By Robert C. Griggs and Anthony A. Amato (Eds.)
This quantity offers clinicians and scientists with the newest info in regards to the muscular dystrophies, paying unique awareness to the way in which developments in molecular and phone biology, biochemistry, and different organic sciences supply complete insights right into a staff of problems that experience in simple terms been studied for the earlier twenty years.
Information on either pathogenesis and clients for remedy are coated, with an emphasis on scientific implications, either now and within the foreseeable destiny. medical knowledge is mixed with helpful views from the main hugely skilled physicians, specialists, and scientists to convey an authoritative and whole exam of the muscular dystrophies, their analysis, and coverings protocols. Insights from this instruction manual will either increase and ahead efforts for practitioners who take care of, and deal with, sufferers with this team of disorders.
* invaluable insights into the muscular dystrophies, together with therapy, prognosis, and care and sufferer management
* A accomplished compilation of the mixed knowledge of the main extremely popular physicians, specialists, and scientists learning the muscular dystrophies
* An evaluate of how advances in molecular and phone biology, biochemistry, and different organic sciences proceed to strengthen the examine of those problems
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Additional info for Muscular Dystrophies
Sample text
2008). DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy. Ann Neurol 63: 81–89. Guy-Coichard C, Nguyen DT, Delorme T et al. (2008). Pain in hereditary neuromuscular disorders and myasthenia gravis: a national survey of frequency, characteristics, and impact. J Pain Symptom Manage 35: 40–50. Haldane JB (2004). The rate of spontaneous mutation of a human gene. 1935. J Genet 83: 235–244. Harper CM, Ambler G, Edge G (2004). The prognostic value of pre-operative predicted forced vital capacity in corrective spinal surgery for Duchenne’s muscular dystrophy.
Hum Mutat 29: 728–737. Khurana TS, Davies KE (2003). Pharmacological strategies for muscular dystrophy. Nat Rev Drug Discov 2: 379–390. Khurana TS, Prendergast RA, Alameddine HS et al. (1995). Absence of extraocular muscle pathology in Duchenne’s muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing. J Exp Med 182: 467–475. Kimura S, Ito K, Ueno H et al. (2009). A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness. Brain Dev 31: 169–172.
Eur J Paediatr Neurol 9: 387–393. Beggs AH, Kunkel LM (1990). Improved diagnosis of Duchenne/Becker muscular dystrophy. J Clin Invest 85: 613–619. Beggs AH, Koenig M, Boyce FM et al. (1990). Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet 86: 45–48. Berko BA, Swift M (1987). X-linked dilated cardiomyopathy. N Engl J Med 316 (19): 1186–1191. Beroud C, Carrie A, Beldjord C et al. (2004). Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene.