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Similar articles for PubMed (Select 23348287)

1.

Pfeiffer syndrome: analysis of a clinical series and development of a classification system.

Greig AV, Wagner J, Warren SM, Grayson B, McCarthy JG.

J Craniofac Surg. 2013 Jan;24(1):204-15. doi: 10.1097/SCS.0b013e31826704be.

PMID:
23348287
2.

Upper extremity anomalies in Pfeiffer syndrome and mutational correlations.

Cerrato FE, Nuzzi LC, Theman TA, Taghinia A, Upton J, Labow BI.

Plast Reconstr Surg. 2014 May;133(5):654e-661e. doi: 10.1097/PRS.0000000000000107.

PMID:
24776567
4.

Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classification.

Robin NH, Scott JA, Arnold JE, Goldstein JA, Shilling BB, Marion RW, Cohen MM Jr.

Am J Med Genet. 1998 Jan 23;75(3):240-4.

PMID:
9475589
5.

Reossification of cranium and zygomatic arch after monobloc frontofacial distraction advancement for syndromic craniosynostosis.

Oyama A, Arnaud E, Marchac D, Renier D.

J Craniofac Surg. 2009 Sep;20 Suppl 2:1905-9. doi: 10.1097/SCS.0b013e3181b6c634.

PMID:
19816373
6.

Pfeiffer syndrome: a clinical review.

Moore MH, Cantrell SB, Trott JA, David DJ.

Cleft Palate Craniofac J. 1995 Jan;32(1):62-70.

PMID:
7727489
7.

Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.

Piccione M, Antona V, Niceta M, Fabiano C, Martines M, Bianchi A, Corsello G.

Eur J Pediatr. 2009 Sep;168(9):1135-9. doi: 10.1007/s00431-008-0884-x. Epub 2008 Dec 6.

PMID:
19066959
8.

FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report.

Hackett A, Rowe L.

Clin Dysmorphol. 2006 Oct;15(4):207-10.

PMID:
16957473
9.

Pfeiffer syndrome: a treatment evaluation.

Fearon JA, Rhodes J.

Plast Reconstr Surg. 2009 May;123(5):1560-9. doi: 10.1097/PRS.0b013e3181a2057e.

PMID:
19407629
10.

Pyrexia after transcranial surgery for Pfeiffer syndrome.

Tamada I, David DJ, Anderson PJ.

J Craniofac Surg. 2009 Mar;20(2):414-6. doi: 10.1097/SCS.0b013e31819b9656.

PMID:
19242364
11.

Pfeiffer syndrome.

Vogels A, Fryns JP.

Orphanet J Rare Dis. 2006 Jun 1;1:19. Review.

12.

Surgical treatment of isolated and syndromic craniosynostosis. Results and complications in 283 consecutive cases.

Esparza J, Hinojosa J, García-Recuero I, Romance A, Pascual B, Martínez de Aragón A.

Neurocirugia (Astur). 2008 Dec;19(6):509-29.

13.

Tracheal cartilaginous sleeve with cricoid cartilage involvement in Pfeiffer syndrome.

Elloy MD, Cochrane LA, Wyatt M.

J Craniofac Surg. 2006 Mar;17(2):272-4.

PMID:
16633174
14.

Audiologic findings in Pfeiffer syndrome.

Desai U, Rosen H, Mulliken JB, Gopen Q, Meara JG, Rogers GF.

J Craniofac Surg. 2010 Sep;21(5):1411-8. doi: 10.1097/SCS.0b013e3181ebcf58.

PMID:
20856029
15.

Tracheal anomalies in Pfeiffer syndrome.

Hockstein NG, McDonald-McGinn D, Zackai E, Bartlett S, Huff DS, Jacobs IN.

Arch Otolaryngol Head Neck Surg. 2004 Nov;130(11):1298-302.

PMID:
15545585
16.

Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect?

Escobar V, Bixler D.

Birth Defects Orig Artic Ser. 1977;13(3C):139-54.

PMID:
890108
17.

Variable expression in Pfeiffer syndrome.

Sanchex HM, De Negrotti TC.

J Med Genet. 1981 Feb;18(1):73-5.

18.

Monobloc and midface distraction osteogenesis in pediatric patients with severe syndromal craniosynostosis.

Meling TR, Tveten S, Due-Tonnessen BJ, Skjelbred P, Helseth E.

Pediatr Neurosurg. 2000 Aug;33(2):89-94.

PMID:
11070435
19.

Obstructive sleep apnea in children with syndromic craniosynostosis: long-term respiratory outcome of midface advancement.

Bannink N, Nout E, Wolvius EB, Hoeve HL, Joosten KF, Mathijssen IM.

Int J Oral Maxillofac Surg. 2010 Feb;39(2):115-21. doi: 10.1016/j.ijom.2009.11.021. Epub 2010 Jan 6.

PMID:
20056390
20.

Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.

Chen CP, Lin SP, Su YN, Chien SC, Tsai FJ, Wang W.

Genet Couns. 2008;19(2):165-72. Review.

PMID:
18618990
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