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

Year Number of Results
1796 1
1800 1
1801 1
1816 1
1817 4
1818 1
1819 1
1820 1
1822 1
1827 1
1829 1
1830 1
1837 1
1838 1
1841 2
1842 1
1844 1
1847 3
1856 2
1858 2
1859 2
1860 1
1865 1
1866 1
1868 2
1869 2
1871 3
1872 2
1874 2
1879 2
1880 1
1882 2
1883 2
1884 1
1885 1
1886 2
1890 2
1891 2
1892 5
1893 4
1894 5
1895 2
1896 1
1897 4
1898 3
1899 3
1900 3
1901 1
1903 2
1904 1
1905 1
1908 1
1909 2
1910 1
1911 3
1912 4
1913 3
1914 3
1915 2
1916 3
1917 3
1918 1
1920 3
1921 3
1922 1
1923 1
1924 2
1925 2
1926 3
1927 5
1928 4
1929 6
1930 7
1931 6
1932 6
1933 8
1934 7
1935 5
1936 2
1937 5
1938 6
1939 5
1940 3
1941 4
1942 2
1943 3
1944 2
1945 2
1946 46
1947 47
1948 54
1949 51
1950 47
1951 59
1952 58
1953 45
1954 48
1955 46
1956 48
1957 65
1958 50
1959 43
1960 66
1961 67
1962 69
1963 102
1964 103
1965 125
1966 133
1967 129
1968 129
1969 147
1970 143
1971 161
1972 167
1973 171
1974 206
1975 212
1976 233
1977 232
1978 274
1979 261
1980 253
1981 246
1982 252
1983 265
1984 315
1985 360
1986 345
1987 422
1988 538
1989 518
1990 571
1991 583
1992 606
1993 656
1994 693
1995 660
1996 723
1997 782
1998 731
1999 767
2000 853
2001 910
2002 859
2003 914
2004 973
2005 1034
2006 1096
2007 1161
2008 1432
2009 1558
2010 1733
2011 1951
2012 2070
2013 2319
2014 2849
2015 3138
2016 3387
2017 3388
2018 3578
2019 3796
2020 4268
2021 4614
2022 4451
2023 4052
2024 4759
2025 3868

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71,399 results

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Page 1
Kennedy's disease (spinal and bulbar muscular atrophy): a clinically oriented review of a rare disease.
Breza M, Koutsis G. Breza M, et al. J Neurol. 2019 Mar;266(3):565-573. doi: 10.1007/s00415-018-8968-7. Epub 2018 Jul 13. J Neurol. 2019. PMID: 30006721 Review.
Spinal and bulbar muscular atrophy (SBMA), also known as Kennedy's disease, is a rare, X-linked hereditary lower motor neuron disease, characterized by progressive muscular weakness. ...Kennedy's disease mimics are also discussed, as are ongoing and recently complet …
Spinal and bulbar muscular atrophy (SBMA), also known as Kennedy's disease, is a rare, X-linked hereditary lower motor neuron disease …
Kennedy's disease: an under-recognized motor neuron disorder.
Malek EG, Salameh JS, Makki A. Malek EG, et al. Acta Neurol Belg. 2020 Dec;120(6):1289-1295. doi: 10.1007/s13760-020-01472-6. Epub 2020 Aug 24. Acta Neurol Belg. 2020. PMID: 32839928 Review.
Kennedy's disease or spinal bulbar muscular atrophy is a rare, inherited and slowly progressive multisystem disease mostly manifesting with a motor neuron disease phenotype leading to disability. ...
Kennedy's disease or spinal bulbar muscular atrophy is a rare, inherited and slowly progressive multisystem disease mostly manifestin …
Kennedy's disease.
Au KM, Lau KK, Chan AY, Sheng B, Li HL. Au KM, et al. Hong Kong Med J. 2003 Jun;9(3):217-20. Hong Kong Med J. 2003. PMID: 12777661 Free article.
Kennedy's disease is an X-linked, neurodegenerative disorder, characterised by lower motor neuron syndrome. This report gives the clinical details of six male patients with Kennedy's disease diagnosed at Princess Margaret Hospital. Three were initially diagnosed wit …
Kennedy's disease is an X-linked, neurodegenerative disorder, characterised by lower motor neuron syndrome. This report gives the cli …
Kennedy's disease: pathogenesis and clinical approaches.
Greenland KJ, Zajac JD. Greenland KJ, et al. Intern Med J. 2004 May;34(5):279-86. doi: 10.1111/j.1444-0903.2004.00588.x. Intern Med J. 2004. PMID: 15151675 Review.
Kennedy's disease, also known as spinal and bulbar muscular atrophy, is a progressive degenerative condition affecting lower motor neurons. ...The causative protein in Kennedy's disease, with a polyglutamine expansion residing in the first N-terminal domain, is the …
Kennedy's disease, also known as spinal and bulbar muscular atrophy, is a progressive degenerative condition affecting lower motor ne …
Congenital Syphilis-An Illustrative Review.
Sankaran D, Partridge E, Lakshminrusimha S. Sankaran D, et al. Children (Basel). 2023 Jul 29;10(8):1310. doi: 10.3390/children10081310. Children (Basel). 2023. PMID: 37628309 Free PMC article. Review.
Update on the Genetics of Osteogenesis Imperfecta.
Jovanovic M, Marini JC. Jovanovic M, et al. Calcif Tissue Int. 2024 Dec;115(6):891-914. doi: 10.1007/s00223-024-01266-5. Epub 2024 Aug 11. Calcif Tissue Int. 2024. PMID: 39127989 Free PMC article. Review.
The Kennedy Center at Vanderbilt University.
Camarata S. Camarata S. Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):441. doi: 10.1016/s0736-5748(02)00073-4. Int J Dev Neurosci. 2002. PMID: 12175884 Review. No abstract available.
Diet in the Treatment of Epilepsy.
Westmark CJ. Westmark CJ. Nutrients. 2021 Mar 12;13(3):917. doi: 10.3390/nu13030917. Nutrients. 2021. PMID: 33809037 Free PMC article.
In Reply.
Guglielminotti J, Li G. Guglielminotti J, et al. Obstet Gynecol. 2024 Aug 1;144(2):e43-e44. doi: 10.1097/AOG.0000000000005657. Obstet Gynecol. 2024. PMID: 39024613 No abstract available.
In Reply.
Main EK, Fuller M, Bauer ME. Main EK, et al. Obstet Gynecol. 2024 Aug 1;144(2):e42-e43. doi: 10.1097/AOG.0000000000005655. Obstet Gynecol. 2024. PMID: 39024611 No abstract available.
71,399 results
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