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
1955 1
1975 1
1977 1
1980 1
1981 1
1982 1
1985 1
1988 1
1992 1
1993 1
1994 2
1996 2
1998 3
1999 4
2001 6
2002 4
2003 2
2004 2
2005 3
2006 4
2007 5
2008 7
2009 12
2010 7
2011 4
2012 5
2013 3
2014 7
2015 9
2016 6
2017 7
2018 5
2019 13
2020 9
2021 4
2022 3
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

135 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Skeletal dysplasia-intellectual disability syndrome"
Page 1
Vitamin D Deficiency and Sarcopenia in Older Persons.
Remelli F, Vitali A, Zurlo A, Volpato S. Remelli F, et al. Nutrients. 2019 Nov 21;11(12):2861. doi: 10.3390/nu11122861. Nutrients. 2019. PMID: 31766576 Free PMC article. Review.
Therefore, older people with vitamin D deficiency might be at risk of sarcopenia, a geriatric syndrome characterized by the progressive loss of skeletal muscle mass and strength often complicated by adverse events, such as falls, disability hospitalization an …
Therefore, older people with vitamin D deficiency might be at risk of sarcopenia, a geriatric syndrome characterized by the progressi …
Sarcopenia in Asia: consensus report of the Asian Working Group for Sarcopenia.
Chen LK, Liu LK, Woo J, Assantachai P, Auyeung TW, Bahyah KS, Chou MY, Chen LY, Hsu PS, Krairit O, Lee JS, Lee WJ, Lee Y, Liang CK, Limpawattana P, Lin CS, Peng LN, Satake S, Suzuki T, Won CW, Wu CH, Wu SN, Zhang T, Zeng P, Akishita M, Arai H. Chen LK, et al. J Am Med Dir Assoc. 2014 Feb;15(2):95-101. doi: 10.1016/j.jamda.2013.11.025. J Am Med Dir Assoc. 2014. PMID: 24461239
Sarcopenia, a newly recognized geriatric syndrome, is characterized by age-related decline of skeletal muscle plus low muscle strength and/or physical performance. ...In addition to sarcopenia screening for community-dwelling older people, AWGS recommends sarcopenia …
Sarcopenia, a newly recognized geriatric syndrome, is characterized by age-related decline of skeletal muscle plus low muscle …
A randomized controlled study for the treatment of middle-aged and old-aged lumbar disc herniation by Shis spine balance manipulation combined with bone and muscle guidance.
Xu J, Ding X, Wu J, Zhou X, Jin K, Yan M, Ma J, Wu X, Ye J, Mo W. Xu J, et al. Medicine (Baltimore). 2020 Dec 18;99(51):e23812. doi: 10.1097/MD.0000000000023812. Medicine (Baltimore). 2020. PMID: 33371159 Free PMC article. Clinical Trial.
This study will be performed to investigate the effect of a combination of Shi-style spine balance manipulation and Daoyin therapy on LDH in middle-aged and elderly patients. In this non-blinded, randomized controlled trial, 72 eligible patients will be randomly …
This study will be performed to investigate the effect of a combination of Shi-style spine balance manipulation and Daoyin therapy on LDH in …
Elosulfase alfa.
Haddley K. Haddley K. Drugs Today (Barc). 2014 Jul;50(7):475-83. doi: 10.1358/dot.2014.50.7.2177904. Drugs Today (Barc). 2014. PMID: 25101330 Review.
Mucopolysaccharidosis type IVA (MPS IVA), also known as Morquio A syndrome, is an inherited, lysosomal storage disorder caused by genetic mutations in N-acetylgalactosamine-6-sulfatase (GALNS) enzyme gene. GALNS is essential for breakdown of glycosaminoglycans. The disease …
Mucopolysaccharidosis type IVA (MPS IVA), also known as Morquio A syndrome, is an inherited, lysosomal storage disorder caused by gen …
Effect of manual physiotherapy in homogeneous individuals with subacromial shoulder impingement: A randomized controlled trial.
Land H, Gordon S, Watt K. Land H, et al. Physiother Res Int. 2019 Apr;24(2):e1768. doi: 10.1002/pri.1768. Epub 2019 Jan 25. Physiother Res Int. 2019. PMID: 30680850 Clinical Trial.
STUDY DESIGN: Single-centre, prospective, double-blinded, randomized controlled trial. METHOD: Eligible individuals with clearly defined extrinsic SSI were randomized to each group. ...The trial is registered with the Australian New Zealand Clinical …
STUDY DESIGN: Single-centre, prospective, double-blinded, randomized controlled trial. METHOD: Eligible individuals with clear …
Trigger Point Management.
Shipton B, Sagar S, Mall JK. Shipton B, et al. Am Fam Physician. 2023 Feb;107(2):159-164. Am Fam Physician. 2023. PMID: 36791442
Trigger points producing myofascial pain syndromes are common in primary care. Located within skeletal muscle, trigger points are taut, band-like nodules capable of producing pain and disability. Some evidence from clinical trials supports massage, phy …
Trigger points producing myofascial pain syndromes are common in primary care. Located within skeletal muscle, trigger points …
The Strengthening Exercises in Shoulder Impingement trial (The SExSI-trial) investigating the effectiveness of a simple add-on shoulder strengthening exercise programme in patients with long-lasting subacromial impingement syndrome: Study protocol for a pragmatic, assessor blinded, parallel-group, randomised, controlled trial.
Clausen MB, Bandholm T, Rathleff MS, Christensen KB, Zebis MK, Graven-Nielsen T, Hölmich P, Thorborg K. Clausen MB, et al. Trials. 2018 Mar 2;19(1):154. doi: 10.1186/s13063-018-2509-7. Trials. 2018. PMID: 29499710 Free PMC article.
The randomisation sequence is computer generated, with permuted blocks of random sizes. ...TRIAL REGISTRATION: The trial is pre-registered at ClinicalTrials.gov with the ID NCT02747251 on April 19, 2016....
The randomisation sequence is computer generated, with permuted blocks of random sizes. ...TRIAL REGISTRATION: The t …
Fetal Valproate Syndrome.
Mutlu-Albayrak H, Bulut C, Çaksen H. Mutlu-Albayrak H, et al. Pediatr Neonatol. 2017 Apr;58(2):158-164. doi: 10.1016/j.pedneo.2016.01.009. Epub 2016 Jun 17. Pediatr Neonatol. 2017. PMID: 27422007 Free article.
METHODS: Herein, we describe four cases with typically similar facial features of fetal valproate syndrome accompanied to minor skeletal abnormalities. RESULTS: The first case was a 16-month-old girl, presenting with facial dysmorphism, and finger abnormalities. ... …
METHODS: Herein, we describe four cases with typically similar facial features of fetal valproate syndrome accompanied to minor sk …
Metabolic arthropathies.
Timsit MA, Bardin T. Timsit MA, et al. Curr Opin Rheumatol. 1994 Jul;6(4):448-53. doi: 10.1097/00002281-199407000-00017. Curr Opin Rheumatol. 1994. PMID: 8068518 Review.
Among hemoglobinopathies, sickle-cell disease is frequently the source of rheumatic syndromes, as emphasized in recent epidemiologic studies. Avascular necrosis is one of the most common features and may be disabling, leading to total joint replacement of the hip or …
Among hemoglobinopathies, sickle-cell disease is frequently the source of rheumatic syndromes, as emphasized in recent epidemiologic …
Treatment of Satoyoshi syndrome: a systematic review.
Solís-García Del Pozo J, de Cabo C, Solera J. Solís-García Del Pozo J, et al. Orphanet J Rare Dis. 2019 Jun 19;14(1):146. doi: 10.1186/s13023-019-1120-7. Orphanet J Rare Dis. 2019. PMID: 31217029 Free PMC article. Review.
BACKGROUND: Satoyoshi syndrome is a multisystemic rare disease of unknown etiology, although an autoimmune basis is presumed. Its main symptoms are: painful muscle spasms, diarrhea, alopecia and skeletal abnormalities. Clinical course without treatment may re …
BACKGROUND: Satoyoshi syndrome is a multisystemic rare disease of unknown etiology, although an autoimmune basis is presumed. Its mai …
135 results