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Items: 1 to 50 of 247

1.

Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.

Bao EL, Lareau CA, Brugnara C, Fulcher IR, Barau C, Moutereau S, Habibi A, Badaoui B, Berkenou J, Bartolucci P, Galactéros F, Platt OS, Mahaney M, Sankaran VG.

Am J Hematol. 2019 Jan 25. doi: 10.1002/ajh.25421. [Epub ahead of print]

PMID:
30680775
2.

Shape oscillations of single blood drops: applications to human blood and sickle cell disease.

Hosseinzadeh VA, Brugnara C, Holt RG.

Sci Rep. 2018 Nov 14;8(1):16794. doi: 10.1038/s41598-018-34600-7.

3.

Resolution of sickle cell disease-associated inflammation and tissue damage with 17R-resolvin D1.

Matte A, Recchiuti A, Federti E, Koehl B, Mintz T, El Nemer W, Tharaux PL, Brousse V, Andolfo I, Lamolinara A, Weinberg O, Siciliano A, Norris PC, Riley IR, Iolascon A, Serhan CN, Brugnara C, De Franceschi L.

Blood. 2019 Jan 17;133(3):252-265. doi: 10.1182/blood-2018-07-865378. Epub 2018 Nov 7.

PMID:
30404812
4.

Erythrocytes lacking the Langereis blood group protein ABCB6 are resistant to the malaria parasite Plasmodium falciparum.

Egan ES, Weekes MP, Kanjee U, Manzo J, Srinivasan A, Lomas-Francis C, Westhoff C, Takahashi J, Tanaka M, Watanabe S, Brugnara C, Gygi SP, Tani Y, Duraisingh MT.

Commun Biol. 2018 May 3;1:45. doi: 10.1038/s42003-018-0046-2. eCollection 2018.

5.

Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.

Andolfo I, Russo R, Rosato BE, Manna F, Gambale A, Brugnara C, Iolascon A.

Am J Hematol. 2018 Dec;93(12):1509-1517. doi: 10.1002/ajh.25276. Epub 2018 Oct 2.

PMID:
30187933
6.

A common functional PIEZO1 deletion allele associates with red blood cell density in sickle cell disease patients.

Ilboudo Y, Bartolucci P, Garrett ME, Ashley-Koch A, Telen M, Brugnara C, Galactéros F, Lettre G.

Am J Hematol. 2018 Nov;93(11):E362-E365. doi: 10.1002/ajh.25245. Epub 2018 Sep 9. No abstract available.

PMID:
30105803
7.

Sickle cell dehydration: Pathophysiology and therapeutic applications.

Brugnara C.

Clin Hemorheol Microcirc. 2018;68(2-3):187-204. doi: 10.3233/CH-189007.

PMID:
29614632
8.

Positive Iron Balance in Chronic Kidney Disease: How Much is Too Much and How to Tell?

Wish JB, Aronoff GR, Bacon BR, Brugnara C, Eckardt KU, Ganz T, Macdougall IC, Núñez J, Perahia AJ, Wood JC.

Am J Nephrol. 2018;47(2):72-83. doi: 10.1159/000486968. Epub 2018 Feb 13.

9.

Iron balance and iron supplementation for the female athlete: A practical approach.

Pedlar CR, Brugnara C, Bruinvels G, Burden R.

Eur J Sport Sci. 2018 Mar;18(2):295-305. doi: 10.1080/17461391.2017.1416178. Epub 2017 Dec 27. Review.

PMID:
29280410
10.

Revised prevalence estimate of possible Hereditary Xerocytosis as derived from a large U.S. Laboratory database.

Kaufman HW, Niles JK, Gallagher DR, Rivera A, Alper SL, Brugnara C, Snyder LM.

Am J Hematol. 2018 Jan;93(1):E9-E12. doi: 10.1002/ajh.24923. Epub 2017 Nov 23. No abstract available.

11.

Automated cell counts on CSF samples: A multicenter performance evaluation of the GloCyte system.

Hod EA, Brugnara C, Pilichowska M, Sandhaus LM, Luu HS, Forest SK, Netterwald JC, Reynafarje GM, Kratz A.

Int J Lab Hematol. 2018 Feb;40(1):56-65. doi: 10.1111/ijlh.12728. Epub 2017 Sep 7.

PMID:
28880455
12.

Genome-wide association study of erythrocyte density in sickle cell disease patients.

Ilboudo Y, Bartolucci P, Rivera A, Sedzro JC, Beaudoin M, Trudel M, Alper SL, Brugnara C, Galactéros F, Lettre G.

Blood Cells Mol Dis. 2017 Jun;65:60-65. doi: 10.1016/j.bcmd.2017.05.005. Epub 2017 May 13.

PMID:
28552477
13.

Erythrocytes from hereditary xerocytosis patients heterozygous for KCNN4 V282M exhibit increased spontaneous Gardos channel-like activity inhibited by senicapoc.

Rivera A, Vandorpe DH, Shmukler BE, Gallagher DR, Fikry CC, Kuypers FA, Brugnara C, Snyder LM, Alper SL.

Am J Hematol. 2017 Jun;92(6):E108-E110. doi: 10.1002/ajh.24716. Epub 2017 Apr 29. No abstract available.

14.

Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci.

Canver MC, Lessard S, Pinello L, Wu Y, Ilboudo Y, Stern EN, Needleman AJ, Galactéros F, Brugnara C, Kutlar A, McKenzie C, Reid M, Chen DD, Das PP, A Cole M, Zeng J, Kurita R, Nakamura Y, Yuan GC, Lettre G, Bauer DE, Orkin SH.

Nat Genet. 2017 Apr;49(4):625-634. doi: 10.1038/ng.3793. Epub 2017 Feb 20.

15.

Diagnosis of iron deficiency anemia using density-based fractionation of red blood cells.

Hennek JW, Kumar AA, Wiltschko AB, Patton MR, Lee SY, Brugnara C, Adams RP, Whitesides GM.

Lab Chip. 2016 Oct 5;16(20):3929-3939.

PMID:
27713998
16.

Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia.

Andolfo I, Russo R, Manna F, De Rosa G, Gambale A, Zouwail S, Detta N, Pardo CL, Alper SL, Brugnara C, Sharma AK, De Franceschi L, Iolascon A.

Haematologica. 2016 Aug;101(8):909-17. doi: 10.3324/haematol.2016.142372. Epub 2016 May 5.

17.

Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells.

Giani FC, Fiorini C, Wakabayashi A, Ludwig LS, Salem RM, Jobaliya CD, Regan SN, Ulirsch JC, Liang G, Steinberg-Shemer O, Guo MH, Esko T, Tong W, Brugnara C, Hirschhorn JN, Weiss MJ, Zon LI, Chou ST, French DL, Musunuru K, Sankaran VG.

Cell Stem Cell. 2016 Jan 7;18(1):73-78. doi: 10.1016/j.stem.2015.09.015. Epub 2015 Oct 22.

18.

The American Journal of Hematology turns 40.

Brugnara C.

Am J Hematol. 2016 Jan;91(1):4. doi: 10.1002/ajh.24237. No abstract available.

19.

The Clinically Tested Gardos Channel Inhibitor Senicapoc Exhibits Antimalarial Activity.

Tubman VN, Mejia P, Shmukler BE, Bei AK, Alper SL, Mitchell JR, Brugnara C, Duraisingh MT.

Antimicrob Agents Chemother. 2015 Oct 12;60(1):613-6. doi: 10.1128/AAC.01668-15. Print 2016 Jan.

20.

Diagnosis of iron-deficient states.

Archer NM, Brugnara C.

Crit Rev Clin Lab Sci. 2015;52(5):256-72. doi: 10.3109/10408363.2015.1038744. Epub 2015 Aug 14. Review.

PMID:
26292073
21.

Diagnosis of iron-deficient states.

Archer NM, Brugnara C.

Crit Rev Clin Lab Sci. 2015 Aug 14:1-17. [Epub ahead of print]

PMID:
26274917
22.

Rapamycin improves TIE2-mutated venous malformation in murine model and human subjects.

Boscolo E, Limaye N, Huang L, Kang KT, Soblet J, Uebelhoer M, Mendola A, Natynki M, Seront E, Dupont S, Hammer J, Legrand C, Brugnara C, Eklund L, Vikkula M, Bischoff J, Boon LM.

J Clin Invest. 2015 Sep;125(9):3491-504. doi: 10.1172/JCI76004. Epub 2015 Aug 10.

23.

Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).

Andolfo I, Russo R, Manna F, Shmukler BE, Gambale A, Vitiello G, De Rosa G, Brugnara C, Alper SL, Snyder LM, Iolascon A.

Am J Hematol. 2015 Oct;90(10):921-6. doi: 10.1002/ajh.24117.

24.

2015 Clinical trials update in sickle cell anemia.

Archer N, Galacteros F, Brugnara C.

Am J Hematol. 2015 Oct;90(10):934-50. doi: 10.1002/ajh.24116. Review.

25.

Malaria. A forward genetic screen identifies erythrocyte CD55 as essential for Plasmodium falciparum invasion.

Egan ES, Jiang RH, Moechtar MA, Barteneva NS, Weekes MP, Nobre LV, Gygi SP, Paulo JA, Frantzreb C, Tani Y, Takahashi J, Watanabe S, Goldberg J, Paul AS, Brugnara C, Root DE, Wiegand RC, Doench JG, Duraisingh MT.

Science. 2015 May 8;348(6235):711-4. doi: 10.1126/science.aaa3526.

26.

Dietary ω-3 fatty acids protect against vasculopathy in a transgenic mouse model of sickle cell disease.

Kalish BT, Matte A, Andolfo I, Iolascon A, Weinberg O, Ghigo A, Cimino J, Siciliano A, Hirsch E, Federti E, Puder M, Brugnara C, De Franceschi L.

Haematologica. 2015 Jul;100(7):870-80. doi: 10.3324/haematol.2015.124586. Epub 2015 May 1.

27.

The utility of the DDAVP challenge test in children with low von Willebrand factor.

Archer NM, Samnaliev M, Grace R, Brugnara C.

Br J Haematol. 2015 Sep;170(6):884-6. doi: 10.1111/bjh.13331. Epub 2015 Mar 2. No abstract available.

28.

Automated hematology analyzers: state of the art.

Kratz A, Brugnara C.

Clin Lab Med. 2015 Mar;35(1):xiii-xiv. doi: 10.1016/j.cll.2014.11.004. Epub 2014 Nov 28. No abstract available.

PMID:
25676382
29.

Clinical utility of reticulocyte parameters.

Piva E, Brugnara C, Spolaore F, Plebani M.

Clin Lab Med. 2015 Mar;35(1):133-63. doi: 10.1016/j.cll.2014.10.004. Epub 2014 Nov 26. Review.

PMID:
25676377
30.

Reductions in red blood cell 2,3-diphosphoglycerate concentration during continuous renal replacment therapy.

Sharma S, Brugnara C, Betensky RA, Waikar SS.

Clin J Am Soc Nephrol. 2015 Jan 7;10(1):74-9. doi: 10.2215/CJN.02160214. Epub 2014 Dec 23.

31.

Evaluation of a density-based rapid diagnostic test for sickle cell disease in a clinical setting in Zambia.

Kumar AA, Chunda-Liyoka C, Hennek JW, Mantina H, Lee SY, Patton MR, Sambo P, Sinyangwe S, Kankasa C, Chintu C, Brugnara C, Stossel TP, Whitesides GM.

PLoS One. 2014 Dec 9;9(12):e114540. doi: 10.1371/journal.pone.0114540. eCollection 2014.

32.

American Journal of Hematology, getting ready for the 40th birthday in 2016.

Brugnara C.

Am J Hematol. 2015 Jan;90(1):1. doi: 10.1002/ajh.23906. No abstract available.

33.

Density-based separation in multiphase systems provides a simple method to identify sickle cell disease.

Kumar AA, Patton MR, Hennek JW, Lee SY, D'Alesio-Spina G, Yang X, Kanter J, Shevkoplyas SS, Brugnara C, Whitesides GM.

Proc Natl Acad Sci U S A. 2014 Oct 14;111(41):14864-9. doi: 10.1073/pnas.1414739111. Epub 2014 Sep 2.

34.

Optical assay of erythrocyte function in banked blood.

Bhaduri B, Kandel M, Brugnara C, Tangella K, Popescu G.

Sci Rep. 2014 Sep 5;4:6211. doi: 10.1038/srep06211.

35.

Aging-like phenotype and defective lineage specification in SIRT1-deleted hematopoietic stem and progenitor cells.

Rimmelé P, Bigarella CL, Liang R, Izac B, Dieguez-Gonzalez R, Barbet G, Donovan M, Brugnara C, Blander JM, Sinclair DA, Ghaffari S.

Stem Cell Reports. 2014 Jun 6;3(1):44-59. doi: 10.1016/j.stemcr.2014.04.015. eCollection 2014 Jul 8.

36.

Hereditary xerocytosis revisited.

Archer NM, Shmukler BE, Andolfo I, Vandorpe DH, Gnanasambandam R, Higgins JM, Rivera A, Fleming MD, Sachs F, Gottlieb PA, Iolascon A, Brugnara C, Alper SL, Nathan DG.

Am J Hematol. 2014 Dec;89(12):1142-6. doi: 10.1002/ajh.23799. Epub 2014 Jul 21. No abstract available.

37.

FOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis.

Zhang X, Campreciós G, Rimmelé P, Liang R, Yalcin S, Mungamuri SK, Barminko J, D'Escamard V, Baron MH, Brugnara C, Papatsenko D, Rivella S, Ghaffari S.

Am J Hematol. 2014 Oct;89(10):954-63. doi: 10.1002/ajh.23786. Epub 2014 Jul 22.

38.

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.

39.

Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice.

Franco SS, De Falco L, Ghaffari S, Brugnara C, Sinclair DA, Matte' A, Iolascon A, Mohandas N, Bertoldi M, An X, Siciliano A, Rimmelé P, Cappellini MD, Michan S, Zoratti E, Anne J, De Franceschi L.

Haematologica. 2014 Feb;99(2):267-75. doi: 10.3324/haematol.2013.090076. Epub 2013 Aug 23.

40.

Dehydrated stomatocytic anemia due to the heterozygous mutation R2456H in the mechanosensitive cation channel PIEZO1: a case report.

Shmukler BE, Vandorpe DH, Rivera A, Auerbach M, Brugnara C, Alper SL.

Blood Cells Mol Dis. 2014 Jan;52(1):53-4. doi: 10.1016/j.bcmd.2013.07.015. Epub 2013 Aug 23. No abstract available.

PMID:
23973043
41.

Expansion of host cellular niche can drive adaptation of a zoonotic malaria parasite to humans.

Lim C, Hansen E, DeSimone TM, Moreno Y, Junker K, Bei A, Brugnara C, Buckee CO, Duraisingh MT.

Nat Commun. 2013;4:1638. doi: 10.1038/ncomms2612.

42.

Strain-specific variations in cation content and transport in mouse erythrocytes.

Rivera A, Zee RY, Alper SL, Peters LL, Brugnara C.

Physiol Genomics. 2013 May 1;45(9):343-50. doi: 10.1152/physiolgenomics.00143.2012. Epub 2013 Mar 12.

43.

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

Andolfo I, Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A.

Blood. 2013 May 9;121(19):3925-35, S1-12. doi: 10.1182/blood-2013-02-482489. Epub 2013 Mar 11.

44.

Red cell indices in classification and treatment of anemias: from M.M. Wintrobes's original 1934 classification to the third millennium.

Brugnara C, Mohandas N.

Curr Opin Hematol. 2013 May;20(3):222-30. doi: 10.1097/MOH.0b013e32835f5933. Review.

PMID:
23449069
45.

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

Andolfo I, Alper SL, Delaunay J, Auriemma C, Russo R, Asci R, Esposito MR, Sharma AK, Shmukler BE, Brugnara C, De Franceschi L, Iolascon A.

Am J Hematol. 2013 Jan;88(1):66-72. doi: 10.1002/ajh.23357. Epub 2012 Nov 24.

46.

Iron deficiency: what are the future trends in diagnostics and therapeutics?

Brugnara C, Adamson J, Auerbach M, Kane R, Macdougall I, Mast A.

Clin Chem. 2013 May;59(5):740-5. doi: 10.1373/clinchem.2012.182071. Epub 2012 Nov 13. No abstract available.

47.

Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts.

Shah DI, Takahashi-Makise N, Cooney JD, Li L, Schultz IJ, Pierce EL, Narla A, Seguin A, Hattangadi SM, Medlock AE, Langer NB, Dailey TA, Hurst SN, Faccenda D, Wiwczar JM, Heggers SK, Vogin G, Chen W, Chen C, Campagna DR, Brugnara C, Zhou Y, Ebert BL, Danial NN, Fleming MD, Ward DM, Campanella M, Dailey HA, Kaplan J, Paw BH.

Nature. 2012 Nov 22;491(7425):608-12. doi: 10.1038/nature11536. Epub 2012 Nov 7. Erratum in: Nature. 2013 Apr 18;496(7445):386.

48.

Pharmacological inhibition of calpain-1 prevents red cell dehydration and reduces Gardos channel activity in a mouse model of sickle cell disease.

De Franceschi L, Franco RS, Bertoldi M, Brugnara C, Matté A, Siciliano A, Wieschhaus AJ, Chishti AH, Joiner CH.

FASEB J. 2013 Feb;27(2):750-9. doi: 10.1096/fj.12-217836. Epub 2012 Oct 19.

49.

Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis.

Bartolucci P, Brugnara C, Teixeira-Pinto A, Pissard S, Moradkhani K, Jouault H, Galacteros F.

Blood. 2012 Oct 11;120(15):3136-41. doi: 10.1182/blood-2012-04-424184. Epub 2012 Aug 23. Erratum in: Blood. 2014 Mar 20;123(12):1972.

50.

Calpain-1 knockout reveals broad effects on erythrocyte deformability and physiology.

Wieschhaus A, Khan A, Zaidi A, Rogalin H, Hanada T, Liu F, De Franceschi L, Brugnara C, Rivera A, Chishti AH.

Biochem J. 2012 Nov 15;448(1):141-52. doi: 10.1042/BJ20121008.

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