Výsledky vyhledávání - "van, Noesel MM"

Akademický článek

Treatment at Relapse for Synovial Sarcoma of Children, Adolescents and Young Adults: From the State of Art to Future Clinical Perspectives

Autor: Ferrari A, Berlanga P, Gatz SA, Schoot RA, van Noesel MM, Hovsepyan S, Chiaravalli S, Bergamaschi L, Minard-Colin V, Corradini N, Alaggio R, Gasparini P, Brennan B, Casanova M, Pasquali S, Orbach D

Publikováno v: Cancer Management and Research, Vol Volume 15, Pp 1183-1196 (2023)

Andrea Ferrari,1 Pablo Berlanga,2 Susanne Andrea Gatz,3 Reineke A Schoot,4 Max M van Noesel,4,5 Shushan Hovsepyan,6 Stefano Chiaravalli,1 Luca Bergamaschi,1 Veronique Minard-Colin,2 Nadege Corradini,7 Rita Alaggio,8 Patrizia Gasparini,9 Bernadette Br

Externí odkaz: https://doaj.org/article/3e6e0b9c0f6443eebf852be4af465b32

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Akademický článek

Pediatric Non-Rhabdomyosarcoma Soft Tissue Sarcomas: Standard of Care and Treatment Recommendations from the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG)

Autor: Ferrari A, Brennan B, Casanova M, Corradini N, Berlanga P, Schoot RA, Ramirez-Villar GL, Safwat A, Guillen Burrieza G, Dall'Igna P, Alaggio R, Lyngsie Hjalgrim L, Gatz SA, Orbach D, van Noesel MM

Publikováno v: Cancer Management and Research, Vol Volume 14, Pp 2885-2902 (2022)

Andrea Ferrari,1 Bernadette Brennan,2 Michela Casanova,1 Nadege Corradini,3 Pablo Berlanga,4 Reineke A Schoot,5 Gema L Ramirez-Villar,6 Akmal Safwat,7 Gabriela Guillen Burrieza,8 Patrizia Dall’Igna,9 Rita Alaggio,10 Lisa Lyngsie Hjalgrim,11 Susanne

Externí odkaz: https://doaj.org/article/3925a99ee9c148ecb40828b0dd804014

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Single-cell atlas of developing murine adrenal gland reveals relation of Schwann cell precursor signature to neuroblastoma phenotype

Autor: Hanemaaijer, ES, Margaritis, T, Sanders, K, Bos, FL, Candelli, T, Al-Saati, H, van, Noesel MM, Meyer-Wentrup, FAG, van, de Wetering M, Holstege, FCP, Clevers, H, Interne geneeskunde GD, dCSCA AVR, dCSCA RMSC-2, Faculteit Diergeneeskunde, CS_Cancer

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, 118(5). National Academy of Sciences
Proceedings of the National Academy of Sciences

Significance Neuroblastoma is a childhood malignancy that originates from neural crest cells. We present a single-cell transcriptome and localization atlas of the developing adrenal gland and identify seven different cell clusters that make up the ad

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c3a84e7c4fb288538e4594a29283370
https://pubmed.ncbi.nlm.nih.gov/33500353

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Giant Intraparenchymal Schwannoma with Bone Remodeling: Case Report of a 17-year-old Boy

Autor: Tas Ml, Van de Sande Maj, Hehir-Kwa Jy, Van den Boogaard Ml, Schild Gg, Molenaar Jj, Martin Hsiu Chu Lin, Jen Tsung Yang, Ming Hsueh Lee, Koster J, Bovée Jvmg, Van Noesel Mm, Flucke Ue, Yu Jen Kuo

Publikováno v: Biomedical Journal of Scientific & Technical Research. 27

Intracranial schwannomas account for 8% of all primary brain tumours [1] and are derived from Schwann cells in the peripheral...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::af755e8f87f1a7e8dbf0f016964a0a9c
https://doi.org/10.26717/bjstr.2020.27.004579

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ZFP42: A New Tumor Predisposition Gene? Presentation of a Patient with two Neoplasms in Childhood

Autor: Tas Ml, Van de Sande Maj, Molenaar Jj, Schild Gg, Bovée Jvmg, Koster J, Hehir-Kwa Jy, Van Noesel Mm, Van den Boogaard Ml, Flucke Ue

Publikováno v: Biomedical Journal of Scientific & Technical Research. 27

Neuroblastoma is a developmental malignancy of the neural crest [1]. Tumors typically arise in young children...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0b3b10226859109ec999152759c85067
https://doi.org/10.26717/bjstr.2020.27.004578

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Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas

Autor: Theo J. M. Hulsebos, van Noesel Mm, Andries Westerveld, M. Luijten, S. Redeker, Dirk Troost

Publikováno v: European journal of human genetics, 8(12), 939-945. Nature Publishing Group

Neurofibromatosis type 1 (NF1) is a frequent hereditary disorder. One of the characteristic features of this disease is the development of neurofibromas. Since the NF1 gene is supposed to be a tumour suppressor gene, these neurofibromas should develo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6c53c4eb797b9f18c77a5034d06d6cd
https://pubmed.ncbi.nlm.nih.gov/11175282

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