Zobrazeno 1 - 10 of 33 pro vyhledávání: '"María del Mar Mañú-Pereira"'
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Akademický článek
The variable manifestations of disease in pyruvate kinase deficiency and their management
Autor: Hanny Al-Samkari, Eduard J. van Beers, Kevin H.M. Kuo, Wilma Barcellini, Paola Bianchi, Andreas Glenthøj, María del Mar Mañú Pereira, Richard van Wijk, Bertil Glader, Rachael F. Grace
Publikováno v: Haematologica, Vol 105, Iss 9 (2020)
Pyruvate kinase deficiency (PKD) is the most common cause of chronic hereditary non-spherocytic hemolytic anemia and results in a broad spectrum of disease. The diagnosis of PKD requires a high index of suspicion and judicious use of laboratory tests
Externí odkaz: https://doaj.org/article/5415c1f489f3422aa3d91370036814c5
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4
Akademický článek
Recommendations for centres of expertise in rare anaemias. The ENERCA White Book
Autor: Joan-Lluis Vives Corrons, María del Mar Mañú Pereira, Carlos Romeo-Casabona, Pilar Nicolás, Béatrice Gulbis, Androulla Eleftheriou, Michael Angastiniotis, Patricia Aguilar Martínez, Paola Bianchi, Richard Van Wijk, Hermann Heimpel, Barbara De la Salle, Andrea Mosca
Publikováno v: Thalassemia Reports, Vol 4, Iss 3 (2014)
The Community added value of Centres of Expertise (CoE) and European Reference Networks (ERN) is particularly high for rare diseases (RD) due to the rarity of these conditions, which implies both a small number of patients and scarcity of expertise w
Externí odkaz: https://doaj.org/article/8dfd18cd6843465cb8188620f60bf6bd
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5
Akademický článek
e-ENERCA: telemedicine platform for rare anaemias
Autor: Béatrice Gulbis, María del Mar Mañú Pereira, Emilio J. Armaza Armaza, Pilar Nicolás, for the ENERCA working group
Publikováno v: Thalassemia Reports, Vol 4, Iss 3 (2014)
The creation of a telemedicine, tele-expertise platform opens a new challenge within the European Network for Rare and Congenital Anaemias (ENERCA; www.enerca.org). This is a cornerstone in the field of rare anaemias, in which national expertise is u
Externí odkaz: https://doaj.org/article/edc16b4accef42d1b9b2f12b256def51
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6
ERN-EuroBloodNet European Registry of Patients Affected by Red Blood Cell Disorders and COVID-19
Autor: Teresa Ferreira Faria, Eduardo J. Bardón-Cancho, Pablo Velasco, Ioannis Lafiatis, Fleur Samantha Benghiat, Saveria Campisi, Ersi Voskaridou, Sabrina Bagnato, Michael D. Diamantidis, Achille Iolascon, Marie-Agnès Azerad, Beatriz Ponce-Salas, María del Mar Mañú Pereira, Andrea Piolatto, Christopher J. Saunders, Anna Spasiano, Polyxeni Delaporta, Pagona Flevari, Rosamaria Rosso, Mariane de Montalembert, Eftichia Stiakaki, David Beneitez-Pastor, Bart J. Biemond, Simona Raso, Anna Ruiz-Llobet, Erfan Nur, Ali T. Taher, Joachim B. Kunz, Raffaella Colombatti, Mikael Lorite, Paula Gonzalez Urdiales, An Van Damme, Noémi B. A. Roy, Andreas Glenthøj, Jean-Louis H. Kerkhoffs, Tatiana Besse-Hammer, Elisa Bertoni, Alexis Rodriguez, Alessia Pepe, Laurence Dedeken, Maria Elena Guerzoni, Veerle Labarque, Tommaso Casini, María Argüello Marina, Alessandra Quota, Ann Van de Velde, Filomena Longo, Roberta Russo, Maria Jose Teles, Soteroula Christou
Publikováno v: Blood
PV, NR and MMP contributed equally Introduction Patients with red blood cell disorders (RBCD), chronic life threating multisystemic disorders in their severe forms, are likely to be at increased risk of complications from SARS-Cov-2 (Covid-19), but e
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab9ff86ea27012d50014bbc13e59a380
http://europepmc.org/articles/PMC8701690
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7
Limited Access to Transcranial Doppler Screening and Stroke Prevention for Children with Sickle Cell Disease in Europe: Results of a Multinational Eurobloodnet Survey
Autor: Vincenzo Voi, Maddalena Casale, Corrina McMahon, Raffaella Colombatti, Baba Inusa, Mariane de Montalembert, María del Mar Mañú Pereira, Daniela Cuzzubbo, Victoria Gutierrez-Valle
Publikováno v: Blood. 138:915-915
Background: Children with sickle cell disease (SCD) are at increased risk of cerebrovascular events such as stroke, silent infarcts and neurocognitive impairment. The role of Transcranial Doppler ultrasound scanning (TCD) to identify sickle cell anem
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::346e88fb00e7689c1a77fa720b881ed5
https://doi.org/10.1182/blood-2021-147298
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9
Pathophysiology of Anemia in HIV-Infected Children Exposed to Malaria
Autor: John J. Aponte, Llorenç Quintó, Tacilta Nhampossa, Montserrat Renom, María Rupérez, Pedro L. Alonso, Eusebio Macete, Ariel H. Achtman, Louis Schofield, Ruth Aguilar, Cinta Moraleda, María Del Mar Mañú Pereira, Clara Menéndez, Augusto Nhabomba
Publikováno v: Am J Trop Med Hyg
Anemia is a common condition in HIV-infected children; however, its pathophysiology and the contribution of frequent causes of anemia such as iron deficiency (ID) and malaria are poorly understood. We carried out an ancillary study on the effect of H
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6338cfdc842800720bfdaf4413424fb
https://pubmed.ncbi.nlm.nih.gov/33534758
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