Lazarou LP - Search Results

1

A comparison of methods for EGFR mutation testing in non-small cell lung cancer.

Young EC, Owens MM, Adebiyi I, Bedenham T, Butler R, Callaway J, Cranston T, Crosby C, Cree IA, Dutton L, Faulkes C, Faulkner C, Howard E, Knight J, Huang Y, Lavender L, Lazarou LP, Liu H, Mair D, Milano A, Sandell S, Skinner A, Wallace A, Williams M, Spivey V, Goodall J, Frampton J, Ellard S; Clinical Molecular Genetics Society (CMGS) Scientific Subcommittee. Young EC, et al. Among authors: lazarou lp. Diagn Mol Pathol. 2013 Dec;22(4):190-5. doi: 10.1097/PDM.0b013e318294936c. Diagn Mol Pathol. 2013. PMID: 24193010

2

Improvement in the quality of molecular analysis of EGFR in non-small-cell lung cancer detected by three rounds of external quality assessment.

Deans ZC, Bilbe N, O'Sullivan B, Lazarou LP, de Castro DG, Parry S, Dodson A, Taniere P, Clark C, Butler R. Deans ZC, et al. Among authors: lazarou lp. J Clin Pathol. 2013 Apr;66(4):319-25. doi: 10.1136/jclinpath-2012-201227. Epub 2013 Feb 1. J Clin Pathol. 2013. PMID: 23378269

3

MECP2 triplication in 3 brothers - a rarely described cause of familial neurological regression in boys.

Tang SS, Fernandez D, Lazarou LP, Singh R, Fallon P. Tang SS, et al. Among authors: lazarou lp. Eur J Paediatr Neurol. 2012 Mar;16(2):209-12. doi: 10.1016/j.ejpn.2011.07.011. Epub 2011 Aug 6. Eur J Paediatr Neurol. 2012. PMID: 21821449

4

An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene.

Millar DS, Tysoe C, Lazarou LP, Pilz DT, Mohammed S, Anderson K, Chuzhanova N, Cooper DN, Butler R. Millar DS, et al. Among authors: lazarou lp. Hum Genomics. 2010 Aug;4(6):384-93. doi: 10.1186/1479-7364-4-6-384. Hum Genomics. 2010. PMID: 20846927 Free PMC article.

5

Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene.

Rosser LG, McKee S, Millar DS, Archer H, Hughes J, Butler R, Chuzhanova N, Cooper DN, Lazarou LP. Rosser LG, et al. Among authors: lazarou lp. Genomic Med. 2008 Dec;2(3-4):77-81. doi: 10.1007/s11568-008-9026-9. Epub 2008 Sep 20. Genomic Med. 2008. PMID: 18810657 Free PMC article.

6

High frequency of genomic deletions--and a duplication--in the LIS1 gene in lissencephaly: implications for molecular diagnosis.

Mei D, Lewis R, Parrini E, Lazarou LP, Marini C, Pilz DT, Guerrini R. Mei D, et al. Among authors: lazarou lp. J Med Genet. 2008 Jun;45(6):355-61. doi: 10.1136/jmg.2007.056507. Epub 2008 Feb 19. J Med Genet. 2008. PMID: 18285425

7

Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene.

Ørstavik KH, Knudsen GP, Nordgarden H, Ormerod E, Strømme P, Lazarou LP, Rosser LG, Prescott T, Houge G. Ørstavik KH, et al. Among authors: lazarou lp. Am J Med Genet A. 2007 Jul 1;143A(13):1510-3. doi: 10.1002/ajmg.a.31797. Am J Med Genet A. 2007. PMID: 17568423

8

Mutations in TITF-1 are associated with benign hereditary chorea.

Breedveld GJ, van Dongen JW, Danesino C, Guala A, Percy AK, Dure LS, Harper P, Lazarou LP, van der Linde H, Joosse M, Grüters A, MacDonald ME, de Vries BB, Arts WF, Oostra BA, Krude H, Heutink P. Breedveld GJ, et al. Among authors: lazarou lp. Hum Mol Genet. 2002 Apr 15;11(8):971-9. doi: 10.1093/hmg/11.8.971. Hum Mol Genet. 2002. PMID: 11971878

9

Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindred.

Hateboer N, Buchalter M, Davies SJ, Lazarou LP, Ravine D. Hateboer N, et al. Among authors: lazarou lp. Am J Kidney Dis. 2000 Apr;35(4):753-60. doi: 10.1016/s0272-6386(00)70026-6. Am J Kidney Dis. 2000. PMID: 10739800

10

Familial phenotype differences in PKD11.

Hateboer N, Lazarou LP, Williams AJ, Holmans P, Ravine D. Hateboer N, et al. Among authors: lazarou lp. Kidney Int. 1999 Jul;56(1):34-40. doi: 10.1046/j.1523-1755.1999.00541.x. Kidney Int. 1999. PMID: 10411677 Free article.

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