| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Yuko Nitahara-Kasahara, Soya Nakayama, Koichi Kimura, Sho Yamaguchi, Yuko Kakiuchi, Chikako Nito, Masahiro Hayashi, Tomoyuki Nakaishi, Yasuyoshi Ueda, Takashi Okad. Immunomodulatory amnion-derived mesenchymal stromal cells preserve muscle function in a mouse model of Duchenne muscular dystrophy. Stem cell research & therapy. vol 14. issue 1. 2023-04-27. PMID:37106393. |
duchenne muscular dystrophy (dmd) is an incurable genetic disease characterized by degeneration and necrosis of myofibers, chronic inflammation, and progressive muscle weakness resulting in premature mortality. |
2023-04-27 |
2023-08-14 |
mouse |
| Sean Y Ng, Andrew I Mikhail, Stephanie R Mattina, Alexander Manta, Ian J Diffey, Vladimir Ljubici. Acute, next-generation AMPK activation initiates a disease-resistant gene expression program in dystrophic skeletal muscle. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 37. issue 5. 2023-04-05. PMID:37016990. |
duchenne muscular dystrophy (dmd) is a life-limiting neuromuscular disorder characterized by muscle weakness and wasting. |
2023-04-05 |
2023-08-14 |
mouse |
| Grant Patterson, Haley Conner, Mecham Groneman, Cyril Blavo, Mayur S Parma. Duchenne muscular dystrophy: Current treatment and emerging exon skipping and gene therapy approach. European journal of pharmacology. 2023-03-24. PMID:36963652. |
duchenne muscular dystrophy (dmd) is an x-linked recessive neuromuscular disorder that causes debilitating muscle weakness and atrophy due to a loss of the dystrophin protein. |
2023-03-24 |
2023-08-14 |
Not clear |
| Marielle G Contesse, Jason Hodges, Hannah Staunton, Linda P Lowes, Bassem Elmankabadi, Sonya J Elder, Maitea Guridi Ormazabal, Laura Dalle Pazze, Mindy G Leffle. Home-based video assessment of ease of movement for patients with Duchenne: Interviews with physical therapists to select movement tasks. Physiotherapy research international : the journal for researchers and clinicians in physical therapy. 2023-01-31. PMID:36718112. |
patients with duchenne muscular dystrophy (dmd) change their movement patterns to compensate for muscle weakness. |
2023-01-31 |
2023-08-14 |
Not clear |
| Jacob A Kaslow, Andrew G Sokolow, Thomas Donnelly, Maciej S Buchowski, Larry W Markham, W Bryan Burnette, Jonathan H Soslo. Spirometry Correlates with Physical Activity in Patients with Duchenne Muscular Dystrophy. Pediatric pulmonology. 2022-12-26. PMID:36571207. |
duchenne muscular dystrophy (dmd) is associated with progressive muscle weakness and respiratory decline. |
2022-12-26 |
2023-08-14 |
Not clear |
| Leighton Schreyer, Jack Reilly, Haley McConkey, Jennifer Kerkhof, Michael A Levy, Jonathan Hu, Mona Hnaini, Bekim Sadikovic, Craig Campbel. The discovery of the DNA methylation episignature for Duchenne muscular dystrophy. Neuromuscular disorders : NMD. 2022-12-26. PMID:36572586. |
duchenne muscular dystrophy (dmd) is an x-linked recessive neuromuscular disorder characterized by progressive muscle weakness due to loss of function mutations in the dystrophin gene. |
2022-12-26 |
2023-08-14 |
Not clear |
| Cintia Gomez Limia, Megan Baird, Maura Schwartz, Smita Saxena, Kathrin Meyer, Nicolas Wei. Emerging Perspectives on Gene Therapy Delivery for Neurodegenerative and Neuromuscular Disorders. Journal of personalized medicine. vol 12. issue 12. 2022-12-23. PMID:36556200. |
neuromuscular disorders (nmds) are a group of diseases in which patients show primary progressive muscle weaknesses, including duchenne muscular dystrophy (dmd), pompe disease, and spinal muscular atrophy (sma). |
2022-12-23 |
2023-08-14 |
Not clear |
| Susan Sienko, Cathleen Buckon, Anita Bagley, Eileen Fowler, Kent Heberer, Loretta Staudt, Mitell Sison-Williamson, Craig McDonald, Michael Sussma. Kinematic changes in gait in boys with Duchenne Muscular Dystrophy: Utility of the Gait Deviation Index, the Gait Profile Score and the Gait Variable Scores. Gait & posture. vol 100. 2022-12-18. PMID:36529026. |
in boys with dmd, muscle weakness progresses in a proximal to distal pattern, leading to gait abnormalities at all joints, in all planes of motion. |
2022-12-18 |
2023-08-14 |
Not clear |
| Agnieszka Sobierajska-Rek, Eliza Wasilewska, Karolina Śledzińska, Joanna Jabłońska-Brudło, Sylwia Małgorzewicz, Andrzej Wasilewski, Dominika Szalewsk. The Association between the Respiratory System and Upper Limb Strength in Males with Duchenne Muscular Dystrophy: A New Field for Intervention? International journal of environmental research and public health. vol 19. issue 23. 2022-12-11. PMID:36497753. |
progressive, irreversible muscle weakness is the leading symptom of duchenne muscular dystrophy (dmd), often resulting in death from respiratory muscle failure. |
2022-12-11 |
2023-08-14 |
Not clear |
| Purva S Shahade, Purva H Mundada, Snehal S Sama. Perks of Rehabilitation in Improving Motor Function in a Nine-Year-Old Male With Duchenne Muscular Dystrophy: A Case Report. Cureus. vol 14. issue 10. 2022-11-18. PMID:36397889. |
it primarily affects males and is characterized by motor delays, muscle weakness, respiratory impairment, and loss of ambulation. a case study of a nine-year-old male diagnosed with dmd is presented. |
2022-11-18 |
2023-08-14 |
Not clear |
| Rebecca A Ellwood, Luke Slade, Jonathan Lewis, Roberta Torregrossa, Surabhi Sudevan, Mathew Piasecki, Matthew Whiteman, Timothy Etheridge, Nathaniel J Szewczy. Sulfur amino acid supplementation displays therapeutic potential in a C. elegans model of Duchenne muscular dystrophy. Communications biology. vol 5. issue 1. 2022-11-17. PMID:36385509. |
mutations in the dystrophin gene cause duchenne muscular dystrophy (dmd), a common muscle disease that manifests with muscle weakness, wasting, and degeneration. |
2022-11-17 |
2023-08-14 |
caenorhabditis_elegans |
| Yuri Fujikura, Keitaro Yamanouchi, Hidetoshi Sugihara, Masaki Hatakeyama, Tomoki Abe, Satoru Ato, Katsutaka Oish. Ketogenic diet containing medium-chain triglyceride ameliorates transcriptome disruption in skeletal muscles of rat models of duchenne muscular dystrophy. Biochemistry and biophysics reports. vol 32. 2022-11-17. PMID:36386439. |
duchenne muscular dystrophy (dmd) is a myopathy characterized by progressive muscle weakness caused by a mutation in the dystrophin gene on the x chromosome. |
2022-11-17 |
2023-08-14 |
rat |
| Abdulaziz S AlSaman, Fouad Al Ghamdi, Ahmed K Bamaga, Nahla AlShaikh, Mohammed Al Muqbil, Osama Muthaffar, Fahad A Bashiri, Baleegh Ali, Arzu Mulayim, Elena Heider, Abdullah A Alshahrani, Mohammed A Al Muhaize. Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia. Frontiers in pediatrics. vol 10. 2022-10-24. PMID:36275069. |
duchenne muscular dystrophy (dmd) is a rare neuromuscular disorder that is characterized by progressive muscle weakness, resulting in disability and premature death. |
2022-10-24 |
2023-08-14 |
Not clear |
| Dorota Gruber, Michele Lloyd-Puryear, Niki Armstrong, Mena Scavina, Norma P Tavakoli, Amy M Brower, Michele Caggana, Wendy K Chun. Newborn screening for Duchenne muscular dystrophy-early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy. American journal of medical genetics. Part C, Seminars in medical genetics. 2022-09-24. PMID:36152336. |
dmd is a multi-system disease resulting in muscle weakness with progressive deterioration of skeletal, heart, and smooth muscle, and learning disabilities. |
2022-09-24 |
2023-08-14 |
Not clear |
| Paul Ritter, Stefanie Nübler, Andreas Buttgereit, Lucas R Smith, Alexander Mühlberg, Julian Bauer, Mena Michael, Lucas Kreiß, Michael Haug, Elisabeth Barton, Oliver Friedric. Myofibrillar Lattice Remodeling Is a Structural Cytoskeletal Predictor of Diaphragm Muscle Weakness in a Fibrotic International journal of molecular sciences. vol 23. issue 18. 2022-09-23. PMID:36142754. |
myofibrillar lattice remodeling is a structural cytoskeletal predictor of diaphragm muscle weakness in a fibrotic duchenne muscular dystrophy (dmd) is a degenerative genetic myopathy characterized by complete absence of dystrophin. |
2022-09-23 |
2023-08-14 |
Not clear |
| b' Mariana De Abreu Rays Dazzi, Cristina Dos Santos Cardoso De S\\xc3\\xa. Gait and Sit-To-Stand Motor Compensation Strategies in Children and Adolescents With Duchenne Muscular Dystrophy. Perceptual and motor skills. 2022-09-19. PMID:36121164.' |
duchenne muscular dystrophy (dmd), the most common form of muscular dystrophies, is characterized by progressive and generalized muscle weakness. |
2022-09-19 |
2023-08-14 |
Not clear |
| Mariana Angélica de Souza, Edson Zangiacomi Martinez, Elisângela Aparecida da Silva Lizzi, Ananda Cezarani, Gabriela Barroso de Queiroz Davoli, Marjory Irineu Bená, Cláudia Ferreira da Rosa Sobreira, Ana Claudia Mattiello-Sverzu. Alternative instrument for the evaluation of handgrip strength in Duchenne muscular dystrophy. BMC pediatrics. vol 22. issue 1. 2022-06-10. PMID:35689212. |
the commonly used dynamometers can be ineffective in evaluating handgrip in patients with duchenne muscular dystrophy (dmd), especially children with generalized muscle weakness. |
2022-06-10 |
2023-08-14 |
Not clear |
| Giulia Ricci, Luca Bello, Francesca Torri, Erika Schirinzi, Elena Pegoraro, Gabriele Sicilian. Therapeutic opportunities and clinical outcome measures in Duchenne muscular dystrophy. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2022-05-24. PMID:35608735. |
duchenne muscular dystrophy (dmd) is a devastatingly severe genetic muscle disease characterized by childhood-onset muscle weakness, leading to loss of motor function and premature death due to respiratory and cardiac insufficiency. |
2022-05-24 |
2023-08-13 |
Not clear |
| Miguel A Lopez Perez, Kassidy K Banford, Noah L Weislede. The Differential Contribution of TRIM72/MG53 Protein Domains in Plasma Membrane Repair. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 36 Suppl 1. 2022-05-13. PMID:35553558. |
duchenne muscular dystrophy (dmd) is a fatal x-linked genetic disease that is hallmarked by progressive muscle weakness and degeneration. |
2022-05-13 |
2023-08-13 |
mouse |
| Aoife D Slyne, Ken D O'Halloran, David P Burn. Accessory Muscle Support of Breathing in Young Dystrophin-deficient mdx Mice. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 36 Suppl 1. 2022-05-13. PMID:35553932. |
dmd is characterized by severe and progressive skeletal muscle weakness, which extends to the respiratory muscles. |
2022-05-13 |
2023-08-13 |
mouse |