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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|April 17, 2025
Safety and quality of life of PSMA-PET- and MRI-based focal dose escalated radiotherapy for intermediate- and high-risk prostate cancer: Primary endpoint analysis of the bi-centric phase II HypoFocal trial (ARO2020-01)Simon K B Spohn, Constantinos Zamboglou, Sophia L Bürkle, et al.
Leukemia|June 1, 2002
BFM-oriented treatment for children with acute lymphoblastic leukemia without cranial irradiation and treatment reduction for standard risk patients: results of DCLSG protocol ALL-8 (1991-1996)W A Kamps, J P M Bökkerink, F G A J Hakvoort-Cammel, et al.
Leukemia|October 12, 2007
Prognostic significance of molecular-cytogenetic abnormalities in pediatric T-ALL is not explained by immunophenotypic differencesM van Grotel, J P P Meijerink, E R van Wering, et al.
Frontiers in Molecular Neuroscience|November 3, 2017
Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I DefectTom E J Theunissen, Mike Gerards, Debby M E I Hellebrekers, et al.
Haematologica|September 8, 2006
The outcome of molecular-cytogenetic subgroups in pediatric T-cell acute lymphoblastic leukemia: a retrospective study of patients treated according to DCOG or COALL protocolsMartine van Grotel, Jules P P Meijerink, H Berna Beverloo, et al.
Blood|August 10, 1999
Intensive treatment of children with acute lymphoblastic leukemia according to ALL-BFM-86 without cranial radiotherapy: results of Dutch Childhood Leukemia Study Group Protocol ALL-7 (1988-1991)W A Kamps, J P Bökkerink, K Hählen, et al.
Leukemia|December 3, 2011
Polymorphisms in the TLR6 gene associated with the inverse association between childhood acute lymphoblastic leukemia and atopic diseaseK G E Miedema, W J E Tissing, E M Te Poele, et al.
Cancer Research|February 11, 1998
A lack of neuroblastoma in Down syndrome: a study from 11 European countriesD Satgé, A J Sasco, N L Carlsen, et al.
The Journal of Pediatrics|January 14, 2017
Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome SequencingTom E J Theunissen, Suzanne C E H Sallevelt, Debby M E I Hellebrekers, et al.
Human Molecular Genetics|July 11, 2006
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulationValerie L R M Verstraeten, Jos L V Broers, Maurice A M van Steensel, et al.
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