Gallagher PG - Search Results

1

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.

2

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.

Eber SW, Gonzalez JM, Lux ML, Scarpa AL, Tse WT, Dornwell M, Herbers J, Kugler W, Ozcan R, Pekrun A, Gallagher PG, Schröter W, Forget BG, Lux SE. Eber SW, et al. Among authors: gallagher pg. Nat Genet. 1996 Jun;13(2):214-8. doi: 10.1038/ng0696-214. Nat Genet. 1996. PMID: 8640229

3

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.

4

A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis.

Gallagher PG, Ferreira JD, Costa FF, Saad ST, Forget BG. Gallagher PG, et al. Br J Haematol. 2000 Dec;111(4):1190-3. doi: 10.1046/j.1365-2141.2000.02441.x. Br J Haematol. 2000. PMID: 11167760 Free article.

5

Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expression.

Gallagher PG, Sabatino DE, Basseres DS, Nilson DM, Wong C, Cline AP, Garrett LJ, Bodine DM. Gallagher PG, et al. J Biol Chem. 2001 Nov 9;276(45):41683-9. doi: 10.1074/jbc.M105844200. Epub 2001 Aug 29. J Biol Chem. 2001. PMID: 11527968 Free article.

6

A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis.

Gallagher PG, Nilson DG, Wong C, Weisbein JL, Garrett-Beal LJ, Eber SW, Bodine DM. Gallagher PG, et al. Hum Mol Genet. 2005 Sep 1;14(17):2501-9. doi: 10.1093/hmg/ddi254. Epub 2005 Jul 21. Hum Mol Genet. 2005. PMID: 16037067 Free article.

7

Hematologically important mutations: ankyrin variants in hereditary spherocytosis.

Gallagher PG. Gallagher PG. Blood Cells Mol Dis. 2005 Nov-Dec;35(3):345-7. doi: 10.1016/j.bcmd.2005.08.008. Epub 2005 Oct 11. Blood Cells Mol Dis. 2005. PMID: 16223590

8

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis.

Edelman EJ, Maksimova Y, Duru F, Altay C, Gallagher PG. Edelman EJ, et al. Among authors: gallagher pg. Blood. 2007 Jun 15;109(12):5491-3. doi: 10.1182/blood-2006-09-046573. Epub 2007 Feb 27. Blood. 2007. PMID: 17327413 Free PMC article.

9

A decline in the frequency of neonatal exchange transfusions and its effect on exchange-related morbidity and mortality.

Steiner LA, Bizzarro MJ, Ehrenkranz RA, Gallagher PG. Steiner LA, et al. Among authors: gallagher pg. Pediatrics. 2007 Jul;120(1):27-32. doi: 10.1542/peds.2006-2910. Pediatrics. 2007. PMID: 17606558

10

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.

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