Cargando…

Reduced bone mineral density in adolescents with Duchenne Muscular Dystrophy (DMD) and scoliosis

SUMMARY: Duchenne muscular dystrophy is a progressive disease usually associated with loss of ambulation and progressive scoliosis. Immobilisation and glucocorticoid treatment are predisposing factors for reduced bone mineral density (BMD). Analysis of quantitative computed tomography revealed low B...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tsaknakis, K., Jäckle, K., Lüders, K. A., Lorenz, H. M., Braunschweig, L., Hell, A. K.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer London 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463342/ https://www.ncbi.nlm.nih.gov/pubmed/35583603 http://dx.doi.org/10.1007/s00198-022-06416-9

Ejemplares similares

Reduced Volumetric Bone Mineral Density of the Spine in Adolescent Rett Girls with Scoliosis
por: Tsaknakis, Konstantinos, et al.
Publicado: (2022)

Symptomatic therapy of Duchenne Muscular Dystrophy (DMD)
por: Rüdel, Reinhardt
Publicado: (2012)

Vascular therapy for Duchenne muscular dystrophy (DMD)
por: Thapa, Sangharsha, et al.
Publicado: (2023)

Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
por: Rodger, Sunil, et al.
Publicado: (2012)

Duchenne Muscular Dystrophy (DMD) Protein-Protein Interaction Mapping
por: REZAEI TAVIRANI, Mostafa, et al.
Publicado: (2017)

Duchenne muscular dystrophy (DMD) cardiomyocyte-secreted exosomes promote the pathogenesis of DMD-associated cardiomyopathy
por: Gartz, Melanie, et al.
Publicado: (2020)

Bone Mineral Density and Bone Metabolism in Patients with Duchenne Muscular Dystrophy
por: BARZEGAR, Mohammad, et al.
Publicado: (2018)

Assessment of diaphragmatic thickness by ultrasonography in Duchenne muscular dystrophy (DMD) patients
por: Laviola, Marianna, et al.
Publicado: (2018)

Spinal Deformity Correction in Duchenne Muscular Dystrophy (DMD): Comparing the Outcome of Two Instrumentation Techniques
por: Debnath, Ujjwal Kanti, et al.
Publicado: (2011)

Targeting Duchenne muscular dystrophy by skipping DMD exon 45 with base editors
por: Gapinske, Michael, et al.
Publicado: (2023)

Effects of Bisphosphonate Therapy on Bone Mineral Density in Boys with Duchenne Muscular Dystrophy
por: Ronsley, Rebecca, et al.
Publicado: (2020)

Cardiovascular phenotype of the Dmd(mdx) rat – a suitable animal model for Duchenne muscular dystrophy
por: Szabó, Petra Lujza, et al.
Publicado: (2021)

A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20
por: Mata López, Sara, et al.
Publicado: (2018)

Chronic Hypoxia Impairs Muscle Function in the Drosophila Model of Duchenne's Muscular Dystrophy (DMD)
por: Mosqueira, Matias, et al.
Publicado: (2010)

Ventilatory Chemosensory Drive Is Blunted in the mdx Mouse Model of Duchenne Muscular Dystrophy (DMD)
por: Mosqueira, Matias, et al.
Publicado: (2013)

Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies
por: Ling, Chao, et al.
Publicado: (2019)

Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy
por: Wu, Jiangfen, et al.
Publicado: (2023)

Risk of Obstructive Sleep Apnea in Saudi Male Boys with Duchenne Muscular Dystrophy (DMD)
por: Bamaga, Ahmed, et al.
Publicado: (2023)

Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
por: Dwianingsih, Ery Kus, et al.
Publicado: (2023)

Can radial bone mineral density predict spinal bone mineral density in patients with advanced Duchenne muscular dystrophy?
por: Kim, Eunyoung, et al.
Publicado: (2018)

Screening of Duchenne Muscular Dystrophy (DMD) Mutations and Investigating Its Mutational Mechanism in Chinese Patients
por: Chen, Chen, et al.
Publicado: (2014)

Aquatic therapy for boys with Duchenne muscular dystrophy (DMD): an external pilot randomised controlled trial
por: Hind, Daniel, et al.
Publicado: (2017)

Perspectives on Everyday Life Challenges of Danish Young People With Duchenne Muscular Dystrophy (DMD) on Corticosteroids
por: Handberg, Charlotte, et al.
Publicado: (2022)

Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells
por: Cardone, Nastasia, et al.
Publicado: (2023)

Clinical Heterogeneity of Duchenne Muscular Dystrophy (DMD): Definition of Sub-Phenotypes and Predictive Criteria by Long-Term Follow-Up
por: Desguerre, Isabelle, et al.
Publicado: (2009)

Systemic deletion of DMD exon 51 rescues clinically severe Duchenne muscular dystrophy in a pig model lacking DMD exon 52
por: Stirm, Michael, et al.
Publicado: (2023)

Current Practices in Treating Cardiomyopathy and Heart Failure in Duchenne Muscular Dystrophy (DMD): Understanding Care Practices in Order to Optimize DMD Heart Failure Through ACTION
por: Villa, Chet, et al.
Publicado: (2022)

Neurodevelopmental Needs in Young Boys with Duchenne Muscular Dystrophy (DMD): Observations from the Cooperative International Neuromuscular Research Group (CINRG) DMD Natural History Study (DNHS).
por: Thangarajh, Mathula, et al.
Publicado: (2018)

Delay in Diagnosis of Duchenne Muscular Dystrophy
por: Rao, Vamshi K., et al.
Publicado: (2015)

A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy
por: Wong, Tatianna Wai Ying, et al.
Publicado: (2020)

The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
por: Bladen, Catherine L, et al.
Publicado: (2015)

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations
por: Okubo, Mariko, et al.
Publicado: (2016)

Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy
por: Donandt, Tina, et al.
Publicado: (2022)

The relationship between scoliosis and upper extremity functions in patients with Duchenne muscular dystrophy
por: Erdinç Gündüz, Nihan, et al.
Publicado: (2021)

Duchenne and Becker muscular dystrophy in adolescents: current perspectives
por: Andrews, Jennifer G, et al.
Publicado: (2018)

The Relationship Between Bone Mineral Density and Cardiovascular Function in Duchenne Muscular Dystrophy: A Retrospective Cohort Study
por: Kervin, Tara, et al.
Publicado: (2018)

Development of a New Quality of Life Measure for Duchenne Muscular Dystrophy Using Mixed Methods: The DMD-QoL
por: Powell, Philip A., et al.
Publicado: (2021)

Newborn screening for Duchenne muscular dystrophy‐early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy
por: Gruber, Dorota, et al.
Publicado: (2022)

Molecular characterization and reclassification of a 1.18 Mbp DMD duplication following positive carrier screening for Duchenne/Becker muscular dystrophy
por: Zepeda‐Mendoza, Cinthya J., et al.
Publicado: (2022)

Magnetically Controlled Devices Parallel to the Spine in Children with Spinal Muscular Atrophy
por: Lorenz, Heiko M., et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_bbujrejur3k3d5u3o92snoe5fe