McAndrew PE - Search Results

1

Collaboration between civilian and military healthcare professionals: a better way for planning, preparing, and responding to all hazard domestic events.

Marklund LA, Graham AM, Morton PG, Hurst CG, Motola I, Robinson DW, Kelley VA, Elenberg KJ, Russler MF, Boehm DE Jr, Higgins DM, McAndrew PE, Williamson HM, Atwood RD, Huebner KD, Brotons AA, Miller GT, Rimpel LY, Harris LL, Santiago M, Cantrell L. Marklund LA, et al. Among authors: mcandrew pe. Prehosp Disaster Med. 2010 Sep-Oct;25(5):399-412. doi: 10.1017/s1049023x00008451. Prehosp Disaster Med. 2010. PMID: 21053185 Review.

2

Mutation detection in the ABCC6 gene and genotype-phenotype analysis in a large international case series affected by pseudoxanthoma elasticum.

Pfendner EG, Vanakker OM, Terry SF, Vourthis S, McAndrew PE, McClain MR, Fratta S, Marais AS, Hariri S, Coucke PJ, Ramsay M, Viljoen D, Terry PF, De Paepe A, Uitto J, Bercovitch LG. Pfendner EG, et al. Among authors: mcandrew pe. J Med Genet. 2007 Oct;44(10):621-8. doi: 10.1136/jmg.2007.051094. Epub 2007 Jul 6. J Med Genet. 2007. PMID: 17617515 Free PMC article.

3

Rapid and robust screening of the Menkes disease/occipital horn syndrome gene.

Liu PC, McAndrew PE, Kaler SG. Liu PC, et al. Among authors: mcandrew pe. Genet Test. 2002 Winter;6(4):255-60. doi: 10.1089/10906570260471778. Genet Test. 2002. PMID: 12537648

4

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7.

Rochette CF, Surh LC, Ray PN, McAndrew PE, Prior TW, Burghes AH, Vanasse M, Simard LR. Rochette CF, et al. Among authors: mcandrew pe. Neurogenetics. 1997 Sep;1(2):141-7. doi: 10.1007/s100480050021. Neurogenetics. 1997. PMID: 10732817

5

Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number.

Parsons DW, McAndrew PE, Iannaccone ST, Mendell JR, Burghes AH, Prior TW. Parsons DW, et al. Among authors: mcandrew pe. Am J Hum Genet. 1998 Dec;63(6):1712-23. doi: 10.1086/302160. Am J Hum Genet. 1998. PMID: 9837824 Free PMC article.

6

Diagnosis of spinal muscular atrophy in an SMN non-deletion patient using a quantitative PCR screen and mutation analysis.

Parsons DW, McAndrew PE, Allinson PS, Parker WD Jr, Burghes AH, Prior TW. Parsons DW, et al. Among authors: mcandrew pe. J Med Genet. 1998 Aug;35(8):674-6. doi: 10.1136/jmg.35.8.674. J Med Genet. 1998. PMID: 9719377 Free PMC article.

7

Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy.

Bartolo C, McAndrew PE, Sosolik RC, Cawley KA, Balcerzak SP, Brandt JT, Prior TW. Bartolo C, et al. Among authors: mcandrew pe. Arch Pathol Lab Med. 1998 Jul;122(7):633-7. Arch Pathol Lab Med. 1998. PMID: 9674544

8

Identification and characterization of RPTP rho, a novel RPTP mu/kappa-like receptor protein tyrosine phosphatase whose expression is restricted to the central nervous system.

McAndrew PE, Frostholm A, White RA, Rotter A, Burghes AH. McAndrew PE, et al. Brain Res Mol Brain Res. 1998 May;56(1-2):9-21. doi: 10.1016/s0169-328x(98)00014-x. Brain Res Mol Brain Res. 1998. PMID: 9602027

9

Novel receptor protein tyrosine phosphatase (RPTPrho) and acidic fibroblast growth factor (FGF-1) transcripts delineate a rostrocaudal boundary in the granule cell layer of the murine cerebellar cortex.

McAndrew PE, Frostholm A, Evans JE, Zdilar D, Goldowitz D, Chiu IM, Burghes AH, Rotter A. McAndrew PE, et al. J Comp Neurol. 1998 Feb 22;391(4):444-55. doi: 10.1002/(sici)1096-9861(19980222)391:4<444::aid-cne3>3.0.co;2-0. J Comp Neurol. 1998. PMID: 9486824

10

The survival motor neuron protein in spinal muscular atrophy.

Coovert DD, Le TT, McAndrew PE, Strasswimmer J, Crawford TO, Mendell JR, Coulson SE, Androphy EJ, Prior TW, Burghes AH. Coovert DD, et al. Among authors: mcandrew pe. Hum Mol Genet. 1997 Aug;6(8):1205-14. doi: 10.1093/hmg/6.8.1205. Hum Mol Genet. 1997. PMID: 9259265

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