Gallagher PG - Search Results

1

Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.

Bianchi P, Fermo E, Lezon-Geyda K, van Beers EJ, Morton HD, Barcellini W, Glader B, Chonat S, Ravindranath Y, Newburger PE, Kollmar N, Despotovic JM, Verhovsek M, Sharma M, Kwiatkowski JL, Kuo KHM, Wlodarski MW, Yaish HM, Holzhauer S, Wang H, Kunz J, Addonizio K, Al-Sayegh H, London WB, Andres O, van Wijk R, Gallagher PG, Grace RFF. Bianchi P, et al. Among authors: gallagher pg. Am J Hematol. 2020 May;95(5):472-482. doi: 10.1002/ajh.25753. Epub 2020 Mar 6. Am J Hematol. 2020. PMID: 32043619 Free PMC article.

2

Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosis.

Tse WT, Gallagher PG, Jenkins PB, Wang Y, Benoit L, Speicher D, Winkelmann JC, Agre P, Forget BG, Marchesi SL. Tse WT, et al. Among authors: gallagher pg. Am J Hematol. 1997 Mar;54(3):233-41. doi: 10.1002/(sici)1096-8652(199703)54:3<233::aid-ajh10>3.0.co;2-e. Am J Hematol. 1997. PMID: 9067503 Free article.

3

Genetic basis of the polymorphisms of the alphaI domain of spectrin.

Gallagher PG, Romana M, Wong C, Forget BG. Gallagher PG, et al. Am J Hematol. 1997 Oct;56(2):107-11. doi: 10.1002/(sici)1096-8652(199710)56:2<107::aid-ajh6>3.0.co;2-2. Am J Hematol. 1997. PMID: 9326352 Free article.

4

Exclusion of the stomatin, alpha-adducin and beta-adducin loci in a large kindred with dehydrated hereditary stomatocytosis.

Innes DS, Sinard JH, Gilligan DM, Snyder LM, Gallagher PG, Morrow JS. Innes DS, et al. Among authors: gallagher pg. Am J Hematol. 1999 Jan;60(1):72-4. doi: 10.1002/(sici)1096-8652(199901)60:1<72::aid-ajh13>3.0.co;2-8. Am J Hematol. 1999. PMID: 9883810 Free article.

5

Update on the clinical spectrum and genetics of red blood cell membrane disorders.

Gallagher PG. Gallagher PG. Curr Hematol Rep. 2004 Mar;3(2):85-91. Curr Hematol Rep. 2004. PMID: 14965483 Review.

6

Red cell membrane disorders.

Gallagher PG. Gallagher PG. Hematology Am Soc Hematol Educ Program. 2005:13-8. doi: 10.1182/asheducation-2005.1.13. Hematology Am Soc Hematol Educ Program. 2005. PMID: 16304353

7

Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.

dos Santos CO, Zhou S, Secolin R, Wang X, Cunha AF, Higgs DR, Kwiatkowski JL, Thein SL, Gallagher PG, Costa FF, Weiss MJ. dos Santos CO, et al. Among authors: gallagher pg. Am J Hematol. 2008 Feb;83(2):103-8. doi: 10.1002/ajh.21041. Am J Hematol. 2008. PMID: 17874450 Free article.

8

Ankyrin-linked hereditary spherocytosis in an African-American kindred.

Sangerman J, Maksimova Y, Edelman EJ, Morrow JS, Forget BG, Gallagher PG. Sangerman J, et al. Among authors: gallagher pg. Am J Hematol. 2008 Oct;83(10):789-94. doi: 10.1002/ajh.21254. Am J Hematol. 2008. PMID: 18704959 Free PMC article.

9

Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes.

Weinstein JS, Lezon-Geyda K, Maksimova Y, Craft S, Zhang Y, Su M, Schulz VP, Craft J, Gallagher PG. Weinstein JS, et al. Among authors: gallagher pg. Blood. 2014 Dec 11;124(25):3719-29. doi: 10.1182/blood-2014-06-582700. Epub 2014 Oct 20. Blood. 2014. PMID: 25331115 Free PMC article.

10

A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Christensen RD, Yaish HM, Gallagher PG. Christensen RD, et al. Among authors: gallagher pg. Pediatrics. 2015 Jun;135(6):1107-14. doi: 10.1542/peds.2014-3516. Pediatrics. 2015. PMID: 26009624 Free PMC article. Review.

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