Cargando…

Compliance to DMD Care Considerations in the Netherlands

BACKGROUND AND OBJECTIVE: To optimize care for patients with DMD, it is essential to know to what extent current care complies with the recommended monitoring frequencies suggested by the DMD care considerations. The objective of this study was to investigate the current care for patients with DMD i...

Descripción completa

Detalles Bibliográficos
Autores principales:	Heutinck, Lotte, Houwen-van Opstal, Saskia L.S., Krom, Yvonne D., Niks, Erik H., Verschuuren, Jan J.G.M., Jansen, Merel, de Groot, Imelda J.M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	IOS Press 2021
Materias:	Research Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673507/ https://www.ncbi.nlm.nih.gov/pubmed/34120911 http://dx.doi.org/10.3233/JND-210670

Ejemplares similares

Clinical Management of Duchenne Muscular Dystrophy in the Netherlands: Barriers to and Proposals for the Implementation of the International Clinical Practice Guidelines
por: Heutinck, Lotte, et al.
Publicado: (2021)

Occurrence of symptoms in different stages of Duchenne muscular dystrophy and their impact on social participation
por: Houwen‐van Opstal, Saskia L. S., et al.
Publicado: (2021)

Exon skipping for DMD
por: Aartsma-Rus, Annemieke, et al.
Publicado: (2012)

The Dilemma of Choice for Duchenne Patients Eligible for Exon 51 Skipping The European Experience
por: Aartsma-Rus, Annemieke, et al.
Publicado: (2023)

The neurocognitive profile of adults with Becker muscular dystrophy in the Netherlands
por: Koeks, Zaıda, et al.
Publicado: (2022)

Association of Elbow Flexor MRI Fat Fraction With Loss of Hand-to-Mouth Movement in Patients With Duchenne Muscular Dystrophy
por: Naarding, Karin J., et al.
Publicado: (2021)

DMD Genotypes and Motor Function in Duchenne Muscular Dystrophy: A Multi-institution Meta-analysis With Implications for Clinical Trials
por: Muntoni, Francesco, et al.
Publicado: (2023)

Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy
por: Naarding, Karin J., et al.
Publicado: (2020)

The Black Box of Technological Outcome Measures: An Example in Duchenne Muscular Dystrophy
por: Naarding, Karin J., et al.
Publicado: (2022)

DMD & BMD – CLINICAL: P.51 DMD Hub: demonstrating impact for DMD trials
por: Heslop, E., et al.
Publicado: (2020)

Physical training in boys with Duchenne Muscular Dystrophy: the protocol of the No Use is Disuse study
por: Jansen, Merel, et al.
Publicado: (2010)

Multi‐parametric MR in Becker muscular dystrophy patients
por: Hooijmans, Melissa T., et al.
Publicado: (2020)

Age-Related Longitudinal Changes in Metabolic Energy Expenditure during Walking in Boys with Duchenne Muscular Dystrophy
por: Brehm, Merel-Anne, et al.
Publicado: (2014)

Pseudoexons of the DMD Gene
por: Keegan, Niall P.
Publicado: (2020)

Repurposing Pathogenic Variants of DMD Gene and its Isoforms for DMD Exon Skipping Intervention
por: Tyagi, Rahul, et al.
Publicado: (2019)

Are Soy Products Effective in DMD?
por: Winder, Steve J, et al.
Publicado: (2018)

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

The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine
por: Iskandar, Kristy, et al.
Publicado: (2019)

Guidelines for Corticosteroid use in Treatment of DMD
por: Rao, Vamshi K.
Publicado: (2016)

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)

Matrilineal analysis of mutations in the DMD gene in a multigenerational South Indian cohort using DMD gene panel sequencing
por: Shastry, Arun, et al.
Publicado: (2021)

P4 Cost Analysis of Post-COVID-19 Healthcare Consumption in the Netherlands
por: Fens, T, et al.
Publicado: (2022)

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

Early Identification of DMD in the Setting of West Syndrome
por: Razeq, Ahmed, et al.
Publicado: (2021)

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

Daniel Frank Whitten, D.M.D.
Publicado: (1891)

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)

Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype
por: Brioschi, Simona, et al.
Publicado: (2012)

Long-Read Sequencing Revealed Extragenic and Intragenic Duplications of Exons 56–61 in DMD in an Asymptomatic Male and a DMD Patient
por: Bai, Ying, et al.
Publicado: (2022)

Update on Standard Operating Procedures in Preclinical Research for DMD and SMA Report of TREAT-NMD Alliance Workshop, Schiphol Airport, 26 April 2015, The Netherlands
por: van Putten, Maaike, et al.
Publicado: (2018)

184th ENMC international workshop: Pain and fatigue in neuromuscular disorders(): 20–22 May 2011, Naarden, The Netherlands
por: de Groot, Imelda J.M., et al.
Publicado: (2013)

Bovine-associated MRSA ST398 in The Netherlands
por: Tavakol, Mehri, et al.
Publicado: (2012)

Regulation of DMD pathology by an ankyrin-encoded miRNA
por: Alexander, Matthew S, et al.
Publicado: (2011)

A promising preclinical test for DMD in dog models
Publicado: (2014)

LINC complex alterations in DMD and EDMD/CMT fibroblasts
por: Taranum, Surayya, et al.
Publicado: (2012)

Second-generation compound for the modulation of utrophin in the therapy of DMD
por: Guiraud, Simon, et al.
Publicado: (2015)

New insights into DMD using mouse and canine models
Publicado: (2013)

Skipping Multiple Exons to Treat DMD—Promises and Challenges
por: Aslesh, Tejal, et al.
Publicado: (2018)

Humanizing the mdx mouse model of DMD: the long and the short of it
por: Yucel, Nora, et al.
Publicado: (2018)

Breakpoint junction features of seven DMD deletion mutations
por: Keegan, Niall P., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_bis02qbfkjp6g5een428ndaeu5