Mills P - Search Results

1

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME. Pilz DT, et al. Among authors: mills p. Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029. Hum Mol Genet. 1998. PMID: 9817918

2

The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene.

Cardoso C, Leventer RJ, Matsumoto N, Kuc JA, Ramocki MB, Mewborn SK, Dudlicek LL, May LF, Mills PL, Das S, Pilz DT, Dobyns WB, Ledbetter DH. Cardoso C, et al. Among authors: mills pl. Hum Mol Genet. 2000 Dec 12;9(20):3019-28. doi: 10.1093/hmg/9.20.3019. Hum Mol Genet. 2000. PMID: 11115846

3

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

Matsumoto N, Leventer RJ, Kuc JA, Mewborn SK, Dudlicek LL, Ramocki MB, Pilz DT, Mills PL, Das S, Ross ME, Ledbetter DH, Dobyns WB. Matsumoto N, et al. Among authors: mills pl. Eur J Hum Genet. 2001 Jan;9(1):5-12. doi: 10.1038/sj.ejhg.5200548. Eur J Hum Genet. 2001. PMID: 11175293

4

X-linked malformations of cortical development.

Leventer RJ, Mills PL, Dobyns WB. Leventer RJ, et al. Among authors: mills pl. Am J Med Genet. 2000 Fall;97(3):213-20. doi: 10.1002/1096-8628(200023)97:3<213::AID-AJMG1039>3.0.CO;2-W. Am J Med Genet. 2000. PMID: 11449490 Review.

5

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

Demelas L, Serra G, Conti M, Achene A, Mastropaolo C, Matsumoto N, Dudlicek LL, Mills PL, Dobyns WB, Ledbetter DH, Das S. Demelas L, et al. Among authors: mills pl. Neurology. 2001 Jul 24;57(2):327-30. doi: 10.1212/wnl.57.2.327. Neurology. 2001. PMID: 11468322

6

Urorectal septal defects in a female and her offspring.

Mills PL, Pergament E. Mills PL, et al. Am J Med Genet. 1997 Jun 13;70(3):250-2. doi: 10.1002/(sici)1096-8628(19970613)70:3<250::aid-ajmg7>3.0.co;2-#. Am J Med Genet. 1997. PMID: 9188661

7

Characterization of mutations in fifty North American patients with X-linked myotubular myopathy.

Herman GE, Kopacz K, Zhao W, Mills PL, Metzenberg A, Das S. Herman GE, et al. Hum Mutat. 2002 Feb;19(2):114-21. doi: 10.1002/humu.10033. Hum Mutat. 2002. PMID: 11793470

8

Effect of family history on disclosure patterns of cystic fibrosis carrier status.

Ormond KE, Mills PL, Lester LA, Ross LF. Ormond KE, et al. Am J Med Genet C Semin Med Genet. 2003 May 15;119C(1):70-7. doi: 10.1002/ajmg.c.10008. Am J Med Genet C Semin Med Genet. 2003. PMID: 12704640

9

Sympathetic overactivity and nocturnal diuresis in obstructive sleep apnea alter the response to hypertension therapy.

Ziegler MG, Milic M, Dimsdale JE, Mills PJ. Ziegler MG, et al. Among authors: mills pj. Clin Hypertens. 2024 Jun 1;30(1):14. doi: 10.1186/s40885-024-00272-x. Clin Hypertens. 2024. PMID: 38822391 Free PMC article.

10

A Randomized Controlled Trial of the Implementation of BREASTChoice, a Multilevel Breast Reconstruction Decision Support Tool With Personalized Risk Predictiona.

Politi MC, Myckatyn TM, Cooksey K, Olsen MA, Smith RM, Foraker R, Parrish K, Phommasathit C, Brock G, Janse S, Guglielmino J, Peled A, Mills PB, Jackson S, Lee CN. Politi MC, et al. Among authors: mills pb. Ann Surg. 2024 May 27. doi: 10.1097/SLA.0000000000006354. Online ahead of print. Ann Surg. 2024. PMID: 38801247

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