Philippa G Sprinz
Overview
Explore the profile of Philippa G Sprinz including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
257
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Recent Articles
1.
MacDonell-Yilmaz R, Sampino E, Moynihan L, Chang W, Sprinz P
J Pediatr Hematol Oncol
. 2023 Jul;
45(6):e764-e767.
PMID: 37494613
Background: Therapy options for relapsed/refractory acute myelogenous leukemia (AML) are limited. Palliative chemotherapy options have been explored in adult patients, but little evidence exists in children. Objectives: Describe the clinical...
2.
3.
Gale H, Bobbitt C, Setty B, Sprinz P, Doros G, Williams D, et al.
J Ultrasound Med
. 2016 Jun;
35(8):1735-45.
PMID: 27353067
Objectives: To update the imaging literature regarding spleen appearances in young patients with sickle cell disease (SCD). Methods: We conducted a retrospective study and included 112 patients age 0 to...
4.
Kavanagh P, Sprinz P, Wolfgang T, Killius K, Champigny M, Sobota A, et al.
Pediatrics
. 2015 Sep;
136(4):e1016-25.
PMID: 26391933
Objectives: Vaso-occlusive episodes (VOEs) account for the majority of emergency department (ED) visits for children with sickle cell disease (SCD). We hypothesized that addressing key barriers to VOE care would...
5.
Gale H, Setty B, Sprinz P, Doros G, Williams D, Morrison T, et al.
Emerg Radiol
. 2015 Jun;
22(5):543-51.
PMID: 26109240
The purpose of this study is to describe gallbladder imaging findings in patients with sickle cell disease, and to determine how they correspond with occurrence of complications, need for cholecystectomy,...
6.
Sobota A, Kavanagh P, Adams W, McClure E, Farrell D, Sprinz P
Pediatr Blood Cancer
. 2014 Dec;
62(4):654-7.
PMID: 25545967
Background: Children with sickle cell disease (SCD) are at increased risk of complications from influenza. However, despite widespread recommendations that these patients receive an annual influenza immunization, reported vaccination rates...
7.
Chawla A, Sprinz P, Welch J, Heeney M, Usmani N, Pashankar F, et al.
Pediatrics
. 2013 Mar;
131(4):e1168-73.
PMID: 23460681
Objective: Historically, many children and adolescents with sickle cell disease (SCD) were underweight. Treatment advances like hydroxyurea have been associated with improved growth. We hypothesized that increased hemoglobin (Hb) levels...
8.
Kavanagh P, Sprinz P, Vinci S, Bauchner H, Wang C
Pediatrics
. 2011 Nov;
128(6):e1552-74.
PMID: 22123880
Objective: Sickle cell disease (SCD) affects 70 000 to 100 000 people in the United States, and 2000 infants are born with the disease each year. The purpose of this...
9.
Wang C, Kavanagh P, Little A, Holliman J, Sprinz P
Pediatrics
. 2011 Aug;
128(3):484-93.
PMID: 21844055
Objective: To develop a set of quality-of-care indicators for the management of children with sickle cell disease (SCD) who are cared for in a variety of settings by addressing the...
10.
Amendah D, Mvundura M, Kavanagh P, Sprinz P, Grosse S
Am J Prev Med
. 2010 Mar;
38(4 Suppl):S550-6.
PMID: 20331957
Background: Although it is known that people with sickle cell disease (SCD) have relatively high utilization of medical care, most previous estimates of SCD-attributable expenditures have been limited to either...