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Items: 1 to 20 of 51

1.

Views of parents of children with sickle cell disease on pre-implantation genetic diagnosis.

Darbari I, O'Brien JE, Hardy SJ, Speller-Brown B, Thaniel L, Martin B, Darbari DS, Nickel RS.

Pediatr Blood Cancer. 2018 Aug;65(8):e27102. doi: 10.1002/pbc.27102. Epub 2018 Apr 18.

PMID:
29667775
2.

Diverse manifestations of acute sickle cell hepatopathy in pediatric patients with sickle cell disease: A case series.

Pecker LH, Patel N, Creary S, Darbari A, Meier ER, Darbari DS, Fasano RM.

Pediatr Blood Cancer. 2018 Aug;65(8):e27060. doi: 10.1002/pbc.27060. Epub 2018 Apr 18.

PMID:
29667721
3.

Pain and opioid use after reversal of sickle cell disease following HLA-matched sibling haematopoietic stem cell transplant.

Darbari DS, Liljencrantz J, Ikechi A, Martin S, Roderick MC, Fitzhugh CD, Tisdale JF, Thein SL, Hsieh M.

Br J Haematol. 2018 Mar 12. doi: 10.1111/bjh.15169. [Epub ahead of print] No abstract available.

PMID:
29527656
4.

A phase 1 dose-finding study of intravenous L-citrulline in sickle cell disease: a potential novel therapy for sickle cell pain crisis.

Majumdar S, Tirona R, Mashegu H, Desai J, Shannon NT, Summar M, Cunningham G, Darbari D, Nickel R, Campbell A, Barr FE.

Br J Haematol. 2018 Feb 7. doi: 10.1111/bjh.15124. [Epub ahead of print] No abstract available.

PMID:
29411862
5.

Inhaled corticosteroid use to prevent severe vaso-occlusive episode recurrence in children between 1 and 4 years of age with sickle cell disease: a multicenter feasibility trial.

Vance Utset L, Ivy Z, Willen SM, Rodeghier M, Watt A, Schilling L, Jenkins CL, Pepper S, Speller-Brown B, Darbari DS, Majumdar S, Adisa O, DeBaun MR.

Am J Hematol. 2018 Aug;93(4):E101-E103. doi: 10.1002/ajh.25033. Epub 2018 Feb 5. No abstract available.

PMID:
29322539
6.

Pain-measurement tools in sickle cell disease: where are we now?

Darbari DS, Brandow AM.

Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):534-541. doi: 10.1182/asheducation-2017.1.534. Review.

PMID:
29222302
7.

Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia.

Darbari DS, Vaughan KJ, Roskom K, Seamon C, Diaw L, Quinn M, Conrey A, Schechter AN, Haythornthwaite JA, Waclawiw MA, Wallen GR, Belfer I, Taylor JG 6th.

Scand J Pain. 2017 Oct;17:279-286. doi: 10.1016/j.sjpain.2017.08.001. Epub 2017 Sep 30.

PMID:
28969994
8.

Determining the longitudinal validity and meaningful differences in HRQL of the PedsQLâ„¢ Sickle Cell Disease Module.

Panepinto JA, Paul Scott J, Badaki-Makun O, Darbari DS, Chumpitazi CE, Airewele GE, Ellison AM, Smith-Whitley K, Mahajan P, Sarnaik SA, Charles Casper T, Cook LJ, Leonard J, Hulbert ML, Powell EC, Liem RI, Hickey R, Krishnamurti L, Hillery CA, Brousseau DC; Pediatric Emergency Care Applied Research Network (PECARN).

Health Qual Life Outcomes. 2017 Jun 12;15(1):124. doi: 10.1186/s12955-017-0700-2.

9.

AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain.

Dampier C, Palermo TM, Darbari DS, Hassell K, Smith W, Zempsky W.

J Pain. 2017 May;18(5):490-498. doi: 10.1016/j.jpain.2016.12.016. Epub 2017 Jan 5.

10.

Hydroxyurea therapy in sickle cell disease: An alternative approach to preoperative red cell transfusion.

Okoye NC, Meier ER, Darbari DS.

J Natl Med Assoc. 2015 Jun;107(2):102-3. doi: 10.1016/S0027-9684(15)30031-6. Epub 2015 Dec 2. No abstract available.

PMID:
27269497
11.

Provider Perspective on Integrative Medicine for Pediatric Sickle Cell Disease-related Pain.

Neri CM, Beeson T, Mead H, Darbari DS, Meier ER.

Glob Adv Health Med. 2016 Jan;5(1):44-50. doi: 10.7453/gahmj.2015.101. Epub 2016 Jan 1.

12.

Frequency of Hospitalizations for Pain and Association With Altered Brain Network Connectivity in Sickle Cell Disease.

Darbari DS, Hampson JP, Ichesco E, Kadom N, Vezina G, Evangelou I, Clauw DJ, Taylor Vi JG, Harris RE.

J Pain. 2015 Nov;16(11):1077-86. doi: 10.1016/j.jpain.2015.07.005. Epub 2015 Aug 18.

13.

A multicenter randomized controlled trial of intravenous magnesium for sickle cell pain crisis in children.

Brousseau DC, Scott JP, Badaki-Makun O, Darbari DS, Chumpitazi CE, Airewele GE, Ellison AM, Smith-Whitley K, Mahajan P, Sarnaik SA, Casper TC, Cook LJ, Dean JM, Leonard J, Hulbert ML, Powell EC, Liem RI, Hickey R, Krishnamurti L, Hillery CA, Nimmer M, Panepinto JA; Pediatric Emergency Care Applied Research Network (PECARN).

Blood. 2015 Oct 1;126(14):1651-7. doi: 10.1182/blood-2015-05-647107. Epub 2015 Jul 31.

14.

Dexmedetomidine as an Adjuvant to Analgesic Strategy During Vaso-Occlusive Episodes in Adolescents with Sickle-Cell Disease.

Sheehy KA, Finkel JC, Darbari DS, Guerrera MF, Quezado ZM.

Pain Pract. 2015 Nov;15(8):E90-7. doi: 10.1111/papr.12336. Epub 2015 Jul 23.

15.

Measuring Transition Readiness: A Correlational Study of Perceptions of Parent and Adolescents and Young Adults with Sickle Cell Disease.

Speller-Brown B, Patterson Kelly K, VanGraafeiland B, Feetham S, Sill A, Darbari D, Meier ER.

J Pediatr Nurs. 2015 Sep-Oct;30(5):788-96. doi: 10.1016/j.pedn.2015.06.008. Epub 2015 Jul 18.

PMID:
26195300
16.

Effect of cytomegalovirus co-infection on normalization of selected T-cell subsets in children with perinatally acquired HIV infection treated with combination antiretroviral therapy.

Kapetanovic S, Aaron L, Montepiedra G, Anthony P, Thuvamontolrat K, Pahwa S, Burchett S, Weinberg A, Kovacs A; Pediatric AIDS Clinical Trials Group Protocol 366.

PLoS One. 2015 Mar 20;10(3):e0120474. doi: 10.1371/journal.pone.0120474. eCollection 2015.

17.

Inflammatory bowel disease in sickle cell disease: diagnostic and treatment challenges.

Azar JM, Darbari DS, Meier ER, Conklin LS, Darbari A.

J Pediatr Gastroenterol Nutr. 2014 Nov;59(5):e47. doi: 10.1097/MPG.0000000000000534. No abstract available.

PMID:
25347161
18.

Sleep disturbance, depression and pain in adults with sickle cell disease.

Wallen GR, Minniti CP, Krumlauf M, Eckes E, Allen D, Oguhebe A, Seamon C, Darbari DS, Hildesheim M, Yang L, Schulden JD, Kato GJ, Taylor JG 6th.

BMC Psychiatry. 2014 Jul 21;14:207. doi: 10.1186/1471-244X-14-207.

19.

Thinking beyond sickling to better understand pain in sickle cell disease.

Darbari DS, Ballas SK, Clauw DJ.

Eur J Haematol. 2014 Aug;93(2):89-95. doi: 10.1111/ejh.12340. Epub 2014 May 16. Review.

20.

Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia.

Darbari DS, Nouraie M, Taylor JG, Brugnara C, Castro O, Ballas SK.

Eur J Haematol. 2014 Apr;92(4):341-5. doi: 10.1111/ejh.12245. Epub 2014 Jan 30.

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