Publications in OpenAlex of which a co-author is affiliated to this organization
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| Title | DOI |
|---|---|
| https://doi.org/10.1016/j.joms.2016.09.044 | Do Antibiotics Decrease the Risk of Inflammatory Complications After Third Molar Removal in Community Practices? |
| https://doi.org/10.1016/j.nmd.2018.06.005 | Sensitivity and clinical utility of the anti-cytosolic 5′-nucleotidase 1A (cN1A) antibody test in sporadic inclusion body myositis: Report of 40 patients from a single neuromuscular center |
| Prevalence of overweight and abdominal obesity in Greek children 6-12 years old: Results from the National Epidemiological Survey. | |
| https://doi.org/10.1097/wco.0000000000000241 | Viral vector-mediated gene therapies |
| https://doi.org/10.1136/medethics-2016-103917 | Fair, just and compassionate: A pilot for making allocation decisions for patients requesting experimental drugs outside of clinical trials |
| https://doi.org/10.1172/jci.insight.146511 | Micro-dystrophin gene therapy prevents heart failure in an improved Duchenne muscular dystrophy cardiomyopathy mouse model |
| https://doi.org/10.14310/horm.2002.1410 | Association of physical activity and sedentary lifestyle patterns with obesity and cardiometabolic comorbidities in Greek adults: Data from the National Epidemiological Survey |
| https://doi.org/10.1002/mus.26720 | Delays in diagnosis of Duchenne muscular dystrophy: An evaluation of genotypic and sociodemographic factors |
| https://doi.org/10.1002/mus.25185 | Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal |
| https://doi.org/10.1186/s13023-018-0889-0 | Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease |
| https://doi.org/10.1002/adtp.201900061 | Polyrotaxane Nanocarriers Can Deliver CRISPR/Cas9 Plasmid to Dystrophic Muscle Cells to Successfully Edit the DMD Gene |
| https://doi.org/10.1007/bf00218376 | Shape and disposition of clefts, tubules, and sarcoplasmic reticulum in long and short sarcomere fibers of crab and crayfish |
| https://doi.org/10.1038/s41526-023-00273-4 | Skeletal muscle gene expression dysregulation in long-term spaceflights and aging is clock-dependent |
| https://doi.org/10.1161/atvbaha.120.314488 | ETV2 (Ets Variant Transcription Factor 2)- Rhoj Cascade Regulates Endothelial Progenitor Cell Migration During Embryogenesis |
| https://doi.org/10.1073/pnas.1808648115 | Engineered DNA plasmid reduces immunity to dystrophin while improving muscle force in a model of gene therapy of Duchenne dystrophy |
| https://doi.org/10.1161/circresaha.120.318170 | Loss of CASK Accelerates Heart Failure Development |
| https://doi.org/10.1186/s13098-015-0081-9 | Health-related quality of life in patients with type 1 diabetes mellitus in the different geographical regions of Brazil: data from the Brazilian Type 1 Diabetes Study Group |
| https://doi.org/10.33233/fb.v21i4.1462 | Abordagem fisioterapêutica na reabilitação da musculatura do assoalho pélvico em mulheres com prolapso genital |
| https://doi.org/10.1126/sciadv.abq7744 | DUX4 double whammy: The transcription factor that causes a rare muscular dystrophy also kills the precursors of the human nose |
| https://doi.org/10.2144/000114576 | Spin Infection Enables Efficient Gene Delivery to Muscle Stem Cells |
| https://doi.org/10.1016/j.ncl.2020.03.007 | Distal Myopathies |
| https://doi.org/10.1186/s13395-019-0218-x | Development of a high-throughput screen to identify small molecule enhancers of sarcospan for the treatment of Duchenne muscular dystrophy |
| https://doi.org/10.1172/jci189075 | Expression of full-length dystrophin reverses muscular dystrophy defects in young and old mdx4cv mice |
| https://doi.org/10.1016/j.jacl.2015.12.008 | Changes in lipid profile after treatment of women with gestational diabetes mellitus |
| https://doi.org/10.3233/jnd-240002 | Meeting Report: 2023 Muscular Dystrophy Association Summit on ‘Safety and Challenges in Gene Therapy of Neuromuscular Diseases’ |
| https://doi.org/10.1210/clinem/dgaf103 | Lipodystrophy Severity Score to Assess Disease Burden in Lipodystrophy |
| https://doi.org/10.21769/bioprotoc.4500 | Generation of iMyoblasts from Human Induced Pluripotent Stem Cells |
| https://doi.org/10.1016/j.gim.2024.101336 | Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets |
| https://doi.org/10.1002/mus.28313 | The Economic Burden of Myasthenia Gravis ( |
| https://doi.org/10.1016/j.nmd.2025.106208 | Consensus recommendations and considerations for the delivery and monitoring of gene therapy in patients with Duchenne muscular dystrophy |
| https://doi.org/10.34119/bjhrv6n4-311 | Electromyographic activation levels of gluteus maximus, hamstrings and quadriceps in squat and hip thrust exercises: a systematic review |
| https://doi.org/10.3233/jnd-230142 | The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot Study |
| https://doi.org/10.1044/2024_ajslp-24-00061 | Features of Swallowing Function in Sporadic Inclusion Body Myositis: Preliminary Evidence Using Well-Tested Assessment Frameworks |
| https://doi.org/10.1016/j.ymthe.2024.12.051 | Heterogeneity, a weak link between constrained AAV dose and long-term efficacy of gene therapy to muscular dystrophy: A critical and prospective review |
| https://doi.org/10.1038/s42003-025-07648-1 | Porcine myogenesis in cloned wildtype and MYF5/MYOD/MYF6-null porcine embryo |
| https://doi.org/10.1038/s41467-025-66061-8 | Transcytotic transportation of size-controlled nanocarriers into dystrophic skeletal muscle leads to therapeutic outcome in mice |
| https://doi.org/10.1016/j.joms.2012.07.047 | Who Is at Fault? |
| https://doi.org/10.1016/j.xhgg.2025.100481 | Comprehensive genotype-phenotype analysis in POLR3-related disorders |
| https://doi.org/10.1016/j.ando.2025.102432 | Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip) Paris, France, 20–21 May 2025 |
| https://doi.org/10.1212/wnl.0000000000214320 | Consensus-Based Expert Recommendations for Diagnosis and Clinical Management of Vanishing White Matter |
| https://doi.org/10.1161/01.res.72.2.349 | Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle. |
| https://doi.org/10.1016/j.joms.2004.10.003 | Office-based ambulatory anesthesia: Factors that influence patient satisfaction or dissatisfaction with deep sedation/general anesthesia |
| https://doi.org/10.1002/ana.21544 | Managing amyotrophic lateral sclerosis: Slowing disease progression and improving patient quality of life |
| https://doi.org/10.1016/0960-8966(94)00062-e | Double trouble: Combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both loci |
| https://doi.org/10.1097/00002060-200211001-00015 | Response to Aerobic Exercise Training in Humans with Neuromuscular Disease |
| https://doi.org/10.5014/ajot.35.2.83 | A Survey of Rationales For and Against Hand Splinting in Hemiplegia |
| https://doi.org/10.1097/01.tp.0000167379.27872.2b | Improved Success of Myoblast Transplantation in mdx Mice by Blocking the Myostatin Signal |
| https://doi.org/10.1113/jp272707 | Validation of ultrasonography for non‐invasive assessment of diaphragm function in muscular dystrophy |
| https://doi.org/10.1002/mus.20877 | Fluorophore‐labeled myosin‐specific antibodies simplify muscle‐fiber phenotyping |
| https://doi.org/10.1097/gim.0b013e3181ef6079 | Carrier testing for spinal muscular atrophy |
| Viral vectors for gene transfer to striated muscle. | |
| https://doi.org/10.1007/978-1-4939-7374-3_18 | AAV6 Vector Production and Purification for Muscle Gene Therapy |
| https://doi.org/10.1093/pm/pny024 | Intravenous Ketamine Infusion for Complex Regional Pain Syndrome: Survey, Consensus, and a Reference Protocol |
| https://doi.org/10.1111/j.1440-1681.2007.04865.x | DIAPHRAGM MUSCLE STRIP PREPARATION FOR EVALUATION OF GENE THERAPIES IN mdx MICE |
| https://doi.org/10.1016/j.joms.2015.10.009 | Complications of Moderate Sedation Versus Deep Sedation/General Anesthesia for Adolescent Patients Undergoing Third Molar Extraction |
| https://doi.org/10.1016/j.scr.2014.12.007 | Sparse feature selection identifies H2A.Z as a novel, pattern-specific biomarker for asymmetrically self-renewing distributed stem cells |
| https://doi.org/10.1111/febs.12295 | The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy |
| https://doi.org/10.1016/j.pmr.2011.11.001 | Hypohomocysteinemia: A Potentially Treatable Cause of Peripheral Neuropathology? |
| https://doi.org/10.1212/wnl.0b013e318282334e | Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data? |
| https://doi.org/10.1002/path.5263 | Morpholino‐induced exon skipping stimulates cell‐mediated and humoral responses to dystrophin in mdx mice |
| https://doi.org/10.1186/s12889-015-1812-4 | Retirement due to disabilities in patients with type 1 diabetes a nationwide multicenter survey in Brazil |
| https://doi.org/10.3109/21678421.2013.778588 | Funding agencies and disease organizations: Resources and recommendations to facilitate ALS clinical research |
| https://doi.org/10.3233/jnd-170240 | The New Zealand Neuromuscular Disease Patient Registry; Five Years and a Thousand Patients |
| https://doi.org/10.1212/01.wnl.0000319661.70648.9b | Congenital muscular dystrophy in a new age |
| https://doi.org/10.1016/j.nmd.2015.03.004 | Dystroglycanopathy muscles lacking functional glycosylation of alpha-dystroglycan retain regeneration capacity |
| https://doi.org/10.1016/0040-8166(79)90062-4 | Chemically skinned mammalian skeletal muscle I. The structure of skinned rabbit psoas |
| https://doi.org/10.1212/wnl.48.2.453 | Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12S rRNA gene |
| https://doi.org/10.1006/bbrc.1995.2697 | A Novel Mitochondrial DNA Point Mutation Associated with Mitochondrial Encephalocardiomyopathy |
| https://doi.org/10.1212/wnl.32.6.584 | Muscle phosphoglycerate rnutase deficiency |
| https://doi.org/10.1097/00007632-198209000-00012 | Spinal Deformities in Patients With Spinal Muscle Atrophy |
| https://doi.org/10.1212/wnl.47.2.579 | Diagnosis of McArdle's disease by molecular genetic analysis of blood |
| https://doi.org/10.1016/0887-8994(96)00163-4 | Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death |
| https://doi.org/10.1016/0027-5107(86)90121-1 | Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical |
| https://doi.org/10.1002/mus.880140603 | Effect of dantrolene in duchenne muscular dystrophy |
| https://doi.org/10.1126/sageke.2003.35.dn2 | Amyotrophic Lateral Sclerosis |
| https://doi.org/10.1016/0003-4975(92)91464-k | Placement of a Greenfield filter in the superior vena cava |
| https://doi.org/10.1159/000243300 | Mitochondrial Defects of Brain and Muscle |
| https://doi.org/10.1016/j.pmr.2012.06.007 | Electrodiagnosis in Neuromuscular Disease |
| https://doi.org/10.2460/ajvr.1999.60.06.734 | Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele |
| https://doi.org/10.1016/j.joms.2008.06.028 | Comparison of Methohexital and Propofol Use in Ambulatory Procedures in Oral and Maxillofacial Surgery |
| https://doi.org/10.1016/j.joms.2017.12.001 | Do Postoperative Antibiotics Decrease the Frequency of Inflammatory Complications Following Third Molar Removal? |
| https://doi.org/10.1016/j.apmr.2014.05.024 | Vestibular Deficits Leading to Disequilibrium and Falls in Ambulatory Amyotrophic Lateral Sclerosis |
| Drug therapy for amyotrophic lateral sclerosis: Where are we now? | |
| https://doi.org/10.1371/journal.pone.0001254 | Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery |
| https://doi.org/10.1016/j.joms.2012.05.001 | Summary of the Proceeding of the Third Molar Multidisciplinary Conference |
| https://doi.org/10.11606/issn.2176-7262.v46i1p24-35 | Avaliação funcional pré e pós-programa de exercício físico de pacientes em hemodiálise |
| https://doi.org/10.1212/wnl.0000000000001910 | Quality improvement in neurology |
| https://doi.org/10.1080/17483107.2017.1413143 | Survey of the functional priorities in patients with disability due to neuromuscular disorders |
| https://doi.org/10.3390/ijns4010006 | Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations |
| https://doi.org/10.1038/s41436-018-0086-5 | MOVR—NeuroMuscular ObserVational Research, a unified data hub for neuromuscular diseases |
| https://doi.org/10.18454/acen.2017.1.6162 | Quantitative sonographic parameters of the peripheral nerves in healthy individuals |
| https://doi.org/10.1002/mus.21939 | Trauma, TDP‐43, and amyotrophic lateral sclerosis |
| https://doi.org/10.1016/j.joms.2016.01.055 | Anesthesia Complications of Diazepam Use for Adolescents Receiving Extraction of Third Molars |
| https://doi.org/10.1016/j.yapd.2020.03.002 | New Developments in Diagnosis, Treatment, and Management of Duchenne Muscular Dystrophy |
| https://doi.org/10.1073/pnas.1802425115 | Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy |
| https://doi.org/10.1016/j.jns.2020.116893 | Modification of non-invasive ventilation for the advanced amyotrophic lateral sclerosis patient during the COVID-19 pandemic - do it now |
| https://doi.org/10.1007/s10597-022-01076-9 | The Mental Health, Substance Use, Physical Health, and Mental Health Treatment Need of Community Individuals Experiencing Homelessness in Hawai‘i |
| https://doi.org/10.1056/nejm198701083160211 | Is Nebulin the Defective Gene Product in Duchenne Muscular Dystrophy? |
| https://doi.org/10.1097/00000542-199307000-00003 | False-negative Results with Muscle Caffeine Halothane Contracture Testing for Malignant Hyperthermia |
| https://doi.org/10.1212/wnl.28.5.447 | Duchenne dystrophy |