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Items: 13


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.


Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias.

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

Front Physiol. 2019 Apr 16;10:386. doi: 10.3389/fphys.2019.00386. eCollection 2019.


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.


Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.

Bianchi P, Fermo E, Glader B, Kanno H, Agarwal A, Barcellini W, Eber S, Hoyer JD, Kuter DJ, Maia TM, Mañu-Pereira MDM, Kalfa TA, Pissard S, Segovia JC, van Beers E, Gallagher PG, Rees DC, van Wijk R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Hematological Diseases.

Am J Hematol. 2019 Jan;94(1):149-161. doi: 10.1002/ajh.25325. Epub 2018 Nov 28.


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.


Heterogeneity of G6PD deficiency prevalence in Mozambique: a school-based cross-sectional survey in three different regions.

Galatas B, Mabote L, Simone W, Matambisso G, Nhamussua L, Mañú-Pereira MD, Menéndez C, Saute F, Macete E, Bassat Q, Alonso P, Aide P.

Malar J. 2017 Jan 19;16(1):36. doi: 10.1186/s12936-016-1674-y.


Low affinity hemoglobinopathy (Hb Vigo) due to a new mutation of beta globin gene (c200 A>T; Lys>Ile). A cause of rare anemia misdiagnosis.

Mañú Pereira MD, Ropero P, Loureiro C, Vives Corrons JL.

Am J Hematol. 2017 Apr;92(4):E38-E40. doi: 10.1002/ajh.24649. Epub 2017 Feb 13. No abstract available.


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.


[Haemoglobin Köln as a cause of haemolytic anaemia and splenomegaly].

Durán Urdániz G, Gil Sáenz FJ, Molina Garicano J, Gimeno Ballester J, Mañú Pereira MM.

An Pediatr (Barc). 2013 Aug;79(2):124-5. doi: 10.1016/j.anpedi.2013.01.007. Epub 2013 Feb 26. Spanish. No abstract available.


Neonatal haemoglobinopathy screening in Spain.

Mañú Pereira M, Corrons JL.

J Clin Pathol. 2009 Jan;62(1):22-5. doi: 10.1136/jcp.2008.058834. Review.


Cell counter-based parameters and formulas in detection of beta-thalassemia trait.

Juncà J, Mañú-Pereira M, Radó-Trilla N, Vives-Corrons JL.

Am J Clin Pathol. 2008 Jul;130(1):147-8; author reply 148. No abstract available.


[Hemoglobinopathy Newcastle: use of chromatography and first case reported in Spain].

Mañú Pereira MM, Coll Sibina MT, García Mateos E, Vives Corrons JL.

Med Clin (Barc). 2008 Apr 5;130(12):455-8. Spanish.


Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin.

Mañú Pereira M, Gelbart T, Ristoff E, Crain KC, Bergua JM, López Lafuente A, Kalko SG, García Mateos E, Beutler E, Vives Corrons JL.

Haematologica. 2007 Nov;92(11):e102-5.

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