Search Results - "Ancochea, A."

Strategic discussion on funding and access to therapies targeting rare diseases in Spain: an expert consensus paper by Zozaya, N, Villaseca, J, Abdalla, F, Ancochea, A, Málaga, I, Trapero-Bertran, M, Martín-Sobrino, N, Delgado, O, Ferré, P, Hidalgo-Vega, A

“…In recent years, significant advances have been made in the field of rare diseases (RDs). However, there is a large number of RDs without specific treatment…”
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Changes over the last 15 years in the psychopharmacological management of persons with borderline personality disorder by Martín‐Blanco, A., Ancochea, A., Soler, J., Elices, M., Carmona, C., Pascual, J. C.

“…Objective To describe the pharmacological management of borderline personality disorder (BPD) in Spain from 2001 through 2016, the factors associated with…”
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P.423 Left behind after suicide. Suicide Survivor Programme, a longitudinal study by Vidal, A. Fernandez, Ávila-Parcet, A., Raventós, B., Casellas, E., Tiana, T., Ancochea, A., Borrás, C., Portella, M., Álvarez, E.

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PRO96 A Multi-Stakeholder Multicriteria Decision Analysis in Rare Diseases: Reimbursement Criteria for Orphan Drugs in Spain (FinMHU-MCDA study) by de Andrés-Nogales, F., Cruz, E., Calleja, M.Á., Delgado, O., Gorgas Torner, M.Q., Espin, J., Mestre-Ferrandiz, J., Palau, F., Ancochea, A., Arce, R., Domínguez-Hernández, R., Casado, M.A.

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P1550: NEW GENERATION EKTACYTOMETRY STUDY OF RED BLOOD CELLS RHEOLOGICAL PARAMETERS IN HEMOGLOBINOPATHIES by Krishnevskaya, E., Molero Magariño, M., Ancochea Serra, Á., Vives Corrons, J.‐L., Hernandez, I., Leguizamón, V.

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Red cell mass measurement in patients with clinically suspected diagnosis of polycythemia vera or essential thrombocythemia by Alvarez-Larrán, Alberto, Ancochea, Agueda, Angona, Anna, Pedro, Carme, García-Pallarols, Francesc, Martínez-Avilés, Luz, Bellosillo, Beatriz, Besses, Carlos

“…The cut off for hemoglobin or hematocrit that indicates the need for an isotopic red cell mass study was investigated in 179 patients with a presumptive…”
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PS1204 SEVERE HEREDITARY HAEMOLYTIC ANAEMIA DUE TO THREE NOVEL SPTA1 MUTATIONS IN TWO COMPOUND HETEROZYGOUS UNRELATED PATIENTS by Krishnevskaya, E., Rodriguez, I. Hernandez, Serra, A. Ancochea, Payán‐Pernía, S., Rizzuto, V., Magariño, M. Molero, Vives‐Corrons, J.‐L.

“…Background: Red blood cell (RBC) membrane defects are a cause of hereditary haemolytic anaemia (HHA) due to mutations in the genes that encode cytoskeletal…”
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Capitalismo, desarrollo y estado. Una revision critica de la teoria del Estado de Schumpeter by Sánchez Ancochea, Diego

“…Las teorías del Estado se pueden beneficiar de una nueva mirada al papel económico del Estado en la obra de los grandes economistas de los siglos XIX y XX. El…”
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