Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1975 1
1977 1
1982 2
1983 1
1991 1
1992 1
1993 2
1994 3
1995 2
1996 5
1997 1
1998 3
1999 5
2000 2
2001 7
2002 8
2003 5
2004 5
2005 9
2006 10
2007 9
2008 4
2009 5
2010 6
2011 8
2012 6
2013 10
2014 14
2015 10
2016 13
2017 11
2018 12
2019 11
2020 19
2021 16
2022 10
2023 9
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

221 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Skeletal dysplasia-intellectual disability syndrome"
Page 1
The relationship between nutrition and frailty: Effects of protein intake, nutritional supplementation, vitamin D and exercise on muscle metabolism in the elderly. A systematic review.
Artaza-Artabe I, Sáez-López P, Sánchez-Hernández N, Fernández-Gutierrez N, Malafarina V. Artaza-Artabe I, et al. Maturitas. 2016 Nov;93:89-99. doi: 10.1016/j.maturitas.2016.04.009. Epub 2016 Apr 14. Maturitas. 2016. PMID: 27125943 Review.
BACKGROUND: Frailty is a geriatric syndrome that predicts the onset of disability, morbidity and mortality in elderly people; it is a state of pre-disability and is reversible. ...Screening and early diagnosis of malnutrition and frailty in elderly peo …
BACKGROUND: Frailty is a geriatric syndrome that predicts the onset of disability, morbidity and mortality in elderly p …
Mitochondrial cytopathies.
El-Hattab AW, Scaglia F. El-Hattab AW, et al. Cell Calcium. 2016 Sep;60(3):199-206. doi: 10.1016/j.ceca.2016.03.003. Epub 2016 Mar 4. Cell Calcium. 2016. PMID: 26996063 Review.
Impaired mitochondrial function in various tissues and organs results in the multi-organ manifestations of mitochondrial diseases including epilepsy, intellectual disability, skeletal and cardiac myopathies, hepatopathies, endocrinopathies, and nephropathies. ...Cur …
Impaired mitochondrial function in various tissues and organs results in the multi-organ manifestations of mitochondrial diseases including …
Exercise and Sarcopenia.
Phu S, Boersma D, Duque G. Phu S, et al. J Clin Densitom. 2015 Oct-Dec;18(4):488-92. doi: 10.1016/j.jocd.2015.04.011. Epub 2015 Jun 10. J Clin Densitom. 2015. PMID: 26071171 Review.
Sarcopenia is a major component of the frailty syndrome and is also a strong predictor of disability, morbidity, and mortality in older persons. ...Among those interventions, physical activity with or without protein supplementation has demonstrated to …
Sarcopenia is a major component of the frailty syndrome and is also a strong predictor of disability, morbidity, and mo …
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.
Detection of diagnostic genetic variants enabled us to distinguish between syndromic and non-syndromic fetal anomalies (eg, congenital heart disease only vs a syndrome with congenital heart disease and learning disability). ...INTERPRETATION: WES facil …
Detection of diagnostic genetic variants enabled us to distinguish between syndromic and non-syndromic fetal anomalies (eg, co …
Impact of osteosarcopenia on disability and mortality among Japanese older adults.
Shimada H, Suzuki T, Doi T, Lee S, Nakakubo S, Makino K, Arai H. Shimada H, et al. J Cachexia Sarcopenia Muscle. 2023 Apr;14(2):1107-1116. doi: 10.1002/jcsm.13209. Epub 2023 Mar 1. J Cachexia Sarcopenia Muscle. 2023. PMID: 36858820 Free PMC article.
Skeletal muscle mass was evaluated using a bioimpedance analysis device. ...Further research is needed to implement these findings in community health activities, such as setting precise cut-off values and constructing accurate disability and mortality prediction …
Skeletal muscle mass was evaluated using a bioimpedance analysis device. ...Further research is needed to implement these findings in …
Translational research into frailty from bench to bedside: Salivary biomarkers for inflammaging.
Niebla-Cárdenas A, Bareke H, Juanes-Velasco P, Landeira-Viñuela A, Hernández ÁP, Montalvillo E, Góngora R, Arroyo-Anlló E, Silvia Puente-González A, Méndez-Sánchez R, Fuentes M. Niebla-Cárdenas A, et al. Exp Gerontol. 2023 Jan;171:112040. doi: 10.1016/j.exger.2022.112040. Epub 2022 Nov 28. Exp Gerontol. 2023. PMID: 36455696 Free article. Review.
Frailty is a complex physiological syndrome associated with adverse ageing and decreased physiological reserves. ...The aim of this review is to describe the current knowledge on the association between frailty and the inflammatory process and discuss methods to identify p …
Frailty is a complex physiological syndrome associated with adverse ageing and decreased physiological reserves. ...The aim of this r …
Chromosome 15q24 microdeletion syndrome.
Magoulas PL, El-Hattab AW. Magoulas PL, et al. Orphanet J Rare Dis. 2012 Jan 4;7:2. doi: 10.1186/1750-1172-7-2. Orphanet J Rare Dis. 2012. PMID: 22216833 Free PMC article. Review.
Chromosome 15q24 microdeletion syndrome is a recently described rare microdeletion syndrome that has been reported in 19 individuals. ...Chromosome 15q24 microdeletion syndrome should be differentiated from other genetic syndromes, particularly velo-ca …
Chromosome 15q24 microdeletion syndrome is a recently described rare microdeletion syndrome that has been reported in 19 indiv …
Frailty in heart failure.
Uchmanowicz I, Łoboz-Rudnicka M, Szeląg P, Jankowska-Polańska B, Łoboz-Grudzień K. Uchmanowicz I, et al. Curr Heart Fail Rep. 2014 Sep;11(3):266-73. doi: 10.1007/s11897-014-0198-4. Curr Heart Fail Rep. 2014. PMID: 24733407 Review.
Considering the increasing age of individuals affected with heart failure (HF), a specific approach to their treatment is required, with more attention paid to geriatric conditions such as poor mobility, multiple disabilities, and cognitive impairment. Frailty is a distinc …
Considering the increasing age of individuals affected with heart failure (HF), a specific approach to their treatment is required, with mor …
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cavé H, Zenker M, Tartaglia M. Motta M, et al. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. Am J Hum Genet. 2021. PMID: 34626534 Free PMC article.
The clinical phenotype of the four affected individuals included developmental delay, intellectual disability, cardiac defects, short stature, skeletal anomalies, and a typical facial gestalt as major features, without the occurrence of the distinctive skin signs ch …
The clinical phenotype of the four affected individuals included developmental delay, intellectual disability, cardiac defects, short …
Frailty and prognosis in advanced heart failure.
Boxer RS, Shah KB, Kenny AM. Boxer RS, et al. Curr Opin Support Palliat Care. 2014 Mar;8(1):25-9. doi: 10.1097/SPC.0000000000000027. Curr Opin Support Palliat Care. 2014. PMID: 24346236 Review.
PURPOSE OF REVIEW: The frailty syndrome is characterized by an increased vulnerability to physiologic stress. Frailty is distinct from disability and disease states; however, there is a strong relationship between frailty and heart failure and the pathophysiology's …
PURPOSE OF REVIEW: The frailty syndrome is characterized by an increased vulnerability to physiologic stress. Frailty is distinct fro …
221 results