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Keimzelltumoren bei Kindern und Jugendlichen. Int J Cancer Germ-cell tumors in childhood and adolescence. Gene therapy holds great promise for FA, but previous attempts to use retroviral vectors in humans have proven ineffective given the impaired proliferation potential of human FA hematopoietic progenitors HPCs. Ui gleich 2 katzen und a Hai a no.

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    To study the association of PSI with disease stage at diagnosis, tumour control and survival in children with medulloblastoma, prospectively collected data on PSI, clinical, and biological features were analysed in patients diagnosed at the age of years and treated within the prospective randomised multicentre trial HIT' Intracranial ependymomas in children.

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    Radiation therapy of optico-hypothalamic gliomas OHG --radiographic response, vision and late toxicity. Determination of the relative allele expression showed that the Grace RF, Long M, Kalish LA, Neufeld EJ Applicability of international consensus terminology and criteria for immune thrombocytopenia to a clinical pediatric population.

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    Quatscha hilft dir ganz locker das Eis zu brechen! The aim of this study was to determine the prognostic relevance of molecular-cytogenetic abnormalities in pediatric patients using quantitative real-time polymerase chain reaction and fluorescence in situ hybridization. Development of lentiviral vectors with optimized transcriptional activity for the gene therapy of patients with fanconi anemia. Simultaneously, transition into a myelodysplastic syndrome MDS occurred.

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    Patients with lower-stage disease tended towards a longer median PSI than those with higher-stage disease M0 stage, 2.

    To accommodate for the characteristics of pediatric MDS, a simple classification scheme based on morphological features and conforming with the WHO suggestions was proposed. Hemangiomas in infancy and childhood.

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    Median follow-up was 79 months range, 4 months to months. Part A To accommodate for the characteristics of pediatric MDS, a simple classification scheme based on morphological features and conforming with the WHO suggestions was proposed.

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    1. The predominant site for the tumour was the femur, followed by the tibia. Subgroups of T-cell acute lymphoblastic leukemia T-ALLdefined according to recurrent cytogenetic aberrations, may have different prognoses.

    2. Patients' characteristics before and after transplant were provided by the European group blood and marrow transplant registry and were analyzed in collaboration with the European Fanconi Anemia Registry.

    3. Most DBA cases are caused by heterozygous null mutations in genes encoding ribosomal proteins.

    4. Quatscha hilft dir ganz locker das Eis zu brechen! Nine patients are alive with no evidence of disease recurrence at a median of 62 months from diagnosis range, 28 to monthsincluding three patients with metastatic disease and two infants who did not receive any radiotherapy.

    5. This study shows the dramatic impact of preexisting congenital malformations on the outcome of FA patients transplanted with HLA-matched unrelated donors.