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

Year Number of Results
1963 6
1964 3
1965 3
1967 11
1968 11
1969 9
1970 13
1971 14
1972 29
1973 12
1974 13
1975 17
1976 11
1977 11
1978 13
1979 13
1980 14
1981 8
1982 10
1983 15
1984 22
1985 19
1986 20
1987 33
1988 58
1989 45
1990 51
1991 49
1992 40
1993 71
1994 75
1995 84
1996 79
1997 75
1998 85
1999 96
2000 103
2001 134
2002 78
2003 78
2004 76
2005 88
2006 92
2007 92
2008 95
2009 102
2010 105
2011 102
2012 98
2013 127
2014 138
2015 119
2016 126
2017 112
2018 94
2019 87
2020 107
2021 126
2022 93
2023 82
2024 29

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3,342 results

Results by year

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Page 1
Congenital malformations.
Corsello G, Giuffrè M. Corsello G, et al. J Matern Fetal Neonatal Med. 2012 Apr;25 Suppl 1:25-9. doi: 10.3109/14767058.2012.664943. Epub 2012 Mar 14. J Matern Fetal Neonatal Med. 2012. PMID: 22356564 Free article. Review.
Schwartz-Jampel syndrome and perlecan deficiency.
Stum M, Davoine CS, Fontaine B, Nicole S. Stum M, et al. Acta Myol. 2005 Oct;24(2):89-92. Acta Myol. 2005. PMID: 16550923 Review.
Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disorder characterized by the association of myotonia with chondrodysplasia. ...
Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disorder characterized by the association of myotonia with
Acrodysostosis.
Silve C, Clauser E, Linglart A. Silve C, et al. Horm Metab Res. 2012 Sep;44(10):749-58. doi: 10.1055/s-0032-1316330. Epub 2012 Jul 19. Horm Metab Res. 2012. PMID: 22815067 Review.
KATP channels in lymphatic function.
Davis MJ, Kim HJ, Nichols CG. Davis MJ, et al. Am J Physiol Cell Physiol. 2022 Oct 1;323(4):C1018-C1035. doi: 10.1152/ajpcell.00137.2022. Epub 2022 Jul 4. Am J Physiol Cell Physiol. 2022. PMID: 35785984 Free PMC article. Review.
This review summarizes and critiques the evidence for the expression of specific K(ATP) channel subunits in lymphatic smooth muscle and endothelium, the roles that they play in normal lymphatic function, and their possible involvement in multiple diseases, including metabolic …
This review summarizes and critiques the evidence for the expression of specific K(ATP) channel subunits in lymphatic smooth muscle and endo …
Sclerostin deficiency in humans.
van Lierop AH, Appelman-Dijkstra NM, Papapoulos SE. van Lierop AH, et al. Bone. 2017 Mar;96:51-62. doi: 10.1016/j.bone.2016.10.010. Epub 2016 Oct 11. Bone. 2017. PMID: 27742500 Review.
Fibrous dysplasia.
Lietman SA, Levine MA. Lietman SA, et al. Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2:389-96. Pediatr Endocrinol Rev. 2013. PMID: 23858622 Review.
Fibrous dysplasia is usually an isolated skeletal finding but can sometimes occur as a component of a multisystem developmental disorder known as McCune-Albright syndrome (MAS) that is also associated with endocrine hyperfunction (e.g. precocious puberty) and caf au lait c …
Fibrous dysplasia is usually an isolated skeletal finding but can sometimes occur as a component of a multisystem developmental disorder kno …
Schwartz-Jampel syndrome.
Pascuzzi RM. Pascuzzi RM. Semin Neurol. 1991 Sep;11(3):267-73. doi: 10.1055/s-2008-1041231. Semin Neurol. 1991. PMID: 1947489 Review. No abstract available.
Schwartz-Jampel syndrome: a review of the literature and case report.
Mallineni SK, Yiu CK, King NM. Mallineni SK, et al. Spec Care Dentist. 2012 Jun;32(3):105-11. doi: 10.1111/j.1754-4505.2012.00249.x. Epub 2012 Apr 26. Spec Care Dentist. 2012. PMID: 22591433 Review.
Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive skeletal dysplasia associated with myotonia. ...
Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive skeletal dysplasia associated with myotonia. ...
Craniofacial Fibrous Dysplasia: Clinical and Therapeutic Implications.
Szymczuk V, Taylor J, Boyce AM. Szymczuk V, et al. Curr Osteoporos Rep. 2023 Apr;21(2):147-153. doi: 10.1007/s11914-023-00779-6. Epub 2023 Feb 28. Curr Osteoporos Rep. 2023. PMID: 36849642 Free PMC article. Review.
Disease presents along a broad spectrum and may be associated with extraskeletal features as part of McCune-Albright syndrome (MAS). The craniofacial skeleton is one of the most commonly impacted areas in FD, and its functional and anatomical complexities create unique cha …
Disease presents along a broad spectrum and may be associated with extraskeletal features as part of McCune-Albright syndrome (MAS). …
3,342 results