, B.A.4
-
7
-
-
0031923323
-
Identification of a genetic cause for isolated unilateral coronal synostosis: A unique mutation in the fibroblast growth factor receptor 3
-
DOI 10.1016/S0022-3476(98)70366-X
-
Gripp K.W., McDonald-McGinn D.M., Gaudenz K., Whitaker L.A., Bartlett S.P., Glat P.M., Cassileth L.B., Mayro R., Zackai E.H., Muenke M. Identification of a genetic cause for isolated unilateral coronal synostosis:A unique mutation in the fibroblast growth factor receptor 3. J Pediatr. 1998;132:714-716. (Pubitemid 28194597)
-
(1998)
Journal of Pediatrics
, vol.132
, Issue.4
, pp. 714-716
-
-
Gripp, K.W.1
McDonald-Mcginn, D.M.2
Gaudenz, K.3
Whitaker, L.A.4
Bartlett, S.P.5
Glat, P.M.6
Cassileth, L.B.7
Mayro, R.8
Zackai, E.H.9
Muenke, M.10
-
8
-
-
0028080497
-
Frontal plagiocephaly. Diagnosis and treatment
-
Hansen M., Mulliken J.B. Frontal plagiocephaly. Diagnosis and treatment. Clin Plast Surg. 1994;21:543-553.
-
(1994)
Clin Plast Surg.
, vol.21
, pp. 543-553
-
-
Hansen, M.1
Mulliken, J.B.2
-
9
-
-
33645422454
-
Prenatal diagnosis of achondroplasia presenting with multiple-suture synostosis:A novel association
-
Karadimas C., Trouvas D., Haritatos G., Makatsoris C., Dedoulis E., Velissariou V., Antoniadi T., Hatzaki A., Petersen M.B. Prenatal diagnosis of achondroplasia presenting with multiple-suture synostosis:A novel association. Prenat Diagn. 2006;26:258-261.
-
(2006)
Prenat Diagn.
, vol.26
, pp. 258-261
-
-
Karadimas, C.1
Trouvas, D.2
Haritatos, G.3
Makatsoris, C.4
Dedoulis, E.5
Velissariou, V.6
Antoniadi, T.7
Hatzaki, A.8
Petersen, M.B.9
-
10
-
-
0030071923
-
Plagiocephaly: Differential diagnosis based on endocranial morphology
-
DOI 10.1097/00006534-199602000-00003
-
Lo L.J., Marsh J.L., Pilgram T.K., Vannier M.W. Plagiocephaly: Differential diagnosis based on endocranial morphology. Plast Reconstr Surg. 1996;97:282-291. (Pubitemid 26042486)
-
(1996)
Plastic and Reconstructive Surgery
, vol.97
, Issue.2
, pp. 282-291
-
-
Lo, L.-J.1
Marsh, J.L.2
Pilgram, T.K.3
Vannier, M.W.4
-
12
-
-
16944367030
-
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
-
Muenke M., Gripp K.W., McDonald-McGinn D.M., Gaudenz K., Whitaker L.A., Bartlett S.P., Markowitz R.I., Robin N.H., Nwokoro N., Mulvihill J.J., 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. (Pubitemid 27097603)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.3
, pp. 555-564
-
-
Muenke, M.1
Gripp, K.W.2
McDonald-McGinn, D.M.3
Gaudenz, K.4
Whitaker, L.A.5
Bartlett, S.P.6
Markowitz, R.I.7
Robin, N.H.8
Nwokoro, N.9
Mulvihill, J.J.10
Losken, H.W.11
Mulliken, J.B.12
Guttmacher, A.E.13
Wilroy, R.S.14
Clarke, L.A.15
Hollway, G.16
Ades, L.C.17
Haan, E.A.18
Mulley, J.C.19
Cohen Jr., M.M.20
Bellus, G.A.21
Francomano, C.A.22
Moloney, D.M.23
Wall, S.A.24
Wilkie, A.O.M.25
Zackai, E.H.26
more..
-
13
-
-
0030888218
-
Craniofrontonasal dysplasia
-
Orr D.J., Slaney S., Ashworth G.J., Poole M.D. Craniofrontonasal dysplasia. Br J Plast Surg. 1997;50:153-161. (Pubitemid 27190008)
-
(1997)
British Journal of Plastic Surgery
, vol.50
, Issue.3
, pp. 153-161
-
-
Orr, D.J.A.1
Slaney, S.2
Ashworth, G.J.3
Poole, M.D.4
-
14
-
-
0037105791
-
Unilateral fusion of the frontosphenoidal suture: A rare cause of synostotic frontal plagiocephaly
-
Rogers G.F., Proctor M.R., Mulliken J.B. Unilateral fusion of the frontosphenoidal suture:A rare cause of synostotic frontal plagiocephaly. Plast Reconstr Surg. 2002;110:1011-1021. (Pubitemid 34913335)
-
(2002)
Plastic and Reconstructive Surgery
, vol.110
, Issue.4
, pp. 1011-1021
-
-
Rogers, G.F.1
Proctor, M.R.2
Mulliken, J.B.3
-
15
-
-
0029940878
-
The "back to sleep campaign" and deformational plagiocephaly:Is there a cause for concern?
-
Turk A.E., McCarthy J.G., Thorne C.H., Wisoff J.H. The "back to sleep campaign" and deformational plagiocephaly:Is there a 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
-
16
-
-
0034464005
-
The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: The achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans
-
DOI 10.1210/er.21.1.23
-
Vajo Z., Francomano C.A., Wilkin D.J. The molecular and genetic basis of fibroblast growth factor receptor 3 disorders:The achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000;21:23-39. (Pubitemid 32260394)
-
(2000)
Endocrine Reviews
, vol.21
, Issue.1
, pp. 23-39
-
-
Vajo, Z.1
Francomano, C.A.2
Wilkin, D.J.3
|