Publicacions
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Payan-Pernia, S, Ruiz-Llobet A, Sevilla, AFR, Egido, J, Castan, JAB and Moreno, JA.
Sickle cell nephropathy. Clinical manifestations and new mechanisms involved in kidney injury
Nefrologia . 41(4): 373-382. Nº de cites: 2
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Gassiot S, Ruiz-Llobet A, Suleman W, Sarrate E and Berrueco R.
Thrombin generation in children using ThromboScreen reagent kit with ST Genesia-A pilot study
CLINICAL AND LABORATORY HAEMATOLOGY . 43(6): 1612-1619. Nº de cites: 2
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Berrueco R, Sebastián E, Solsona M, González de Pablo J, Ruiz-Llobet A, Mesegue-Meda M, Gálvez E and Sevilla J.
Secondary immune thrombocytopenia in children: Characteristics and outcome of a large cohort from two Spanish centres
ACTA PAEDIATRICA . 110(6): 1952-1958. Nº de cites: 3
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Vilaseca M, Burgos-Fernandez FJ, Rey-Barroso L, Roldan-Molina M, Gassiot S, Sarrate E, Isola I and Ruiz-Llobet A.
Hyperspectral imaging for skin cancer and blood disorders diagnosis.
Asian Journal of Physics . 29(10-12): 1-20.
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Bardón Cancho EJ, García-Morín M, Beléndez C, Velasco P, Benéitez D, Ruiz-Llobet A, Berrueco R, Argilés B, Cervera Á, Salinas JA, Vecilla C, Gondra A, Vallés G, Murciano T, Bermúdez M and Cela E.
Update of the Spanish registry of haemoglobinopathies in children and adults
MEDICINA CLINICA . 155(3): 95-103. Nº de cites: 15
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Rey-Barroso L, Roldan-Molina M, Burgos-Fernández FJ, Gassiot S, Ruiz-Llobet A, Isola I and Vilaseca MA.
Spectroscopic Evaluation of Red Blood Cells of Thalassemia Patients with Confocal Microscopy: A Pilot Study
SENSORS . 20(14): . Nº de cites: 6
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Bogliolo M, Pujol R, Aza-Carmona M, Muñoz-Subirana N, Rodriguez-Santiago B, Casado JA, Rio P, Bauser C, Reina-Castillón J, Lopez-Sanchez M, Gonzalez-Quereda L, Gallano P, Català-Temprano A, Ruiz-Llobet A, Badell I, Diaz-Heredia C, Hladun R, Senent L, Argiles B, Bergua Burgues JM, Bañez F, Arrizabalaga B, López Almaraz R, Lopez M, Figuera Á, Molinés A, Pérez de Soto I, Hernando I, Muñoz JA, Del Rosario Marin M, Balmaña J, Stjepanovic N, Carrasco E, Cuesta I, Cosuelo JM, Regueiro A, Moraleda Jimenez J, Galera-Miñarro AM, Rosiñol L, Carrió A, Beléndez-Bieler C, Escudero Soto A, Cela E, de la Mata G, Fernández-Delgado R, Garcia-Pardos MC, Sáez-Villaverde R, Barragaño M, Portugal R, Lendinez F, Hernadez I, Vagace JM, Tapia M, Nieto J, Garcia M, Gonzalez M, Vicho C, Galvez E, Valiente A, Antelo ML, Ancliff P, Garcia F, Dopazo J, Sevilla J, Paprotka T, Pérez-Jurado LA, Bueren J and Surralles J.
Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies
JOURNAL OF MEDICAL GENETICS . 57(4): 258-268. Nº de cites: 20
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Ruiz-Llobet A, Isola I, Gassiot S, Català-Temprano A, Díaz-Ricart M, Martinez-Monseny T, Serrano M and Berrueco R.
Platelet Dysfunction in Noonan and 22q11.2 Deletion Syndromes in Childhood
THROMBOSIS AND HAEMOSTASIS . 120(3): 457-465. Nº de cites: 4
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Pérez-Grijalba V, Arbizu J, Romero J, Prieto E, Pesini P, Sarasa L, Guillen F, Monleón I, San-José I, Martínez-Lage P, Munuera-del Cerro JL, Hernández I, Buendía M, Sotolongo-Grau O, Alegret M, Ruiz-Llobet A, Tárraga L, Boada M and Sarasa M.
Plasma A beta 42/40 ratio alone or combined with FDG-PET can accurately predict amyloid-PET positivity: a cross-sectional analysis from the AB255 Study
ALZHEIMERS RESEARCH & THERAPY . 11(1): 96-96. Nº de cites: 41
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Arias-Salgado EG, Galvez E, Planas-Cerezales L, Pintado-Berninches L, Vallespin E, Martinez P, Carrillo J, Iarriccio L, Ruiz-Llobet A, Català-Temprano A, Badell-Serra I, Gonzalez-Granado LI, Martín-Nalda A, Martínez-Gallo M, Galera-Miñarro A, Rodríguez-Vigil C, Bastos-Oreiro M, Perez de Nanclares G, Leiro-Fernández V, Uria ML, Diaz-Heredia C, Valenzuela C, Martín S, López-Muñiz B, Lapunzina P, Sevilla J, Molina-Molina M, Perona R and Sastre L.
Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes.
ORPHANET JOURNAL OF RARE DISEASES . 14(1): 82-82. Nº de cites: 21