https://www.parentprojectmd.org/
Parent Project Muscular Dystrophy (PPMD) | Fighting to End Duchenne
Jan 20, 2026 - Parent Project Muscular Dystrophy (PPMD) fights to end Duchenne muscular dystrophy. We accelerate research, raise our voices to impact policy, demand optimal...
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https://www.mda.org/
Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) has been at the center of progress for people living with muscular dystrophy, ALS, and over 300 other neuromuscular...
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https://mdaquest.org/
Home - Quest | Muscular Dystrophy Association
Jun 29, 2026 - Quest is the largest adaptive lifestyle content platform for the neuromuscular disease community and the disability community at large. Quest includes MDA's...
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https://muscle.ca/
Home - Muscular Dystrophy Canada
Jan 5, 2026 - You are not alone. Muscular Dystrophy Canada is here to support individuals and families living with neuromuscular disorders.
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https://musculardystrophynews.com/
Muscular Dystrophy News Home | Muscular Dystrophy News
Jun 22, 2026 - The Web's Daily Resource for Muscular Dystrophy News
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https://research.monash.edu/en/projects/using-zebrafish-congenital-muscular-dystrophy-models-to-find-nove/
Using zebrafish congenital muscular dystrophy models to find novel therapies - Monash University
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https://www.justgiving.com/fundraising/team-univ
University College, Oxford is fundraising for Muscular Dystrophy UK
Help University College, Oxford raise money to support Muscular Dystrophy UK
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https://www.podcasts.ox.ac.uk/keywords/muscular-dystrophy
muscular dystrophy | University of Oxford Podcasts
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https://stemcell.ucla.edu/news/ucla-based-startup-new-muscular-dystrophy-treatment-personal-mission
For UCLA-based startup, new muscular dystrophy treatment is a personal mission
Courtney Young helped develop the gene therapy at the heart of a biotech startup, MyoGene Bio, when she was a doctoral student at UCLA from 2013 to 2018. But...
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https://pubmed.ncbi.nlm.nih.gov/15789136/?dopt=Abstract&holding=idemdclib_fft&otool=idemdclib
A new LMNA mutation causing limb girdle muscular dystrophy 1B
A new LMNA mutation causing limb girdle muscular dystrophy 1B
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https://experts.umn.edu/en/publications/xanthine-oxidase-is-hyper-active-in-duchenne-muscular-dystrophy/
Xanthine oxidase is hyper-active in Duchenne muscular dystrophy - Experts@Minnesota
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https://gov.alaska.gov/muscular-dystrophy-awareness-month-2/
Muscular Dystrophy Awareness Month - Mike Dunleavy
Aug 1, 2021 - WHEREAS, Muscular Dystrophy is a group of hereditary genetic disorders characterized by the weakening and wasting of muscle structures that vary in inheritance...
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https://www.vyondys53.com/
VYONDYS 53 (golodirsen) | Duchenne Muscular Dystrophy Treatment
Vyondys 53, an FDA-approved Duchenne muscular dystrophy treatment for patients who have a genetic mutation in the dystrophin gene that can be treated by...
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https://medlineplus.gov/genetics/condition/rigid-spine-muscular-dystrophy/
Rigid spine muscular dystrophy: MedlinePlus Genetics
Rigid spine muscular dystrophy (RSMD) is a form of congenital muscular dystrophy. Explore symptoms, inheritance, genetics of this condition.
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https://kidshealth.org/CHOC/en/parents/md-factsheet.html
Muscular Dystrophy Factsheet (for Schools) (for Parents) - CHOC Childrens
What teachers should know about muscular dystrophy, and how to help students with MD do their best in school.
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https://www.sciencedaily.com/releases/2009/10/091021011145.htm
Muscular Dystrophy: Exon Skipping Shows Dramatic Effects In Preventing, Treating Muscle-wasting...
Researchers have released details of a breakthrough which holds promise of a new therapeutic approach for the treatment of Duchenne muscular dystrophy (DMD),...
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https://data.mendeley.com/datasets/w9x5p9f5hm/1
Awareness of muscular dystrophy in primary health care workers in Haryana. - Mendeley Data
Muscles gradually deteriorate as a result of a group of inherited degenerative disorders called the muscular dystrophies. They may be X-linked, autosomal...
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https://pubmed.ncbi.nlm.nih.gov/11222452/
Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK population
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commonly presents with ptosis and dysphagia. The genetic basis...
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https://aggiecollaborate.tamu.edu/investigating-lymphatic-dysfunction-in-duchenne-muscular-dystrophy/
Investigating lymphatic dysfunction in Duchenne muscular dystrophy - Aggie Collaborate
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https://gov.alaska.gov/muscular-dystrophy-awareness-month/
Muscular Dystrophy Awareness Month - Mike Dunleavy
Aug 1, 2019 - WHEREAS, muscular dystrophy is a group of hereditary disorders characterized by a weakening and wasting away of muscles that vary in inheritance pattern, age...
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https://healthcare.utah.edu/neurosciences/neurology/muscular-dystrophy-clinic
Muscular Dystrophy | University of Utah Health
Mar 25, 2026 - Our Muscular Dystrophy Clinic treats over 40 types of neuromuscular disorders. We treat both adults and children. Our goal is to give you the highest quality...
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https://scholarworks.indianapolis.iu.edu/items/18265326-e12c-4ff8-ac75-b4d1c06024b4
Duchenne Muscular Dystrophy Patients: Troponin Leak in Asymptomatic and Implications for Drug...
Background: Cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD), but studies suggest heart failure biomarkers correlate poorly...
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https://pubmed.ncbi.nlm.nih.gov/3239379/
Skeletal muscle pathology in ovine congenital progressive muscular dystrophy. 2. Myofiber...
Fiber-type proportions were determined in 12 skeletal muscles (peronaeus tertius, tibialis cranialis, tensor fascia lata, psoas major, extensor digitorum...
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https://pmc.ncbi.nlm.nih.gov/articles/PMC8665435/
Life Expectancy in Duchenne Muscular Dystrophy: Reproduced Individual Patient Data Meta-analysis -...
Duchenne muscular dystrophy (DMD) is a rare progressive disease that is often diagnosed in early childhood and leads to considerably reduced life expectancy;...
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https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2020.00721/full
Frontiers | Genetic Modifiers of Duchenne Muscular Dystrophy in Chinese Patients
Background Duchenne muscular dystrophy (DMD) is a fatal, X-linked recessive muscle disorder characterized by heterogeneous progression and severity. We aimed...
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https://www.kasslab.johnshopkins.edu/
Mechanosensing and Muscular Dystrophy | The Kass Lab
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https://wiki.ubc.ca/Course:KIN366/ConceptLibrary/Muscular_Dystrophy
Course:KIN366/ConceptLibrary/Muscular Dystrophy - UBC Wiki
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https://essentials-review.teachable.com/courses/nclex-insight-online-academy/lectures/31358410
Muscular Dystrophy | NCLEX Insight Online Academy
This course shows you how to pass the NCLEX Exam. We provide all the essential content you need to know to pass your NCLEX Exam.
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https://kidshealth.org/CareSource/en/parents/becker-md.html
Becker Muscular Dystrophy (for Parents) - CareSource
Becker muscular dystrophy is a genetic disorder that gradually makes the body's muscles weaker and smaller. It causes less severe problems than the most common...
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https://www.urmc.rochester.edu/conditions-and-treatments/muscular-dystrophy
Muscular Dystrophy | Rochester, NY | Expert Treatment | URochester Medicine
University of Rochester Medicine offers expert muscular dystrophy care with genetic testing, physical therapy, infusion therapy, and access to clinical trials.
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Muscular Dystrophy in Children: Care Instructions
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https://www.justgiving.com/fundraising/maxbarnett
Max Barnett is fundraising for Muscular Dystrophy UK
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https://www.sciencedaily.com/releases/2008/03/080316161133.htm
New Treatment Strategy Possible For Muscular Dystrophy, Mouse Studies Show | ScienceDaily
An investigational antiviral drug currently undergoing human trials in Europe for treating hepatitis C infections may have potential to reduce muscle cell...
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https://rarediseases.info.nih.gov/diseases/3854/muscular-dystrophy-white-matter-spongiosis-syndrome
Muscular dystrophy-white matter spongiosis syndrome | About the Disease | GARD
Find symptoms and other information about Muscular dystrophy-white matter spongiosis syndrome.
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https://www.semanticscholar.org/topic/MUSCULAR-DYSTROPHY%2C-LIMB-GIRDLE%2C-TYPE-2Z-%281-family%29/8317116
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z (1 family) | Semantic Scholar
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https://www.healthcare.uiowa.edu/path_handbook/Appendix/Outreach/md_test_support.html
Muscular Dystrophy Biopsy Testing and Clinical Support
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https://ja.dh.duke.edu/content/2018-parent-project-muscular-dystrophy-ppmd-duchenne-clinician-conference
2018 Parent Project Muscular Dystrophy (PPMD) Duchenne Clinician Conference | DUKEHealth JA
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https://www.urmc.rochester.edu/neurology/wellstone-mdcrc/projects
UR Wellstone Research Projects - Wellstone Muscular Dystrophy Research Center - Neurology -...
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https://pure.psu.edu/en/publications/cerebro-ocular-dysplasia-muscular-dystrophy-cod-md-syndrome/
Cerebro-ocular dysplasia -Muscular dystrophy (COD-MD) syndrome - Penn State
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https://www.sciencedaily.com/releases/2007/04/070402102250.htm
Switching Genes To Overdrive Improves Muscular Dystrophy Symptoms In Mice | ScienceDaily
Scientists have shown in a laboratory study that revving up a crucial set of muscle genes counteracts the damage caused by a form of muscular dystrophy.
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https://health.economictimes.indiatimes.com/news/industry/protein-can-improve-muscle-function-in-duchenne-muscular-dystrophy-study/100501857
Protein can improve muscle function in Duchenne muscular dystrophy: Study, ETHealthworld
Duchenne Muscular Dystrophy: DMD, caused by mutations in the dystrophin gene, is an inheritable neuromuscular disorder that occurs in one out of 3,600 male...
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https://experts.arizona.edu/en/publications/noninvasive-respiratory-care-received-by-individuals-with-duchenn/
Noninvasive respiratory care received by individuals with duchenne muscular dystrophy since...
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https://videocast.nih.gov/watch/b8089eeb-d5db-11f0-9cf9-12c45c580ad9
NIH VideoCast - Muscular Dystrophy Coordinating Committee - March 2019
Muscular Dystrophy Coordinating Committee March 20 2019 standing meeting
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https://www.mdff.org/
Muscular Dystrophy Family Foundation | Donate Today
Jul 10, 2026 - The MDFF provides support and services, including financial assistance, to families affected by muscular dystrophy, ALS, and other neuromuscular diseases.
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https://pubmed.ncbi.nlm.nih.gov/33917623/
Role of Cdkn2a in the Emery-Dreifuss Muscular Dystrophy Cardiac Phenotype
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https://rarediseases.info.nih.gov/diseases/5900/becker-muscular-dystrophy
Becker muscular dystrophy | About the Disease | GARD
Find symptoms and other information about Becker muscular dystrophy.
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https://experts.umn.edu/en/organisations/greg-marzolf-jr-muscular-dystrophy-center/
Greg Marzolf Jr Muscular Dystrophy Center - Experts@Minnesota
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https://kidshealth.org/ChildrensAlabamaXML/en/parents/becker-md.html
Becker Muscular Dystrophy (for Parents) - Children's Health System - Alabama (iFrame)
Becker muscular dystrophy is a genetic disorder that gradually makes the body's muscles weaker and smaller. It causes less severe problems than the most common...
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https://kidshealth.org/HumanaOhio/en/parents/muscular-dystrophy.html
Muscular Dystrophy (for Parents) - Humana - Ohio
Muscular dystrophy is a disorder that weakens a person's muscles over time. People who have the disease can gradually lose the ability to do everyday tasks.
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https://profiles.wustl.edu/en/publications/quantitative-ultrasound-assessment-of-duchenne-muscular-dystrophy/
Quantitative ultrasound assessment of duchenne muscular dystrophy using edge detection analysis -...
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https://commondataelements.ninds.nih.gov/Congenital%20Muscular%20Dystrophy
Congenital Muscular Dystrophy | NINDS CDE
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https://agerrtc.washington.edu/taxonomy/term/12?page=1
Muscular dystrophy | Rehabilitation Research and Training Center on Aging With Physical Disabilities
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https://pmc.ncbi.nlm.nih.gov/articles/PMC10258980/
Orthogonal proteomics methods warrant the development of Duchenne muscular dystrophy biomarkers -...
Molecular components in blood, such as proteins, are used as biomarkers to detect or predict disease states, guide clinical interventions and aid in the...
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https://coronationstreetupdates.blogspot.com/2016/10/coronation-street-praised-for-muscular.html
Coronation Street Blog: Coronation Street praised for muscular dystrophy storyline
Corrie spoilers, news, reviews, updates, original and exclusive competitions and content. Everything a Coronation Street fan could desire - and more!
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https://www.news-medical.net/news/20100827/Nationwide-Childrens-Hospital-designated-as-Wellstone-Muscular-Dystrophy-Cooperative-Research-Center.aspx
Nationwide Children's Hospital designated as Wellstone Muscular Dystrophy Cooperative Research...
Jun 18, 2019 - A $7 million grant from the National Institutes of Health (NIH) will help researchers at Nationwide Children's Hospital translate new scientific findings and...
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Indian Muscular Dystrophy Society & Research Center (IMDSRC)
Support, awareness and advocacy for muscular dystrophy families.
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https://www.mrl.ucsb.edu/index.php/research/seminars/bottlebrush-block-copolymer-prevents-disease-onset-duchenne-muscular-dystrophy
Bottlebrush Block Copolymer Prevents Disease Onset in Duchenne Muscular Dystrophy | Material...
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https://www.kqed.org/futureofyou/152831/disappointing-patients-fda-panel-rejects-muscular-dystrophy-drug
Disappointing Patients, an FDA Panel Rejects Muscular Dystrophy Drug | KQED
While not binding, the panel's view carries weight in FDA's final decision whether to approve a drug.
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https://www.urmc.rochester.edu/highland/departments-centers/neurology/conditions-we-treat/muscular-dystrophy
Muscular Dystrophy - Neurology - Highland Hospital - URochester Medicine
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https://agerrtc.washington.edu/node/21
Aging with muscular dystrophy: pathophysiology and clinical management. | Rehabilitation Research...
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https://www.mda.org/science/movr2
MOVR Update: MOVR 2.0 is Coming! | Muscular Dystrophy Association
Apr 9, 2026 - MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
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https://experts.arizona.edu/en/projects/arizona-muscular-dystrophy-surveillance-and-research-program/
Arizona Muscular Dystrophy Surveillance and Research Program - University of Arizona
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https://pubmed.ncbi.nlm.nih.gov/23525014/
Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in...
Overexpression of facioscapulohumeral muscular dystrophy region gene 1 (FRG1) in mice, frogs and worms leads to muscular and vascular abnormalities....
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https://www.researchandmarkets.com/reports/6212481/becker-muscular-dystrophy-market-global
Becker Muscular Dystrophy Market - A Global and Regional Analysis: Focus on Country and Regional...
Becker Muscular Dystrophy Market - A Global and Regional Analysis: Focus on Country and Regional Analysis, 2025-2035
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https://www.justgiving.com/page/sara-gifford-hull-1685457588094
sara gifford-hull is fundraising for Muscular Dystrophy UK
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https://www.justgiving.com/page/sid-keyte-1728302625514
Sid Keyte is fundraising for Muscular Dystrophy UK
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https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2024.1522203/full
Frontiers | Facioscapulohumeral muscular dystrophy type 1 combined with becker muscular dystrophy:...
Facioscapulohumeral muscular dystrophy type 1 (FSHD1) and Becker muscular dystrophy (BMD) are distinct disorders caused by different genetic variations and e...
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https://www.buildfortheboys.ie/
Duchenne Muscular Dystrophy | Build For The Boys
Help raise funds Donate today Build for the boys Duchenne
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https://dmd.nl/
Leiden Muscular Dystrophy Pages
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https://post.health.ufl.edu/2015/10/20/a-major-center-for-muscular-dystrophy/?contrast=1
A major center for muscular dystrophy - The POST (Simplified View)
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https://childnervoussystem.blogspot.com/2020/09/duchenne-muscular-dystrophy-new.html
pediatric neurology: Duchenne muscular dystrophy. New treatments.
Smith EC, Conklin LS, Hoffman EP, Clemens PR, Mah JK, Finkel RS, Guglieri M, Tulinius M, Nevo Y, Ryan MM, Webster R, Castro D, Kuntz NL, Ker...
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https://pubmed.ncbi.nlm.nih.gov/9673987/
Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31
A genome scan with highly polymorphic markers has established linkage for tibial muscular dystrophy (TMD), a recently described late onset distal myopathy, to...
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https://kidshealth.org/ChildrensAlabamaXML/en/parents/md-factsheet.html
Muscular Dystrophy Factsheet (for Schools) (for Parents) - Children's Health System - Alabama...
What teachers should know about muscular dystrophy, and how to help students with MD do their best in school.
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https://www.prnewswire.com/news-releases/parent-project-muscular-dystrophy-expands-leadership-team-to-accelerate-progress-for-duchenne-becker-community-302532498.html
Parent Project Muscular Dystrophy Expands Leadership Team to Accelerate Progress for Duchenne,...
/PRNewswire/ -- Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), is...
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https://blogs.bmj.com/jmg/2011/10/04/genetic-diagnosis-of-duchenne-muscular-dystrophy-using-next-generation-sequencing-technology-comprehensive-mutational-search-in-a-single-platform/
Genetic diagnosis of Duchenne muscular dystrophy using next-generation sequencing technology:...
Feb 25, 2026 - Next generation sequencing technology(NGS) can be a useful tool for genetic diagnosis of certain diseases where laborious sequencing efforts are required...
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https://mda.org.nz/
Muscular Dystrophy New Zealand
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https://pubmed.ncbi.nlm.nih.gov/12868502/
Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to...
Facioscapulohumeral muscular dystrophy is an autosomal dominant disorder resulting from an unusual genetic mechanism. The mutation, a deletion of 3.3 kb...
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https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/1407/
"Quality improvement in neurology: muscular dystrophy quality measures." by Pushpa Narayanaswami,...
By Pushpa Narayanaswami, Richard Dubinsky, David Wang, et al., Published on 09/08/15
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https://elbiruniblogspotcom.blogspot.com/2012/05/cdc-facts-muscular-dystrophy-ncbddd.html
CIENCIASMEDICASNEWS: CDC - Facts, Muscular Dystrophy - NCBDDD
CDC - Facts, Muscular Dystrophy - NCBDDD Facts about Muscular Dystrophy Muscular dystrophies (MDs) are a group of disorders that result i...
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https://sciencedaily.com/releases/2025/03/250305224003.htm
Scientists unlock clues to new treatments for muscular dystrophy | ScienceDaily
Researchers combined advanced imaging techniques and theoretical physics to observe and explain how nanoclusters of the protein emerin form inside living...
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https://www.urmc.rochester.edu/neurology/wellstone-mdcrc/links
Related Links - Wellstone Muscular Dystrophy Research Center - Neurology - URochester Medicine
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https://videocast.nih.gov/watch/d091a633-d5db-11f0-9cf9-12c45c580ad9
NIH VideoCast - Muscular Dystrophy Coordinating Committee Meeting
The purpose of this meeting is to bring together committee members, representing government agencies, patient advocacy groups, other voluntary health...
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https://www.mda.org/disease/charcot-marie-tooth
Charcot-Marie-Tooth Disease (CMT) - Diseases | Muscular Dystrophy Association
Jul 1, 2021 - MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
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https://dukespace.lib.duke.edu/items/3714d4bf-88e9-41ae-81df-9ccfdf0516bc
Genetic Correction of Duchenne Muscular Dystrophy using Engineered Nucleases
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https://parentprojectmusculardystrophy2.my.site.com/grants/s/?
Parent Project Muscular Dystrophy Grants Portal
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https://experts.colorado.edu/display/meshid_C10.668.491.175.500.400
Neuromuscular Diseases - Muscular Dystrophy, Facioscapulohumeral | CU Experts | CU Boulder
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https://www.sciencedaily.com/releases/2009/12/091231164749.htm
Unusual protein modification involved in muscular dystrophy, cancer | ScienceDaily
With the discovery of a new type of chemical modification on an important muscle protein, a new study improves understanding of certain muscular dystrophies...
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https://pmc.ncbi.nlm.nih.gov/articles/PMC6415693/
CRISPR Correction of Duchenne Muscular Dystrophy - PMC
The ability to efficiently modify the genome using CRISPR technology has rapidly revolutionized biology and genetics and will soon transform medicine. Duchenne...
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https://rarediseases.info.nih.gov/diseases/17653/miyoshi-muscular-dystrophy-3
Miyoshi muscular dystrophy 3 | About the Disease | GARD
Find symptoms and other information about Miyoshi muscular dystrophy 3.
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https://research.monash.edu/en/publications/a-review-of-nutrition-in-duchenne-muscular-dystrophy/
A review of nutrition in Duchenne muscular dystrophy - Monash University
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https://kidshealth.org/RadyChildrens/en/parents/muscular-dystrophy.html
Muscular Dystrophy (for Parents) - Rady Children's Hospital - San Diego
Muscular dystrophy is a disorder that weakens a person's muscles over time. People who have the disease can gradually lose the ability to do everyday tasks.
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https://justgiving.com/page/lew-mathias-mduk
Lew Mathias is fundraising for Muscular Dystrophy UK
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Andrea Hornby is fundraising for Muscular Dystrophy UK
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https://www.prnewswire.com/news/parent-project-muscular-dystrophy-%28ppmd%29/
Parent Project Muscular Dystrophy (PPMD) News and Press Releases | PR Newswire
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https://www.semanticscholar.org/topic/Muscular-Dystrophy%2C-Oculopharyngeal/345834
Muscular Dystrophy, Oculopharyngeal | Semantic Scholar
An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in...
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https://www.sciencedaily.com/releases/2020/02/200224131133.htm
Releasing brakes: Potential new methods for Duchenne muscular dystrophy therapies | ScienceDaily
Testing of small molecules in mouse models for Duchenne muscular dystrophy shows promise for restoration of muscle structure and function.
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Em Runton is fundraising for Muscular Dystrophy UK
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Progress Made Toward Early Identification Of Muscular Dystrophy | ScienceDaily
New muscular dystrophy (MD) research is moving doctors and scientists closer to disease diagnosis in advance of patient symptoms. Since it is now clear that...
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https://www.sciencedaily.com/releases/2011/12/111213190025.htm
Some muscular dystrophy patients at increased risk for cancer | ScienceDaily
People who have the most common type of adult muscular dystrophy also have a higher risk of getting cancer, according to a paper published today in the Journal...
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Living with Muscular Dystrophy | Muscular Dystrophy | CDC
Paul, Carly, Connor, and Kevin share their stories about living with muscular dystrophy.
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