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1826 2
1827 1
1830 1
1832 1
1849 1
1850 1
1852 2
1857 3
1858 1
1859 2
1860 1
1861 2
1862 1
1865 1
1866 1
1870 1
1872 1
1873 1
1874 3
1875 4
1880 1
1883 1
1884 5
1885 3
1886 3
1887 2
1888 1
1890 1
1891 1
1892 5
1893 1
1894 2
1895 3
1896 3
1897 5
1898 3
1900 2
1901 1
1903 2
1904 1
1905 3
1906 1
1908 4
1909 3
1910 3
1911 5
1912 3
1913 4
1914 4
1915 3
1916 2
1917 2
1918 5
1919 6
1920 3
1921 3
1922 11
1923 8
1924 11
1925 12
1926 14
1927 9
1928 13
1929 19
1930 6
1931 8
1932 13
1933 16
1934 10
1935 18
1936 18
1937 8
1938 9
1939 4
1940 6
1941 9
1942 8
1943 6
1944 16
1945 15
1946 84
1947 101
1948 79
1949 96
1950 84
1951 116
1952 93
1953 111
1954 68
1955 105
1956 75
1957 69
1958 94
1959 84
1960 81
1961 112
1962 104
1963 107
1964 153
1965 144
1966 176
1967 178
1968 178
1969 192
1970 194
1971 229
1972 209
1973 224
1974 215
1975 246
1976 246
1977 246
1978 235
1979 290
1980 297
1981 271
1982 290
1983 289
1984 334
1985 329
1986 365
1987 420
1988 433
1989 426
1990 507
1991 540
1992 536
1993 530
1994 540
1995 598
1996 629
1997 647
1998 689
1999 766
2000 855
2001 939
2002 1009
2003 1086
2004 1159
2005 1313
2006 1478
2007 1511
2008 1654
2009 1676
2010 1836
2011 2069
2012 2360
2013 2554
2014 2974
2015 3782
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2017 4467
2018 4929
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90,293 results

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Page 1
Alexander's Disease: Potential Drug Targets and Future Directions.
Zavala E, Zimmerman T. Zavala E, et al. Mol Neurobiol. 2025 Nov;62(11):15010-15023. doi: 10.1007/s12035-025-05083-1. Epub 2025 May 31. Mol Neurobiol. 2025. PMID: 40448810 Free PMC article. Review.
Alexander's disease is a rare neurodegenerative disorder primarily characterized by upregulation of the GFAP gene and the formation of Rosenthal fibers. ...
Alexander's disease is a rare neurodegenerative disorder primarily characterized by upregulation of the GFAP gene and the form
Leo Alexander's Blueprint of the Nuremberg Code.
Weisleder P. Weisleder P. Pediatr Neurol. 2022 Jan;126:120-124. doi: 10.1016/j.pediatrneurol.2021.10.015. Epub 2021 Oct 30. Pediatr Neurol. 2022. PMID: 34844134
Authorship of the Code has been the subject of dispute, with both Ivy and Alexander claiming sole authorship. METHODS: In the summer of 2017, I visited Duke University Medical Center's Archives and surveyed the contents of boxes labeled "Alexander's papers." …
Authorship of the Code has been the subject of dispute, with both Ivy and Alexander claiming sole authorship. METHODS: In the summer …
Alexander's law in vestibular neuritis.
Shikino K, Ikusaka M. Shikino K, et al. BMJ Case Rep. 2021 Jan 11;14(1):e239705. doi: 10.1136/bcr-2020-239705. BMJ Case Rep. 2021. PMID: 33431477 Free PMC article. No abstract available.
Alexander's Law revisited.
Jeffcoat B, Shelukhin A, Fong A, Mustain W, Zhou W. Jeffcoat B, et al. J Neurophysiol. 2008 Jul;100(1):154-9. doi: 10.1152/jn.00055.2008. Epub 2008 Apr 30. J Neurophysiol. 2008. PMID: 18450584 Free article.
Alexander's Law states that the slow-phase velocity of the nystagmus caused by unilateral vestibular lesion increases with gaze in the beat direction. ...Furthermore, we examined the two hypotheses of Alexander's Law proposed in the two studies. One hy
Alexander's Law states that the slow-phase velocity of the nystagmus caused by unilateral vestibular lesion increases with gaz
Alexander's disease: reassessment of a neonatal form.
Singh N, Bixby C, Etienne D, Tubbs RS, Loukas M. Singh N, et al. Childs Nerv Syst. 2012 Dec;28(12):2029-31. doi: 10.1007/s00381-012-1868-8. Epub 2012 Aug 14. Childs Nerv Syst. 2012. PMID: 22890470 Review.
INTRODUCTION: Alexander disease is a disorder caused by a mutation and accumulation of the glial fibrillary acidic protein. ...RESULTS AND DISCUSSION: Though the neonatal form of Alexander disease is not well acknowledged, a uniform and distinct presentation of the …
INTRODUCTION: Alexander disease is a disorder caused by a mutation and accumulation of the glial fibrillary acidic protein. ...RESULT …
Alexander's disease: clinical, pathologic, and genetic features.
Johnson AB, Brenner M. Johnson AB, et al. J Child Neurol. 2003 Sep;18(9):625-32. doi: 10.1177/08830738030180090901. J Child Neurol. 2003. PMID: 14572141 Review.
Alexander's disease, a rare and fatal disorder of the central nervous system, most commonly affects infants and young children but can also occur in older children and sometimes adults. ...
Alexander's disease, a rare and fatal disorder of the central nervous system, most commonly affects infants and young children
Alexander's Law During High-Speed, Yaw-Axis Rotation: Adaptation or Saturation?
Lädrach C, Zee DS, Wyss T, Wimmer W, Korda A, Salmina C, Caversaccio MD, Mantokoudis G. Lädrach C, et al. Front Neurol. 2020 Nov 23;11:604502. doi: 10.3389/fneur.2020.604502. eCollection 2020. Front Neurol. 2020. PMID: 33329363 Free PMC article.
Objective: Alexander's law (AL) states the intensity of nystagmus increases when gaze is toward the direction of the quick phase. ...
Objective: Alexander's law (AL) states the intensity of nystagmus increases when gaze is toward the direction of the quick pha …
Alexander's disease: clues to diagnosis.
Pridmore CL, Baraitser M, Harding B, Boyd SG, Kendall B, Brett EM. Pridmore CL, et al. J Child Neurol. 1993 Apr;8(2):134-44. doi: 10.1177/088307389300800205. J Child Neurol. 1993. PMID: 8505475 Review.
The clinical, radiologic, neurophysiologic, and pathologic findings in 10 children with histologically proven Alexander's disease are described, and the presence of two broad clinical subgroups is confirmed. ...
The clinical, radiologic, neurophysiologic, and pathologic findings in 10 children with histologically proven Alexander's dise …
Studying the Structural Organization of Polyribosomes with Alexander S. Spirin.
Klaholz BP. Klaholz BP. Biochemistry (Mosc). 2021 Sep;86(9):1053-1059. doi: 10.1134/S0006297921090030. Biochemistry (Mosc). 2021. PMID: 34565311 Free article. Review.
- we asked through a longstanding collaboration between my research group and that of Alexander S. Spirin. Indeed, it was: we found that double-row polyribosomes can have both circular and linear arrangements of their mRNA [Afonina, Z. ...Our joint fruitful exchange …
- we asked through a longstanding collaboration between my research group and that of Alexander S. Spirin. Indeed, it was: we …
Leukodystrophy Imaging: Insights for Diagnostic Dilemmas.
Thakkar RN, Patel D, Kioutchoukova IP, Al-Bahou R, Reddy P, Foster DT, Lucke-Wold B. Thakkar RN, et al. Med Sci (Basel). 2024 Jan 25;12(1):7. doi: 10.3390/medsci12010007. Med Sci (Basel). 2024. PMID: 38390857 Free PMC article. Review.
The leukodystrophies discussed in this paper include X-linked adrenoleukodystrophy, metachromatic leukodystrophy, Krabbe's disease, Pelizaeus-Merzbacher disease, Alexander's disease, Canavan disease, and Aicardi-Goutieres Syndrome....
The leukodystrophies discussed in this paper include X-linked adrenoleukodystrophy, metachromatic leukodystrophy, Krabbe's disease, Pelizaeu …
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