| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| H Stedman, S Sarka. Molecular genetics in muscular dystrophy research: revolutionary progress. Muscle & nerve. vol 11. issue 7. 1988-09-22. PMID:3043215. |
the contribution of "reverse genetic" strategies to neuromuscular disease research is evident in the progression of breakthroughs that have recently culminated in the cloning of the duchenne muscular dystrophy (dmd) cdna. |
1988-09-22 |
2023-08-11 |
Not clear |
| S R Braun, R L Sufit, R Giovannoni, M O'Connor, H Peter. Intermittent negative pressure ventilation in the treatment of respiratory failure in progressive neuromuscular disease. Neurology. vol 37. issue 12. 1987-12-28. PMID:3683880. |
five men with degenerative neuromuscular diseases (three with amyotrophic lateral sclerosis [als] and two with duchenne's muscular dystrophy [dmd]) who had respiratory failure were treated with intermittent negative pressure ventilation (npv). |
1987-12-28 |
2023-08-11 |
Not clear |
| E Bakker, C Van Broeckhoven, E J Bonten, M J van de Vooren, H Veenema, W Van Hul, G J Van Ommen, A Vandenberghe, P L Pearso. Germline mosaicism and Duchenne muscular dystrophy mutations. Nature. vol 329. issue 6139. 1987-11-09. PMID:2889144. |
duchenne muscular dystrophy (dmd) is a severe x-linked neuromuscular disease with an incidence of approximately 1 in 3,500 newborn boys. |
1987-11-09 |
2023-08-11 |
Not clear |
| G R Freidenberg, J M Olefsk. Dissociation of insulin resistance and decreased insulin receptor binding in Duchenne muscular dystrophy. The Journal of clinical endocrinology and metabolism. vol 60. issue 2. 1985-02-21. PMID:3965491. |
duchenne muscular dystrophy (dmd) is an x-linked inherited neuromuscular disease characterized by progressive weakness and severe muscle wasting. |
1985-02-21 |
2023-08-11 |
human |
| R S Shalev, O Shalev, N Amir, S Porat, G Fawlewski De Leo. Erythrocyte (Ca2+ + Mg2+)-ATPase activity and calcium homeostasis in Duchenne muscular dystrophy. Journal of the neurological sciences. vol 63. issue 3. 1984-07-20. PMID:6144734. |
it is inferred that the increase in intramuscular calcium in dmd muscle, which is also found in other neuromuscular diseases, may be a non-specific finding in the diseased muscle and part of the final common pathway leading toward cellular degeneration and death. |
1984-07-20 |
2023-08-12 |
Not clear |
| K Nørregaard-Hansen, O Hein-Sørense. Significance of serum myoglobin in neuromuscular diseases and in carrier detection of Duchenne muscular dystrophy. Acta neurologica Scandinavica. vol 66. issue 2. 1982-12-18. PMID:7136489. |
in a retrospective study, the serum myoglobin concentration (s-myoglobin) was determined in patients with neuromuscular diseases and in carriers of duchenne muscular dystrophy (dmd). |
1982-12-18 |
2023-08-12 |
Not clear |
| K Nørregaard-Hansen, O Hein-Sørense. Significance of serum myoglobin in neuromuscular diseases and in carrier detection of Duchenne muscular dystrophy. Acta neurologica Scandinavica. vol 66. issue 2. 1982-12-18. PMID:7136489. |
sera from 70 patients with various neuromuscular diseases and from 17 female relatives of patients with dmd were analysed. |
1982-12-18 |
2023-08-12 |
Not clear |
| A Takagi, S Ishiura, I Nonaka, H Sugit. Myosin light chain components in single muscle fibers of Duchenne muscular dystrophy. Muscle & nerve. vol 5. issue 5. 1982-12-02. PMID:6889680. |
single muscle fibers were prepared from biopsy specimens of duchenne muscular dystrophy (dmd), normal, and neuromuscular disease controls. |
1982-12-02 |
2023-08-12 |
Not clear |
| J K Tomkins, S P Collins, W D Baker, A D Kidma. In vitro skeletal muscle protein and RNA incorporation in neuromuscular disease. Journal of the neurological sciences. vol 54. issue 1. 1982-07-08. PMID:6176687. |
skeletal muscle of duchenne muscular dystrophy (dmd) patients, dmd carriers and of patients with other neuromuscular diseases was sampled at diagnostic muscle biopsy. |
1982-07-08 |
2023-08-12 |
Not clear |
| A Takagi, I Nonak. Duchenne muscular dystrophy: unusual activation of single fibers in vitro. Muscle & nerve. vol 4. issue 1. 1981-07-23. PMID:7231441. |
single skinned fibers were prepared from muscle biopsies of patients with duchenne muscular dystrophy (dmd) and other neuromuscular diseases. |
1981-07-23 |
2023-08-12 |
Not clear |
| M J Dunn, A H Burghes, V Dubowit. Erythrocyte ghost Na+,K+-adenosine triphosphatase in Duchenne muscular dystrophy. Journal of the neurological sciences. vol 46. issue 2. 1980-08-15. PMID:6247454. |
erythrocyte ghost membranes have been prepared by two different methods from patients with duchenne muscular dystrophy (dmd), carriers of dmd, patients with other neuromuscular diseases, and normal individuals. |
1980-08-15 |
2023-08-12 |
Not clear |
| Y Wakayama, A Hodson, E Bonilla, D Pleasure, D L Schotlan. Freeze-fracture studies of erythrocyte plasma membrane in human neuromuscular diseases. Neurology. vol 29. issue 5. 1979-07-16. PMID:571565. |
freeze-fracture studies were conducted in erythrocyte plasma membrane from 8 patients with duchenne muscular dystrophy (dmd), 8 age-matched controls, 3 adult controls, 10 patients with myotonic muscular dystrophy, and 26 other neuromuscular disease controls. |
1979-07-16 |
2023-08-11 |
human |