T Olive
Overview
Explore the profile of T Olive including associated specialties, affiliations and a list of published articles.
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Articles
49
Citations
144
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Recent Articles
1.
Diaz de Heredia C, Gonzalez M, Verdeguer A, Elorza I, Rodriguez A, Martinez A, et al.
Bone Marrow Transplant
. 2014 Mar;
49(6):767-72.
PMID: 24614843
Outcomes of unrelated cord blood transplants (UCBT) were assessed in 172 consecutive children, median age 5 years (range: 0.5-18), with haematological malignancies treated at nine Spanish hospitals between February 1996...
2.
Hladun R, Elorza I, Olive T, Dapena J, Llort A, Sanchez de Toledo J, et al.
An Pediatr (Barc)
. 2013 Feb;
79(2):75-82.
PMID: 23402775
Background: The prevalence of hemoglobinopathies in Spain is increasing as a result of immigration. Thalassemia major presents with chronic hemolytic anemia that requires regular red blood cell transfusions within the...
3.
Barcelo Canellas C, Marhuenda Irastorza C, Olive T, Moreno Montero A, Guillen Burrieza G, Gaethe J, et al.
Cir Pediatr
. 2008 Nov;
21(4):219-22.
PMID: 18998372
Objective: Pneumatosis intestinalis (PI) is a radiological sign that can be accompanied by pneumoperitoneum. It is not exclusive of neonatal necrotizing enterocolitis. It can also appear after bone marrow transplantation....
4.
Diaz de Heredia C, Ortega J, Diaz M, Olive T, Badell I, Gonzalez-Vicent M, et al.
Bone Marrow Transplant
. 2007 Dec;
41(7):627-33.
PMID: 18084339
HCT is currently the treatment of choice for children with severe primary immunodeficiencies (PIDs). Frequently, these patients lack an HLA-identical sibling donor, and umbilical cord blood (UCB) transplantation may be...
5.
Munoz A, Olive T, Martinez A, Bureo E, Maldonado M, Diaz de Heredia C, et al.
Pediatr Hematol Oncol
. 2007 Aug;
24(6):393-402.
PMID: 17710656
Allogeneic stem cell transplantation is the only curative treatment for Wiskott-Aldrich syndrome. The authors retrospectively analyzed the outcome with this procedure in 13 patients with severe Wiskott-Aldrich syndrome transplanted in...
6.
Ferreira R, Vastert S, Abinun M, Foster H, Modesto C, Olive T, et al.
Bone Marrow Transplant
. 2006 Jun;
38(3):249-51.
PMID: 16770315
No abstract available.
7.
Jacome A, Navarro S, Casado J, Rio P, Madero L, Estella J, et al.
Hum Gene Ther
. 2006 Feb;
17(2):245-50.
PMID: 16454658
Fanconi anemia (FA) is an inherited DNA repair disorder characterized by genetic instability of cells lacking a functional FA/BRCA pathway. Previous studies have shown that in vitro stimulation of bone...
8.
Sardon O, Garcia Pardos C, Mintegui J, Perez Ruiz E, Coll M, Chabas A, et al.
An Pediatr (Barc)
. 2005 Jul;
63(1):61-7.
PMID: 15989873
We performed a prospective study of two patients with Hurler's syndrome (aged 4.8 years and 17 months at the beginning of the intervention) under enzyme replacement therapy with human recombinant...
9.
Ortega J, Olive T, de Heredia C, Llort A
Bone Marrow Transplant
. 2005 Apr;
35 Suppl 1:S83-7.
PMID: 15812538
Malignant diseases (MD) occurring after stem cell transplantation (SCT) are of particular concern as increasing number of patients survive and remain free of their original disease. The cumulative incidence at...
10.
Badell I, Munoz A, Ortega J, Martinez A, Madero L, Bureo E, et al.
Bone Marrow Transplant
. 2005 Mar;
35(9):895-901.
PMID: 15778727
We present a retrospective study of long-term outcome and predictive factors of survival and relapse in 219 paediatric patients with acute lymphoblastic leukaemia (ALL) in second remission. They received allogeneic...