Estepp JH - Search Results

1

Pharmacogenetics for Safe Codeine Use in Sickle Cell Disease.

Gammal RS, Crews KR, Haidar CE, Hoffman JM, Baker DK, Barker PJ, Estepp JH, Pei D, Broeckel U, Wang W, Weiss MJ, Relling MV, Hankins J. Gammal RS, et al. Among authors: estepp jh. Pediatrics. 2016 Jul;138(1):e20153479. doi: 10.1542/peds.2015-3479. Pediatrics. 2016. PMID: 27335380 Free PMC article.

2

Protection from sickle cell retinopathy is associated with elevated HbF levels and hydroxycarbamide use in children.

Estepp JH, Smeltzer MP, Wang WC, Hoehn ME, Hankins JS, Aygun B. Estepp JH, et al. Br J Haematol. 2013 May;161(3):402-5. doi: 10.1111/bjh.12238. Epub 2013 Feb 6. Br J Haematol. 2013. PMID: 23384083 Free article.

3

Improved hydroxyurea effect with the use of text messaging in children with sickle cell anemia.

Estepp JH, Winter B, Johnson M, Smeltzer MP, Howard SC, Hankins JS. Estepp JH, et al. Pediatr Blood Cancer. 2014 Nov;61(11):2031-6. doi: 10.1002/pbc.25177. Epub 2014 Aug 17. Pediatr Blood Cancer. 2014. PMID: 25132074

4

MAGiC: VOC remains but kids with SCA appear.

Estepp JH. Estepp JH. Blood. 2015 Oct 1;126(14):1637-8. doi: 10.1182/blood-2015-08-662502. Blood. 2015. PMID: 26429963 Free article.

5

The clinical severity of hemoglobin S/Black (^A γδβ)⁰ -thalassemia.

Cancio MI, Aygun B, Chui DHK, Rothman JA, Scott JP, Estepp JH, Hankins JS. Cancio MI, et al. Among authors: estepp jh. Pediatr Blood Cancer. 2017 Nov;64(11):10.1002/pbc.26596. doi: 10.1002/pbc.26596. Epub 2017 Apr 28. Pediatr Blood Cancer. 2017. PMID: 28453928 Free PMC article.

6

A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapy.

Estepp JH, Smeltzer MP, Kang G, Li C, Wang WC, Abrams C, Aygun B, Ware RE, Nottage K, Hankins JS. Estepp JH, et al. Am J Hematol. 2017 Dec;92(12):1333-1339. doi: 10.1002/ajh.24906. Epub 2017 Sep 28. Am J Hematol. 2017. PMID: 28913922 Free PMC article.

7

Sickle Cell Clinical Research and Intervention Program (SCCRIP): A lifespan cohort study for sickle cell disease progression from the pediatric stage into adulthood.

Hankins JS, Estepp JH, Hodges JR, Villavicencio MA, Robison LL, Weiss MJ, Kang G, Schreiber JE, Porter JS, Kaste SC, Saving KL, Bryant PC, Deyo JE, Nottage KA, King AA, Brandow AM, Lebensburger JD, Adesina O, Chou ST, Zemel BS, Smeltzer MP, Wang WC, Gurney JG. Hankins JS, et al. Among authors: estepp jh. Pediatr Blood Cancer. 2018 Sep;65(9):e27228. doi: 10.1002/pbc.27228. Epub 2018 May 24. Pediatr Blood Cancer. 2018. PMID: 29797644

8

Vaso-occlusive crisis as a predictor of symptomatic avascular necrosis in children with sickle cell disease.

Mesleh Shayeb A, Smeltzer MP, Kaste SC, Brown A, Estepp JH, Nottage KA. Mesleh Shayeb A, et al. Among authors: estepp jh. Pediatr Blood Cancer. 2018 Dec;65(12):e27435. doi: 10.1002/pbc.27435. Epub 2018 Sep 5. Pediatr Blood Cancer. 2018. PMID: 30183122

9

Hydroxyurea prevents onset and progression of albuminuria in children with sickle cell anemia.

Zahr RS, Hankins JS, Kang G, Li C, Wang WC, Lebensburger J, Estepp JH. Zahr RS, et al. Among authors: estepp jh. Am J Hematol. 2019 Jan;94(1):E27-E29. doi: 10.1002/ajh.25329. Epub 2018 Nov 29. Am J Hematol. 2019. PMID: 30359463 Free PMC article. No abstract available.

10

Complexities of genetic diagnosis illustrated by an atypical case of congenital hypoplastic anemia.

Claassen D, Boals M, Bowling KM, Cooper GM, Cox J, Hershfield M, Lewis S, Wlodarski M, Weiss MJ, Estepp JH. Claassen D, et al. Among authors: estepp jh. Cold Spring Harb Mol Case Stud. 2018 Dec 17;4(6):a003384. doi: 10.1101/mcs.a003384. Print 2018 Dec. Cold Spring Harb Mol Case Stud. 2018. PMID: 30559313 Free PMC article.

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