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
1989 1
1990 2
1991 2
1992 2
1993 5
1994 3
1995 4
1996 4
1997 2
1998 2
1999 3
2000 3
2001 3
2002 2
2003 5
2004 5
2005 7
2006 5
2007 4
2008 8
2009 8
2010 13
2011 9
2012 10
2013 8
2014 8
2015 8
2016 12
2017 9
2018 8
2019 10
2020 12
2021 12
2022 12
2023 9
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

206 results

Results by year

Filters applied: . Clear all
Page 1
Facioscapulohumeral Muscular Dystrophy.
Mul K. Mul K. Continuum (Minneap Minn). 2022 Dec 1;28(6):1735-1751. doi: 10.1212/CON.0000000000001155. Continuum (Minneap Minn). 2022. PMID: 36537978 Review.
PURPOSE OF REVIEW: This article reviews the current knowledge on the clinical characteristics and disease mechanism of facioscapulohumeral muscular dystrophy (FSHD), as well as advances in targeted therapy development. ...
PURPOSE OF REVIEW: This article reviews the current knowledge on the clinical characteristics and disease mechanism of facioscapulohumera …
Muscular Dystrophies.
Carter JC, Sheehan DW, Prochoroff A, Birnkrant DJ. Carter JC, et al. Clin Chest Med. 2018 Jun;39(2):377-389. doi: 10.1016/j.ccm.2018.01.004. Clin Chest Med. 2018. PMID: 29779596 Review.
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care of a pulmonologist. ...The authors present an overview of the muscular dystrophies, including their basic features, common clinical phenotype …
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care of a pul …
Facioscapulohumeral muscular dystrophy: the road to targeted therapies.
Tihaya MS, Mul K, Balog J, de Greef JC, Tapscott SJ, Tawil R, Statland JM, van der Maarel SM. Tihaya MS, et al. Nat Rev Neurol. 2023 Feb;19(2):91-108. doi: 10.1038/s41582-022-00762-2. Epub 2023 Jan 10. Nat Rev Neurol. 2023. PMID: 36627512 Review.
Advances in the molecular understanding of facioscapulohumeral muscular dystrophy (FSHD) have revealed that FSHD results from epigenetic de-repression of the DUX4 gene in skeletal muscle, which encodes a transcription factor that is active in early embryonic …
Advances in the molecular understanding of facioscapulohumeral muscular dystrophy (FSHD) have revealed that FSHD result …
The muscular dystrophies.
Emery AE. Emery AE. Lancet. 2002 Feb 23;359(9307):687-95. doi: 10.1016/S0140-6736(02)07815-7. Lancet. 2002. PMID: 11879882 Review.
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable distribution and severity. They can be subdivided into several groups, including congenital forms, in accordance with the distribution of predomin …
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable distri …
Facioscapulohumeral muscular dystrophy.
Tawil R. Tawil R. Handb Clin Neurol. 2018;148:541-548. doi: 10.1016/B978-0-444-64076-5.00035-1. Handb Clin Neurol. 2018. PMID: 29478599 Review.
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy with a distinctive pattern of skeletal muscle weakness and a wide spectrum of disease severity. ...
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy with …
Facioscapulohumeral Muscular Dystrophy.
DeSimone AM, Pakula A, Lek A, Emerson CP Jr. DeSimone AM, et al. Compr Physiol. 2017 Sep 12;7(4):1229-1279. doi: 10.1002/cphy.c160039. Compr Physiol. 2017. PMID: 28915324 Review.
Facioscapulohumeral Muscular Dystrophy is a common form of muscular dystrophy that presents clinically with progressive weakness of the facial, scapular, and humeral muscles, with later involvement of the trunk and lower extremities. While typic …
Facioscapulohumeral Muscular Dystrophy is a common form of muscular dystrophy that presents clinically wi …
Facioscapulohumeral Muscular Dystrophy: Update on Pathogenesis and Future Treatments.
Hamel J, Tawil R. Hamel J, et al. Neurotherapeutics. 2018 Oct;15(4):863-871. doi: 10.1007/s13311-018-00675-3. Neurotherapeutics. 2018. PMID: 30361930 Free PMC article. Review.
A reliable model of a disease pathomechanism is the first step to develop targeted treatment. In facioscapulohumeral muscular dystrophy (FSHD), the third most common muscular dystrophy, recent advances in understanding the complex genetics and e …
A reliable model of a disease pathomechanism is the first step to develop targeted treatment. In facioscapulohumeral muscular …
Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals.
Hangül C, Karaüzüm SB, Akkol EK, Demir-Dora D, Çetin Z, Saygılı Eİ, Evcili G, Sobarzo-Sánchez E. Hangül C, et al. Curr Neuropharmacol. 2021;19(12):2276-2295. doi: 10.2174/1570159X19666210726151924. Curr Neuropharmacol. 2021. PMID: 34315378 Free PMC article. Review.
Facioscapulohumeral Muscular Dystrophy (FSHD) is in the top three list of all dystrophies with an approximate 1:8000 incidence. ...
Facioscapulohumeral Muscular Dystrophy (FSHD) is in the top three list of all dystrophies with an approximate 1:8000 in …
Cellular and animal models for facioscapulohumeral muscular dystrophy.
DeSimone AM, Cohen J, Lek M, Lek A. DeSimone AM, et al. Dis Model Mech. 2020 Oct 28;13(10):dmm046904. doi: 10.1242/dmm.046904. Dis Model Mech. 2020. PMID: 33174531 Free PMC article. Review.
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy and presents with weakness of the facial, scapular and humeral muscles, which frequently progresses to the lower limbs and truncal areas, causing …
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy and p …
Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review.
Chen TH, Wu YZ, Tseng YH. Chen TH, et al. Int J Mol Sci. 2020 Oct 21;21(20):7783. doi: 10.3390/ijms21207783. Int J Mol Sci. 2020. PMID: 33096728 Free PMC article. Review.
Facioscapulohumeral muscular dystrophy (FSHD)-the worldwide third most common inherited muscular dystrophy caused by the heterozygous contraction of a 3.3 kb tandem repeat (D4Z4) on a chromosome with a 4q35 haplotype-is a progressive genetic myo …
Facioscapulohumeral muscular dystrophy (FSHD)-the worldwide third most common inherited muscular dystrophy …
206 results