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Items: 29

1.

Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.

Bianchi P, Fermo E, Lezon-Geyda K, van Beers EJ, Morton HD, Barcellini W, Glader B, Chonat S, Ravindranath Y, Newburger PE, Kollmar N, Despotovic JM, Verhovsek M, Sharma M, Kwiatkowski JL, Kuo KHM, Wlodarski MW, Yaish HM, Holzhauer S, Wang H, Kunz J, Addonizio K, Al-Sayegh H, London WB, Andres O, van Wijk R, Gallagher PG, Grace RFF.

Am J Hematol. 2020 Feb 11. doi: 10.1002/ajh.25753. [Epub ahead of print]

PMID:
32043619
2.

Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal.

Thein SL, Pirenne F, Fasano RM, Habibi A, Bartolucci P, Chonat S, Hendrickson JE, Stowell SR.

Haematologica. 2020 Mar;105(3):539-544. doi: 10.3324/haematol.2019.224709. Epub 2020 Feb 6. No abstract available.

3.

Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis.

Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA.

Front Physiol. 2019 Oct 18;10:1331. doi: 10.3389/fphys.2019.01331. eCollection 2019.

4.

Examining the Role of Complement in Predicting, Preventing, and Treating Hemolytic Transfusion Reactions.

Arthur CM, Chonat S, Fasano R, Yee MEM, Josephson CD, Roback JD, Stowell SR.

Transfus Med Rev. 2019 Oct;33(4):217-224. doi: 10.1016/j.tmrv.2019.09.006. Epub 2019 Oct 18. Review.

PMID:
31679762
5.

Complement Mediated Hemolytic Anemia Secondary to Plasmodium ovale Infection in a Child.

Graciaa S, Russell R, Chonat S.

J Pediatr Hematol Oncol. 2019 Oct;41(7):557-558. doi: 10.1097/MPH.0000000000001584. No abstract available.

PMID:
31589179
6.

The Spectrum of SPTA1-Associated Hereditary Spherocytosis.

Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA.

Front Physiol. 2019 Jul 3;10:815. doi: 10.3389/fphys.2019.00815. eCollection 2019. Erratum in: Front Physiol. 2019 Oct 18;10:1331.

7.

Challenges in preventing and treating hemolytic complications associated with red blood cell transfusion.

Chonat S, Arthur CM, Zerra PE, Maier CL, Jajosky RP, Yee MEM, Miller MJ, Josephson CD, Roback JD, Fasano R, Stowell SR.

Transfus Clin Biol. 2019 May;26(2):130-134. doi: 10.1016/j.tracli.2019.03.002. Epub 2019 Mar 25. Review.

PMID:
30979566
8.

Challenges in the treatment and prevention of delayed hemolytic transfusion reactions with hyperhemolysis in sickle cell disease patients.

Dean CL, Maier CL, Chonat S, Chang A, Carden MA, El Rassi F, McLemore ML, Stowell SR, Fasano RM.

Transfusion. 2019 May;59(5):1698-1705. doi: 10.1111/trf.15227. Epub 2019 Mar 8.

PMID:
30848512
9.

Clinical presentation of delayed hemolytic transfusion reactions and hyperhemolysis in sickle cell disease.

Fasano RM, Miller MJ, Chonat S, Stowell SR.

Transfus Clin Biol. 2019 May;26(2):94-98. doi: 10.1016/j.tracli.2019.02.002. Epub 2019 Feb 22. Review.

PMID:
30837199
10.

Marginal Zone B Cells Induce Alloantibody Formation Following RBC Transfusion.

Patel SR, Gibb DR, Girard-Pierce K, Zhou X, Rodrigues LC, Arthur CM, Bennett AL, Jajosky RP, Fuller M, Maier CL, Zerra PE, Chonat S, Smith NH, Tormey CA, Hendrickson JE, Stowell SR.

Front Immunol. 2018 Nov 16;9:2516. doi: 10.3389/fimmu.2018.02516. eCollection 2018.

11.

Complement serves as a switch between CD4+ T cell-independent and -dependent RBC antibody responses.

Mener A, Patel SR, Arthur CM, Chonat S, Wieland A, Santhanakrishnan M, Liu J, Maier CL, Jajosky RP, Girard-Pierce K, Bennett A, Zerra PE, Smith NH, Hendrickson JE, Stowell SR.

JCI Insight. 2018 Nov 15;3(22). pii: 121631. doi: 10.1172/jci.insight.121631.

12.

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study.

van Beers EJ, van Straaten S, Morton DH, Barcellini W, Eber SW, Glader B, Yaish HM, Chonat S, Kwiatkowski JL, Rothman JA, Sharma M, Neufeld EJ, Sheth S, Despotovic JM, Kollmar N, Pospíšilová D, Knoll CM, Kuo K, Pastore YD, Thompson AA, Newburger PE, Ravindranath Y, Wang WC, Wlodarski MW, Wang H, Holzhauer S, Breakey VR, Verhovsek M, Kunz J, McNaull MA, Rose MJ, Bradeen HA, Addonizio K, Li A, Al-Sayegh H, London WB, Grace RF.

Haematologica. 2019 Feb;104(2):e51-e53. doi: 10.3324/haematol.2018.196295. Epub 2018 Sep 13. No abstract available.

13.

Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease.

Chonat S, Quarmyne MO, Bennett CM, Dean CL, Joiner CH, Fasano RM, Stowell SR.

Haematologica. 2018 Oct;103(10):e483-e485. doi: 10.3324/haematol.2018.194670. Epub 2018 May 24. No abstract available.

14.

Congenital dyserythropoietic anaemia type I diagnosed in a young adult with a history of splenectomy in childhood for presumed haemolytic anaemia.

Chonat S, McLemore ML, Bunting ST, Nortman S, Zhang K, Kalfa TA.

Br J Haematol. 2018 Jul;182(1):10. doi: 10.1111/bjh.15217. Epub 2018 Apr 20. No abstract available.

PMID:
29676459
15.

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.

Grace RF, Bianchi P, van Beers EJ, Eber SW, Glader B, Yaish HM, Despotovic JM, Rothman JA, Sharma M, McNaull MM, Fermo E, Lezon-Geyda K, Morton DH, Neufeld EJ, Chonat S, Kollmar N, Knoll CM, Kuo K, Kwiatkowski JL, Pospíšilová D, Pastore YD, Thompson AA, Newburger PE, Ravindranath Y, Wang WC, Wlodarski MW, Wang H, Holzhauer S, Breakey VR, Kunz J, Sheth S, Rose MJ, Bradeen HA, Neu N, Guo D, Al-Sayegh H, London WB, Gallagher PG, Zanella A, Barcellini W.

Blood. 2018 May 17;131(20):2183-2192. doi: 10.1182/blood-2017-10-810796. Epub 2018 Mar 16.

PMID:
29549173
16.

Transfusion-transmitted malaria masquerading as sickle cell crisis with multisystem organ failure.

Maier CL, Gross PJ, Dean CL, Chonat S, Ip A, McLemore M, El Rassi F, Stowell SR, Josephson CD, Fasano RM.

Transfusion. 2018 Jun;58(6):1550-1554. doi: 10.1111/trf.14566. Epub 2018 Mar 9.

PMID:
29524230
17.

Recipient priming to one RBC alloantigen directly enhances subsequent alloimmunization in mice.

Patel SR, Bennett A, Girard-Pierce K, Maier CL, Chonat S, Arthur CM, Zerra PE, Mener A, Stowell SR.

Blood Adv. 2018 Jan 23;2(2):105-115. doi: 10.1182/bloodadvances.2017010124.

18.

Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients.

Lesmana H, Dyer L, Li X, Denton J, Griffiths J, Chonat S, Seu KG, Heeney MM, Zhang K, Hopkin RJ, Kalfa TA.

Hum Mutat. 2018 Mar;39(3):389-393. doi: 10.1002/humu.23392. Epub 2018 Jan 11.

19.

Hereditary xerocytosis: Diagnostic considerations.

Risinger M, Glogowska E, Chonat S, Zhang K, Dagaonkar N, Joiner CH, Quinn CT, Kalfa TA, Gallagher PG.

Am J Hematol. 2018 Mar;93(3):E67-E69. doi: 10.1002/ajh.24996. Epub 2017 Dec 23. No abstract available.

20.

Current Standards of Care and Long Term Outcomes for Thalassemia and Sickle Cell Disease.

Chonat S, Quinn CT.

Adv Exp Med Biol. 2017;1013:59-87. doi: 10.1007/978-1-4939-7299-9_3. Review.

21.

Extracellular fluid tonicity impacts sickle red blood cell deformability and adhesion.

Carden MA, Fay ME, Lu X, Mannino RG, Sakurai Y, Ciciliano JC, Hansen CE, Chonat S, Joiner CH, Wood DK, Lam WA.

Blood. 2017 Dec 14;130(24):2654-2663. doi: 10.1182/blood-2017-04-780635. Epub 2017 Oct 4.

22.

Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab.

Chonat S, Chandrakasan S, Kalinyak KA, Ingala D, Gruppo R, Kalfa TA.

Br J Haematol. 2016 Nov;175(4):744-747. doi: 10.1111/bjh.13884. Epub 2015 Dec 21. No abstract available.

23.

Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.

Niss O, Chonat S, Dagaonkar N, Almansoori MO, Kerr K, Rogers ZR, McGann PT, Quarmyne MO, Risinger M, Zhang K, Kalfa TA.

Blood Cells Mol Dis. 2016 Oct;61:4-9. doi: 10.1016/j.bcmd.2016.07.003. Epub 2016 Jul 17.

24.

Absent left common and left external iliac artery presenting in a neonate.

Patel M, Chonat S, Olomu I, Arrington S, Kadrofske M.

J Perinatol. 2013 May;33(5):407-9. doi: 10.1038/jp.2012.132. No abstract available.

PMID:
23624970
25.

Cutaneous lesions in transient abnormal myelopoiesis.

Winckworth LC, Chonat S, Uthaya S.

J Paediatr Child Health. 2012 Feb;48(2):184-5. doi: 10.1111/j.1440-1754.2011.02407.x. No abstract available.

PMID:
22320276
26.

Co-occurrence of Chiari malformations and sickle cell disease-a diagnostic dilemma: a report of 4 cases and review of literature.

Chonat S, Saah E, Gera R, Scott-Emuakpor A, Kulkarni R.

J Pediatr Hematol Oncol. 2011 Dec;33(8):624-5. doi: 10.1097/MPH.0b013e3182346ec3. Review.

PMID:
22042280
27.

Nutritional outcomes in surgical neonates after hospital discharge.

Winckworth LC, Chonat S, Chuang SL.

Pediatr Surg Int. 2011 May;27(5):553-4. doi: 10.1007/s00383-011-2893-5. Epub 2011 Mar 27. No abstract available.

PMID:
21442424
28.

Use of premedication for intubation in tertiary neonatal units in the United Kingdom.

Chaudhary R, Chonat S, Gowda H, Clarke P, Curley A.

Paediatr Anaesth. 2009 Jul;19(7):653-8. doi: 10.1111/j.1460-9592.2008.02829.x. Epub 2009 May 15.

PMID:
19490437
29.

Variations in practice among paediatric consultants when referring unexpected neonatal deaths to a coroner.

Chonat S, Lakshman R, Clements M, Iles R.

Arch Dis Child Fetal Neonatal Ed. 2007 May;92(3):F234. No abstract available.

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