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Quoted phrase not found in phrase index: "Cowden syndrome 7"
Page 1
Nervous system (NS) Tumors in Cancer Predisposition Syndromes.
Patil P, Pencheva BB, Patil VM, Fangusaro J. Patil P, et al. Neurotherapeutics. 2022 Oct;19(6):1752-1771. doi: 10.1007/s13311-022-01277-w. Epub 2022 Sep 2. Neurotherapeutics. 2022. PMID: 36056180 Free PMC article. Review.
These fundamental discoveries have also broadened the horizon of novel therapeutic possibilities and have helped to be better predictors of prognosis and survival. The treatment paradigm of specific NS tumors may also vary based on the patient's cancer predispositio …
These fundamental discoveries have also broadened the horizon of novel therapeutic possibilities and have helped to be better predictors …
Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
Boland CR, Idos GE, Durno C, Giardiello FM, Anderson JC, Burke CA, Dominitz JA, Gross S, Gupta S, Jacobson BC, Patel SG, Shaukat A, Syngal S, Robertson DJ. Boland CR, et al. Gastroenterology. 2022 Jun;162(7):2063-2085. doi: 10.1053/j.gastro.2022.02.021. Epub 2022 Apr 26. Gastroenterology. 2022. PMID: 35487791
The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign and malignant intestinal and extraintestinal tumors. They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN …
The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant disorders associated with an increased risk of benign an …
Gastrointestinal Polyposis in Cowden Syndrome.
Shaco-Levy R, Jasperson KW, Martin K, Samadder NJ, Burt RW, Ying J, Bronner MP. Shaco-Levy R, et al. J Clin Gastroenterol. 2017 Aug;51(7):e60-e67. doi: 10.1097/MCG.0000000000000703. J Clin Gastroenterol. 2017. PMID: 27661969
BACKGROUND: The gastrointestinal manifestations of Cowden Syndrome, an important heritable and multiorgan cancer syndrome, are not well defined. ...These features should warrant consideration of Cowden syndrome....
BACKGROUND: The gastrointestinal manifestations of Cowden Syndrome, an important heritable and multiorgan cancer syndrome …
Lhermitte-Duclos disease.
Kumar R, Vaid VK, Kalra SK. Kumar R, et al. Childs Nerv Syst. 2007 Jul;23(7):729-32. doi: 10.1007/s00381-006-0271-8. Epub 2007 Jan 13. Childs Nerv Syst. 2007. PMID: 17221273
BACKGROUND: Lhermitte-Duclos disease (LDD; dysplastic gangliocytoma of the cerebellum) is a rare hamartoma of the cerebellum. It was first described by Lhermitte and Duclos in 1920 as "Sur un ganglioneurome diffus du cortex du cervelet" (Lhermitte and Duclos [Bull Assoc Fr …
BACKGROUND: Lhermitte-Duclos disease (LDD; dysplastic gangliocytoma of the cerebellum) is a rare hamartoma of the cerebellum. It was …
Encephalocraniocutaneous lipomatosis.
Gawel J, Schwartz RA, Józwiak S. Gawel J, et al. J Cutan Med Surg. 2003 Jan-Feb;7(1):61-5. doi: 10.1007/s10227-002-1142-x. Epub 2002 Oct 9. J Cutan Med Surg. 2003. PMID: 12362260 Review.
The syndrome is rare, with only 25 cases reported since first communication in 1970. ...OBJECTIVE: We discuss underlying pathophysiology, diagnostic difficulties, differential diagnosis, and therapeutic possibilities of the syndrome. CONCLUSIONS: The syndrome …
The syndrome is rare, with only 25 cases reported since first communication in 1970. ...OBJECTIVE: We discuss underlying pathophysiol …
Colonic manifestations of PTEN hamartoma tumor syndrome: case series and systematic review.
Stanich PP, Pilarski R, Rock J, Frankel WL, El-Dika S, Meyer MM. Stanich PP, et al. World J Gastroenterol. 2014 Feb 21;20(7):1833-8. doi: 10.3748/wjg.v20.i7.1833. World J Gastroenterol. 2014. PMID: 24587660 Free PMC article. Review.
AIM: To investigate our clinical experience with the colonic manifestations of phosphatase and tensin homolog on chromosome ten (PTEN) hamartoma tumor syndrome (PHTS) and to perform a systematic literature review regarding the same. ...CONCLUSION: PHTS has a high pr …
AIM: To investigate our clinical experience with the colonic manifestations of phosphatase and tensin homolog on chromosome ten (PTEN) ha …
Familial syndromes associated with thyroid cancer in the era of personalized medicine.
Richards ML. Richards ML. Thyroid. 2010 Jul;20(7):707-13. doi: 10.1089/thy.2010.1641. Thyroid. 2010. PMID: 20578894 Review.
Most cases of familial thyroid cancer are nonmedullary (NMFTC), and have been shown to be present in familial cancer syndromes such as familial adenomatous polyposis, Cowden syndrome, Carney complex, Pendred syndrome, and Werner syndrome. ...In many ca …
Most cases of familial thyroid cancer are nonmedullary (NMFTC), and have been shown to be present in familial cancer syndromes such as famil …
Current Knowledge of Germline Genetic Risk Factors for the Development of Non-Medullary Thyroid Cancer.
Hińcza K, Kowalik A, Kowalska A. Hińcza K, et al. Genes (Basel). 2019 Jun 26;10(7):482. doi: 10.3390/genes10070482. Genes (Basel). 2019. PMID: 31247975 Free PMC article. Review.
Approximately 5%-15% of NMTC cases are thought to be of familial origin (FNMTC), which is defined as the occurrence of the disease in three or more first-degree relatives of the patient. It is often divided into two groups: Syndrome-associated and non-syndromic. The associ …
Approximately 5%-15% of NMTC cases are thought to be of familial origin (FNMTC), which is defined as the occurrence of the disease in three …
Germline epigenetic regulation of KILLIN in Cowden and Cowden-like syndrome.
Bennett KL, Mester J, Eng C. Bennett KL, et al. JAMA. 2010 Dec 22;304(24):2724-31. doi: 10.1001/jama.2010.1877. JAMA. 2010. PMID: 21177507 Free PMC article.
A large heterogeneous group of individuals with Cowden-like syndrome, who have various combinations of Cowden syndrome features but who do not meet Cowden syndrome diagnostic criteria, have PTEN mutations less than 10% of the time, making …
A large heterogeneous group of individuals with Cowden-like syndrome, who have various combinations of Cowden syndro …
Familial nonmedullary thyroid cancer: a review of the genetics.
Khan A, Smellie J, Nutting C, Harrington K, Newbold K. Khan A, et al. Thyroid. 2010 Jul;20(7):795-801. doi: 10.1089/thy.2009.0216. Thyroid. 2010. PMID: 20465534 Review.
Although nonmedullary thyroid cancer (NMTC) is mostly sporadic, evidence for a familial form, which is not associated with other Mendelian cancer syndromes (e.g., familial adenomatous polyposis and Cowden's syndrome), is well documented and thought to cause more agg …
Although nonmedullary thyroid cancer (NMTC) is mostly sporadic, evidence for a familial form, which is not associated with other Mendelian c …
47 results