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

Year Number of Results
1983 1
1988 2
1989 1
1991 1
1992 2
1993 2
1994 3
1995 3
1996 10
1997 11
1998 6
1999 15
2000 14
2001 14
2002 8
2003 15
2004 17
2005 17
2006 11
2007 13
2008 15
2009 11
2010 14
2011 19
2012 16
2013 14
2014 17
2015 13
2016 21
2017 11
2018 20
2019 14
2020 19
2021 22
2022 12
2023 14
2024 3

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388 results

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Page 1
The Limb-Girdle Muscular Dystrophies.
Johnson NE, Statland JM. Johnson NE, et al. Continuum (Minneap Minn). 2022 Dec 1;28(6):1698-1714. doi: 10.1212/CON.0000000000001178. Continuum (Minneap Minn). 2022. PMID: 36537976 Review.
PURPOSE OF REVIEW: The limb-girdle muscular dystrophies (LGMDs) are a group of inherited muscle disorders with a common feature of limb-girdle pattern of weakness, caused by over 29 individual genes. ...
PURPOSE OF REVIEW: The limb-girdle muscular dystrophies (LGMDs) are a group of inherited muscle disorders with a …
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 spectrum of conditions encapsulated by this subset ranges from severe and fatal congenital muscular dystrop …
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care o …
Anti-HMGCR Myopathy.
Mohassel P, Mammen AL. Mohassel P, et al. J Neuromuscul Dis. 2018;5(1):11-20. doi: 10.3233/JND-170282. J Neuromuscul Dis. 2018. PMID: 29480216 Free PMC article. Review.
After the discovery of anti-HMGCR autoantibodies, several international groups identified and characterized more patients, expanding the phenotypic spectrum of this disease to include pediatric patients and young adults without statin exposure and those with a chronic myopathy re …
After the discovery of anti-HMGCR autoantibodies, several international groups identified and characterized more patients, expanding the phe …
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 p …
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable …
Limb-girdle Muscular Dystrophy and Therapy: Insights into Cell and Gene-based Approaches.
Taheri F, Taghizadeh E, Pour MJR, Rostami D, Renani PG, Rastgar-Moghadam A, Hayat SMG. Taheri F, et al. Curr Gene Ther. 2020;19(6):386-394. doi: 10.2174/1566523220666200218113526. Curr Gene Ther. 2020. PMID: 32067617 Review.
The Limb-Girdle Muscular Dystrophies (LGMD) are genetically heterogeneous disorders, responsible for muscle wasting and severe form of dystrophies. Despite the critical developments in the insight and information of pathomechanisms of limb …
The Limb-Girdle Muscular Dystrophies (LGMD) are genetically heterogeneous disorders, responsible for muscle wast …
Muscle-Related Plectinopathies.
Zrelski MM, Kustermann M, Winter L. Zrelski MM, et al. Cells. 2021 Sep 19;10(9):2480. doi: 10.3390/cells10092480. Cells. 2021. PMID: 34572129 Free PMC article. Review.
The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), which is characterized by skin blistering and progressive muscle weakness. Besides EBS-MD, PLEC mutations lead to EBS with nail dystrophy, …
The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), which …
Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients.
Wang DN, Wang ZQ, Chen YQ, Xu GR, Lin MT, Wang N. Wang DN, et al. Int J Neurosci. 2018 Mar;128(3):199-207. doi: 10.1080/00207454.2017.1380640. Epub 2017 Oct 2. Int J Neurosci. 2018. PMID: 28931339 Review.
BACKGROUND: Limb-girdle muscular dystrophy type 2I (LGMD2I) is an autosomal recessive hereditary disorder caused by mutations in the fukutin-related protein (FKRP) gene. ...
BACKGROUND: Limb-girdle muscular dystrophy type 2I (LGMD2I) is an autosomal recessive hereditary disorder caused …
Sarcoglycanopathies.
Kirschner J, Lochmüller H. Kirschner J, et al. Handb Clin Neurol. 2011;101:41-6. doi: 10.1016/B978-0-08-045031-5.00003-7. Handb Clin Neurol. 2011. PMID: 21496623 Review.
The so-called sarcoglycanopathies form a subgroup of four genetically closely related autosomal recessive limb-girdle muscular dystrophies (LGMD2C-F) caused by mutations of the alpha-, beta-, gamma-, and delta-sarcoglycan genes. ...The disease course i …
The so-called sarcoglycanopathies form a subgroup of four genetically closely related autosomal recessive limb-girdle muscu …
Sarcoglycanopathies: an update.
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Vainzof M, et al. Neuromuscul Disord. 2021 Oct;31(10):1021-1027. doi: 10.1016/j.nmd.2021.07.014. Epub 2021 Jul 28. Neuromuscul Disord. 2021. PMID: 34404573 Review.
Sarcoglycanopathies are the most severe forms of autosomal recessive limb-girdle muscular dystrophies (LGMDs), constituting about 10-25% of LGMDs. ...
Sarcoglycanopathies are the most severe forms of autosomal recessive limb-girdle muscular dystrophies (LGMDs), c …
Limb-girdle muscular dystrophy.
Mathews KD, Moore SA. Mathews KD, et al. Curr Neurol Neurosci Rep. 2003 Jan;3(1):78-85. doi: 10.1007/s11910-003-0042-9. Curr Neurol Neurosci Rep. 2003. PMID: 12507416 Review.
The limb-girdle muscular dystrophies (LGMDs) are a group of muscular dystrophies that share a similar clinical phenotype. ...Some are allelic with other forms of muscular dystrophy; LGMD 1B is allelic with autosomal dominant …
The limb-girdle muscular dystrophies (LGMDs) are a group of muscular dystrophies that share a simi …
388 results