| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Nastasia Cardone, Valentina Taglietti, Serena Baratto, Kaouthar Kefi, Baptiste Periou, Ciryl Gitiaux, Christine Barnerias, Peggy Lafuste, France Leturcq Pharm, Juliette Nectoux Pharm, Chiara Panicucci, Isabelle Desguerre, Claudio Bruno, François-Jerome Authier, Chiara Fiorillo, Frederic Relaix, Edoardo Malfatt. Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells. Acta neuropathologica communications. vol 11. issue 1. 2023-10-20. PMID:37858263. |
duchenne muscular dystrophy (dmd) is a devastating x-linked muscular disease, caused by mutations in the dmd gene encoding dystrophin and affecting 1:5000 boys worldwide. |
2023-10-20 |
2023-11-08 |
Not clear |
| Tetsushi Yamamoto, Yoshinori Nambu, Ryosuke Bo, Shotaro Morichi, Misato Yanagiya, Masafumi Matsuo, Hiroyuki Awan. Electrocardiographic R wave amplitude in V6 lead as a predictive marker of cardiac dysfunction in Duchenne muscular dystrophy. Journal of cardiology. 2023-07-22. PMID:37481234. |
duchenne muscular dystrophy (dmd) is an inherited muscular disease characterized by progressive and fatal muscle weakness. |
2023-07-22 |
2023-08-14 |
Not clear |
| Zhi Jiang, Hongmei Liao, Liwen Wu, Wenjing Hu, Liming Yang, Bo Chen, Zeshu Ning, Jingwen Tang, Rong Xu, Mei Chen, Feng Guo, Shulei Li. Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study. Italian journal of pediatrics. vol 49. issue 1. 2023-07-13. PMID:37443128. |
duchenne muscular dystrophy (dmd) is a rare hereditary muscular disease. |
2023-07-13 |
2023-08-14 |
Not clear |
| Titiksha Sirari, Renu Suthar, Amarjeet Singh, Shankar Prinja, Vishwas Gupta, Manisha Malviya, Akashdeep Singh Chauhan, Naveen Sankhya. Development and Economic Evaluation of a Patient-Centered Care Model for Children With Duchenne Muscular Dystrophy: Protocol for a Quasi-Experimental Study. JMIR research protocols. vol 12. 2023-04-28. PMID:37115592. |
duchenne muscular dystrophy (dmd) is a rare progressive muscular disease that primarily affects boys. |
2023-04-28 |
2023-08-14 |
Not clear |
| Masae Sato, Megumi Goto, Keitaro Yamanouchi, Hidetoshi Sakura. A new immunodeficient Duchenne muscular dystrophy rat model to evaluate engraftment after human cell transplantation. Frontiers in physiology. vol 14. 2023-04-27. PMID:37101699. |
duchenne muscular dystrophy (dmd) is an x-linked fatal muscular disease, affecting one in 3,500 live male births worldwide. |
2023-04-27 |
2023-08-14 |
human |
| Merve Oğuz, Dolunay Gürses, Furkan Ufuk, Münevver Yılmaz, Olcay Güngö. Successful treatment of acute myocardial injury of Duchenne muscular dystrophy with steroids: a case report. Journal of cardiothoracic surgery. vol 18. issue 1. 2023-03-03. PMID:36869352. |
duchenne muscular dystrophy (dmd) is an x-linked muscular disease which is caused by the absence of dystrophin. |
2023-03-03 |
2023-08-14 |
Not clear |
| Catherine I Soderstrom, Jennifer Larsen, Carolina Owen, David Gifondorwa, David Beidler, Florence H Yong, Patricia Conrad, Hendrik Neubert, Steven A Moore, Mohamed Hassanei. Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle Biopsies. The AAPS journal. vol 25. issue 1. 2022-12-20. PMID:36539515. |
duchenne muscular dystrophy (dmd) is a degenerative muscular disease affecting roughly one in 5000 males at birth. |
2022-12-20 |
2023-08-14 |
human |
| Hye-Geum Kim, Bon-Hoon Koo, Seung Woo Lee, Eun-Jin Cheo. Management of Panic Disorder with Neurofeedback in Patients with Muscular Dystrophy: A Case Report. Alpha psychiatry. vol 22. issue 4. 2022-11-25. PMID:36424934. |
duchenne muscular dystrophy (dmd) is the most common hereditary progressive muscular disease. |
2022-11-25 |
2023-08-14 |
Not clear |
| Kristy Iskandar, Agung Triono, Sunartini, Ery Kus Dwianingsih, Braghmandita Widya Indraswari, Ignatia Rosalia Kirana, Gabriele Ivana, Retno Sutomo, Suryono Yudha Patria, Elisabeth Siti Herini, Gunad. Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy. PloS one. vol 17. issue 10. 2022-10-31. PMID:36315559. |
duchenne muscular dystrophy (dmd) is an x-linked recessive progressive muscular disease marked by developmental delays due to mutations in the dmd gene, which encodes dystrophin. |
2022-10-31 |
2023-08-14 |
Not clear |
| Elisa Ferrer-Mallol, Clare Matthews, Madeline Stoodley, Alessandra Gaeta, Elinor George, Emily Reuben, Alex Johnson, Elin Haf Davie. Patient-led development of digital endpoints and the use of computer vision analysis in assessment of motor function in rare diseases. Frontiers in pharmacology. vol 13. 2022-09-29. PMID:36172196. |
working in partnership with patient organisation duchenne uk, we co-developed a video-based approach, delivered through a new mobile health platform (dmd home), to assess motor function in patients with duchenne muscular dystrophy (dmd), a genetic, rare, muscular disease characterized by the progressive loss of muscle function and strength. |
2022-09-29 |
2023-08-14 |
human |
| Yuhui Su, Yafeng Son. The new challenge of "exercise + X″ therapy for Duchenne muscular dystrophy-Individualized identification of exercise tolerance and precise implementation of exercise intervention. Frontiers in physiology. vol 13. 2022-08-22. PMID:35991169. |
duchenne muscular dystrophy (dmd) is an x-linked recessive fatal muscular disease. |
2022-08-22 |
2023-08-14 |
Not clear |
| Panagiota Mitropoulou, Alexander Hobson, Geraint Morton, Brijesh Ananthara. ST-elevation myocardial infarction in a young patient with Duchenne's muscular dystrophy: a case report. European heart journal. Case reports. vol 6. issue 5. 2022-05-18. PMID:35582544. |
duchenne's muscular dystrophy (dmd) is an x-linked muscular disease which is caused by the absence of dystrophin. |
2022-05-18 |
2023-08-13 |
Not clear |
| Caorui Lin, Gang Han, Lulu Jia, Yiwen Zhao, Jun Song, Ning Ran, Toshifumi Yokota, Yiqi Seow, HaiFang Yi. Cardio-respiratory and phenotypic rescue of dystrophin/utrophin-deficient mice by combination therapy. EMBO reports. 2022-04-08. PMID:35393769. |
duchenne muscular dystrophy (dmd) is a systemic progressive muscular disease caused by frame-disrupting mutations in the dmd gene. |
2022-04-08 |
2023-08-13 |
mouse |
| Hirofumi Komaki, Yoshihiro Maegaki, Tsuyoshi Matsumura, Kazuhiro Shiraishi, Hiroyuki Awano, Akinori Nakamura, Satoru Kinoshita, Katsuhisa Ogata, Keiko Ishigaki, Shinji Saitoh, Michinori Funato, Satoshi Kuru, Takahiro Nakayama, Yasuyuki Iwata, Hiroyuki Yajima, Shin'ichi Taked. Early phase 2 trial of TAS-205 in patients with Duchenne muscular dystrophy. Annals of clinical and translational neurology. vol 7. issue 2. 2021-11-10. PMID:31957953. |
duchenne muscular dystrophy (dmd) is a progressive muscular disease characterized by chronic cycles of inflammatory and necrotic processes. |
2021-11-10 |
2023-08-13 |
Not clear |
| Yoshitsugu Aoki, Cristina S J Rocha, Taavi Lehto, Shouta Miyatake, Henrik Johansson, Yasumasa Hashimoto, Joel Z Nordin, Imre Mager, Misako Aoki, McClorey Graham, Chaitra Sathyaprakash, Thomas C Roberts, Matthew J A Wood, Mark A Behlke, Samir El Andalouss. Fine Tuning of Phosphorothioate Inclusion in 2'-O-Methyl Oligonucleotides Contributes to Specific Cell Targeting for Splice-Switching Modulation. Frontiers in physiology. vol 12. 2021-11-02. PMID:34721051. |
splice-switching antisense oligonucleotide- (sso-) mediated correction of framedisrupting mutation-containing premessenger rna (mrna) transcripts using exon skipping is a highly promising treatment method for muscular diseases such as duchenne muscular dystrophy (dmd). |
2021-11-02 |
2023-08-13 |
Not clear |
| Elisa Domi, Malvina Hoxha, Emanuela Prendi, Bruno Zappacost. A Systematic Review on the Role of SIRT1 in Duchenne Muscular Dystrophy. Cells. vol 10. issue 6. 2021-10-27. PMID:34205021. |
duchenne muscular dystrophy (dmd) is a muscular disease characterized by progressive muscle degeneration. |
2021-10-27 |
2023-08-13 |
Not clear |
| Ning Ran, Caorui Lin, Ling Leng, Gang Han, Mengyuan Geng, Yingjie Wu, Scott Bittner, Hong M Moulton, HaiFang Yi. MOTS-c promotes phosphorodiamidate morpholino oligomer uptake and efficacy in dystrophic mice. EMBO molecular medicine. vol 13. issue 2. 2021-10-25. PMID:33337582. |
antisense oligonucleotide (ao)-mediated exon-skipping therapies show promise in duchenne muscular dystrophy (dmd), a devastating muscular disease caused by frame-disrupting mutations in the dmd gene. |
2021-10-25 |
2023-08-13 |
mouse |
| Neepa Gurbani, John E Pascoe, Sherri Katz, Hemant Sawnan. Sleep disordered breathing: Assessment and therapy in the age of emerging neuromuscular therapies. Pediatric pulmonology. vol 56. issue 4. 2021-10-12. PMID:32720756. |
although it may be conventional to relate the use of this term to the most common muscular diseases (duchenne muscular dystrophy [dmd], spinal muscular atrophy [sma], and amyotrophic lateral sclerosis, etc), it is important to extend the term to pathologies manifested by severe neurologic (brain and spinal cord) malformations and injuries. |
2021-10-12 |
2023-08-13 |
Not clear |
| Chia-Wei Lin, Po-Hsiang Tsui, Chun-Hao Lu, Yi-Hsuan Hung, Meng-Ru Tsai, Jeng-Yi Shieh, Wen-Chin Wen. Quantifying Lower Limb Muscle Stiffness as Ambulation Function Declines in Duchenne Muscular Dystrophy with Acoustic Radiation Force Impulse Shear Wave Elastography. Ultrasound in medicine & biology. vol 47. issue 10. 2021-08-30. PMID:34284931. |
duchenne muscular dystrophy (dmd) is a progressive muscular disease, but validated imaging tools to quantify muscle microstructure alteration as mobility declines are lacking. |
2021-08-30 |
2023-08-13 |
Not clear |
| Salvo Danilo Lombardo, Maria Sofia Basile, Rosella Ciurleo, Alessia Bramanti, Antonio Arcidiacono, Katia Mangano, Placido Bramanti, Ferdinando Nicoletti, Paolo Fagon. A Network Medicine Approach for Drug Repurposing in Duchenne Muscular Dystrophy. Genes. vol 12. issue 4. 2021-08-16. PMID:33918694. |
duchenne muscular dystrophy (dmd) is a progressive hereditary muscular disease caused by a lack of dystrophin, leading to membrane instability, cell damage, and inflammatory response. |
2021-08-16 |
2023-08-13 |
human |