| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Simone Nava, Giorgio Conte, Fabio M Triulzi, Giacomo P Comi, Francesca Magri, Daniele Velardo, Claudia M Cinnant. Diffusion tensor imaging reveals subclinical alterations in muscles of patients with becker muscular dystrophy. The British journal of radiology. 2024-04-04. PMID:38574384. |
becker muscular dystrophy (bmd) is a relatively less investigated neuromuscular disease, partially overlapping the phenotype of duchenne dystrophy (dmd). |
2024-04-04 |
2024-04-07 |
Not clear |
| Vahid Omarmeli, Kai-Uwe Lewandrovski, Marjan Assefi, Hanieh Faizmahdavi, Alireza Sharafshah, Nasrin Mansour. A Novel Mutation (Lys31Arg) in the DMD Gene Impacts on Neuromuscular Dysfunctions found by Whole Exome Sequencing and In Silico Analyses in an Iranian Family. Current aging science. 2024-01-24. PMID:38265407. |
duchene muscular disorder (dmd) is a severe x-linked recessive neuromuscular disease. |
2024-01-24 |
2024-01-26 |
Not clear |
| Ying Chen, Chenjie Ling, Mengting Chen, Liqiang Yu, Jing Yang, Qi Fan. Astaxanthin Ameliorates Worsened Muscle Dysfunction of MDX Mice Fed with a High-Fat Diet through Reducing Lipotoxicity and Regulating Gut Microbiota. Nutrients. vol 16. issue 1. 2024-01-11. PMID:38201863. |
duchenne muscular dystrophy (dmd), a severe x-linked inherited neuromuscular disease, has a high prevalence of obesity. |
2024-01-11 |
2024-01-13 |
mouse |
| Tsukasa Tominari, Masaru Takatoya, Toshiya Matsubara, Michio Matsunobe, Daichi Arai, Chiho Matsumoto, Michiko Hirata, Shosei Yoshinouchi, Chisato Miyaura, Yoshifumi Itoh, Hirofumi Komaki, Shin'ichi Takeda, Yoshitsugu Aoki, Masaki Inad. Establishment of a Triple Quadrupole HPLC-MS Quantitation Method for Dystrophin Protein in Mouse and Human Skeletal Muscle. International journal of molecular sciences. vol 25. issue 1. 2024-01-11. PMID:38203473. |
duchenne muscular dystrophy (dmd) is the most common type of neuromuscular disease caused by mutations in the |
2024-01-11 |
2024-01-13 |
mouse |
| Erik Landfeldt, Kim Phung, Farasat Zaman, Eva Åström, Sophia Abner, Hanns Lochmüller, Thomas Sejersen, Leanne M War. Bisphosphonates in Glucocorticoid-Treated Patients With Duchenne Muscular Dystrophy. Neurology. vol 102. issue 2. 2024-01-02. PMID:38165327. |
bisphosphonates are routinely used to treat osteoporosis in patients with duchenne muscular dystrophy (dmd), a rare, severely debilitating neuromuscular disease. |
2024-01-02 |
2024-01-05 |
Not clear |
| Victoria Brown, Elizabeth Merikle, Kelly Johnston, Katherine Gooch, Ivana Audhya, Linda Lowe. A qualitative study to understand the Duchenne muscular dystrophy experience from the parent/patient perspective. Journal of patient-reported outcomes. vol 7. issue 1. 2023-12-12. PMID:38085412. |
duchenne muscular dystrophy (dmd) is a rare, severe, fatal neuromuscular disease characterized by progressive atrophy and muscle weakness, resulting in loss of ambulation, decreased upper body function, and impaired cardiorespiratory function. |
2023-12-12 |
2023-12-17 |
Not clear |
| Dalya Al-Mfarej, Jennifer M Vojtech, Serge H Roy, Elise Townsend, Julie J Keysor, Nancy Kuntz, Vamshi Rao, Joshua C Kline, Bhawna Shiwan. A Virtual Reality Exergame: Clinician-Guided Breathing and Relaxation for Children with Muscular Dystrophy. 2023 IEEE Conference on Virtual Reality and 3D User Interfaces Abstracts and Workshops (VRW). vol 2023. 2023-11-27. PMID:38009078. |
dmd is a rare neuromuscular disease that leads to respiratory muscle dysfunction with anxiety being a common comorbidity. |
2023-11-27 |
2023-11-28 |
human |
| María Rosa Baeza-Barragán, Maria Teresa Labajos Manzanares, Mercedes Cristina Amaya-Álvarez, Fabián Morales Vega, Judit Rodriguez Ruiz, Rocío Martín-Valer. Effectiveness of a 5-Week Virtual Reality Telerehabilitation Program for Children With Duchenne and Becker Muscular Dystrophy: Prospective Quasi-Experimental Study. JMIR serious games. vol 11. 2023-11-22. PMID:37990809. |
duchenne muscular dystrophy (dmd) and becker muscular dystrophy (bmd) are neuromuscular diseases. |
2023-11-22 |
2023-11-29 |
Not clear |
| Elisabeth Wallach, Virginie Ehlinger, Maelle Biotteau, Ulrike Walther-Louvier, Yann Péréon, Carole Vuillerot, Stephanie Fontaine, Pascal Sabouraud, Caroline Espil-Taris, Jean-Marie Cuisset, Vincent Laugel, Eloïse Baudou, Catherine Arnaud, Claude Cance. Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQL BMC pediatrics. vol 23. issue 1. 2023-11-16. PMID:37968589. |
confirmatory validation of the french version of the duchenne muscular dystrophy module of the pediatric quality of life inventory (pedsql duchenne muscular dystrophy (dmd) is a neuromuscular disease that inevitably leads to total loss of autonomy. |
2023-11-16 |
2023-11-20 |
Not clear |
| Rosa Baeza Barragan, Maria Teresa Labajos Manzanares, Mercedes Cristina Amaya Álvarez, Fabian Morales Vega, Judith Rodriguez Ruiz, Rocío Martín Valer. Effectiveness of a 5 weeks telerehabilitation programme with virtual reality glasses in boys with Duchenne and Becker during the COVID-19: A clinical trial. JMIR serious games. 2023-09-30. PMID:37776510. |
duchenne and becker muscular dystrophy (from now "dmd" and "bmd" respectively) are the neuromuscular diseases with the most significant involvement in children. |
2023-09-30 |
2023-10-07 |
Not clear |
| Cara A Timpani, Stephanie Kourakis, Danielle A Debruin, Dean G Campelj, Nancy Pompeani, Narges Dargahi, Angelo Patrick R Bautista, Ryan M Bagaric, Elya J Ritenis, Lauren Sahakian, Didier Debrincat, Nicole Stupka, Patricia Hafner, Peter G Arthur, Jessica R Terrill, Vasso Apostolopoulos, Judy B De Haan, Nuri Gueven, Dirk Fischer, Emma Rybalk. Dimethyl fumarate modulates the dystrophic disease program following short-term treatment. JCI insight. 2023-09-26. PMID:37751291. |
new medicines are urgently required to treat the fatal neuromuscular disease, duchenne muscular dystrophy (dmd). |
2023-09-26 |
2023-10-07 |
mouse |
| Ainoa Tejedera-Villafranca, Marisol Montolio, Javier Ramón-Azcón, Juan M Fernández-Cost. Mimicking sarcolemmal damage Biofabrication. 2023-09-19. PMID:37725998. |
mimicking sarcolemmal damage duchenne muscular dystrophy (dmd) is the most prevalent neuromuscular disease diagnosed in childhood. |
2023-09-19 |
2023-10-07 |
Not clear |
| Mona Hnaini, Matt Downs, Michael R Miller, Craig Campbell, Aaron St-Lauren. Duchenne muscular dystrophy respiratory profiles from real world registry data. Pediatric pulmonology. 2023-08-04. PMID:37539841. |
the canadian neuromuscular disease registry (cndr) has respiratory data from a population of boys with duchenne muscular dystrophy (dmd). |
2023-08-04 |
2023-08-14 |
Not clear |
| Xu Han, Guang Ji, Ning Wang, Le Yi, Yafei Mao, Jinliang Deng, Hongran Wu, Shaojuan Ma, Jingzhe Han, Yi Bu, Pingping Fang, Juyi Liu, Fanzhe Sun, Xueqin Son. Comprehensive analysis of m Journal of translational medicine. vol 21. issue 1. 2023-07-11. PMID:37434186. |
comprehensive analysis of m duchenne muscular dystrophy (dmd) is an x-linked, incurable, degenerative neuromuscular disease that is exacerbated by secondary inflammation. |
2023-07-11 |
2023-08-14 |
Not clear |
| Shohko Sekine, Sayaka Mayama, Nobuaki Nishijima, Takuo Kojima, Yoko Endo-Takahashi, Yuko Ishii, Hitomi Shiono, Saki Akiyama, Akane Sakurai, Sanae Sashida, Nobuhito Hamano, Rui Tada, Ryo Suzuki, Kazuo Maruyama, Yoichi Negish. Development of a Gene and Nucleic Acid Delivery System for Skeletal Muscle Administration via Limb Perfusion Using Nanobubbles and Ultrasound. Pharmaceutics. vol 15. issue 6. 2023-06-28. PMID:37376113. |
strategies for gene and nucleic acid delivery to skeletal muscles have been extensively explored to treat duchenne muscular dystrophy (dmd) and other neuromuscular diseases. |
2023-06-28 |
2023-08-14 |
mouse |
| Anne M Connolly, Craig M Zaidman, John F Brandsema, Han C Phan, Cuixia Tian, Xueping Zhang, Jack Li, Mark D Eisner, Ewa Carrie. Pamrevlumab, a Fully Human Monoclonal Antibody Targeting Connective Tissue Growth Factor, for Non-Ambulatory Patients with Duchenne Muscular Dystrophy. Journal of neuromuscular diseases. 2023-05-30. PMID:37248912. |
duchenne muscular dystrophy (dmd) is a neuromuscular disease stemming from dystrophin gene mutations. |
2023-05-30 |
2023-08-14 |
human |
| Viktorija Cernisova, Ngoc Lu-Nguyen, Jessica Trundle, Shan Herath, Alberto Malerba, Linda Popplewel. Microdystrophin Gene Addition Significantly Improves Muscle Functionality and Diaphragm Muscle Histopathology in a Fibrotic Mouse Model of Duchenne Muscular Dystrophy. International journal of molecular sciences. vol 24. issue 9. 2023-05-14. PMID:37175881. |
duchenne muscular dystrophy (dmd) is a rare neuromuscular disease affecting 1:5000 newborn males. |
2023-05-14 |
2023-08-14 |
mouse |
| Wooi Fang Lim, Carlo Rinald. RNA Transcript Diversity in Neuromuscular Research. Journal of neuromuscular diseases. 2023-05-14. PMID:37182892. |
it is therefore not surprising that splicing mis-regulation is causally associated with a myriad of neuromuscular diseases, including but not limited to amyotrophic lateral sclerosis (als), spinal muscular atrophy (sma), duchenne muscular dystrophy (dmd), and myotonic dystrophy type 1 and 2 (dm1, dm2). |
2023-05-14 |
2023-08-14 |
human |
| Andrew I Mikhail, Sean Y Ng, Stephanie R Mattina, Vladimir Ljubici. AMPK is mitochondrial medicine for neuromuscular disorders. Trends in molecular medicine. 2023-04-20. PMID:37080889. |
here, we survey mitochondrial stresses that are common between, as well as unique to, dmd, dm1, and sma, and which may serve as potential therapeutic targets to mitigate neuromuscular disease. |
2023-04-20 |
2023-08-14 |
Not clear |
| Rachele Rossi, Camilla Johansson, Wendy Heywood, Heloise Vinette, Gabriella Jensen, Hanna Tegel, Albert Jiménez-Requena, Silvia Torelli, Cristina Al-Khalili Szigyarto, Alessandra Ferlin. A Proof of Principle Proteomic Study Detects Dystrophin in Human Plasma: Implications in DMD Diagnosis and Clinical Monitoring. International journal of molecular sciences. vol 24. issue 6. 2023-03-29. PMID:36982290. |
duchenne muscular dystrophy (dmd) is a rare neuromuscular disease caused by pathogenic variations in the |
2023-03-29 |
2023-08-14 |
human |