Zobrazeno 1 - 10
of 27
pro vyhledávání: '"G. A. M. de Vaan"'
Publikováno v:
British Journal of Visual Impairment, 38, 2, pp. 168-183
British Journal of Visual Impairment, 38, 168-183
British Journal of Visual Impairment, 38, 168-183
Contains fulltext : 218473.pdf (Publisher’s version ) (Open Access) Stereotyped and repetitive behaviours are characteristics of autism spectrum disorder (ASD) but also occur in individuals with combined intellectual and sensory disabilities. This
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
Publikováno v:
Pediatric Hematology and Oncology. 11:83-90
The light chain ratios and the concentrations of immunoglobulin G (IgG), IgA, and IgM were measured before, during, and after antileukemic therapy in 10 patients with common acute lymphoblastic leukemia. The concentrations of IgG, IgA, and IgM decrea
Publikováno v:
Acta Paediatrica. 77:224-225
Autor:
G. A. M. de Vaan, Jan A.J.M. Bakkeren, I.S. Klasen, Ásgeir Haraldsson, Corry M.R. Weemaes, F.W.M.B. Preijers
Publikováno v:
European Journal of Pediatrics, 155, 2, pp. 96-98
European Journal of Pediatrics, 155, 96-98
European Journal of Pediatrics, 155, 96-98
We describe a patient with myelodysplastic syndrome with monosomy 7 presenting with a T-cell defect. He suffered from infections from the age of 10 years, when a CD4 deficiency and impaired lymphoproliferative responses in vitro were found. The only
Autor:
WA Kamps, E.F. van Leeuwen, G. A. M. de Vaan, Stefan Suciu, G. Solbu, Karel Hählen, A. J. P. Veerman, E. R. Van Wering, A. van der Does-van den Berg
Publikováno v:
Journal of Clinical Oncology, 14, pp. 911-918
Journal of Clinical Oncology, 14, 3, pp. 911-918
Journal of Clinical Oncology, 14, 911-918
Journal of Clinical Oncology, 14, 3, pp. 911-918
Journal of Clinical Oncology, 14, 911-918
PURPOSE Here we report the results of a nationwide cooperative study in the Netherlands on acute lymphoblastic leukemia (ALL) in children. The aim of the study was to improve the cure rate and to minimize side effects in a group of non-high-risk ALL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1376f126a999db420f57c7628266183
https://hdl.handle.net/2066/189009
https://hdl.handle.net/2066/189009
Publikováno v:
Pediatric Hematology and Oncology, 12, pp. 571-573
Pediatric Hematology and Oncology, 12, 571-573
Pediatric Hematology and Oncology, 12, 571-573
Noonan's syndrome (NS) is a syndrome with multiple congenital anomalies, characterized by craniofacial anomalies, congenital heart disease, skeletal and genital abnormalities, and mild mental retardation. Chromosomal abnormalities have been found in
Publikováno v:
European journal of pediatrics. 151(4)
A girl with acute non-lymphoblastic leukaemia was treated with immunosuppressive chemotherapy. After cessation of therapy she had three consecutive episodes of infection due to Streptococcus pneumoniae from which she recovered and was shown to have d
Publikováno v:
Medical and pediatric oncology. 18(4)
The frequency of naevocytic naevi (moles) in patients with childhood haematologic malignancies was studied. All patients had received multiple chemotherapy. The majority had also received cranial irradiation as part of their central nervous system le
Publikováno v:
Cancer. 43:749-759
About 90% of Caucasian individuals in the general population may observe two transverse palmar flexion creases when their fingers are slightly bent. A small minority may find in one hand a single transverse crease or the usual two creases, of which o