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Year Number of Results
1803 2
1833 1
1846 1
1848 1
1853 2
1854 1
1855 1
1856 2
1857 2
1858 2
1859 2
1860 3
1861 3
1862 2
1863 2
1865 1
1866 1
1867 6
1869 1
1870 2
1873 1
1881 1
1885 8
1890 1
1892 2
1895 2
1896 1
1897 3
1899 1
1900 2
1901 1
1903 6
1904 2
1905 5
1908 23
1909 16
1910 16
1911 13
1912 16
1913 36
1914 16
1915 15
1916 7
1917 28
1918 4
1919 4
1920 12
1921 11
1922 1
1923 14
1924 9
1925 11
1926 12
1927 32
1928 16
1929 18
1930 20
1931 23
1932 33
1933 30
1934 14
1935 13
1936 7
1937 12
1938 12
1939 14
1940 2
1941 3
1942 3
1943 3
1944 6
1945 14
1946 46
1947 47
1948 61
1949 57
1950 101
1951 109
1952 119
1953 125
1954 119
1955 128
1956 130
1957 129
1958 120
1959 121
1960 122
1961 118
1962 102
1963 169
1964 167
1965 186
1966 191
1967 209
1968 251
1969 303
1970 276
1971 263
1972 297
1973 269
1974 312
1975 358
1976 390
1977 438
1978 437
1979 429
1980 442
1981 471
1982 510
1983 512
1984 525
1985 543
1986 575
1987 646
1988 676
1989 702
1990 786
1991 704
1992 789
1993 813
1994 801
1995 922
1996 905
1997 952
1998 1003
1999 1013
2000 1085
2001 1066
2002 1156
2003 1169
2004 1289
2005 1368
2006 1424
2007 1559
2008 1750
2009 1820
2010 1909
2011 2029
2012 2122
2013 2355
2014 2334
2015 2582
2016 2605
2017 2612
2018 2784
2019 2808
2020 3180
2021 3499
2022 3261
2023 3108
2024 1184

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67,917 results

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Page 1
Sturge-Weber Syndrome: A Review.
Higueros E, Roe E, Granell E, Baselga E. Higueros E, et al. Actas Dermosifiliogr. 2017 Jun;108(5):407-417. doi: 10.1016/j.ad.2016.09.022. Epub 2017 Jan 23. Actas Dermosifiliogr. 2017. PMID: 28126187 Free article. Review. English, Spanish.
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ; it affects 1 in every 20,000 to 50,000 newborns. ...Neuroimaging studies show leptomeningeal angiomatosis, supporting diagnosis. Standard treatment for S …
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ; it affects 1 …
Sturge-Weber Syndrome: A Case Report.
Timilsina S, Kunwor B, Thapa Chhetri S, Nepal S, Sedhai K. Timilsina S, et al. JNMA J Nepal Med Assoc. 2023 Nov 1;61(267):890-892. doi: 10.31729/jnma.8344. JNMA J Nepal Med Assoc. 2023. PMID: 38289732 Free PMC article.
We present the case of a five-year-old child diagnosed with Sturge-Weber syndrome. The patient exhibited high-grade fever, headaches, and generalized tonic-clonic seizures. ...This case underscores the importance of early diagnosis and tailored treatment strategies for pat …
We present the case of a five-year-old child diagnosed with Sturge-Weber syndrome. The patient exhibited high-grade fever, headaches, …
The Weber-Fechner law: A misnomer that persists but that should go away.
Algom D. Algom D. Psychol Rev. 2021 Jul;128(4):757-765. doi: 10.1037/rev0000278. Epub 2021 Apr 22. Psychol Rev. 2021. PMID: 34242050
The term "Weber-Fechner law" is arguably the most widely used misnomer in psychological science. ...In truth, the principle, here called the Weber principle, and Weber's law, are different and independent. ...
The term "Weber-Fechner law" is arguably the most widely used misnomer in psychological science. ...In truth, the principle, here cal …
Sturge-Weber syndrome: a review.
Thomas-Sohl KA, Vaslow DF, Maria BL. Thomas-Sohl KA, et al. Pediatr Neurol. 2004 May;30(5):303-10. doi: 10.1016/j.pediatrneurol.2003.12.015. Pediatr Neurol. 2004. PMID: 15165630 Review.
Sturge-Weber syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50,000. ...
Sturge-Weber syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50,000. ...
Weber Syndrome.
Romozzi M, Bramato G, Luigetti M. Romozzi M, et al. Acta Neurol Belg. 2023 Jun;123(3):1101-1103. doi: 10.1007/s13760-021-01861-5. Epub 2022 Jan 7. Acta Neurol Belg. 2023. PMID: 34997560 No abstract available.
Parkes Weber syndrome: a rare cause of foot drop.
Kyriakides DE, Michaelides D, Lambrianides S. Kyriakides DE, et al. BMJ Case Rep. 2023 Oct 4;16(10):e254455. doi: 10.1136/bcr-2022-254455. BMJ Case Rep. 2023. PMID: 37793841
The patient's differential diagnosis based on clinical examination and investigations is discussed leading to a final diagnosis of sciatic neuropathy secondary to an arteriovenous malformation due to Parkes Weber syndrome....
The patient's differential diagnosis based on clinical examination and investigations is discussed leading to a final diagnosis of sciatic n …
Sturge-Weber syndrome and associated congenital vascular disorders: a review.
Nathan N, Thaller SR. Nathan N, et al. J Craniofac Surg. 2006 Jul;17(4):724-8. doi: 10.1097/00001665-200607000-00024. J Craniofac Surg. 2006. PMID: 16877925 Review.
Sturge-Weber syndrome (SWS), Klippel-Trenaunay syndrome (KTS), and Parkes-Weber syndrome (PWS) represent a wide range of congenital vascular abnormality syndromes. ...
Sturge-Weber syndrome (SWS), Klippel-Trenaunay syndrome (KTS), and Parkes-Weber syndrome (PWS) represent a wide range of conge …
Sturge-Weber syndrome.
Baselga E. Baselga E. Semin Cutan Med Surg. 2004 Jun;23(2):87-98. doi: 10.1016/j.sder.2004.01.002. Semin Cutan Med Surg. 2004. PMID: 15295918 Review.
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma and choroidal hemangioma) and leptomeningeal angioma. ...Early neuroimaging features are important to recognize. Management of patients with S …
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma an …
[Sturge-Weber syndrome: about a case].
Doumiri M, Labied M, Salam S, Laoudiyi D, Chbani K, Ouzidane L. Doumiri M, et al. Pan Afr Med J. 2020 Aug 12;36:273. doi: 10.11604/pamj.2020.36.273.24346. eCollection 2020. Pan Afr Med J. 2020. PMID: 33088402 Free PMC article. French.
Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. ...
Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. ...
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