Muscular Dystrophy Association

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https://doi.org/10.1042/bj2580837 Cell fractionation studies indicate that dystrophin is a protein of surface membranes of skeletal muscle
https://doi.org/10.1002/ana.410200210 Adult‐onset autosomal dominant limb‐girdle muscular dystrophy
https://doi.org/10.1093/ptj/66.1.32 Sequential Isokinetic and Manual Muscle Testing in Patients with Neuromuscular Disease
https://doi.org/10.1111/j.1750-3639.1992.tb00682.x Disorders Associated with Depletion of Mitochondrial DNA
https://doi.org/10.1212/wnl.46.3.600 Acute illness myopathy
https://doi.org/10.1111/j.1365-2044.1989.tb11445.x Migration of thoracic epidural catheters
https://doi.org/10.1136/jnnp.47.4.391 Hypersensitivity to DNA-damaging agents in cultured cells from patients with Usher's syndrome and Duchenne muscular dystrophy.
https://doi.org/10.3122/jabfm.2010.06.100056 Characteristics of Medical Professional Liability Claims in Patients Treated by Family Medicine Physicians
https://doi.org/10.1182/blood-2004-12-4603 Donor origin of multipotent adult progenitor cells in radiation chimeras
https://doi.org/10.1016/s0960-8966(97)00076-x Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegia
https://doi.org/10.1002/elps.201100642 Optimization of large gel 2D electrophoresis for proteomic studies of skeletal muscle
https://doi.org/10.1016/j.diabres.2014.10.009 Early age at menarche: A risk factor for overweight or obesity in patients with type 1 diabetes living in urban areas?
https://doi.org/10.1186/1758-5996-6-67 Determinants of intensive insulin therapeutic regimens in patients with type 1 diabetes: data from a nationwide multicenter survey in Brazil
https://doi.org/10.1016/b978-1-56053-604-8.50022-4 Quality of Life and Ethical Issues
https://doi.org/10.1038/35102259 Recognizing risks and potential promise of germline engineering
https://doi.org/10.1371/journal.pone.0206323 Non-invasive tracking of disease progression in young dystrophic muscles using multi-parametric MRI at 14T
https://doi.org/10.1002/jgc4.1156 Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?
https://doi.org/10.1186/s13395-015-0042-x A reporter mouse for optical imaging of inflammation in mdx muscles
https://doi.org/10.5435/jaaos-20-08-s70 Evolution of Acute Orthopaedic Care
https://doi.org/10.33314/jnhrc.v0i0.496 Effect of sitting posture on development of scoliosis in Duchenne Muscular Dystrophy cases.
https://doi.org/10.1016/j.joms.2012.04.021 Preface Proceedings of the Third Molar Multidisciplinary Conference Washington, DC, October 19, 2010
https://doi.org/10.1016/j.joms.2015.03.037 Letter of Welcome
https://doi.org/10.1016/j.joms.2019.09.002 AAOMS Response to Recent Challenges to OMS Office-Based Anesthesia for Pediatric Patients
https://doi.org/10.3233/jnd-221551 The Muscular Dystrophy Association’s neuroMuscular ObserVational Research Data Hub (MOVR): Design, Methods, and Initial Observations
https://doi.org/10.1097/pep.0000000000000537 Stepping Activity in Children With Congenital Myotonic Dystrophy
https://doi.org/10.1210/clinem/dgaf196 Effects of 1-Month Very-Low-Calorie Ketogenic Diet on 24-Hour Energy Metabolism and Body Composition in Women With Obesity
https://doi.org/10.1213/00000539-198304000-00007 In Vitro Contracture Tests for Susceptibility to Malignant Hyperthermia
https://doi.org/10.1016/0305-0491(94)00128-h Comparison of structural protein and proteolytic enzyme levels in degenerating and regenerating rat muscle induced by Notechis scutatus venom
Pain management in epidermolysis bullosa: an intractable problem.
https://doi.org/10.1016/j.nmd.2018.02.002 Whole exome sequencing discloses a pathogenic MTM1 gene mutation and ends the diagnostic odyssey in an older woman with a progressive and seemingly sporadic myopathy: Case report and literature review of MTM1 manifesting female carriers
https://doi.org/10.1542/peds.2018-0333n Evaluating Implementation of the Updated Care Considerations for Duchenne Muscular Dystrophy
https://doi.org/10.1039/c9nr10804a Glial restricted precursor delivery of dendrimer N-acetylcysteine promotes migration and differentiation following transplant in mouse white matter injury model
https://doi.org/10.1016/j.joms.2016.02.017 AAOMS Informational Campaign Communicates the OMS Story
https://doi.org/10.1016/j.eats.2022.04.001 Arthroscopic Internal Fixation of Coracoid Fractures: Surgical Technique Guide
https://doi.org/10.1016/j.joms.2015.04.040 The Faculty Educator Development Award: A 12-Year Perspective on Success, Excellence, and Impact on the Specialty of Oral and Maxillofacial Surgery
https://doi.org/10.1186/s13023-019-1157-7 Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
https://doi.org/10.3389/fcell.2024.1362671 In vivo PSC differentiation as a platform to identify factors for improving the engraftability of cultured muscle stem cells
https://doi.org/10.1212/wnl.28.2.147 Muscle carnitine deficiency and fatal cardiomyopathy
https://doi.org/10.1212/wnl.32.8.898 Cytochrome‐ c ‐oxidase deficiency in a floppy infant
https://doi.org/10.1016/s0021-9258(17)34360-0 31P NMR study of bound reactants and products of yeast 3-phosphoglycerate kinase at equilibrium and the effect of sulfate ion.
https://doi.org/10.1007/bf01812852 Mitochondrial myopathies
https://doi.org/10.1002/cyto.990020503 Isolation of mouse X‐chromosome specific DNA from an X‐enriched lambda phage library derived from flow sorted chromosomes
https://doi.org/10.1212/wnl.43.11.2170 Mitochondria1 involvement in Parkinson's disease
https://doi.org/10.1212/wnl.38.4.609 Effect of chronic treatment with the calcium antagonist diltiazem in Duchenne muscular dystrophy
https://doi.org/10.1002/ana.410110210 Monoclonal antibody analysis of blood T‐cell subsets in myasthenia gravis
https://doi.org/10.1212/wnl.28.12.1298 Thymic and peripheral blood T‐and B‐cell levels in myasthenia gravis
https://doi.org/10.1300/j010v05n04_05 LIVING WITH PROGRESSIVE CHILDHOOD ILLNESS
https://doi.org/10.1016/s0140-6736(84)91019-5 THYMECTOMY IN POLYMYOSITIS
https://doi.org/10.1016/0022-510x(78)90101-6 Susceptibility of human skeletal muscle culture to influenza virus infection
https://doi.org/10.1212/wnl.38.9.1399 Kearns‐Sayre syndrome in twins
https://doi.org/10.1212/wnl.51.4.1228 Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase
https://doi.org/10.1212/wnl.31.9.1198 Polyclonal B‐cell activity in myasthenia gravis
https://doi.org/10.1016/s0030-5898(20)32242-2 Management of Foot Deformity in Duchenne's Pseudohypertrophic Muscular Dystrophy
https://doi.org/10.1016/0022-510x(78)90162-4 Susceptibility of human skeletal muscle culture to influenza virus infection
https://doi.org/10.1111/j.1749-6632.1981.tb33746.x COMPARATIVE IMMUNOGLOBULIN SYNTHESIS BY BLOOD LYMPHOCYTES OF MYASTHENICS AND NORMALS
https://doi.org/10.1016/j.nmd.2008.06.342 T.P.5.01 Phase 2b Study of PTC124 in Duchenne/Becker muscular dystrophy (DMD/BMD): Demographic and other baseline data
Mitochondrial dysfunction as a mechanism of CNS injury.
https://doi.org/10.1145/2517351.2517405 A reliable wireless nurse call system
https://doi.org/10.1097/00007632-198109000-00015 Acute Gastric Volvulus Following Harrington Rod Instrumentation in a Patient With Werdnig-Hoffman Disease
https://doi.org/10.1212/wnl.14.4.355 A previously unreported myopathy in patients with schistosomiasis
https://doi.org/10.1016/b978-1-56053-604-8.50020-0 Respiratory Muscle Aids: Patient Evaluation, Respiratory Aid Protocol, and Outcomes
https://doi.org/10.1590/s2176-94512012000600008 Evaluation of plasticity and radiopacity of elastic separators by means of traction tests and radiography
https://doi.org/10.1097/00002060-200211001-00010 Muscle Fatigue in Animal Models of Neuromuscular Disease
Adult motor neuron disease
https://doi.org/10.1016/j.joms.2012.04.022 Introduction
https://doi.org/10.1177/088307388900400404 Between the Lines: A Message of Hope
https://doi.org/10.1016/s0278-2391(03)00159-9 Private practice versus academia
https://doi.org/10.33588/rn.2802.98367 Encefalomiopatías mitocondriales: ¿Hacia dónde vamos?
https://doi.org/10.1530/rep-19-0382 ETV2 -null porcine embryos survive to post-implantation following incomplete enucleation
https://doi.org/10.1002/(sici)1097-4598(199606)19:6<777::aid-mus15>3.3.co;2-8 Assessment of whole body composition with dual energy X‐ray absorptiometry in Duchenne muscular dystrophy: Correlation of lean body mass with muscle function
https://doi.org/10.1016/j.joms.2015.03.062 What Factors Influence Community Oral and Maxillofacial Surgeons' Choice to Use Capnography in the Office-Based Ambulatory Anesthesia Setting?
https://doi.org/10.1161/circresaha.108.172114 Vascular Endothelial Growth Factor Gene Regulation by HEXIM1 in Heart
https://doi.org/10.1007/978-1-61779-767-5_25 Systemic Delivery of Antisense Oligomer in Animal Models and Its Implications for Treating DMD
Epilepsy in mitochondrial encephalomyopathies.
https://doi.org/10.1016/s1047-9651(18)30249-3 Correlations of Evoked Potentials With Mr Imaging and Mr Spectroscopy in Multiple Sclerosis
https://doi.org/10.5962/bhl.title.15053 Catalogue of the fossils for the Cincinnati group, by Jos. F. James, custodian Cincinnati society of natural history. Published by order of Committee on palaeontology.
https://doi.org/10.1097/wnp.0000000000000415 Charcot–Marie–Tooth Disease Type 1A: Influence of Body Mass Index on Nerve Conduction Studies and on the Charcot–Marie–Tooth Examination Score
Cost of illness for neuromuscular diseases in the U.S
https://doi.org/10.1016/j.joms.2021.05.015 Oral-Maxillofacial Surgery Anesthesia Team Model at a Crossroads Safety in Office-Based Anesthesia – Lessons We Can Learn from Aviation
https://doi.org/10.1108/s1530-353520220000019002 Facing Amyotrophic Lateral Sclerosis Under Lockdown: The Experiences of Minors
https://doi.org/10.2217/nmt.11.37 Als in California: A Report From the First Annual California Als Research Summit
https://doi.org/10.1007/s12663-010-0078-8 Nurturing the Future
https://doi.org/10.1016/j.pmr.2012.12.002 Ambulation in Adults with Central Neurologic Disorders
https://doi.org/10.14219/jada.archive.2010.0236 AAOMS challenges AMA data series comments on OMS, dentistry
https://doi.org/10.1212/wnl.82.10_supplement.p7.008 Muscular Dystrophy Association U.S. Neuromuscular Disease Registry - Preliminary Findings (P7.008)
https://doi.org/10.1038/s41582-024-00978-4 Publisher Correction: The Miami Framework for ALS and related neurodegenerative disorders: an integrated view of phenotype and biology
https://doi.org/10.4000/books.editionscnrs.2942 Rock et télévision : un rendez-vous manqué ? les émissions musicales pour la jeunesse
https://doi.org/10.1016/j.nmd.2019.06.281 EP.49The muscular dystrophy association neuromuscular observational research (MOVR) Data Hub
https://doi.org/10.1212/wnl.32.8.821 Immunocytochemical studies of human peripheral nerve with serum from patients with polyneuropathy and paraproteinemia
https://doi.org/10.1002/cyto.990050202 Development and use of metaphase chromosome flow‐sorting methodology to obtain recombinant phage libraries enriched for parts of the human X chromosome
https://doi.org/10.1016/0022-510x(80)90039-8 Spastic paraplegia-paraparesis
https://doi.org/10.1101/2023.05.16.23289881 Unexpected Death of a Duchenne Muscular Dystrophy Patient in an N-of-1 Trial of rAAV9-delivered CRISPR-transactivator
https://doi.org/10.1111/j.1600-0404.1962.tb01073.x A STUDY OF TRANSIENT MUSCULAR WEAKNESS
https://doi.org/10.1016/0022-510x(79)90224-7 Abnormalities of T-cell subpopulations in the blood and thymus of patients with myasthenia gravis
https://doi.org/10.1097/00006416-198705000-00009 Reflex Sympathetic Dystrophy Syndrome
https://doi.org/10.1111/j.1749-6632.1989.tb54511.x High-dose TRH Treatment of Neuromuscular Diseases: Summary of Mechanisms and Critique of Clinical Studies.
https://doi.org/10.1101/393231 Re-Evaluating One-step Generation of Mice Carrying Conditional Alleles by CRISPR-Cas9-Mediated Genome Editing Technology
https://doi.org/10.1002/jez.1402100308 Neural regulation of cholinesterase in newt skeletal muscle. II. The effects of denervation and of culture in vitro
https://doi.org/10.1111/j.1748-1716.1961.tb02274.x Studies in Neuromuscular Transmission
https://doi.org/10.1212/wnl.19.6.551 Sodium‐potassium adenosine triphosphate in diseased muscle