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Results by year

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

Year Number of Results
1976 1
1977 3
1978 4
1979 6
1980 7
1981 7
1982 6
1983 14
1984 3
1985 8
1986 5
1987 6
1988 8
1989 8
1990 8
1991 11
1992 5
1993 4
1994 8
1995 5
1996 2
1997 7
1998 3
1999 1
2000 5
2001 5
2002 7
2003 5
2004 13
2005 4
2006 5
2007 12
2008 9
2009 9
2010 8
2011 8
2012 7
2013 15
2014 18
2015 15
2016 7
2017 11
2018 11
2019 12
2020 18
2021 9
2022 13
2023 7
2024 3

Search Results

351 results

Results by year

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Page 1
Understanding the floppy baby.
Myers GJ. Myers GJ. Adv Neurol. 1977;17:295-315. Adv Neurol. 1977. PMID: 142421 Review.
Teschler-Nicola/Killian syndrome.
Pagon RA. Pagon RA. J Clin Dysmorphol. 1983 Fall;1(3):18-9. J Clin Dysmorphol. 1983. PMID: 6584556 No abstract available.
Muscle-eye-brain disease (MEB).
Santavuori P, Somer H, Sainio K, Rapola J, Kruus S, Nikitin T, Ketonen L, Leisti J. Santavuori P, et al. Brain Dev. 1989;11(3):147-53. doi: 10.1016/s0387-7604(89)80088-9. Brain Dev. 1989. PMID: 2751061
Pregnancy in 3M syndrome.
Cusimano MC, Chitayat D, Injeyan M, Geary M. Cusimano MC, et al. J Obstet Gynaecol. 2018 Apr;38(3):421-422. doi: 10.1080/01443615.2017.1360849. Epub 2017 Oct 19. J Obstet Gynaecol. 2018. PMID: 29046114 No abstract available.
HECW2-related disorder in four Japanese patients.
Yanagishita T, Hirade T, Shimojima Yamamoto K, Funatsuka M, Miyamoto Y, Maeda M, Yanagi K, Kaname T, Nagata S, Nagata M, Ishihara Y, Miyashita Y, Asano Y, Sakata Y, Kosaki K, Yamamoto T. Yanagishita T, et al. Am J Med Genet A. 2021 Oct;185(10):2895-2902. doi: 10.1002/ajmg.a.62363. Epub 2021 May 28. Am J Med Genet A. 2021. PMID: 34047014
Congenital Hypotonia in Toddlerhood.
Steiner N, Torres A, Reddy A, Augustyn M. Steiner N, et al. J Dev Behav Pediatr. 2017 Sep;38(7):556-557. doi: 10.1097/DBP.0000000000000497. J Dev Behav Pediatr. 2017. PMID: 28816914
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome.
Masnada S, Sarret C, Antonello CE, Fadilah A, Krude H, Mura E, Mordekar S, Nicita F, Olivotto S, Orcesi S, Porta F, Remerand G, Siri B, Wilpert NM, Amir-Yazdani P, Bertini E, Schuelke M, Bernard G, Boespflug-Tanguy O, Tonduti D. Masnada S, et al. Mol Genet Metab. 2022 Jan;135(1):109-113. doi: 10.1016/j.ymgme.2021.12.003. Epub 2021 Dec 16. Mol Genet Metab. 2022. PMID: 34969638
351 results