Literatur

Zuletzt geändert: 02.10.2024 https://kinderkrebsinfo.de/doi/e8952

Autor(en) Titel Quelle Links
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Albrecht S, von Schweinitz D, Waha A, Kraus J, von Deimling A, Pietsch T Loss of maternal alleles on chromosome arm 11p in hepatoblastoma. Cancer Res 1994, 54: 5041    
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Albert MH, Freeman AF Wiskott-Aldrich Syndrome (WAS) and Dedicator of Cytokinesis 8- (DOCK8) Deficiency. Frontiers in pediatrics 2019, 7: 451    
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Alten J, Klapper W, Leuschner I, Eckert C, Beier R, Vallo E, Krause M, Claviez A, Vieth S, Bleckmann K, Möricke A, Schrappe M, Cario G Secondary histiocytic sarcoma may cause apparent persistence or recurrence of minimal residual disease in childhood acute lymphoblastic leukemia. Pediatr Blood Cancer 2015, 62: 1656    
Altintas B, Giri N, McReynolds LJ, Best A, Alter BP Genotype-phenotype and outcome associations in patients with Fanconi anemia: The National Cancer Institute cohort. Haematologica 2022,    
Alvarez O, Rodriguez MM, Jordan L, Sarnaik S Renal medullary carcinoma and sickle cell trait: A systematic review. Pediatric blood & cancer 2015, 62: 1694    
Ambros I, Attarbaschi A, Rumpler S, Luegmayr A, Turkof E, Gadner H, Ambros P Neuroblastoma cells provoke Schwann cell proliferation in vitro. Med Pediatr Oncol 2001, 36: 163    
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Attarbaschi A, Mann G, Dworzak M, Wiesbauer P, Schrappe M, Gadner H Mediastinal mass in childhood T-cell acute lymphoblastic leukemia. Med Pediatr Oncol 2002, 39: 558    
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Attiyeh EF, London WB, Mossé YP, Wang Q, Winter C, Khazi D, McGrady PW, Seeger RC, Look AT, Shimada H, Brodeur GM, Cohn SL, Matthay KK, Maris JM, Children's Oncology Group Chromosome 1p and 11q deletions and outcome in neuroblastoma. The New England journal of medicine 2005 Nov 24; 353: 2243    
Attarbaschi A, Mann G, Panzer-Grümayer R, Röttgers S, Steiner M, König M, Csinady E, Dworzak MN, Seidel M, Janousek D, Möricke A, Reichelt C, Harbott J, Schrappe M, Gadner H, Haas OA Minimal residual disease values discriminate between low and high relapse risk in children with B-cell precursor acute lymphoblastic leukemia and an intrachromosomal amplification of chromosome 21: the Austrian and German acute lymphoblastic leukemia Berlin-Frankfurt-Münster (ALL-BFM) trials. Journal of clinical oncology 2008, 26: 3046    
Attarbaschi A, Panzer-Grümayer R, Mann G, Möricke A, König M, Mecklenbräuker A, Teigler-Schlegel A, Bradtke J, Harbott J, Göhring G, Stanulla M, Schrappe M, Zimmermann M, Haas OA, Austrian and German ALL-BFM (Berlin-Frankfurt-Münster) Study Group Minimal residual disease-based treatment is adequate for relapse-prone childhood acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21: the experience of the ALL-BFM 2000 trial. Klinische Padiatrie 2014, 226(6-7): 338    
Attarbaschi A, Carraro E, Abla O, Barzilai-Birenboim S, Bomken S, Brugieres L, Bubanska E, Burkhardt B, Chiang AK, Csoka M, Fedorova A, Jazbec J, Kabickova E, Krenova Z, Lazic J, Loeffen J, Mann G, Niggli F, Miakova N, Osumi T, Ronceray L, Uyttebroeck A, Williams D, Woessmann W, Wrobel G, Pillon M, European Intergroup for Childhood Non-Hodgkin Lymphoma (EICNHL) and the International Berlin-Frankfurt-Münster (i-BFM) Study Group Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents. Haematologica 2016, 101: 1581    
Attarbaschi A, Mann G, Zimmermann M, Bader P, Barisone E, Basso G, Biondi A, Cario G, Cazzaniga G, Colombini A, Flotho C, Kuhlen M, Lang P, Lauten M, Linderkamp C, Locatelli F, Lo Nigro L, Moericke A, Niggli F, Panzer-Gruemayer R, Parasole R, Peters C, Caterina Putti M, Rizzari C, Suttorp M, Valsecchi MG, Conter V, Schrappe M, on behalf of the AIEOP-BFM (Associazione Italiana di Ematologia e Oncologia Pediatrica & Berlin-Frankfurt-Muenster) Study Group Randomized post-induction and delayed intensification therapy in high-risk pediatric acute lymphoblastic leukemia: long-term results of the international AIEOP-BFM ALL 2000 trial. Leukemia 2019 Dec 5;    
Attarbaschi A, Möricke A, Harrison CJ, Mann G, Baruchel A, De Moerloose B, Conter V, Devidas M, Elitzur S, Escherich G, Hunger SP, Horibe K, Manabe A, Loh ML, Pieters R, Schmiegelow K, Silverman LB, Stary J, Vora A, Pui CH, Schrappe M, Zimmermann M, Ponte-di-Legno Childhood Acute Lymphoblastic Leukemia Working Group Outcomes of Childhood Noninfant Acute Lymphoblastic Leukemia With 11q23/KMT2A Rearrangements in a Modern Therapy Era: A Retrospective International Study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2023, 41: 1404    
Attiyeh EF, London WB, Mossé YP, Wang Q, Winter C, Khazi D, McGrady PW, Seeger RC, Look AT, Shimada H, Brodeur GM, Cohn SL, Matthay KK, Maris JM, Children's Oncology Group Chromosome 1p and 11q deletions and outcome in neuroblastoma. The New England journal of medicine 2005 Nov 24; 353: 2243    
Auerbach AD Fanconi anemia and its diagnosis. Mutat Res 2009, 668(1-2): 4    
Au-Yeung RKH, Richter J, Iaccarino I, Abramov D, Bacon CM, Balagué O, d'Amore ESG, Simonitsch-Klupp I, Hebeda K, Nakazawa A, Oschlies I, Kontny U, Woessmann W, Burkhardt B, Klapper W Molecular features of non-anaplastic peripheral T-cell lymphoma in children and adolescents. Pediatric blood & cancer 2021, 68:e29285    
Au-Yeung RKH, Richter J, Iaccarino I, Abramov D, Bacon CM, Balagué O, d'Amore ESG, Simonitsch-Klupp I, Hebeda K, Nakazawa A, Oschlies I, Kontny U, Woessmann W, Burkhardt B, Klapper W Molecular features of non-anaplastic peripheral T-cell lymphoma in children and adolescents. Pediatric blood & cancer 2021, 68:e29285    
Au-Yeung RKH, Padilla LA, Zimmermann M, Reinke S, Oschlies I, Escherich G, Woessmann W, Burkhardt B, Klapper W Frequency and prognostic implications of KMT2A rearrangements in children with precursor B-cell lymphoma. Leukemia 2023, 37: 488    
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