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Quoted phrase not found in phrase index: "Adult-onset Steinert myotonic dystrophy"
Page 1
Myotonic dystrophy type 1: A comparison between the adult- and late-onset subtype.
Joosten IBT, Horlings CGC, Vosse BAH, Wagner A, Bovenkerk DSH, Evertz R, Vernooy K, van Engelen BGM, Faber CG. Joosten IBT, et al. Muscle Nerve. 2023 Feb;67(2):130-137. doi: 10.1002/mus.27766. Epub 2022 Dec 22. Muscle Nerve. 2023. PMID: 36484161 Free PMC article.
INTRODUCTION/AIMS: Although the extent of muscle weakness and organ complications has not been well studied in patients with late-onset myotonic dystrophy type 1 (DM1), adult-onset DM1 is associated with severe muscle involvement and possible life-thre …
INTRODUCTION/AIMS: Although the extent of muscle weakness and organ complications has not been well studied in patients with late-onset m …
Genetics and muscle pathology in the diagnosis of muscular dystrophies: An update.
Narasimhaiah D, Uppin MS, Ranganath P. Narasimhaiah D, et al. Indian J Pathol Microbiol. 2022 May;65(Supplement):S259-S270. doi: 10.4103/ijpm.ijpm_1074_21. Indian J Pathol Microbiol. 2022. PMID: 35562158 Free article. Review.
Congenital muscular dystrophies (CMD) include dystroglycanopathies, merosin-deficient CMD, collagen VI-deficient CMD, SELENON-related rigid spine muscular dystrophy, and LMNA-related CMD. Childhood and adult-onset muscular dystrophies include dystrophinopathi …
Congenital muscular dystrophies (CMD) include dystroglycanopathies, merosin-deficient CMD, collagen VI-deficient CMD, SELENON-related rigid …
Mechanisms and management of the heart in myotonic dystrophy.
McNally EM, Sparano D. McNally EM, et al. Heart. 2011 Jul;97(13):1094-100. doi: 10.1136/hrt.2010.214197. Heart. 2011. PMID: 21642660 Free PMC article. Review.
Myotonic dystrophy (DM) is the most common form of adult onset muscular dystrophy and is caused by expansion of short nucleotide repeats that, in turn, produce toxic RNA aggregates within cells. ...DM patients are also at risk for cardiomyopathy …
Myotonic dystrophy (DM) is the most common form of adult onset muscular dystrophy and is caused by expans …
Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort.
Chawla T, Reddy N, Jankar R, Vengalil S, Polavarapu K, Arunachal G, Preethish-Kumar V, Nashi S, Bardhan M, Rajeshwaran J, Afsar M, Warrier M, Thomas PT, Thennarasu K, Nalini A. Chawla T, et al. Neurol India. 2024 Jan 1;72(1):83-89. doi: 10.4103/neuroindia.NI_1432_20. Epub 2024 Feb 29. Neurol India. 2024. PMID: 38443007 Free article.
RESULTS: The mean age at symptom onset was 23.1 11.4 years, M: F = 3.8:1, mean duration of illness = 14.3 9.5 years. Clinically 54.2% had adult onset form, juvenile = 27.5%, infantile = 10.8%, late adult onset = 7.5%. ...
RESULTS: The mean age at symptom onset was 23.1 11.4 years, M: F = 3.8:1, mean duration of illness = 14.3 9.5 years. Clinically 54.2% had …
The Dystrophic and Nondystrophic Myotonias.
Sansone VA. Sansone VA. Continuum (Minneap Minn). 2016 Dec;22(6, Muscle and Neuromuscular Junction Disorders):1889-1915. doi: 10.1212/CON.0000000000000414. Continuum (Minneap Minn). 2016. PMID: 27922499 Review.
PURPOSE OF REVIEW: This article describes clinical and electrical myotonia and provides an update on the classification, diagnosis, and management of myotonic disorders. RECENT FINDINGS: In the myotonic dystrophies, antisense oligonucleotides provide a general strat …
PURPOSE OF REVIEW: This article describes clinical and electrical myotonia and provides an update on the classification, diagnosis, and mana …
Cognitive function and its relationship with brain structure in myotonic dystrophy type 1.
Langbehn KE, van der Plas E, Moser DJ, Long JD, Gutmann L, Nopoulos PC. Langbehn KE, et al. J Neurosci Res. 2021 Jan;99(1):190-199. doi: 10.1002/jnr.24595. Epub 2020 Feb 13. J Neurosci Res. 2021. PMID: 32056295 Free PMC article.
Studies have shown relationships between white matter abnormalities and cognitive dysfunction in myotonic dystrophy type 1 (DM1), but comprehensive analysis of potential structure-function relationships are lacking. ...Enlarged hippocampal volume may underlie some a …
Studies have shown relationships between white matter abnormalities and cognitive dysfunction in myotonic dystrophy type 1 (DM …
Individual transcriptomic response to strength training for patients with myotonic dystrophy type 1.
Davey EE, Légaré C, Planco L, Shaughnessy S, Lennon CD, Roussel MP, Shorrock HK, Hung M, Cleary JD, Duchesne E, Berglund JA. Davey EE, et al. JCI Insight. 2023 Jul 24;8(14):e163856. doi: 10.1172/jci.insight.163856. JCI Insight. 2023. PMID: 37318869 Free PMC article.
Myotonic dystrophy type 1 (DM1), the most common form of adult-onset muscular dystrophy, is caused by a CTG expansion resulting in significant transcriptomic dysregulation that leads to muscle weakness and wasting. ...
Myotonic dystrophy type 1 (DM1), the most common form of adult-onset muscular dystrophy, is caused by a C …
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations.
Voermans NC, van der Bilt RC, IJspeert J, Hogrel JY, Jeanpierre M, Behin A, Laforet P, Stojkovic T, van Engelen BG, Padberg GW, Sacconi S, Lemmers RJLF, van der Maarel SM, Eymard B, Bassez G. Voermans NC, et al. J Neurol. 2019 Dec;266(12):2987-2996. doi: 10.1007/s00415-019-09494-8. Epub 2019 Aug 31. J Neurol. 2019. PMID: 31471688 Free PMC article.
OBJECTIVE: To study scapular winging or other forms of scapular dyskinesis (condition of alteration of the normal position and motion of the scapula) in myotonic dystrophy type 1 (DM1), which is generally considered to be a distal myopathy, we performed an observati …
OBJECTIVE: To study scapular winging or other forms of scapular dyskinesis (condition of alteration of the normal position and motion of the …
Encoding of facial expressions in individuals with adult-onset myotonic dystrophy type 1.
Johnson C, Langbehn KE, Long JD, Moser D, Cross S, Gutmann L, Nopoulos PC, van der Plas E. Johnson C, et al. J Clin Exp Neuropsychol. 2020 Nov;42(9):932-940. doi: 10.1080/13803395.2020.1826410. Epub 2020 Oct 7. J Clin Exp Neuropsychol. 2020. PMID: 33028165 Free PMC article.
Introduction: Emotional issues are often reported among individuals with myotonic dystrophy type 1 (DM1) and some studies have suggested that deficits in ability to quickly encode emotions may contribute to these problems. ...The aim of this study was to compare emo …
Introduction: Emotional issues are often reported among individuals with myotonic dystrophy type 1 (DM1) and some studies have …
Longitudinal changes in white matter as measured with diffusion tensor imaging in adult-onset myotonic dystrophy type 1.
Koscik TR, van der Plas E, Long JD, Cross S, Gutmann L, Cumming SA, Monckton DG, Shields RK, Magnotta V, Nopoulos PC. Koscik TR, et al. Neuromuscul Disord. 2023 Aug;33(8):660-669. doi: 10.1016/j.nmd.2023.05.010. Epub 2023 Jun 11. Neuromuscul Disord. 2023. PMID: 37419717
Myotonic dystrophy type 1 is characterized by neuromuscular degeneration. ...
Myotonic dystrophy type 1 is characterized by neuromuscular degeneration. ...
57 results