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EJC paediatric oncology最新文献

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The rare cases of co-occurrences of Down Syndrome Disease and Juvenile Myelomonocytic Leukemia 罕见的唐氏综合症和幼年骨髓单核细胞白血病并发病例
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100090
Barbara Buldini , Manuela Tumino , Elena Varotto , Samuela Francescato , Alberto Peloso , Annamaria Di Meglio , Anna Leszl , Maria Gabelli , Alice Cani , Riccardo Masetti , Alessandra Biffi , Laura Sainati , Silvia Bresolin
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引用次数: 0
INTENSIVE CHEMOTHERAPY AS BRIDGING TO STEM CELL TRANSPLANTATION IN 5 YEAR OLD GIRL WITH JUVENILE MYELOMONOCYTIC LEUKEMIA– CASE REPORT 强化化疗作为干细胞移植的桥梁--5 岁幼年骨髓单核细胞白血病女孩的病例报告
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100103
Bartosz Chyżyński , Katarzyna Pawelec , Marek Ussowicz , Paweł Łaguna
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引用次数: 0
NATURAL HISTORY OF RALD: A 20 YEAR FOLLOW-UP OF A NRAS MUTATED PATIENT EXCLUDING A MALIGNANT PROGRESSION 拉尔德的自然史：对一名排除恶性进展的 Nras 突变患者 20 年的随访
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100104
Enrico Attardi , Beatrice Rivalta , Cristina Cifaldi , Vittorio Rosti , Lucia Pacillo , Hajro Hajrullaj , Silvia Di Cesare , Matteo Luciani , Federica Barzaghi , Andrea Finocchi , Gigliola Di Matteo , Alessandro Aiuti , Franco Locatelli , Maria Teresa Voso , Giuseppe Palumbo , Caterina Cancrini
{"title":"NATURAL HISTORY OF RALD: A 20 YEAR FOLLOW-UP OF A NRAS MUTATED PATIENT EXCLUDING A MALIGNANT PROGRESSION","authors":"Enrico Attardi , Beatrice Rivalta , Cristina Cifaldi , Vittorio Rosti , Lucia Pacillo , Hajro Hajrullaj , Silvia Di Cesare , Matteo Luciani , Federica Barzaghi , Andrea Finocchi , Gigliola Di Matteo , Alessandro Aiuti , Franco Locatelli , Maria Teresa Voso , Giuseppe Palumbo , Caterina Cancrini","doi":"10.1016/j.ejcped.2023.100104","DOIUrl":"https://doi.org/10.1016/j.ejcped.2023.100104","url":null,"abstract":"","PeriodicalId":94314,"journal":{"name":"EJC paediatric oncology","volume":"2 ","pages":"Article 100104"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772610X23001022/pdfft?md5=39adf4a532b24929390f1ecb927b6ff3&pid=1-s2.0-S2772610X23001022-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138738879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
THE INTERFACE OF EPIGENETICS AND ENERGY METABOLISM IN JUVENILE MYELOMONOCYTIC LEUKEMIA 幼年骨髓单核细胞白血病中表观遗传学与能量代谢的相互作用
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100037
Zoé Wehbe , Ruba Hammad , Toni Cathomen , Sheila Bohler , Jovana Rajak , Miriam Erlacher , Foued Ghanjati , Charlotte Niemeyer , Christian Flotho
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引用次数: 0
JUVENILE MYELOMONOCYTIC LEUKEMIA WITH TELOMERE SHORTENING: CASE REPORT 伴有端粒缩短的幼年骨髓单核细胞白血病：病例报告
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100111
Anita Frisanco Oliveira , Rafael Balceiro , Neysimelia Costa Villela , Luiz Fernando Lopes
{"title":"JUVENILE MYELOMONOCYTIC LEUKEMIA WITH TELOMERE SHORTENING: CASE REPORT","authors":"Anita Frisanco Oliveira , Rafael Balceiro , Neysimelia Costa Villela , Luiz Fernando Lopes","doi":"10.1016/j.ejcped.2023.100111","DOIUrl":"https://doi.org/10.1016/j.ejcped.2023.100111","url":null,"abstract":"","PeriodicalId":94314,"journal":{"name":"EJC paediatric oncology","volume":"2 ","pages":"Article 100111"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772610X23001095/pdfft?md5=a014b83200935f28202a8ec746440334&pid=1-s2.0-S2772610X23001095-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138738764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ILLUSTRATION OF CLONAL ARCHITECTURE IN JUVENILE MYELOMONOCYTIC LEUKEMIA BY TARGETED SINGLE-CELL DNA SEQUENCING 通过靶向单细胞 DNA 测序说明幼年骨髓单核细胞白血病的克隆结构
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100064
Foued Ghanjati , Miriam Erlacher , Dirk Lebrecht , Peter Nöllke , Franco Locatelli , European Working Group Of Myelodysplastic Syndromes In Childhood , Charlotte Niemeyer , Christian Flotho
{"title":"ILLUSTRATION OF CLONAL ARCHITECTURE IN JUVENILE MYELOMONOCYTIC LEUKEMIA BY TARGETED SINGLE-CELL DNA SEQUENCING","authors":"Foued Ghanjati , Miriam Erlacher , Dirk Lebrecht , Peter Nöllke , Franco Locatelli , European Working Group Of Myelodysplastic Syndromes In Childhood , Charlotte Niemeyer , Christian Flotho","doi":"10.1016/j.ejcped.2023.100064","DOIUrl":"https://doi.org/10.1016/j.ejcped.2023.100064","url":null,"abstract":"","PeriodicalId":94314,"journal":{"name":"EJC paediatric oncology","volume":"2 ","pages":"Article 100064"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772610X23000624/pdfft?md5=0f7b340a394fcec8960d0774732840f2&pid=1-s2.0-S2772610X23000624-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138738836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES runx1相关家族性血小板紊乱伴血液系统恶性肿瘤易感性的临床表型谱和体细胞变异基因
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100068
Alisa Förster, Melanie Decker, Yvonne L. Behrens, Gudrun Göhring, Brigitte Schlegelberger, Tim Ripperger
{"title":"SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES","authors":"Alisa Förster, Melanie Decker, Yvonne L. Behrens, Gudrun Göhring, Brigitte Schlegelberger, Tim Ripperger","doi":"10.1016/j.ejcped.2023.100068","DOIUrl":"https://doi.org/10.1016/j.ejcped.2023.100068","url":null,"abstract":"","PeriodicalId":94314,"journal":{"name":"EJC paediatric oncology","volume":"2 ","pages":"Article 100068"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772610X23000661/pdfft?md5=9b797bf624a949166df066cb20a6f31b&pid=1-s2.0-S2772610X23000661-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138738840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
CHILDHOOD MYELODYSPLASTIC NEOPLASM: GENETIC VARIANTS AND THEIR IMPACT ON DIAGNOSIS AND PROGNOSIS 儿童骨髓增生异常肿瘤：基因变异及其对诊断和预后的影响
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100085
Viviane Lovatel , Eliane Rodrigues , Gerson Ferreira , Claudia Atayde , Rita De Cássia Tavares , Ana Paula Bueno , Eliana Abdelhay , Teresa Fernandez
{"title":"CHILDHOOD MYELODYSPLASTIC NEOPLASM: GENETIC VARIANTS AND THEIR IMPACT ON DIAGNOSIS AND PROGNOSIS","authors":"Viviane Lovatel , Eliane Rodrigues , Gerson Ferreira , Claudia Atayde , Rita De Cássia Tavares , Ana Paula Bueno , Eliana Abdelhay , Teresa Fernandez","doi":"10.1016/j.ejcped.2023.100085","DOIUrl":"https://doi.org/10.1016/j.ejcped.2023.100085","url":null,"abstract":"","PeriodicalId":94314,"journal":{"name":"EJC paediatric oncology","volume":"2 ","pages":"Article 100085"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772610X23000831/pdfft?md5=46befc1e7d2b8bf2005d05b5c5505bb3&pid=1-s2.0-S2772610X23000831-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138738860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
IDENTIFICATION OF FUNCTIONAL DEFECTS LEADING TO BONE MARROW FAILURE IN GATA2 DEFICIENCY 鉴定导致 Gata2 缺乏症骨髓衰竭的功能缺陷
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100087
Charlotte Wantzen , Baris Yigit , Yuan Suo , Roland Meisel , Shu Zang , Julia Miriam Weiss , Juncal Fernandez-Orth , Miriam Erlacher
{"title":"IDENTIFICATION OF FUNCTIONAL DEFECTS LEADING TO BONE MARROW FAILURE IN GATA2 DEFICIENCY","authors":"Charlotte Wantzen , Baris Yigit , Yuan Suo , Roland Meisel , Shu Zang , Julia Miriam Weiss , Juncal Fernandez-Orth , Miriam Erlacher","doi":"10.1016/j.ejcped.2023.100087","DOIUrl":"https://doi.org/10.1016/j.ejcped.2023.100087","url":null,"abstract":"","PeriodicalId":94314,"journal":{"name":"EJC paediatric oncology","volume":"2 ","pages":"Article 100087"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772610X23000855/pdfft?md5=ed1d5e1a87f8734752564da3255c81aa&pid=1-s2.0-S2772610X23000855-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138738862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
JMML WITH NRAS MUTATION IN ELANE ASSOCIATED SEVERE CONGENITAL NEUTROPENIA 伊兰伴发重度先天性中性粒细胞减少症的JMML与NRAS突变
EJC paediatric oncology
Pub Date : 2023-12-01 DOI: 10.1016/j.ejcped.2023.100102
Hilde Hylland Uhlving , Dorthe Grosen , Mathias Rathe , Mette Klarskov , Henrik Hasle , Tania Nicole Masmas
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引用次数: 0
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