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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2000 1
2001 3
2002 2
2003 1
2004 1
2005 1
2007 1
2008 1
2009 2
2011 2
2012 7
2013 3
2014 4
2015 2
2016 1
2017 3
2018 3
2019 4
2020 1
2021 1
2022 1
2024 0

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39 results

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Page 1
The genetics of paragangliomas.
Burnichon N, Abermil N, Buffet A, Favier J, Gimenez-Roqueplo AP. Burnichon N, et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2012 Dec;129(6):315-8. doi: 10.1016/j.anorl.2012.04.007. Epub 2012 Oct 15. Eur Ann Otorhinolaryngol Head Neck Dis. 2012. PMID: 23078982 Free article. Review.
Identification of a germline mutation on the SDHB gene is a high-risk factor for malignancy and poor prognosis and requires close surveillance of subjects carrying this mutation. The diagnosis of hereditary paraganglioma also allows predictive genetic screening in f …
Identification of a germline mutation on the SDHB gene is a high-risk factor for malignancy and poor prognosis and requires close surveillan …
Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.
Rednam SP, Erez A, Druker H, Janeway KA, Kamihara J, Kohlmann WK, Nathanson KL, States LJ, Tomlinson GE, Villani A, Voss SD, Schiffman JD, Wasserman JD. Rednam SP, et al. Clin Cancer Res. 2017 Jun 15;23(12):e68-e75. doi: 10.1158/1078-0432.CCR-17-0547. Clin Cancer Res. 2017. PMID: 28620007 Review.
Another neuroendocrine-related familial condition is the rapidly expanding hereditary paraganglioma and pheochromocytoma syndrome (HPP). The tumor spectrum for patients with HPP syndrome includes paragangliomas, pheochromocytomas, renal cancer, and gastrointestinal …
Another neuroendocrine-related familial condition is the rapidly expanding hereditary paraganglioma and pheochromocytoma syndr …
Genetic testing by cancer site: urinary tract.
Chan-Smutko G. Chan-Smutko G. Cancer J. 2012 Jul-Aug;18(4):343-9. doi: 10.1097/PPO.0b013e31826246ac. Cancer J. 2012. PMID: 22846736 Review.
The key features of 5 hereditary cancer susceptibility conditions involving an increased risk for RCC are discussed. von Hippel-Lindau disease, hereditary papillary RCC, and hereditary leiomyomatosis and RCC each predispose to a specific histological type of RCC, whereas Birt-Hog …
The key features of 5 hereditary cancer susceptibility conditions involving an increased risk for RCC are discussed. von Hippel-Lindau disea …
Functional consequences of succinate dehydrogenase mutations.
Opocher G, Schiavi F. Opocher G, et al. Endocr Pract. 2011 Jul-Aug;17 Suppl 3:64-71. doi: 10.4158/EP11070.RA. Endocr Pract. 2011. PMID: 21742608 Review.
To explore the genotype-phenotype correlation among the different forms of hereditary paraganglioma. METHODS: We reviewed the pertinent literature on hereditary paragangliomas, which showed the established classification of types 1, 2, 3, and 4 paraganglioma syndrom …
To explore the genotype-phenotype correlation among the different forms of hereditary paraganglioma. METHODS: We reviewed the …
Predisposition to pediatric and hematologic cancers: a moving target.
Malkin D, Nichols KE, Zelley K, Schiffman JD. Malkin D, et al. Am Soc Clin Oncol Educ Book. 2014:e44-55. doi: 10.14694/EdBook_AM.2014.34.e44. Am Soc Clin Oncol Educ Book. 2014. PMID: 24857136 Free article. Review.
In this article, we illustrate the diversity of molecular mechanisms by which these disorders develop in both children and adults with a focus on Li-Fraumeni syndrome, hereditary paraganglioma syndrome, DICER1 syndrome, and multiple endocrine neoplasia syndrome. ...
In this article, we illustrate the diversity of molecular mechanisms by which these disorders develop in both children and adults with a foc …
Genomic imprinting and environment in hereditary paraganglioma.
Baysal BE. Baysal BE. Am J Med Genet C Semin Med Genet. 2004 Aug 15;129C(1):85-90. doi: 10.1002/ajmg.c.30018. Am J Med Genet C Semin Med Genet. 2004. PMID: 15264276 Review.
Hereditary paraganglioma (PGL) is characterized by the development of slow-growing and vascularized tumors in the paraganglionic system. ...
Hereditary paraganglioma (PGL) is characterized by the development of slow-growing and vascularized tumors in the paraganglion …
The role of complex II in disease.
Hoekstra AS, Bayley JP. Hoekstra AS, et al. Biochim Biophys Acta. 2013 May;1827(5):543-51. doi: 10.1016/j.bbabio.2012.11.005. Epub 2012 Nov 20. Biochim Biophys Acta. 2013. PMID: 23174333 Free article. Review.
An array of tumor syndromes caused by complex II-associated gene mutations, in both succinate dehydrogenase and associated accessory factor genes (SDHA, SDHB, SDHC, SDHD, SDHAF1, SDHAF2), have been identified over the last 12 years and include hereditary paraganglioma …
An array of tumor syndromes caused by complex II-associated gene mutations, in both succinate dehydrogenase and associated accessory factor …
Whole-body magnetic resonance imaging (WB-MRI) in oncology: recommendations and key uses.
Petralia G, Padhani AR, Pricolo P, Zugni F, Martinetti M, Summers PE, Grazioli L, Colagrande S, Giovagnoni A, Bellomi M; Italian Working Group on Magnetic Resonance. Petralia G, et al. Radiol Med. 2019 Mar;124(3):218-233. doi: 10.1007/s11547-018-0955-7. Epub 2018 Nov 14. Radiol Med. 2019. PMID: 30430385 Review.
In oncology, the role of WB-MRI has expanded to the point of being recommended in international guidelines for the assessment of several cancer histotypes (multiple myeloma, melanoma, prostate cancer) and cancer-prone syndromes (Li-Fraumeni and hereditary paraganglioma …
In oncology, the role of WB-MRI has expanded to the point of being recommended in international guidelines for the assessment of several can …
New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.
Bertherat J, Gimenez-Roqueplo AP. Bertherat J, et al. Horm Metab Res. 2005 Jun;37(6):384-90. doi: 10.1055/s-2005-870156. Horm Metab Res. 2005. PMID: 16001332 Review.
Up to date, four diagnosis of familal disease (multiple endocrine neoplasia type II, von Hippel Lindau disease, neurofibromatosis type 1 and hereditary paraganglioma) should be discussed and causative mutations in six different phaechomocytoma susceptibility genes ( …
Up to date, four diagnosis of familal disease (multiple endocrine neoplasia type II, von Hippel Lindau disease, neurofibromatosis type 1 and …
39 results