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| Open AccessPractice variation in surgical treatment for lumbar degenerative disc disease: exploring regional and hospital factors influencing surgical rates
- Juliëtte J. C. M. van Munster
- , Ilan J. Y. Halperin
- & Wilco C. Peul
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| Open AccessAmbulatory electrocardiographic longitudinal monitoring in a canine model for Duchenne muscular dystrophy identifies decreased very low frequency power as a hallmark of impaired heart rate variability
- Inès Barthélémy
- , Jin Bo Su
- & Stéphane Blot
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| Open AccessBone scan findings of Paget’s disease of bone in patients with VCP Multisystem Proteinopathy 1
- Rod Carlo Agram Columbres
- , Sarosh Din
- & Virginia Kimonis
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| Open AccessShort-term and mid-term evaluation of three types of minimally invasive lumbar fusion surgery for treatment of L4/L5 degenerative spondylolisthesis
- Zhaojun Song
- , Zhi Zhang
- & Juan Luo
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| Open AccessMendelian randomization study revealed a gut microbiota-neuromuscular junction axis in myasthenia gravis
- Jiaying Shi
- , Ming Yi
- & Yuan Yang
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| Open AccessProteomic and functional characterisation of extracellular vesicles from collagen VI deficient human fibroblasts reveals a role in cell motility
- Carmen Badosa
- , Mónica Roldán
- & Cecilia Jimenez-Mallebrera
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| Open AccessProspective study to evaluate quality of life in amyotrophic lateral sclerosis
- Candela Caballero-Eraso
- , Carlos Carrera-Cueva
- & Luis Jara-Palomares
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| Open AccessDevelopment and characterization of agonistic antibodies targeting the Ig-like 1 domain of MuSK
- Jamie L. Lim
- , Roy Augustinus
- & Maartje G. Huijbers
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| Open AccessElectrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
- Seward B. Rutkove
- , Santiago Callegari
- & Anjali K. Nath
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| Open AccessImprovement of muscle strength in specific muscular regions in nusinersen-treated adult patients with 5q-spinal muscular atrophy
- Olivia Schreiber-Katz
- , Hannah Alexandra Siegler
- & Alma Osmanovic
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| Open AccessThe unconditioned fear response in dystrophin-deficient mice is associated with adrenal and vascular function
- Angus Lindsay
- & Aaron P. Russell
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| Open AccessReal-world data on the incidence and risk of Guillain–Barré syndrome following SARS-CoV-2 vaccination: a prospective surveillance study
- Jongmok Ha
- , Suyeon Park
- & Kunhee Park
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| Open AccessThe diagnostic and prognostic utility of repetitive nerve stimulation in patients with myasthenia gravis
- Matthias Tomschik
- , Eva Renaud
- & Hakan Cetin
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| Open AccessUtilisation of exome sequencing for muscular disorders in Thai paediatric patients: diagnostic yield and mutational spectrum
- Sarinya Summa
- , Chupong Ittiwut
- & Vorasuk Shotelersuk
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| Open AccessEstablishment of quantitative and consistent in vitro skeletal muscle pathological models of myotonic dystrophy type 1 using patient-derived iPSCs
- Ryu Kawada
- , Tatsuya Jonouchi
- & Hidetoshi Sakurai
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| Open AccessTime to diagnosis of Duchenne muscular dystrophy in Austria and Germany
- Miriam Hiebeler
- , Simone Thiele
- & Maggie C. Walter
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| Open AccessQuantitative muscle MRI captures early muscle degeneration in calpainopathy
- Johannes Forsting
- , Marlena Rohm
- & Robert Rehmann
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| Open AccessDual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophy
- Sarah P. Sherlock
- , Jeffrey Palmer
- & Shannon Marraffino
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| Open AccessMagnetic resonance imaging-based lower limb muscle evaluation in Charcot-Marie-Tooth disease type 1A patients and its correlation with clinical data
- Yeo Jin Kim
- , Hyun Su Kim
- & Byung-Ok Choi
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| Open AccessFate of hips complicated by avascular necrosis of the femoral head following reconstructive surgery in nonambulatory patients with cerebral palsy
- Byoung Kyu Park
- , Hoon Park
- & Hyun Woo Kim
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| Open AccessA medium-chain triglyceride containing ketogenic diet exacerbates cardiomyopathy in a CRISPR/Cas9 gene-edited rat model with Duchenne muscular dystrophy
- Yuri Fujikura
- , Koichi Kimura
- & Katsutaka Oishi
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| Open AccessCorticosteroid use and bone health management for Duchenne muscular dystrophy in South Korea
- Jin A Yoon
- , Ho Eun Park
- & Yong Beom Shin
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| Open AccessDynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy
- Xeni Deligianni
- , Francesco Santini
- & Anna Pichiecchio
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| Open AccessChanges in ventilation distribution in children with neuromuscular disease using the insufflator/exsufflator technique: an observational study
- Carmen Casaulta
- , Florence Messerli
- & Thomas Riedel
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| Open AccessThe relevance of migraine in the clinical spectrum of mitochondrial disorders
- Alberto Terrin
- , Luca Bello
- & Elena Pegoraro
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| Open AccessA population-based study of mortality due to muscular dystrophies across a 36-year period in Spain
- Laura Llamosas-Falcón
- , Germán Sánchez-Díaz
- & Verónica Alonso-Ferreira
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| Open AccessWhite matter integrity changes and neurocognitive functioning in adult-late onset DM1: a follow-up DTI study
- Garazi Labayru
- , Borja Camino
- & Andone Sistiaga
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| Open AccessSystematic review and meta-analysis of cognitive impairment in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
- Mehdi Aoun Sebaiti
- , Mathieu Hainselin
- & François Jérôme Authier
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| Open AccessFacioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers
- Anita van den Heuvel
- , Saskia Lassche
- & Silvère M. van der Maarel
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| Open AccessFeeder-supported in vitro exercise model using human satellite cells from patients with sporadic inclusion body myositis
- Yuqing Li
- , Weijian Chen
- & Makoto Kanzaki
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| Open AccessTherapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression
- Anna V. Starikova
- , Victoria V. Skopenkova
- & Maryana V. Bardina
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| Open AccessDistribution of alternative untranslated regions within the mRNA of the CELF1 splicing factor affects its expression
- Arkadiusz Kajdasz
- , Daria Niewiadomska
- & Krzysztof Sobczak
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| Open AccessA proteomics study identifying interactors of the FSHD2 gene product SMCHD1 reveals RUVBL1-dependent DUX4 repression
- Remko Goossens
- , Mara S. Tihaya
- & Silvère M. van der Maarel
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| Open AccessThe effects of molecular crowding and CpG hypermethylation on DNA G-quadruplexes formed by the C9orf72 nucleotide repeat expansion
- Kadir. A. Ozcan
- , Layla T. Ghaffari
- & Aaron R. Haeusler
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| Open AccessPrevalence of sarcopenia in idiopathic dropped head syndrome patients is similar to healthy volunteers
- Tatsuya Igawa
- , Ken Ishii
- & Haruki Funao
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| Open AccessStatistical morphological analysis reveals characteristic paraspinal muscle asymmetry in unilateral lumbar disc herniation
- Yiming Xiao
- , Maryse Fortin
- & Michele C. Battié
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| Open AccessCRISPR mediated targeting of DUX4 distal regulatory element represses DUX4 target genes dysregulated in Facioscapulohumeral muscular dystrophy
- Sunny Das
- & Brian P. Chadwick
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| Open AccessKnockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux
- Gülsüm Kayman Kürekçi
- , Ecem Kural Mangit
- & Pervin R. Dincer
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| Open AccessReappraisal of the incidence, various types and risk factors of malignancies in patients with dermatomyositis and polymyositis in Taiwan
- Jung-Lung Hsu
- , Ming-Feng Liao
- & Long-Sun Ro
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| Open AccessMuscle metabolic remodelling patterns in Duchenne muscular dystrophy revealed by ultra-high-resolution mass spectrometry imaging
- Ivana Dabaj
- , Justine Ferey
- & Abdellah Tebani
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| Open AccessNon-invasive assessment of skeletal muscle fibrosis in mice using nuclear magnetic resonance imaging and ultrasound shear wave elastography
- Aurea B. Martins-Bach
- , Damien Bachasson
- & Pierre G. Carlier
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| Open AccessPMO-based let-7c site blocking oligonucleotide (SBO) mediated utrophin upregulation in mdx mice, a therapeutic approach for Duchenne muscular dystrophy (DMD)
- Kasturi Sengupta
- , Emanuele Loro
- & Tejvir S. Khurana
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| Open AccessActive proportional electromyogram controlled functional electrical stimulation system
- Bethel A. C. Osuagwu
- , Emily Whicher
- & Rebecca Shirley
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| Open AccessEchocardiographic signs of subclinical cardiac function impairment in Duchenne dystrophy gene carriers
- Vladimír Kincl
- , Roman Panovský
- & Lucia Masárová
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| Open AccessA genotyping method combining primer competition PCR with HRM analysis to identify point mutations in Duchenne animal models
- Haizpea Lasa-Fernandez
- , Laura Mosqueira-Martín
- & Ainara Vallejo-Illarramendi
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| Open AccessWnt antagonist FRZB is a muscle biomarker of denervation atrophy in amyotrophic lateral sclerosis
- Thaddaeus Kwan
- , Mohamed Kazamel
- & Peter H. King
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| Open AccessThe D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy
- David W. Hammers
- , Cora C. Hart
- & H. Lee Sweeney
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| Open AccessIntravenous immunoglobulins may prevent prednisone-exacerbation in myasthenia gravis
- Laura Díez-Porras
- , Christian Homedes
- & Carlos Casasnovas
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| Open AccessComputational cognitive modeling and validation of Dp140 induced alteration of working memory in Duchenne Muscular Dystrophy
- Rahul Tyagi
- , Palvi Aggarwal
- & Akshay Anand