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Items: 7

1.

Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis.

Huisjes R, Makhro A, Llaudet-Planas E, Hertz L, Petkova-Kirova P, Verhagen LP, Pignatelli S, Rab MAE, Schiffelers RM, Seiler E, van Solinge WW, Corrons JV, Kaestner L, Mañú-Pereira M, Bogdanov A, van Wijk R.

Haematologica. 2020 Jan 31;105(2):338-347. doi: 10.3324/haematol.2018.188151. Print 2020.

2.

A Previously Unrecognized Ca2+-inhibited Nonselective Cation Channel in Red Blood Cells.

Petkova-Kirova P, Hertz L, Makhro A, Danielczok J, Huisjes R, Llaudet-Planas E, Mañú-Pereira MDM, Vives Corrons JL, van Wijk R, Bogdanova A, Kaestner L.

Hemasphere. 2018 Oct;2(5):e146. doi: 10.1097/HS9.0000000000000146. Epub 2018 Oct 2.

3.

Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.

Llaudet-Planas E, Vives-Corrons JL, Rizzuto V, Gómez-Ramírez P, Sevilla Navarro J, Coll Sibina MT, García-Bernal M, Ruiz Llobet A, Badell I, Velasco-Puyó P, Dapena JL, Mañú-Pereira MM.

Int J Lab Hematol. 2018 Feb;40(1):94-102. doi: 10.1111/ijlh.12746. Epub 2017 Oct 10.

PMID:
29024480
4.

Is Increased Intracellular Calcium in Red Blood Cells a Common Component in the Molecular Mechanism Causing Anemia?

Hertz L, Huisjes R, Llaudet-Planas E, Petkova-Kirova P, Makhro A, Danielczok JG, Egee S, Del Mar Mañú-Pereira M, van Wijk R, Vives Corrons JL, Bogdanova A, Kaestner L.

Front Physiol. 2017 Sep 6;8:673. doi: 10.3389/fphys.2017.00673. eCollection 2017.

5.

Red cell pyruvate kinase deficiency in Spain: A study of 15 cases.

Montllor L, Mañú-Pereira MD, Llaudet-Planas E, Gómez Ramírez P, Sevilla Navarro J, Vives-Corrons JL.

Med Clin (Barc). 2017 Jan 6;148(1):23-27. doi: 10.1016/j.medcli.2016.10.004. Epub 2016 Nov 19. English, Spanish.

PMID:
27871768
6.

Red Cell Properties after Different Modes of Blood Transportation.

Makhro A, Huisjes R, Verhagen LP, Mañú-Pereira Mdel M, Llaudet-Planas E, Petkova-Kirova P, Wang J, Eichler H, Bogdanova A, van Wijk R, Vives-Corrons JL, Kaestner L.

Front Physiol. 2016 Jul 15;7:288. doi: 10.3389/fphys.2016.00288. eCollection 2016.

7.

Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.

Mañú-Pereira Mdel M, Gonzalez-Roca E, van Solinge WW, Llaudet-Planas E, Sevilla J, Montllor L, Mensa-Vilaro A, Ploos van Amstel HK, van Wijk R, Vives-Corrons J.

Am J Hematol. 2015 Dec;90(12):E217-9. doi: 10.1002/ajh.24178. Epub 2015 Nov 17. No abstract available.

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