McAndrew PE[au] - Search Results

Year	Number of Results
1986	1
1995	2
1996	2
1997	3
1998	5
2002	1
2007	1
2010	1
2022	0

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

Myoblast transfer in the treatment of Duchenne's muscular dystrophy.

Mendell JR, Kissel JT, Amato AA, King W, Signore L, Prior TW, Sahenk Z, Benson S, McAndrew PE, Rice R, et al. Mendell JR, et al. Among authors: mcandrew pe. N Engl J Med. 1995 Sep 28;333(13):832-8. doi: 10.1056/NEJM199509283331303. N Engl J Med. 1995. PMID: 7651473 Free article. Clinical Trial.

3

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

4

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.

5

The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African Americans.

McAndrew PE, Brandt JT, Pearl DK, Prior TW. McAndrew PE, et al. Thromb Res. 1996 Jul 15;83(2):195-8. doi: 10.1016/0049-3848(96)00121-1. Thromb Res. 1996. PMID: 8837319

6

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

7

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number.

McAndrew PE, Parsons DW, Simard LR, Rochette C, Ray PN, Mendell JR, Prior TW, Burghes AH. McAndrew PE, et al. Am J Hum Genet. 1997 Jun;60(6):1411-22. doi: 10.1086/515465. Am J Hum Genet. 1997. PMID: 9199562 Free PMC article.

8

An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene.

Parsons DW, McAndrew PE, Monani UR, Mendell JR, Burghes AH, Prior TW. Parsons DW, et al. Among authors: mcandrew pe. Hum Mol Genet. 1996 Nov;5(11):1727-32. doi: 10.1093/hmg/5.11.1727. Hum Mol Genet. 1996. PMID: 8922999

9

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.

10

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

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