| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Z E Davidson, H Trub. A review of nutrition in Duchenne muscular dystrophy. Journal of human nutrition and dietetics : the official journal of the British Dietetic Association. vol 22. issue 5. 2009-11-10. PMID:19743977. |
duchenne muscular dystrophy (dmd) is a recessive x linked genetic disorder characterised by progressive muscle weakness and reduced muscle tone. |
2009-11-10 |
2023-08-12 |
Not clear |
| Herman Vandenburgh, Janet Shansky, Frank Benesch-Lee, Kirsten Skelly, Janelle M Spinazzola, Yero Saponjian, Brian S Tsen. Automated drug screening with contractile muscle tissue engineered from dystrophic myoblasts. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 23. issue 10. 2009-11-05. PMID:19487307. |
since mdx muscle in vivo and dmd patients respond in a similar manner to many of these compounds, the in vitro assay will be a useful tool for the rapid identification of new potential treatments for muscle weakness in dmd and other muscle disorders. |
2009-11-05 |
2023-08-12 |
Not clear |
| James A Ridgley, Gavin J Pinniger, Peter W Hamer, Miranda D Ground. The physiological effects of IGF-1 (class 1:Ea transgene) over-expression on exercise-induced damage and adaptation in dystrophic muscles of mdx mice. Pflugers Archiv : European journal of physiology. vol 457. issue 5. 2009-07-24. PMID:18726613. |
duchenne muscular dystrophy (dmd) is a genetic disorder in which muscle weakness and fragility contribute to ongoing muscle degeneration. |
2009-07-24 |
2023-08-12 |
mouse |
| Olga L Gurvich, Baijayanta Maiti, Robert B Weiss, Gaurav Aggarwal, Michael T Howard, Kevin M Flaniga. DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6. Human mutation. vol 30. issue 4. 2009-07-06. PMID:19206170. |
mutations in the dmd gene result in two common phenotypes associated with progressive muscle weakness: the more severe duchenne muscular dystrophy (dmd) and the milder becker muscular dystrophy (bmd). |
2009-07-06 |
2023-08-12 |
Not clear |
| Eppie M Yiu, Andrew J Kornber. Duchenne muscular dystrophy. Neurology India. vol 56. issue 3. 2009-06-04. PMID:18974549. |
duchenne muscular dystrophy (dmd), an x-linked disorder, is the most common muscular dystrophy in children, presenting in early childhood and characterized by proximal muscle weakness and calf hypertrophy in affected boys. |
2009-06-04 |
2023-08-12 |
Not clear |
| Nathaly Gaudreault, Denis Gravel, Sylvie Nadea. Evaluation of plantar flexion contracture contribution during the gait of children with Duchenne muscular dystrophy. Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology. vol 19. issue 3. 2009-06-02. PMID:17977021. |
we believe that the passive moments can compensate for the presence of progressive muscle weakness in the children with dmd and help these children with gait. |
2009-06-02 |
2023-08-12 |
human |
| Myriam Srour, Bassam A Bejjani, Emily A Rorem, Nicholas Hall, Lisa G Shaffer, Michael I Shevel. An instructive case of an 8-year-old boy with intellectual disability. Seminars in pediatric neurology. vol 15. issue 4. 2009-02-19. PMID:19073314. |
given the familial and therapeutic implications for accurate diagnosis of dmd mutations, this case raises the possible need for screening boys with global developmental delay/intellectual disability even in the absence of any overt muscle weakness and further shows the utility of comparative genomic hybridization (cgh) analysis in the evaluation of patients with nonsyndromic mental retardation. |
2009-02-19 |
2023-08-12 |
Not clear |
| Alexandre Briguet, Michael Erb, Isabelle Courdier-Fruh, Patrizia Barzaghi, Gesa Santos, Holger Herzner, Cyrille Lescop, Hervé Siendt, Marco Henneboehle, Philipp Weyermann, Josef P Magyar, Judith Dubach-Powell, Günther Metz, Thomas Meie. Effect of calpain and proteasome inhibition on Ca2+-dependent proteolysis and muscle histopathology in the mdx mouse. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 22. issue 12. 2008-12-31. PMID:18728218. |
dystrophin deficiency is the underlying molecular cause of progressive muscle weakness observed in duchenne muscular dystrophy (dmd). |
2008-12-31 |
2023-08-12 |
mouse |
| M Marini, A A Salmi, M S Watihayati, M D SMardziah, M K Zahri, B P Hoh, R Ankathil, P S Lai, B A Zilfali. Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy. The Medical journal of Malaysia. vol 63. issue 1. 2008-11-26. PMID:18935728. |
duchenne muscular dystrophy (dmd) is an x-linked recessive genetic disorder characterized by rapidly progressive muscle weakness. |
2008-11-26 |
2023-08-12 |
Not clear |
| Orvar Eeg-Olofsson, Hannu Kalimo, Karin Edebol Eeg-Olofsson, Sten Jagell, Lena Marklund, Linda Simonsson, Niklas Dah. Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. vol 12. issue 5. 2008-11-06. PMID:18833644. |
a boy showed muscle weakness from the age of 10 months and presented typical signs of dmd at the age of 18 months. |
2008-11-06 |
2023-08-12 |
Not clear |
| Mariz Vainzof, Danielle Ayub-Guerrieri, Paula C G Onofre, Poliana C M Martins, Vanessa F Lopes, Dinorah Zilberztajn, Lucas S Maia, Karen Sell, Lydia U Yamamot. Animal models for genetic neuromuscular diseases. Journal of molecular neuroscience : MN. vol 34. issue 3. 2008-06-20. PMID:18202836. |
the canine golden retriever md model represents a more clinically similar model of dmd due to its larger size and significant muscle weakness. |
2008-06-20 |
2023-08-12 |
mouse |
| M Toussaint, P Soudon, W Kinnea. Effect of non-invasive ventilation on respiratory muscle loading and endurance in patients with Duchenne muscular dystrophy. Thorax. vol 63. issue 5. 2008-05-28. PMID:18057095. |
respiratory muscle weakness in patients with duchenne muscular dystrophy (dmd) leads to respiratory failure for which non-invasive positive pressure ventilation (nippv) is an effective treatment. |
2008-05-28 |
2023-08-12 |
Not clear |
| Denis Duboc, Christophe Meune, Bertrand Pierre, Karim Wahbi, Bruno Eymard, Annick Toutain, Carole Berard, Guy Vaksmann, Simon Weber, Henri-Marc Bécan. Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up. American heart journal. vol 154. issue 3. 2007-09-05. PMID:17719312. |
duchenne muscular dystrophy (dmd), an x-linked disorder due to lack of dystrophin, is associated with muscle weakness and myocardial dysfunction. |
2007-09-05 |
2023-08-12 |
Not clear |
| Patrick E Baker, Jessica A Kearney, Bendi Gong, Anita P Merriam, Donald E Kuhn, John D Porter, Jill A Rafael-Fortne. Analysis of gene expression differences between utrophin/dystrophin-deficient vs mdx skeletal muscles reveals a specific upregulation of slow muscle genes in limb muscles. Neurogenetics. vol 7. issue 2. 2007-03-27. PMID:16525850. |
dystrophin-deficient mdx mice are characterized by skeletal muscle weakness and degeneration but they appear outwardly normal in contrast to dmd patients. |
2007-03-27 |
2023-08-12 |
mouse |
| Ellen Sterrenburg, Caroline G C van der Wees, Stefan J White, Rolf Turk, Renée X de Menezes, Gert-Jan B van Ommen, Johan T den Dunnen, Peter A C 't Hoe. Gene expression profiling highlights defective myogenesis in DMD patients and a possible role for bone morphogenetic protein 4. Neurobiology of disease. vol 23. issue 1. 2006-09-06. PMID:16679024. |
duchenne muscular dystrophy (dmd) is characterized by progressive muscle weakness and wasting. |
2006-09-06 |
2023-08-12 |
Not clear |
| Marianne Jover, Christina Schmitz, Emmanuelle Bosdure, Brigitte Chabrol, Christine Assaiant. Anticipatory postural adjustments in a bimanual load-lifting task in children with Duchenne muscular dystrophy. Neuroscience letters. vol 403. issue 3. 2006-09-01. PMID:16750880. |
the muscle weakness did not impair (1) the proprioceptive afference and the motor efference constituting the unloading reflex; and (2) the use of an anticipatory function in children with dmd. |
2006-09-01 |
2023-08-12 |
Not clear |
| Jonathan B Strobe. Therapeutics in duchenne muscular dystrophy. NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics. vol 3. issue 2. 2006-05-03. PMID:16554260. |
duchenne muscular dystrophy (dmd) is a fatal disorder affecting approximately 1 in 3,500 live born males, characterized by progressive muscle weakness. |
2006-05-03 |
2023-08-12 |
Not clear |
| Edo M Hoogerwaard, Ieke B Ginjaar, Egbert Bakker, Marianne de Visse. Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy. Neurology. vol 65. issue 12. 2006-04-14. PMID:16380627. |
associations between clinical phenotype (muscle weakness, dilated cardiomyopathy) and dystrophin abnormalities in muscle tissue among definite carriers of duchenne (dmd) and becker muscular dystrophy (bmd) were investigated. |
2006-04-14 |
2023-08-12 |
Not clear |
| Leanne M Gauld, Alison Boynton, Grant A Betts, Heather Johnsto. Spirometry is affected by intelligence and behavior in Duchenne muscular dystrophy. Pediatric pulmonology. vol 40. issue 5. 2006-03-16. PMID:16145697. |
children with duchenne muscular dystrophy (dmd) have progressive respiratory muscle weakness. |
2006-03-16 |
2023-08-12 |
Not clear |
| Mitra Lavasani, Aiping Lu, Hairong Peng, James Cummins, Johnny Huar. Nerve growth factor improves the muscle regeneration capacity of muscle stem cells in dystrophic muscle. Human gene therapy. vol 17. issue 2. 2006-03-10. PMID:16454652. |
researchers have attempted to use gene- and cell-based therapies to restore dystrophin and alleviate the muscle weakness that results from duchenne muscular dystrophy (dmd). |
2006-03-10 |
2023-08-12 |
mouse |