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Results: 15

Related Articles by Review for PubMed (Select 19816260)

1.

Cleft palate in Pfeiffer syndrome.

Stoler JM, Rosen H, Desai U, Mulliken JB, Meara JG, Rogers GF.

J Craniofac Surg. 2009 Sep;20(5):1375-7. doi: 10.1097/SCS.0b013e3181ae42e4.

PMID:
19816260
2.

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
3.

[From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].

van Ravenswaaij-Arts CM, van den Ouweland AM, Hoogeboom AJ, Herbergs J, Pals G.

Ned Tijdschr Geneeskd. 2002 Jan 12;146(2):63-6. Review. Dutch.

PMID:
11820058
4.

Pfeiffer syndrome.

Vogels A, Fryns JP.

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

5.

Development of the lip and palate: FGF signalling.

Stanier P, Pauws E.

Front Oral Biol. 2012;16:71-80. doi: 10.1159/000337618. Epub 2012 Jun 25. Review.

PMID:
22759671
6.

Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails.

Wilkinson CC, Manchester DK, Keating RF, Ketch LL, Winston KR.

Childs Nerv Syst. 2012 Aug;28(8):1221-6. doi: 10.1007/s00381-012-1813-x. Epub 2012 Jun 4. Review.

PMID:
22661218
7.

Palatal and oral manifestations of Muenke syndrome (FGFR3-related craniosynostosis).

Agochukwu NB, Solomon BD, Doherty ES, Muenke M.

J Craniofac Surg. 2012 May;23(3):664-8. doi: 10.1097/SCS.0b013e31824db8bb. Review.

8.

Craniosynostosis and related limb anomalies.

Wilkie AO, Oldridge M, Tang Z, Maxson RE Jr.

Novartis Found Symp. 2001;232:122-33; discussion 133-43. Review.

PMID:
11277076
9.

Pfeiffer syndrome type 2: further delineation and review of the literature.

Plomp AS, Hamel BC, Cobben JM, Verloes A, Offermans JP, Lajeunie E, Fryns JP, de Die-Smulders CE.

Am J Med Genet. 1998 Jan 23;75(3):245-51. Review.

PMID:
9475590
10.

Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature.

Nazzaro A, Della Monica M, Lonardo F, Di Blasi A, Baffico M, Baldi M, Nazzaro G, De Placido G, Scarano G.

Prenat Diagn. 2004 Nov;24(11):918-22. Review.

PMID:
15565658
11.

Syndromic craniosynostosis: from history to hydrogen bonds.

Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV.

Orthod Craniofac Res. 2007 May;10(2):67-81. Review.

PMID:
17552943
12.

Molecular genetics of craniosynostotic syndromes.

Müller U, Steinberger D, Kunze S.

Graefes Arch Clin Exp Ophthalmol. 1997 Sep;235(9):545-50. Review.

PMID:
9342602
13.

Pfeiffer syndrome: systemic and ocular implications.

Harb E, Kran B.

Optometry. 2005 Jul;76(7):352-62. Review.

PMID:
16038862
14.

A case of Pfeiffer syndrome.

Park MS, Yoo JE, Chung J, Yoon SH.

J Korean Med Sci. 2006 Apr;21(2):374-8. Review.

15.

Pfeiffer syndrome type II discovered perinatally: Report of an observation and review of the literature.

Ben Hamouda H, Tlili Y, Ghanmi S, Soua H, Jerbi S, Souissi MM, Hamza H, Sfar MT.

Diagn Interv Imaging. 2012 Oct;93(10):785-9. doi: 10.1016/j.diii.2012.06.002. Epub 2012 Aug 21. Review. No abstract available.

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