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1800 1
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1828 1
1837 1
1845 1
1848 1
1863 1
1872 1
1873 1
1878 1
1880 3
1881 1
1885 1
1888 2
1889 2
1891 1
1892 2
1893 2
1894 4
1895 2
1896 1
1897 3
1898 2
1899 1
1900 5
1901 1
1902 2
1904 1
1905 1
1906 3
1907 5
1909 4
1910 7
1911 2
1912 1
1913 2
1914 1
1916 1
1918 1
1919 1
1920 2
1921 1
1923 1
1924 3
1925 4
1926 4
1927 5
1928 4
1929 3
1930 5
1931 1
1932 2
1933 2
1935 5
1936 1
1938 1
1939 1
1940 1
1945 1
1946 9
1947 3
1948 5
1949 7
1950 6
1951 7
1952 11
1953 11
1954 15
1955 14
1956 14
1957 6
1958 14
1959 13
1960 12
1961 17
1962 12
1963 17
1964 23
1965 18
1966 28
1967 25
1968 28
1969 42
1970 37
1971 41
1972 44
1973 41
1974 63
1975 45
1976 68
1977 62
1978 61
1979 78
1980 95
1981 71
1982 78
1983 98
1984 102
1985 109
1986 102
1987 133
1988 122
1989 128
1990 109
1991 128
1992 136
1993 142
1994 145
1995 115
1996 158
1997 144
1998 162
1999 166
2000 192
2001 193
2002 198
2003 233
2004 232
2005 302
2006 349
2007 331
2008 335
2009 390
2010 404
2011 441
2012 441
2013 472
2014 581
2015 619
2016 571
2017 618
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2020 704
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2024 231

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13,204 results

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Page 1
Repetitive Sleep Starts in Allan-Herndon-Dudley Syndrome.
Solazzi R, Nanni G, Esposito S, Estienne M, Freri E, Zibordi F, Canafoglia L, Castellotti B, Granata T. Solazzi R, et al. Pediatr Neurol. 2023 Oct;147:24-27. doi: 10.1016/j.pediatrneurol.2023.06.012. Epub 2023 Jun 22. Pediatr Neurol. 2023. PMID: 37542971
Allan-Herndon-Dudley syndrome (AHDS) is caused by mutations in the SLC16A2 gene, encoding for the monocarboxylate transporter 8 (MCT8). ...
Allan-Herndon-Dudley syndrome (AHDS) is caused by mutations in the SLC16A2 gene, encoding for the monocarboxylate transporter 8 (MCT8 …
Allan William Cripps: a mucosal immunologist and mentor from beginning to end.
Gleeson M, West NP. Gleeson M, et al. Immunol Cell Biol. 2023 Nov-Dec;101(10):916-920. doi: 10.1111/imcb.12706. Epub 2023 Oct 27. Immunol Cell Biol. 2023. PMID: 37885423
Allan Cripps was internationally recognized in the field of mucosal immunology, in particular the relationship between respiratory diseases and mucosal immunization strategies. ...Allan published over 400 papers and mentored over 40 research higher degree candidates …
Allan Cripps was internationally recognized in the field of mucosal immunology, in particular the relationship between respiratory di …
Allan-Herndon-Dudley syndrome in a female patient and related mechanisms.
Olivati C, Favilla BP, Freitas EL, Santos B, Melaragno MI, Meloni VA, Piazzon F. Olivati C, et al. Mol Genet Metab Rep. 2022 May 7;31:100879. doi: 10.1016/j.ymgmr.2022.100879. eCollection 2022 Jun. Mol Genet Metab Rep. 2022. PMID: 35782622 Free PMC article.
Allan-Herndon-Dudley syndrome (AHDS) is characterized by neuropsychomotor developmental delay/intellectual disability, neurological impairment with a movement disorder, and an abnormal thyroid hormone profile. ...
Allan-Herndon-Dudley syndrome (AHDS) is characterized by neuropsychomotor developmental delay/intellectual disability, neurological i …
Triac in the treatment of Allan-Herndon-Dudley syndrome.
Bauer AJ. Bauer AJ. Lancet Diabetes Endocrinol. 2019 Sep;7(9):661-663. doi: 10.1016/S2213-8587(19)30217-7. Epub 2019 Jul 31. Lancet Diabetes Endocrinol. 2019. PMID: 31377264 No abstract available.
Analysis of temporal structure of laser chaos by Allan variance.
Asuke N, Chauvet N, Röhm A, Kanno K, Uchida A, Niiyama T, Sunada S, Horisaki R, Naruse M. Asuke N, et al. Phys Rev E. 2023 Jan;107(1-1):014211. doi: 10.1103/PhysRevE.107.014211. Phys Rev E. 2023. PMID: 36797858
Allan variance has been widely utilized for evaluating the stability of the time series generated by atomic clocks and lasers, in time regimes ranging from short to extremely long. ...This study demonstrates that Allan variance can help in understanding and characte …
Allan variance has been widely utilized for evaluating the stability of the time series generated by atomic clocks and lasers, in tim …
Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss.
Gagliardi L, Nataren N, Feng J, Schreiber AW, Hahn CN, Conwell LS, Coman D, Scott HS. Gagliardi L, et al. Am J Med Genet A. 2015 Aug;167A(8):1872-6. doi: 10.1002/ajmg.a.37075. Epub 2015 Apr 6. Am J Med Genet A. 2015. PMID: 25850411
The Allan-Herndon-Dudley syndrome is caused by mutations in the thyroid hormone transporter, Monocarboxylate transporter 8 (MCT8). It is characterized by profound intellectual disability and abnormal thyroid function. We report on a patient with Allan-Herndon-Dudley …
The Allan-Herndon-Dudley syndrome is caused by mutations in the thyroid hormone transporter, Monocarboxylate transporter 8 (MCT8). It …
James Nicholas Allan.
Williams S, Madew L. Williams S, et al. Med J Aust. 1977 Oct 8;2(15):508. doi: 10.5694/j.1326-5377.1977.tb117762.x. Med J Aust. 1977. PMID: 340860 No abstract available.
Allan-Herndon syndrome. I. Clinical studies.
Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT Jr, Herndon CN. Stevenson RE, et al. Am J Hum Genet. 1990 Sep;47(3):446-53. Am J Hum Genet. 1990. PMID: 2393019 Free PMC article.
A large family with X-linked mental retardation, originally reported in 1944 by Allan, Herndon, and Dudley, has been reinvestigated. Twenty-nine males have been affected in seven generations. ...High-resolution chromosomes, serum creatine kinase, and amino acids are normal …
A large family with X-linked mental retardation, originally reported in 1944 by Allan, Herndon, and Dudley, has been reinvestigated. …
Leg-lengthening.
ALLAN FG. ALLAN FG. Br Med J. 1951 Feb 3;1(4700):218-22. doi: 10.1136/bmj.1.4700.218. Br Med J. 1951. PMID: 14821373 Free PMC article. No abstract available.
The chapterhouse.
Allan R. Allan R. Clin Med (Lond). 2009 Apr;9(2):100-1. doi: 10.7861/clinmedicine.9-2-101. Clin Med (Lond). 2009. PMID: 19435108 Free PMC article. No abstract available.
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