Wall S - Search Results

1

Psychosocial Impact of Coronal Access Scars in Craniosynostosis Procedures on Patients and Their Families.

Shaw AV, Kennedy-Williams P, Care H, Dalton L, Wall S, Johnson D. Shaw AV, et al. Among authors: wall s. J Craniofac Surg. 2022 Jan-Feb 01;33(1):168-173. doi: 10.1097/SCS.0000000000008181. J Craniofac Surg. 2022. PMID: 34560731

2

Craniosynostosis: novel insights into pathogenesis and treatment.

Wilkie AO, Wall SA. Wilkie AO, et al. Among authors: wall sa. Curr Opin Neurol. 1996 Apr;9(2):146-52. Curr Opin Neurol. 1996. PMID: 8782984 Review.

3

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SR, Walsh S, Barrow M, Njølstad PR, Kunz J, Ashworth GJ, Wall SA, Kearney L, Wilkie AO. Johnson D, et al. Among authors: wall sa. Am J Hum Genet. 1998 Nov;63(5):1282-93. doi: 10.1086/302122. Am J Hum Genet. 1998. PMID: 9792856 Free PMC article.

4

De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome.

Oldridge M, Zackai EH, McDonald-McGinn DM, Iseki S, Morriss-Kay GM, Twigg SR, Johnson D, Wall SA, Jiang W, Theda C, Jabs EW, Wilkie AO. Oldridge M, et al. Among authors: wall sa. Am J Hum Genet. 1999 Feb;64(2):446-61. doi: 10.1086/302245. Am J Hum Genet. 1999. PMID: 9973282 Free PMC article.

5

A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?

Johnson D, Wall SA, Mann S, Wilkie AO. Johnson D, et al. Among authors: wall sa. Eur J Hum Genet. 2000 Aug;8(8):571-7. doi: 10.1038/sj.ejhg.5200499. Eur J Hum Genet. 2000. PMID: 10951518

6

Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.

Kan SH, Elanko N, Johnson D, Cornejo-Roldan L, Cook J, Reich EW, Tomkins S, Verloes A, Twigg SR, Rannan-Eliya S, McDonald-McGinn DM, Zackai EH, Wall SA, Muenke M, Wilkie AO. Kan SH, et al. Among authors: wall sa. Am J Hum Genet. 2002 Feb;70(2):472-86. doi: 10.1086/338758. Epub 2002 Jan 4. Am J Hum Genet. 2002. PMID: 11781872 Free PMC article.

7

FGFR3 P250R mutation increases the risk of reoperation in apparent 'nonsyndromic' coronal craniosynostosis.

Thomas GP, Wilkie AO, Richards PG, Wall SA. Thomas GP, et al. J Craniofac Surg. 2005 May;16(3):347-52; discussion 353-4. doi: 10.1097/01.scs.0000157024.56055.f2. J Craniofac Surg. 2005. PMID: 15915095

8

Strabismus in unicoronal synostosis: ipsilateral or contralateral?

Macintosh C, Wall S, Leach C. Macintosh C, et al. Among authors: wall s. J Craniofac Surg. 2007 May;18(3):465-9. doi: 10.1097/scs.0b01e3180515d94. J Craniofac Surg. 2007. PMID: 17538304

9

A paramedian cleft of the lower lip.

Morritt DG, Goodacre TE, Wall SA. Morritt DG, et al. J Craniofac Surg. 2007 May;18(3):704-6. doi: 10.1097/scs.0b013e318052e2ce. J Craniofac Surg. 2007. PMID: 17538343

10

The increase of metopic synostosis: a pan-European observation.

van der Meulen J, van der Hulst R, van Adrichem L, Arnaud E, Chin-Shong D, Duncan C, Habets E, Hinojosa J, Mathijssen I, May P, Morritt D, Nishikawa H, Noons P, Richardson D, Wall S, van der Vlugt J, Renier D. van der Meulen J, et al. Among authors: wall s. J Craniofac Surg. 2009 Mar;20(2):283-6. doi: 10.1097/scs.0b013e31818436be. J Craniofac Surg. 2009. PMID: 19326483

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