Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Intralobar Nephrogenic Rest"'
Autor:
Chaima Mrad, Hubert Ducou Le Pointe, Marie-Dominique Tabone, Aurore Coulomb, Sabine Irtan, Georges Audry
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e740-e742
Botryoid growth pattern (BGP) is a polypoid mass growing into the renal pelvis, rarely seen in bilateral Wilms tumors where it represents a surgical challenge. We report our experience of nephron sparing surgery in 3 patients with BGP in bilateral Wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63cb61b23dc4f4a48e1d30435b19f77d
https://doi.org/10.1097/mph.0000000000002337
https://doi.org/10.1097/mph.0000000000002337
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 7:119-124
Nephrogenic rests and nephroblastomatosis describe persistence of embryonic renal parenchyma (metanephric blastema) beyond 36 weeks of gestation, when nephrogenesis is normally complete. This persistent metanephric blastema may transform into the Wil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::944471ef37db1bc3fd073213ea8b56df
https://doi.org/10.21682/2311-1267-2020-7-3-119-124
https://doi.org/10.21682/2311-1267-2020-7-3-119-124
Autor:
Frederik Braun, Tobias B. Haack, Ulrike Schara, Petra Stöbe, Andreas Roos, Andrea Gangfuß, Bernd Schweiger
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 12, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Diaphanospondylodysostosis (DSD) is a rare congenital, lethal skeletal disorder caused by recessively inherited mutations in the BMPER gene, which encodes the bone morphogenetic protein‐binding endothelial cell precursor‐derived regula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::033f184b5692a3534f18f6bcc620733e
https://www.ncbi.nlm.nih.gov/pubmed/34288564
https://www.ncbi.nlm.nih.gov/pubmed/34288564
Autor:
Shih-Hsiang Chen, Chao-Jan Wang, Tang-Her Jaing, Chao-Ping Yang, Jin-Yao Lai, Chuen Hsueh, Iou-Jih Hung
Publikováno v:
Asia-Pacific Journal of Clinical Oncology. 12:300-307
Aims Wilms tumor (WT) is rare in Asia. Treatment of bilateral WT is challenging, and the treatment outcome of bilateral WT is rarely reported in low incidence areas. Methods We enrolled patients with bilateral WT registered in Chang Gung Memorial Hos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce3708d6d5897612a47f4f5faecb370a
https://doi.org/10.1111/ajco.12501
https://doi.org/10.1111/ajco.12501
Autor:
Neil J. Sebire, Richard D. Williams, Kathy Pritchard-Jones, John R. Apps, Federica Ceroni, Gordan M. Vujanic, Veronica Moroz
Publikováno v:
Pediatric bloodcancer. 64(11)
BACKGROUND: Nephrogenic rests (NRs) are abnormally persistent foci of embryonal cells, thought to be the precursor lesion of Wilms tumors (WTs). To date, their presence has not been systematically examined in WTs treated with preoperative chemotherap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da1ca182b962440df852980b5beef451
https://pubmed.ncbi.nlm.nih.gov/28383760
https://pubmed.ncbi.nlm.nih.gov/28383760
Autor:
Elanthenral Sigamani, Mohammad Nahidul Wari, Sandeep Agarwala, Sameer Bakhshi, Amit K. Dinda, Arundhati Sharma, Venkateswaran K. Iyer
Publikováno v:
Pediatric Surgery International. 29:223-227
11p13 and 11p15 loss of heterozygosity (LOH) in Wilms tumor (WT), the commonest molecular pathogenetic event in WT, shows variation in different parts of the world. The present study looked for the presence of 11p13 and 11p15 LOH as well as nephrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::203a70afb871ba3f4f2d08aa0d5e0707
https://doi.org/10.1007/s00383-012-3254-8
https://doi.org/10.1007/s00383-012-3254-8
Autor:
E. Cristy Ruteshouser, Elizabeth J. Perlman, Paul E. Grundy, Jeffrey S. Dome, Vicki Huff, Lawrence J. Jennings, Samantha Gadd, Chiang Ching Huang, Daniel M. Green, J. Bruce Beckwith, Norman E. Breslow
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 14, Iss 8, Pp 742-756 (2012)
Wilms tumors (WT) have provided broad insights into the interface between development and tumorigenesis. Further understanding is confounded by their genetic, histologic, and clinical heterogeneity, the basis of which remains largely unknown. We eval
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87124416f17f69951f9b0f0f38492cae
http://www.sciencedirect.com/science/article/pii/S147655861280008X
http://www.sciencedirect.com/science/article/pii/S147655861280008X
Autor:
Kentaro Mizuno, Shoichiro Iwatsuki, Yutaro Hayashi, Yoshiyuki Kojima, Kenjiro Kohri, Keiichi Tozawa
Publikováno v:
Urology. 76:149-152
Nephrogenic rests are nodular collections of undifferentiated renal blastema cells in the postnatal kidney that are recognized as putative precursor lesions of Wilms tumor. In this study, we report the case of a 3-year-old boy who was diagnosed with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6e9d0f56ee7019e763ab5f47a82384
https://doi.org/10.1016/j.urology.2009.09.012
https://doi.org/10.1016/j.urology.2009.09.012
Autor:
Anthony E. Reeve, Ryuji Fukuzawa
Publikováno v:
Journal of Pediatric Hematology/Oncology. 29:589-594
Perilobar (PLNR) and intralobar nephrogenic rests (ILNR) are distinct precursor lesions of Wilms tumors that have different structural, clinical, genetic, and epidemiologic features. Wilms tumors in East-Asian children have unique epidemiologic featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dd8fe5f4f031e1e758b7a97760d81bf
https://doi.org/10.1097/01.mph.0000212981.67114.ec
https://doi.org/10.1097/01.mph.0000212981.67114.ec
Autor:
Jaime M. Guidry Auvil, Stefan T. Arold, Chih Hao Hsu, Tanja Davidsen, Daoud Meerzaman, Marco A. Marra, Oliver A. Hampton, Charles G. Mullighan, Nicole Ross, Cu Nguyen, Elizabeth J. Perlman, Andrew J. Mungall, Samantha Gadd, Vicki Huff, Yussanne Ma, Daniela S. Gerhard, D Wheeler, Jeffrey S. Dome, Anand Radhakrishnan, Malcolm A. Smith, Jing Ma, Richard A. Moore, James M. Anderson, Lawrence J. Jennings, Julie M. Gastier-Foster
Publikováno v:
Nature Communications
Wilms tumour is an embryonal tumour of childhood that closely resembles the developing kidney. Genomic changes responsible for the development of the majority of Wilms tumours remain largely unknown. Here we identify recurrent mutations within Wilms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a908df8a3d5bc981191cef01d64548d
https://doi.org/10.1038/ncomms10013
https://doi.org/10.1038/ncomms10013