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Items: 1 to 20 of 30

1.

Variation in Gamma-Globin Expression before and after Induction with Hydroxyurea Associated with BCL11A, KLF1 and TAL1.

Grieco AJ, Billett HH, Green NS, Driscoll MC, Bouhassira EE.

PLoS One. 2015 Jun 8;10(6):e0129431. doi: 10.1371/journal.pone.0129431. eCollection 2015.

2.

Parental and other factors associated with hydroxyurea use for pediatric sickle cell disease.

Oyeku SO, Driscoll MC, Cohen HW, Trachtman R, Pashankar F, Mullen C, Giardina PJ, Velazco N, Racine AD, Green NS.

Pediatr Blood Cancer. 2013 Apr;60(4):653-8. doi: 10.1002/pbc.24381. Epub 2012 Nov 5.

3.

Comparison of hematologic measurements between local and central laboratories: data from the BABY HUG trial.

Kalpatthi R, Thompson B, Lu M, Wang WC, Patel N, Kutlar A, Howard T, Luchtman-Jones L, Miller ST; BABY HUG Investigators.

Clin Biochem. 2013 Feb;46(3):278-81. doi: 10.1016/j.clinbiochem.2012.10.032. Epub 2012 Oct 31.

4.

Increased prevalence of osteonecrosis of the femoral head in children and adolescents with sickle-cell disease.

Mahadeo KM, Oyeku S, Taragin B, Rajpathak SN, Moody K, Santizo R, Driscoll MC.

Am J Hematol. 2011 Sep;86(9):806-8. doi: 10.1002/ajh.22103. No abstract available.

5.

Biomarkers of splenic function in infants with sickle cell anemia: baseline data from the BABY HUG Trial.

Rogers ZR, Wang WC, Luo Z, Iyer RV, Shalaby-Rana E, Dertinger SD, Shulkin BL, Miller JH, Files B, Lane PA, Thompson BW, Miller ST, Ware RE; BABY HUG.

Blood. 2011 Mar 3;117(9):2614-7. doi: 10.1182/blood-2010-04-278747. Epub 2011 Jan 7.

6.

Multiagent induction and maintenance therapy for patients with refractory immune thrombocytopenic purpura (ITP).

Boruchov DM, Gururangan S, Driscoll MC, Bussel JB.

Blood. 2007 Nov 15;110(10):3526-31. Epub 2007 Aug 13.

7.

Sickle cell disease.

Driscoll MC.

Pediatr Rev. 2007 Jul;28(7):259-68. Review. No abstract available.

PMID:
17601938
8.

Hydroxyurea therapy lowers TCD velocities in children with sickle cell disease.

Kratovil T, Bulas D, Driscoll MC, Speller-Brown B, McCarter R, Minniti CP.

Pediatr Blood Cancer. 2006 Dec;47(7):894-900.

PMID:
16526051
9.

Transcranial Doppler Changes in Children With Sickle Cell Disease on Transfusion Therapy.

Minniti CP, Gidvani VK, Bulas D, Brown WA, Vezina G, Driscoll MC.

J Pediatr Hematol Oncol. 2004 Oct;26(10):626-630.

PMID:
27811602
10.

Transcranial Doppler changes in children with sickle cell disease on transfusion therapy.

Minniti CP, Gidvani VK, Bulas D, Brown WA, Vezina G, Driscoll MC.

J Pediatr Hematol Oncol. 2004 Oct;26(10):626-30.

PMID:
15454832
11.

Pseudotumor cerebri in children with sickle cell disease: a case series.

Henry M, Driscoll MC, Miller M, Chang T, Minniti CP.

Pediatrics. 2004 Mar;113(3 Pt 1):e265-9.

PMID:
14993587
12.

Stroke risk in siblings with sickle cell anemia.

Driscoll MC, Hurlet A, Styles L, McKie V, Files B, Olivieri N, Pegelow C, Berman B, Drachtman R, Patel K, Brambilla D.

Blood. 2003 Mar 15;101(6):2401-4.

13.

Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control study.

Tang DC, Prauner R, Liu W, Kim KH, Hirsch RP, Driscoll MC, Rodgers GP.

Am J Hematol. 2001 Nov;68(3):164-9.

PMID:
11754397
14.

The methylenetetrahydrofolate reductase gene C677T mutant and ischemic stroke in sickle cell disease.

Driscoll MC, Prauner R.

Thromb Haemost. 1999 Dec;82(6):1780-1. No abstract available.

PMID:
10613678
15.
16.

Heteroduplex analysis in hemophilia B: detection of two novel factor IX gene mutations.

Driscoll MC, Chu A, Hilgartner MW.

Am J Hematol. 1996 Apr;51(4):324-7.

17.

Polymerase chain reaction detection of the Dde I polymorphism in the factor 9 gene for fragile X linkage analysis.

Dobkin CS, Driscoll MC, Ferrando C.

Am J Med Genet. 1991 Feb-Mar;38(2-3):378-9.

PMID:
2018077
18.

A deletion of the human beta-globin locus activation region causes a major alteration in chromatin structure and replication across the entire beta-globin locus.

Forrester WC, Epner E, Driscoll MC, Enver T, Brice M, Papayannopoulou T, Groudine M.

Genes Dev. 1990 Oct;4(10):1637-49.

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