Zobrazeno 1 - 10
of 39
pro vyhledávání: '"M.H. van Weel-Sipman"'
Autor:
Karel Hählen, M.H. van Weel-Sipman, G. A. M. de Vaan, A. J. P. Veerman, J.F. van Weerden, A. van der Does-van den Berg
Publikováno v:
Pediatric Research, 38, 5, pp. 802-807
Pediatric Research, 38, pp. 802-807
Pediatric Research, 38, 802-807
Scopus-Elsevier
Pediatric Research, 38, pp. 802-807
Pediatric Research, 38, 802-807
Scopus-Elsevier
Late events and side effects are reported in 392 children cured of leukemia. They originated from 1193 consecutively newly diagnosed children between 1972 and 1982, in first continuous complete remission for at least 6 y after diagnosis, and were tre
Autor:
J.D.J. Bakker, J.L.W.T. Lie, R M Egeler, Robbert G. M. Bredius, M.H. van Weel-Sipman, Jaak M. Vossen, A E Donker, Martin B. A. Heemskerk, Machteld Oudshoorn
Publikováno v:
Bone Marrow Transplantation, 45(1), 87-95
The transplant policy for unrelated donor (UD) BMT at Leiden Paediatrics' SCT-Centre consisted of the use of (1) fully HLA-matched donors or, if not available, HLA-class I matched and/or cytotoxic T-lymphocyte precursor (CTLp)-negative donors and (2)
Autor:
H. Struikmans, C Emmens, Henk B. Kal, T Révész, A. van der Does-van den Berg, M.H. van Weel-Sipman, M L van Kempen-Harteveld, Jaak M. Vossen, I. van der Tweel, Evert M. Noordijk
Publikováno v:
Bone marrow transplantation. 31(12)
This is a retrospective analysis of 188 children who underwent total body irradiation (TBI) in one or two fractions before bone marrow transplantation (BMT) for a hematological disorder. While 139 children had eye shielding during TBI to decrease cat
Publikováno v:
International journal of oral and maxillofacial surgery. 31(2)
Panoramic radiographs (orthopantomogram [OPT]) are, beside clinical examination, helpful in detecting possible dental foci of infections before bone marrow transplantation (BMT). The value of an OPT in paediatric BMT-recipients was assessed by the re
Publikováno v:
Bone marrow transplantation. 26(1)
We describe an infant with severe combined immunodeficiency syndrome and an alpha-thalassemia trait who developed a renal Fanconi syndrome after his first stem cell transplantation. This syndrome consists of a generalized failure of proximal tubular
Autor:
Guy Massa, M.H. van Weel-Sipman, J.M. Wit, J. M. J. J. Vossen, Wilma Oostdijk, Boudewijn Bakker
Publikováno v:
European journal of pediatrics. 159(1-2)
Pubertal development after total-body irradiation (TBI) was investigated in 40 children (21 boys) treated with allogeneic bone marrow transplantation (BMT) for haematological malignancies at a mean age of 11.3 years. The mean age at the last visit wa
Autor:
E.Th. van't Veer-Korthof, J. M. J. J. Vossen, H. van den Berg, M.H. van Weel-Sipman, E. J. A. Gerritsen, R.P. Kamphuis, Evert M. Noordijk
Publikováno v:
Radiotherapy and Oncology. 18:155-157
Twenty-seven children, surviving disease-free for more than 1 year after allogeneic bone marrow transplantation (BMT) for hematological malignancy were evaluated for the long-term effects on endocrine function, sexual development, physical growth, ap
Publikováno v:
Bone marrow transplantation. 21(5)
Fanconi anaemia (FA) is an accepted indication for treatment with allogeneic HLA-identical BMT. Most patients, however, lack a suitable HLA-identical donor. In our centre, six FA patients were transplanted with a matched unrelated donor. Due to hyper
Autor:
Wilma Oostdijk, J. Van den Broeck, M.H. van Weel-Sipman, J.M. Wit, J. M. J. J. Vossen, A.Clement-De Boers
Publikováno v:
The Journal of pediatrics. 129(4)
AIM: To analyze final height and hormonal function in long-term survivors of bone marrow transplantation (BMT). PATIENTS: Group 1 consisted of 16 patients (10 boys) with a hematologic malignancy, mostly leukemia, conditioned for BMT with total body i
Autor:
M.H. van Weel-Sipman
Publikováno v:
Pediatric Research. 41:777-777
Progressive organdysfunction is the consequence of iron-deposition caused by multiple transfusions in patients with transfusion dependend anaemia's like homozygous β-thalassaemia or Diamond-Blackfan anaemia (DBA). Regular chelation with deferioxamin