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

Year Number of Results
1966 1
1970 1
1971 1
1972 1
1973 1
1974 2
1976 2
1977 1
1980 2
1981 5
1982 1
1983 1
1984 1
1985 2
1986 1
1987 1
1988 3
1989 3
1990 1
1991 4
1992 3
1993 2
1994 2
1995 6
1996 6
1997 6
1998 6
1999 6
2000 9
2001 5
2002 8
2003 9
2004 5
2005 6
2006 8
2007 7
2008 5
2009 5
2010 6
2011 8
2012 11
2013 16
2014 19
2015 13
2016 12
2017 14
2018 9
2019 8
2020 15
2021 5
2022 3
2023 3
2024 2

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256 results

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Quoted phrase not found in phrase index: "Developmental anomaly of metabolic origin"
Page 1
Risk factors for Down syndrome.
Coppedè F. Coppedè F. Arch Toxicol. 2016 Dec;90(12):2917-2929. doi: 10.1007/s00204-016-1843-3. Epub 2016 Sep 7. Arch Toxicol. 2016. PMID: 27600794 Review.
In addition, full trisomy for chromosome 21 should be further divided into cases of maternal origin, the majority, and cases of paternal origin, less than 10 %. Among cases of maternal origin, a further stratification should be performed into errors that have …
In addition, full trisomy for chromosome 21 should be further divided into cases of maternal origin, the majority, and cases of pater …
A review of factors influencing the incidence and severity of plaque-induced gingivitis.
Trombelli L, Farina R. Trombelli L, et al. Minerva Stomatol. 2013 Jun;62(6):207-34. Minerva Stomatol. 2013. PMID: 23828258 Review. English, Italian.
The reported significant differences in gingival inflammatory response under quantitatively and/or qualitatively almost identical bacterial challenge suggest that the gingival response to plaque accumulation may be an individual trait, possibly genetic in origin. The most …
The reported significant differences in gingival inflammatory response under quantitatively and/or qualitatively almost identical bacterial …
Folate deficiency and folic acid supplementation: the prevention of neural-tube defects and congenital heart defects.
Czeizel AE, Dudás I, Vereczkey A, Bánhidy F. Czeizel AE, et al. Nutrients. 2013 Nov 21;5(11):4760-75. doi: 10.3390/nu5114760. Nutrients. 2013. PMID: 24284617 Free PMC article. Review.
The aim of this review paper is to show the characteristics of common and severe neural-tube defects together with congenital heart defects (CHD) as vitamin deficiencies play a role in their origin. The findings of the Hungarian intervention (randomized doubl …
The aim of this review paper is to show the characteristics of common and severe neural-tube defects together with congenital heart d …
Fetal cytomegalovirus infection.
Leruez-Ville M, Ville Y. Leruez-Ville M, et al. Best Pract Res Clin Obstet Gynaecol. 2017 Jan;38:97-107. doi: 10.1016/j.bpobgyn.2016.10.005. Epub 2016 Oct 20. Best Pract Res Clin Obstet Gynaecol. 2017. PMID: 27923540 Review.
Cytomegalovirus (CMV) congenital infection affects 0.7% of live births worldwide and is the leading cause of congenital neurological handicap of infectious origin. ...This review provides an update on the evidence for diagnosis, prognosis and treatment of …
Cytomegalovirus (CMV) congenital infection affects 0.7% of live births worldwide and is the leading cause of congenital neurol …
11-Keto-testosterone and other androgens of adrenal origin.
Stárka L, Dušková M, Vítků J. Stárka L, et al. Physiol Res. 2020 Sep 30;69(Suppl 2):S187-S192. doi: 10.33549/physiolres.934516. Physiol Res. 2020. PMID: 33094617 Free PMC article. Review.
Until recently, the androgenic potency of these adrenal-derived compounds were not well known, but some recent studies have shown that the production of 11-oxo- and 11beta-hydroxy-derived testosterone and dihydrotestosterone evidently have high androgenic activity. This fact has …
Until recently, the androgenic potency of these adrenal-derived compounds were not well known, but some recent studies have shown that the p …
Genetic and environmental origins of hypospadias.
Thorup J, Nordenskjöld A, Hutson JM. Thorup J, et al. Curr Opin Endocrinol Diabetes Obes. 2014 Jun;21(3):227-32. doi: 10.1097/MED.0000000000000063. Curr Opin Endocrinol Diabetes Obes. 2014. PMID: 24722170 Review.
Mechanistic Target of Rapamycin (mTOR) Inhibitors.
Wang D, Eisen HJ. Wang D, et al. Handb Exp Pharmacol. 2022;272:53-72. doi: 10.1007/164_2021_553. Handb Exp Pharmacol. 2022. PMID: 35091825
Everolimus is approved by the FDA to treat postmenopausal advanced hormone receptor-positive, HER2-negative breast cancer in women, progressive neuroendocrine tumors of pancreatic origin (PNET), advanced renal cell carcinoma (RCC), renal angiomyolipoma (AML) and tuberous s …
Everolimus is approved by the FDA to treat postmenopausal advanced hormone receptor-positive, HER2-negative breast cancer in women, progress …
New and Emerging Targeted Therapies for Vascular Malformations.
Van Damme A, Seront E, Dekeuleneer V, Boon LM, Vikkula M. Van Damme A, et al. Am J Clin Dermatol. 2020 Oct;21(5):657-668. doi: 10.1007/s40257-020-00528-w. Am J Clin Dermatol. 2020. PMID: 32557381 Review.
They have historically been managed by surgery and sclerotherapy. Extensive insight into the genetic origin and molecular mechanism of development has been accumulated over the last 20 years. ...Disease responses of vascular malformations to sirolimus have now been reporte …
They have historically been managed by surgery and sclerotherapy. Extensive insight into the genetic origin and molecular mechanism o …
New approaches to the Klinefelter syndrome.
Nieschlag E, Werler S, Wistuba J, Zitzmann M. Nieschlag E, et al. Ann Endocrinol (Paris). 2014 May;75(2):88-97. doi: 10.1016/j.ando.2014.03.007. Epub 2014 Apr 30. Ann Endocrinol (Paris). 2014. PMID: 24793990 Review.
The Klinefelter syndrome (KS), with an incidence of 1 to 2 per 1000 male neonates, is one of the most frequent congenital chromosome disorders. The 47,XXY karyotype causes infertility, testosterone deficiency and a spectrum of further symptoms and comorbidities. ...The …
The Klinefelter syndrome (KS), with an incidence of 1 to 2 per 1000 male neonates, is one of the most frequent congenital chromosome …
Genomic imprinting syndromes and cancer.
Lim DH, Maher ER. Lim DH, et al. Adv Genet. 2010;70:145-75. doi: 10.1016/B978-0-12-380866-0.60006-X. Adv Genet. 2010. PMID: 20920748 Review.
Genomic imprinting represents a form of epigenetic control of gene expression in which one allele of a gene is preferentially expressed according to the parent-of-origin of the allele. Genomic imprinting plays an important role in normal growth and development. ...
Genomic imprinting represents a form of epigenetic control of gene expression in which one allele of a gene is preferentially expressed acco …
256 results