Zobrazeno 1 - 10
of 30
pro vyhledávání: '"J J, Ortega Aramburu"'
Autor:
P, Bastida Vilá, C, Palacio García, M, Solsona Riera, J J, Ortega Aramburu, J, Sánchez de Toledo Codina
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 63(5)
Early response to induction treatment is one of the most important prognostic factors in children with acute lymphoblastic leukemia (ALL). Cytological remission is currently achieved in 95-98 % of these patients, although a significant proportion wil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69d79905ef39235a5c944eb6ed69ce66
https://pubmed.ncbi.nlm.nih.gov/16266612
https://pubmed.ncbi.nlm.nih.gov/16266612
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 61(6)
Transient neonatal leukemia or transient neonatal myeloproliferative disorder is commonly associated with Down syndrome. It usually resolves spontaneously in 4-5 months. However, 25 % of patients will subsequently develop acute megakaryoblastic leuke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d66572604fb33a1b7fa1e3b75a04d1ef
https://pubmed.ncbi.nlm.nih.gov/15574256
https://pubmed.ncbi.nlm.nih.gov/15574256
Autor:
A, Díaz Conradi, C, Díaz de Heredia, J, Tusell Puigbert, S, Quintana Riera, L, Tobeña Boada, J J, Ortega Aramburu
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 59(1)
Immune thrombocytopenic purpura (ITP) is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis. In chronic forms the platelet count remains low for six months after diagnosis and in recurrent forms the drop in platele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a53cb27a33e5b0dc37c030e91e0bc265
https://pubmed.ncbi.nlm.nih.gov/12887867
https://pubmed.ncbi.nlm.nih.gov/12887867
Autor:
J M, Tusell Puigbert, C, Aulesa Martínez, M, Aguirre Canyadell, I, Nicolau Fusté, P, Valentín Valentín, J J, Ortega Aramburu
Publikováno v:
Anales espanoles de pediatria. 53(1)
It has been suggested that the cause of Perthes disease may be intravascular thrombosis induced by a potential congenital hemostatic disorder leading to conditions of thrombophilia or hyperfibrinolysis.Complete study of hemostasis with coagulation an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f07357360c36ce31e86504c84a6c04f3
https://pubmed.ncbi.nlm.nih.gov/10998397
https://pubmed.ncbi.nlm.nih.gov/10998397
Autor:
A, Muñoz Villa, J J, Ortega Aramburu, E, Bureo Dacal, I, Badell Serra, L, Madero López, T, Olive Oliveras, J, Cubells Riero, M S, Maldonado Regalado, M, Ramírez Orellana
Publikováno v:
Anales espanoles de pediatria. 50(1)
The objective of this study was to evaluate retrospectively the efficacy of allogeneic BMT in the treatment of childhood severe acquired aplastic anemia (SAAA).Twenty-seven children aged 2 to 16 years (median 11 years) received a BMT from an HLA iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e8740cae234d2a70a9064c13835a817
https://pubmed.ncbi.nlm.nih.gov/10083639
https://pubmed.ncbi.nlm.nih.gov/10083639
Autor:
F, Castillo Salinas, C, Díaz de Heredia Rubio, S, Salcedo Abizanda, A, Ferrer Comalat, P, Bastida Vila, J J, Ortega Aramburu, G, Peguero Monforte
Publikováno v:
Anales espanoles de pediatria. 49(6)
To assess the therapeutic effect of G-CSF in newborns with neutropenia.Newborn with evidence of both peripheral neutropenia and decreased granulocytic precursors in tibial bone marrow aspirate were included in the study. G-CSF was perfused intravenou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3a672177c01c43a8becec313a635c6e
https://pubmed.ncbi.nlm.nih.gov/9972625
https://pubmed.ncbi.nlm.nih.gov/9972625
Autor:
C, Rodríguez Galindo, J J, Ortega Aramburu, J L, Alonso, M, Albisu, J, Casaldáliga, C, Díaz de Heredia, T, Olivé, P, Bastida
Publikováno v:
Medicina clinica. 102(19)
The current treatment of thalassaemia maior (TM) is based on a hypertransfusion regimen, with deferoxamine (DFO) chelation therapy to minimize the consequences of iron overload. To evaluate the long-term efficacy of chelation therapy, a group of 9 pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ce5eaa0f12db43d5c2d192737793499
https://pubmed.ncbi.nlm.nih.gov/8041200
https://pubmed.ncbi.nlm.nih.gov/8041200
Publikováno v:
Anales espanoles de pediatria. 35(3)
Changes in treatment of ANLL in children over 23 years (1968-90) and advances made in the last ten years in a pediatric hematological unit are reported herein. Of 124 patients under 15 years of age, 18 of whom were infants, 118 were evaluable. Of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7f5265b76c5193b68be96ea09f34ce88
https://pubmed.ncbi.nlm.nih.gov/1741570
https://pubmed.ncbi.nlm.nih.gov/1741570
Publikováno v:
Anales espanoles de pediatria. 33(4)
Bone marrow transplant has proved to be an effective treatment in some hereditary metabolic diseases and, especially, in mucopolysdaccharidosis (MPS). A 9-year-old girl, of consanguineous parents, with MPS Type I, Hurler-Scheie syndrome, received a B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3b7ffa7106f01b3283367f4652d0d1f
https://pubmed.ncbi.nlm.nih.gov/2126172
https://pubmed.ncbi.nlm.nih.gov/2126172
Publikováno v:
Anales espanoles de pediatria. 33(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69e241b222962de255b843e1132e6a9c
https://pubmed.ncbi.nlm.nih.gov/2177315
https://pubmed.ncbi.nlm.nih.gov/2177315