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

Year Number of Results
1981 1
1983 1
1987 1
1990 1
1991 1
1992 1
1993 1
1995 1
1996 2
1998 2
1999 2
2000 2
2001 4
2002 4
2003 1
2004 7
2005 4
2006 1
2007 6
2008 4
2009 4
2010 6
2011 5
2012 11
2013 5
2014 5
2015 6
2016 7
2017 5
2018 9
2019 4
2020 5
2021 13
2022 12
2023 6
2024 2

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131 results

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Page 1
Imaging of Tumor Syndromes.
Batchala PP, Eluvathingal Muttikkal TJ, Mukherjee S. Batchala PP, et al. Radiol Clin North Am. 2021 May;59(3):471-500. doi: 10.1016/j.rcl.2021.01.009. Radiol Clin North Am. 2021. PMID: 33926690 Review.
Phakomatoses and Endocrine Gland Tumors: Noteworthy and (Not so) Rare Associations.
Chevalier B, Dupuis H, Jannin A, Lemaitre M, Do Cao C, Cardot-Bauters C, Espiard S, Vantyghem MC. Chevalier B, et al. Front Endocrinol (Lausanne). 2021 May 6;12:678869. doi: 10.3389/fendo.2021.678869. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34025587 Free PMC article. Review.
Phakomatoses encompass a group of rare genetic diseases, such as von Hippel-Lindau syndrome (VHL), neurofibromatosis type 1 (NF1), tuberous sclerosis complex (TSC) and Cowden syndrome (CS). ...
Phakomatoses encompass a group of rare genetic diseases, such as von Hippel-Lindau syndrome (VHL), neurofibromat …
Multiple endocrine neoplasias.
Hoff AO, Cote GJ, Gagel RF. Hoff AO, et al. Annu Rev Physiol. 2000;62:377-411. doi: 10.1146/annurev.physiol.62.1.377. Annu Rev Physiol. 2000. PMID: 10845096 Review.
The multiple endocrine neoplasia syndromes form a distinct group of genetic tumor syndromes. They include multiple endocrine neoplasia types 1 and 2, von Hippel Lindau syndrome, neurofibromatosis, and Carney complex. ...
The multiple endocrine neoplasia syndromes form a distinct group of genetic tumor syndromes. They include multiple endocrine neoplasia types …
Update on Paragangliomas and Pheochromocytomas.
Lam AK. Lam AK. Turk Patoloji Derg. 2015;31 Suppl 1:105-12. doi: 10.5146/tjpath.2015.01318. Turk Patoloji Derg. 2015. PMID: 26177321 Free article. Review.
The classical syndromes comprise - neurofibromatosis, multiple neuroendocrine neoplasia (MEN) (II and III) syndromes and von Hippel-Lindau syndrome. Also, mutations in succinate dehydrogenase genes contribute to the understanding of hereditary paragang …
The classical syndromes comprise - neurofibromatosis, multiple neuroendocrine neoplasia (MEN) (II and III) syndromes and von Hippe …
Imaging Diagnosis of Von Hippel-Lindau Syndrome.
Xu N, Duan W, Zhang R, Yang B. Xu N, et al. J Craniofac Surg. 2019 Oct;30(7):e674-e677. doi: 10.1097/SCS.0000000000005760. J Craniofac Surg. 2019. PMID: 31574790
Gynecologic Manifestations of Less Commonly Encountered Hereditary Syndromes.
DeLair DF, Soslow RA. DeLair DF, et al. Surg Pathol Clin. 2016 Jun;9(2):269-87. doi: 10.1016/j.path.2016.01.008. Epub 2016 Apr 11. Surg Pathol Clin. 2016. PMID: 27241108 Review.
Recent advances in disorders, such as hereditary leiomyomatosis, renal cell carcinoma syndrome and tuberous sclerosis complex, are discussed as well as lesions that occur in von Hippel-Lindau syndrome, nevoid basal cell carcinoma syndrome, Cowden syndr …
Recent advances in disorders, such as hereditary leiomyomatosis, renal cell carcinoma syndrome and tuberous sclerosis complex, are discussed …
Multiple endocrine neoplasia syndromes.
Callender GG, Rich TA, Perrier ND. Callender GG, et al. Surg Clin North Am. 2008 Aug;88(4):863-95, viii. doi: 10.1016/j.suc.2008.05.001. Surg Clin North Am. 2008. PMID: 18672144 Review.
However, several other hereditary conditions should also be considered in the category of MEN: von Hippel-Lindau syndrome, the familial paraganglioma syndromes, Cowden syndrome, Carney complex, and hyperparathyroidism jaw-tumor syndrome. ...
However, several other hereditary conditions should also be considered in the category of MEN: von Hippel-Lindau syn …
The phakomatoses.
Korf BR. Korf BR. Clin Dermatol. 2005 Jan-Feb;23(1):78-84. doi: 10.1016/j.clindermatol.2004.09.007. Clin Dermatol. 2005. PMID: 15708292 Review.
He included 3 disorders in the group-neurofibromatosis, tuberous sclerosis complex, and von Hippel-Lindau syndrome--on the basis of the occurrence of patchy ophthalmologic manifestations in each disorder. ...
He included 3 disorders in the group-neurofibromatosis, tuberous sclerosis complex, and von Hippel-Lindau syndrome …
131 results