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

Year Number of Results
1822 1
1846 1
1858 1
1867 1
1871 2
1873 1
1875 2
1877 1
1883 1
1890 1
1891 1
1893 3
1894 5
1895 1
1896 3
1897 1
1898 1
1899 1
1900 1
1901 1
1902 2
1903 1
1906 1
1907 2
1908 1
1909 2
1913 2
1918 1
1922 2
1923 1
1924 2
1925 1
1926 1
1927 1
1928 1
1929 2
1930 2
1931 2
1932 1
1933 1
1934 1
1935 1
1939 2
1940 1
1941 1
1943 1
1945 4
1946 12
1947 4
1948 10
1949 8
1950 15
1951 13
1952 14
1953 24
1954 17
1955 16
1956 20
1957 28
1958 14
1959 29
1960 15
1961 19
1962 20
1963 27
1964 24
1965 22
1966 31
1967 17
1968 25
1969 34
1970 31
1971 33
1972 32
1973 25
1974 41
1975 167
1976 166
1977 182
1978 174
1979 204
1980 210
1981 207
1982 268
1983 300
1984 285
1985 327
1986 364
1987 387
1988 418
1989 512
1990 551
1991 632
1992 724
1993 793
1994 947
1995 1072
1996 1167
1997 1377
1998 1464
1999 1527
2000 1683
2001 1708
2002 1861
2003 1845
2004 2000
2005 2098
2006 2399
2007 2365
2008 2598
2009 2738
2010 2871
2011 3014
2012 3217
2013 3205
2014 3420
2015 3347
2016 3323
2017 3163
2018 3261
2019 3113
2020 3493
2021 3635
2022 3542
2023 3219
2024 1244

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76,202 results

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Page 1
Sporadic Desmoid Tumours: Systematic Review with Reflection on the Role of Cryoablation.
Cazzato RL, Gantzer J, de Marini P, Garnon J, Koch G, Buy X, Autrusseau PA, Auloge P, Dalili D, Kurtz JE, Gangi A. Cazzato RL, et al. Cardiovasc Intervent Radiol. 2022 May;45(5):613-621. doi: 10.1007/s00270-022-03091-5. Epub 2022 Mar 2. Cardiovasc Intervent Radiol. 2022. PMID: 35237861 Review.
Desmoid tumours (DT) are rare locally infiltrative soft-tissue tumours which do not metastasise. DT arise sporadically or are associated with familial syndromes, with different clinical and genetic patterns. In recent years there has been an increasing therapeutic role of …
Desmoid tumours (DT) are rare locally infiltrative soft-tissue tumours which do not metastasise. DT arise sporadically or are associa …
Inheritable and sporadic non-autoimmune hyperthyroidism.
Ferraz C, Paschke R. Ferraz C, et al. Best Pract Res Clin Endocrinol Metab. 2017 Mar;31(2):265-275. doi: 10.1016/j.beem.2017.04.005. Epub 2017 Apr 22. Best Pract Res Clin Endocrinol Metab. 2017. PMID: 28648513 Review.
They can be inherited in an autosomal dominant manner (familial or hereditary, FNAH), or may occur sporadically as a de novo condition, also called: persistent sporadic congenital non-autoimmune hyperthyroidism (PSNAH). These three conditions: autonomic adenoma, FNA …
They can be inherited in an autosomal dominant manner (familial or hereditary, FNAH), or may occur sporadically as a de novo conditio …
Sporadic and Familial Adenomatous Polyposis-associated Foveolar-type Adenoma of the Stomach.
Naka T, Hashimoto T, Cho H, Tanabe N, Yoshida T, Yatabe Y, Yoshikawa T, Abe S, Sekine S. Naka T, et al. Am J Surg Pathol. 2023 Jan 1;47(1):91-101. doi: 10.1097/PAS.0000000000001949. Epub 2022 Aug 15. Am J Surg Pathol. 2023. PMID: 35968980
However, the molecular features of FA and the relationship between sporadic and syndromic lesions remain unclear. In this study, we performed clinicopathological, immunohistochemical, and genetic analyses of 18 sporadic and 30 FAP-associated FAs. ...Furthermore, fla …
However, the molecular features of FA and the relationship between sporadic and syndromic lesions remain unclear. In this study, we p …
c-MET inhibition: novel treatment for sporadic and MEN1-associated GEP NETs.
Lee ME, Tepede AA, Mandl A, Weinstein LS, Del Rivero J, Agarwal SK, Blau JE. Lee ME, et al. J Mol Endocrinol. 2020 Aug;65(2):R1-R17. doi: 10.1530/JME-20-0020. J Mol Endocrinol. 2020. PMID: 32384260 Review.
Gastroenteropancreatic neuroendocrine tumors (GEP NETs) comprise a heterogenous and diverse group of neoplasms arising from a common neuroendocrine cell origin. The majority of these tumors occur sporadically while ~20% manifest within the context of hereditary syndromes. …
Gastroenteropancreatic neuroendocrine tumors (GEP NETs) comprise a heterogenous and diverse group of neoplasms arising from a common neuroen …
Genomic profiling of sporadic multiple meningiomas.
Erson-Omay EZ, Vetsa S, Vasandani S, Barak T, Nadar A, Marianayagam NJ, Yalcin K, Miyagishima D, Aguilera SM, Robert S, Mishra-Gorur K, Fulbright RK, McGuone D, Günel M, Moliterno J. Erson-Omay EZ, et al. BMC Med Genomics. 2022 May 14;15(1):112. doi: 10.1186/s12920-022-01258-0. BMC Med Genomics. 2022. PMID: 35568945 Free PMC article.
BACKGROUND: Multiple meningiomas (MMs) rarely occur sporadically. It is unclear whether each individual tumor in a single patient behaves similarly. Moreover, the molecular mechanisms underlying the formation of sporadic MMs and clonal formation etiology of these tu …
BACKGROUND: Multiple meningiomas (MMs) rarely occur sporadically. It is unclear whether each individual tumor in a single patient beh …
The comparable tumour microenvironment in sporadic and NF2-related schwannomatosis vestibular schwannoma.
Gregory GE, Jones AP, Haley MJ, Hoyle C, Zeef LAH, Lin IH, Coope DJ, King AT, Evans DG, Paszek P, Couper KN, Brough D, Pathmanaban ON. Gregory GE, et al. Brain Commun. 2023 Jul 21;5(4):fcad197. doi: 10.1093/braincomms/fcad197. eCollection 2023. Brain Commun. 2023. PMID: 37680691 Free PMC article.
A comparison of the tumour microenvironment in sporadic and NF2-related schwannomatosis tumours is therefore required to underpin the development of immunotherapeutic targets, identify the possibility of extrapolating ex vivo data from sporadic vestibular schwannoma …
A comparison of the tumour microenvironment in sporadic and NF2-related schwannomatosis tumours is therefore required to underpin the …
Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome).
Bresler SC, Padwa BL, Granter SR. Bresler SC, et al. Head Neck Pathol. 2016 Jun;10(2):119-24. doi: 10.1007/s12105-016-0706-9. Epub 2016 Mar 14. Head Neck Pathol. 2016. PMID: 26971503 Free PMC article. Review.
The disorder is caused by defects in hedgehog signaling which result in constitutive pathway activity and tumor cell proliferation. As sporadic basal cell carcinomas also commonly harbor hedgehog pathway aberrations, therapeutic agents targeting key signaling constituents …
The disorder is caused by defects in hedgehog signaling which result in constitutive pathway activity and tumor cell proliferation. As sp …
Genomic rearrangements and sporadic disease.
Lupski JR. Lupski JR. Nat Genet. 2007 Jul;39(7 Suppl):S43-7. doi: 10.1038/ng2084. Nat Genet. 2007. PMID: 17597781 Review.
Many clinical phenotypes occur sporadically despite genetics contributing partly or entirely to their cause. To what extent are de novo mutations the cause of sporadic traits? Locus-specific mutation rates for genomic rearrangements appear to be two to four orders o …
Many clinical phenotypes occur sporadically despite genetics contributing partly or entirely to their cause. To what extent are de no …
Genetic mutations in sporadic pituitary adenomas--what to screen for?
Lecoq AL, Kamenický P, Guiochon-Mantel A, Chanson P. Lecoq AL, et al. Nat Rev Endocrinol. 2015 Jan;11(1):43-54. doi: 10.1038/nrendo.2014.181. Epub 2014 Oct 28. Nat Rev Endocrinol. 2015. PMID: 25350067 Review.
The prevalence of symptomatic pituitary adenomas is approximately 1:1,000 in the general population. The vast majority of these tumours occur sporadically and are not part of syndromic disorders. However, germline mutations in genes known to predispose individuals to famil …
The prevalence of symptomatic pituitary adenomas is approximately 1:1,000 in the general population. The vast majority of these tumours occu …
Presentation, imaging, patterns of care, growth, and outcome in sporadic and von Hippel-Lindau-associated central nervous system hemangioblastomas.
Takami H, Graffeo CS, Perry A, Brown DA, Meyer FB, Burns TC, Parney IF. Takami H, et al. J Neurooncol. 2022 Sep;159(2):221-231. doi: 10.1007/s11060-022-04021-8. Epub 2022 Jul 28. J Neurooncol. 2022. PMID: 35902552 Review.

RESULTS: Two hundred and eighty five hemangioblastomas were treated in 184 unique patients (115 sporadic, 69 VHL). Compared to sporadic patients, VHL patients were younger (36.7 vs 51.7 years; p < 0.0001), were treated while asymptomatic more commonly (47.3 vs 4.

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RESULTS: Two hundred and eighty five hemangioblastomas were treated in 184 unique patients (115 sporadic, 69 VHL). Compared to spo …
76,202 results
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