Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Manuel Vázquez-Donsión"'
Autor:
Manuel Vázquez Donsión, Gema Ariceta Iraola, Marta Gil Calvo, Jose Miguel Couselo Sánchez, Adela Urisarri-Ruiz de Cortázar
Publikováno v:
Pediatric Nephrology. 24:1081-1084
Congenital renal anomalies, Williams Syndrome and non-Hodgkin lymphoma all occur separately at low incidence, so their simultaneous presence in the same patient is exceptional. We present a young patient manifesting all three conditions. This child i
Autor:
Laura Gonzalez-Calvete, José Miguel Couselo-Sánchez, Rebeca Saborido-Fiaño, Alexandra Regueiro-García, Manuel Vázquez-Donsión, Manuel Fernández-Sanmartín
Publikováno v:
Archivos Argentinos de Pediatria. 113
Hypercalcemia as a paraneoplastic syndrome is rare in children. Therapeutic management is aimed at promoting calciuresis with various pharmacological methods, even with extrarenal purification techniques. The aim of presenting this case is to highlig
Autor:
Alexandra, Regueiro-García, Rebeca, Saborido-Fiaño, Laura, González-Calvete, Manuel, Fernández-Sanmartín, Manuel, Vázquez-Donsión, José Miguel, Couselo-Sánchez
Publikováno v:
Archivos argentinos de pediatria. 113(4)
Hypercalcemia as a paraneoplastic syndrome is rare in children. Therapeutic management is aimed at promoting calciuresis with various pharmacological methods, even with extrarenal purification techniques. The aim of presenting this case is to highlig
Autor:
Ignacio Oulego-Erroz, Manuel Vázquez-Donsión, Jose Miguel Couselo, Marta Bouzón-Alejandro, Mercedes Maneiro-Freire
Publikováno v:
Pediatric bloodcancer. 55(3)
Anaphylactic/anaphylactoid reaction to methotrexate (MTX) is uncommon. It may occur with the first dose (non-allergic reactions) or after a previous exposure to the drug (allergic or specific reactions). Desensitization has been shown effective in ch
CAMT in a female with developmental delay, facial malformations and central nervous system anomalies
Publikováno v:
Pediatric Blood & Cancer. 56:452-453
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare disorder characterized by thrombocytopenia and absence or decline in the number of megakaryocytic precursors in the bone marrow. It is caused by mutations in the thrombopoietin receptor gen