Search Results - "COUSELO, M. J"

Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene by Silva, P, Justicia, A, Regueiro, A, Fariña, S, Couselo, J M, Loidi, L

“…Agammaglobulinemia is a primary immunodeficiency disorder characterized by profoundly low or absent serum antibodies and low or absent circulating B cells. The…”
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Haploidentical stem cell transplantation in a boy with chronic granulomatous disease by Regueiro-García, A, Fariña-Nogueira, S, Porto-Arceo, J Á, Couselo-Sánchez, J M

“…Chronic granulomatous disease is a primary immunodeficiency caused by mutations in any one of the five components of the NADPH oxidase in phagocytic…”
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Metastatic neuroblastoma in infants: are survival rates excellent only within the stringent framework of clinical trials? by Di Cataldo, A., Agodi, A., Balaguer, J., Garaventa, A., Barchitta, M., Segura, V., Bianchi, M., Castel, V., Castellano, A., Cesaro, S., Couselo, J. M., Cruz, O., D’Angelo, P., De Bernardi, B., Donat, J., de Andoin, N. G., Hernandez, M. I., La Spina, M., Lillo, M., Lopez-Almaraz, R., Luksch, R., Mastrangelo, S., Mateos, E., Molina, J., Moscheo, C., Mura, R., Porta, F., Russo, G., Tondo, A., Torrent, M., Vetrella, S., Villegas, J. A., Viscardi, E., Zanazzo, G. A., Cañete, A.

“…Introduction SIOPEN INES protocol yielded excellent 5-year survival rates for MYCN -non-amplified metastatic neuroblastoma. Patients deemed ineligible due to…”
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Bone marrow transplantation in chronic granulomatous disease by CALVINO, M. C, MALDONADO, M. S, OTHEO, E, MUNOZ, A, COUSELO, J. M, BURGALETA, X

“…We present a 5-year-old boy with a severe form of X-linked chronic granulomatous disease and hypersensitivity to sulphamides preventing prophylaxis with…”
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Alloantibody from a patient with severe von Willebrand disease inhibits von willebrand factor-FVIII interaction by BATLLE, J, LOURES, E, VILA, P, HERNANDEZ, M. C, MENDEZ, J. A, TOREA, J, RENDAL, E, COUSELO, M. J, FILGUEIRA, A, LOPEZ-FERNANDEZ, M. F

“…The aim of this study was to analyze the ability of an alloantibody from a patient with severe von Willebrand disease (vWD) to interfere with the vWF domain…”
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Orbital langerhans cell histiocytosis: a multidisciplinary approach by Sevillano, C, Lázaro, V M, Couselo, J M, Freire, J

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Anaphylactic reaction to high-dose methotrexate by Lobelle, C, López Rivas, M, Barreiro, J, Rodicio, M, Couselo, J M

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Autosomal recessive agammaglobulinemia due to defect in [mu] heavy chain caused by a novel mutation in the IGHM gene by Silva, P, Justicia, A, Regueiro, A, Fariña, S, Couselo, J M, Loidi, L

“…Agammaglobulinemia is a primary immunodeficiency disorder characterized by profoundly low or absent serum antibodies and low or absent circulating B cells. The…”
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Henoch-Schönlein purpura in children and adults: Clinical differences in a defined population by García-Porrúa, Carlos, Calviño, Maria C., Llorca, Javier, Couselo, José M., González-Gay, Miguel A.

“…Objective: To examine epidemiologic, clinical, and outcome differences between children and adults with Henoch-Schönlein purpura (HSP) in a well-defined…”
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Allopurinol in Duchenne muscular dystrophy by Castro-Gago, M, Jiménez, J F, Pombo, M, Tojo, R, Couselo, J M, Peña, J

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Osteosarcoma and ATR-16 syndrome: association or coincidence? by Regueiro García, A, Saborido Fiaño, R, González Calvete, L, Vázquez Donsión, M, Couselo Sánchez, J M, Fernández Sanmartín, M

“…ATR-16 syndrome is due to alterations on chromosome 16p13.3, and is usually accompanied by alpha-thalassemia, mild-moderate mental retardation, dysmorphic…”
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Histiocitosis de células de Langerhans orbitaria: un abordaje multidisciplinario by Sevillano, C, Lázaro, V.M, Couselo, J.M, Freire, J

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Bone marrow transplantation in chronic granulomatous disease by Calviño, M C, Maldonado, M S, Otheo, E, Muñoz, A, Couselo, J M, Burgaleta, C

“…We present a 5-year-old boy with a severe form of X-linked chronic granulomatous disease and hypersensitivity to sulphamides preventing prophylaxis with…”
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Letter: 45, X-46, XX-47, XXX mosaicism by Couselo, J M, Ansede, A, Noya, M

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Orbital langerhans cell histiocytosis: a multidisciplinary approach by Sevillano, C, Lázaro, V M, Couselo, J M, Freire, J

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56 NEUROENDOCRINE ALTERATIONS INDUSCED BY CRANIAL IRRADIATION (CR) IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA (LLA) by Pombo, M, Couce, M L, Couselo, J M, Devesa, J

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Growth in children with cancer by Pombo, M, Couce, M L, Barreiro, J, Couselo, J M

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Determination of the mean dose of oral theophylline in asthmatic children (author's transl) by Cabanas, R, Peña, J, Fuster, M, Cortizo, E, Castro-Gago, M, Couselo, J M, Tojo, R

“…The oral dosage of theophylline was adjusted in order to maintain a serum level between 10 and 20 micrograms/ml. in a group of 53 children whose ages were less…”
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Congenital deficiency of factor VII (author's transl) by Castro Gago, M, Fernández Pavon, A, Pavón, P, Couselo, J M, Ferrero, F, Tojo, R

“…Authors report a four month old patient, admitted to hospital because of blood in stools. Diagnosis of congenital deficiency of factor VII was established…”
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Delayed hypersensitivity reaction caused by asparaginase by Couselo, J M, Iglesias Diz, J L

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