Publicacions
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Cruz-Martínez O, Caloretti V, Salvador-Hernandez H, Celis-Passini V, Santa-María López V, Morales-La Madrid A, Suñol M, Puerta P, Muchart-Lopez J, Krauel L and Lavarino C.
Synchronous choroid plexus papilloma and Wilms tumor in a girl, disclosing a Li-Fraumeni syndrome
HEREDITARY CANCER IN CLINICAL PRACTICE . 19(1): 1-1. Nº de cites: 2
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Levine JE, Grupp SA, Pulsipher MA, Dietz AC, Rives-Solà S, Myers GD, August KJ, Verneris MR, Buechner J, Laetsch TW, Bittencourt H, Baruchel A, Boyer MW, De Moerloose B, Qayed M, Davies SM, Phillips CL, Driscoll TA, Bader P, Schlis K, Wood PA, Mody R, Yi L, Leung M, Eldjerou LK, June CH and Maude SL.
Pooled safety analysis of tisagenlecleucel in children and young adults with B cell acute lymphoblastic leukemia
Journal for ImmunoTherapy of Cancer . 9(8): 2287. Nº de cites: 47
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Vega-García N, Benito R, Esperanza-Cebollada E, Llop M, Robledo C, Vicente-Garces C, Alonso J, Barragán E, Fernandez-Isern G, Hernández-Sánchez JM, Martín-Izquierdo M, Maynou-Fernández J, Minguela A, Montaño A, Ortega M, Torrebadell-Burriel M, Cervera J, Sánchez J, Jiménez-Velasco A, Riesco S, Hernández-Rivas JM, Lassaletta Á, Fernández JM, Rives-Solà S, Dapena JL, Ramírez M and Camós-Guijosa M.
Helpful Criteria When Implementing NGS Panels in Childhood Lymphoblastic Leukemia
Journal of Personalized Medicine . 10(4): 244. Nº de cites: 1
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Turrubiartes-Martinez, E, Bodega-Mayor, I, Delgado-Wicke, P, Molina-Jimenez, F, Casique-Aguirre, D, Gonzalez-Andrade, M, Rapado, I, Camós-Guijosa M, Diaz-de-Heredia, C, Barragan, E, Ramirez-Orellana, M, Aguado, B, Figuera, A, Martinez-Lopez, J and Fernandez-Ruiz, E.
TYK2 Variants in B-Acute Lymphoblastic Leukaemia
GENES . 11(12): . Nº de cites: 5
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Cuadros M, García DJ, Andrades A, Arenas AM, Coira IF, Baliñas-Gavira C, Peinado P, Rodríguez MI, Álvarez-Pérez JC, Ruiz-Cabello F, Camós-Guijosa M, Jiménez-Velasco A and Medina PP.
LncRNA-mRNA Co-Expression Analysis Identifies AL133346.1/CCN2 as Biomarkers in Pediatric B-Cell Acute Lymphoblastic Leukemia
Cancers . 12(12): 3803. Nº de cites: 7
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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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Parisi C, Candela-Cantó SA, Serrano M, Català-Temprano A, Aparicio J and Hinojosa J.
Life-threatening secondary hemophagocytic lymphohistiocytosis following vagal nerve stimulator infection in a child with CHD2 myoclonic encephalopathy: a case report
CHILDS NERVOUS SYSTEM . 36(11): 2851-2856. Nº de cites: 4
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Salvador, PP, Benjamin, RS, Manel, BG, Angel, FRS, Montserrat, TE, Badell-Serra I, Jordi, SC and Jorge, SG.
APPLICATION OF THE CLINICAL EXOMA "SANT PAU" FOR THE DIAGNOSIS OF HEMOLITIC ANEMIAS AND HEREDITARY IRON METABOLISM DISORDERS
HAEMATOLOGICA . 105: 33-33.
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Kozyra EJ, Pastor VB, Lefkopoulos S, Sahoo SS, Busch H, Voss RK, Erlacher M, Lebrecht D, Szvetnik EA, Hirabayashi S, Pasauliene R, Pedace L, Tartaglia M, Klemann C, Metzger P, Boerries M, Català-Temprano A, Hasle H, de Haas V, Kállay K, Masetti R, De Moerloose B, Dworzak M, Schmugge M, Smith O, Starý J, Mejstrikova E, Ussowicz M, Morris E, Singh P, Collin M, Derecka M, Göhring G, Flotho C, Strahm B, Locatelli F, Niemeyer CM, Trompouki E, Wlodarski MW and European Working Group of MDS in Childhood (EWOG-MDS).
Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency
Leukemia . 34(10): 2673-2687. Nº de cites: 36
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Montaño A, Hernández-Sánchez J, Forero-Castro M, Matorra-Miguel M, Lumbreras E, Miguel C, Santos S, Ramírez-Maldonado V, Fuster JL, de Las Heras N, García-de Coca A, Sierra M, Dávila J, de la Fuente I, Olivier C, Olazabal J, Martínez J, Vega-García N, González T, Hernández-Rivas JM and Benito R.
Comprehensive Custom NGS Panel Validation for the Improvement of the Stratification of B-Acute Lymphoblastic Leukemia Patients
Journal of Personalized Medicine . 10(3): 137. Nº de cites: 8