155 related articles for article (PubMed ID: 20592905)
1. A Korean family with the Muenke syndrome.
Yu JE; Park DH; Yoon SH
J Korean Med Sci; 2010 Jul; 25(7):1086-9. PubMed ID: 20592905
[TBL] [Abstract][Full Text] [Related]
2. Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis.
González-Del Angel A; Estandía-Ortega B; Alcántara-Ortigoza MA; Martínez-Cruz V; Gutiérrez-Tinajero DJ; Rasmussen A; Gómez-González CS
Am J Med Genet A; 2016 Dec; 170(12):3189-3196. PubMed ID: 27568649
[TBL] [Abstract][Full Text] [Related]
3. Muenke syndrome: An international multicenter natural history study.
Kruszka P; Addissie YA; Yarnell CM; Hadley DW; Guillen Sacoto MJ; Platte P; Paelecke Y; Collmann H; Snow N; Schweitzer T; Boyadjiev SA; Aravidis C; Hall SE; Mulliken JB; Roscioli T; Muenke M
Am J Med Genet A; 2016 Apr; 170A(4):918-29. PubMed ID: 26740388
[TBL] [Abstract][Full Text] [Related]
4. [Typical features of craniofacial growth of the FGFR3-associated coronal synostosis syndrome (so-called Muenke craniosynostosis)].
Reinhart E; Eulert S; Bill J; Würzler K; Phan The L; Reuther J
Mund Kiefer Gesichtschir; 2003 May; 7(3):132-7. PubMed ID: 12764678
[TBL] [Abstract][Full Text] [Related]
5. A familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation--case report and review of the literature.
Aravidis C; Konialis CP; Pangalos CG; Kosmaidou Z
J Matern Fetal Neonatal Med; 2014 Sep; 27(14):1502-6. PubMed ID: 24168007
[TBL] [Abstract][Full Text] [Related]
6. Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
Doherty ES; Lacbawan F; Hadley DW; Brewer C; Zalewski C; Kim HJ; Solomon B; Rosenbaum K; Domingo DL; Hart TC; Brooks BP; Immken L; Lowry RB; Kimonis V; Shanske AL; Jehee FS; Bueno MR; Knightly C; McDonald-McGinn D; Zackai EH; Muenke M
Am J Med Genet A; 2007 Dec; 143A(24):3204-15. PubMed ID: 18000976
[TBL] [Abstract][Full Text] [Related]
7. Muenke syndrome: Medical and surgical comorbidities and long-term management.
Murali CN; McDonald-McGinn DM; Wenger TL; McDougall C; Stroup BM; Sheppard SE; Taylor J; Bartlett SP; Bhoj EJ; Zackai EH; Santani A
Am J Med Genet A; 2019 Aug; 179(8):1442-1450. PubMed ID: 31111620
[TBL] [Abstract][Full Text] [Related]
8. Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses.
Ohishi A; Nishimura G; Kato F; Ono H; Maruwaka K; Ago M; Suzumura H; Hirose E; Uchida Y; Fukami M; Ogata T
Am J Med Genet A; 2017 Jan; 173(1):157-162. PubMed ID: 27683237
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations.
Ko JM; Jeong SY; Yang JA; Park DH; Yoon SH
Plast Reconstr Surg; 2012 May; 129(5):814e-821e. PubMed ID: 22544111
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic variability in Muenke syndrome-observations from five Danish families.
Öwall L; Kreiborg S; Dunø M; Hermann NV; Darvann TA; Hove H
Clin Dysmorphol; 2020 Jan; 29(1):1-9. PubMed ID: 31609728
[TBL] [Abstract][Full Text] [Related]
11. Molecular analysis of patients with synostotic frontal plagiocephaly (unilateral coronal synostosis).
Mulliken JB; Gripp KW; Stolle CA; Steinberger D; Müller U
Plast Reconstr Surg; 2004 Jun; 113(7):1899-909. PubMed ID: 15253176
[TBL] [Abstract][Full Text] [Related]
12. The natural history of patients treated for FGFR3-associated (Muenke-type) craniosynostosis.
Honnebier MB; Cabiling DS; Hetlinger M; McDonald-McGinn DM; Zackai EH; Bartlett SP
Plast Reconstr Surg; 2008 Mar; 121(3):919-931. PubMed ID: 18317141
[TBL] [Abstract][Full Text] [Related]
13. Clinical characteristics of patients with unicoronal synostosis and mutations of fibroblast growth factor receptor 3: a preliminary report.
Cassileth LB; Bartlett SP; Glat PM; Gripp KW; Muenke M; Zackai EH; Whitaker LA
Plast Reconstr Surg; 2001 Dec; 108(7):1849-54. PubMed ID: 11743367
[TBL] [Abstract][Full Text] [Related]
14. Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome.
Twigg SR; Healy C; Babbs C; Sharpe JA; Wood WG; Sharpe PT; Morriss-Kay GM; Wilkie AO
Dev Dyn; 2009 Feb; 238(2):331-42. PubMed ID: 19086028
[TBL] [Abstract][Full Text] [Related]
15. Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis.
Agochukwu NB; Solomon BD; Gropman AL; Muenke M
Pediatr Neurol; 2012 Nov; 47(5):355-61. PubMed ID: 23044018
[TBL] [Abstract][Full Text] [Related]
16. Phenotype profile of a genetic mouse model for Muenke syndrome.
Nah HD; Koyama E; Agochukwu NB; Bartlett SP; Muenke M
Childs Nerv Syst; 2012 Sep; 28(9):1483-93. PubMed ID: 22872265
[TBL] [Abstract][Full Text] [Related]
17. Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutation.
Lajeunie E; El Ghouzzi V; Le Merrer M; Munnich A; Bonaventure J; Renier D
J Med Genet; 1999 Jan; 36(1):9-13. PubMed ID: 9950359
[TBL] [Abstract][Full Text] [Related]
18. Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome.
Renier D; El-Ghouzzi V; Bonaventure J; Le Merrer M; Lajeunie E
J Neurosurg; 2000 Apr; 92(4):631-6. PubMed ID: 10761652
[TBL] [Abstract][Full Text] [Related]
19. Additional phenotypic features of Muenke syndrome in 2 Dutch families.
de Jong T; Mathijssen IM; Hoogeboom AJ
J Craniofac Surg; 2011 Mar; 22(2):571-5. PubMed ID: 21403557
[TBL] [Abstract][Full Text] [Related]
20. Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
Lowry RB; Jabs EW; Graham GE; Gerritsen J; Fleming J
Am J Med Genet; 2001 Nov; 104(2):112-9. PubMed ID: 11746040
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
