Search Results - "Fonfria, M."

734P Kidney manifestations in patients with hereditary leiomyomatosis and renal cell cancer syndrome (LHRCC) in Spain by Sanchez, A.B., Teule, A., Lastra, E., Balmana, J., Robles, L., García, J.D.D., Ramón y Cajal, T., Llort, G., Fonfria, M., Robledo, M., Castillejo, A., Duran, M., Zuñiga, A., Gómez, L., Garcés, E. Grau, López, A., Bosquet-Sanz, M., Barberá, V., Soto, J.L.

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Apparent Apert syndrome with polydactyly: rare pleiotropic manifestation or new syndrome? by Maroteaux, P, Fonfria, M C

“…Two patients are described with a syndrome which resembles Apert syndrome with polydactyly of hands and feet. This association is apparently rare and we think…”
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Multimodality management of a locally advanced primary oesophageal melanoma with radical surgery and adjuvant chemoimmunoradiotherapy by Díaz, Roberto, Moral, Pedro, Fonfría, María, de Juan, Manuel, Mancheño, Nuria, Tormo, Alejandro

“…We present the case of a 46-year-old woman diagnosed with a primary oesophageal melanoma (PEM), who was treated with radical surgery followed by combined…”
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