Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas-Reference-Cited by-同舟云学术

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Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas

Published:2011-04-05 Issue:4 Volume:17 Page:801-808
ISSN:1219-4956
Container-title:Pathology & Oncology Research
language:en
Short-container-title:Pathol. Oncol. Res.

Author:

Vicha Ales,Holzerova Milena,Krepelova Anna,Musil Zdenek,Prochazka Pavel,Sumerauer David,Kodet Roman,Eckschlager Tomas,Jarosova Marie

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology,General Medicine,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12253-011-9385-8.pdf

Reference33 articles.

1. Havekes B, Romijn JA, Eisenhofer G et al (2009) Update on pediatric pheochromocytoma. Pediatr Nephrol 24:943–950

2. Lenders JW, Eisenhofer G, Mannelli M et al (2005) Phaeochromocytoma. Lancet 366:665–675

3. Lemeta S, Salmenkivi K, Pylkkanen L et al (2006) Frequent loss of heterozygosity at 6q in pheochromocytoma. Hum Pathol 37:749–754

4. Ciftci AO, Tanyel FC, Senocak ME et al (2001) Pheochromocytoma in children. J Pediatr Surg 36:447–452

5. Ross JH (2000) Pheochromocytoma. Special considerations in children. Urol Clin North Am 27:393–402

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Age-Related Chromosomal Aberrations in Patients with Diffuse Large B-Cell Lymphoma: An In Silico Approach;World Journal of Oncology;2018

2. p.N78S and p.R161Q germline mutations of the VHL gene are present in von Hippel-Lindau syndrome in two pedigrees;Molecular Medicine Reports;2013-07-09

3. Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-Level Uniparental Disomy;American Journal of Medical Genetics Part A;2013-03-26

4. An Unusual Case of Gastrointestinal Bleeding;Case Reports in Pediatrics;2011

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