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Find link is a tool written by Edward Betts.searching for Becker muscular dystrophy 27 found (51 total)
alternate case: becker muscular dystrophy
Biostrophin
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a vehicle for gene therapy, in the treatment of Duchenne and Becker muscular dystrophy. As mutations in the gene which codes for the protein dystrophinMuscular Dystrophy Community Assistance Research and Education Amendments of 2001 (476 words) [view diff] exact match in snippet view article find links to article
Duchenne-Becker muscular dystrophy care considerations for pediatric patients, and (2) develop and disseminate widely Duchenne-Becker muscular dystrophy considerationsPeter Emil Becker (314 words) [view diff] case mismatch in snippet view article find links to article
Daniel Kondziella. "Peter Becker and His Nazi Past The Man Behind Becker Muscular Dystrophy and Becker Myotonia." Journal of Child Neurology (2013). Peter-Emil-Becker-PriceMYF6 (1,166 words) [view diff] exact match in snippet view article find links to article
factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy". Neuromuscular Disorders. 10 (8): 572–577. doi:10.1016/S0960-8966(00)00150-4Gowers's sign (164 words) [view diff] exact match in snippet view article find links to article
conditions associated with proximal muscle weakness, including Becker muscular dystrophy, dermatomyositis and Pompe disease. For this maneuver, the patientAnthony Monaco (498 words) [view diff] exact match in snippet view article find links to article
landmark discovery of the gene responsible for X-linked Duchenne and Becker muscular dystrophy. He subsequently completed a postdoctoral fellowship in LondonGlaxoSmithKline Prize (135 words) [view diff] exact match in snippet view article find links to article
genetics the biochemical abnormality responsible for Duchenne/Becker muscular dystrophy as being the absence of a previously unknown protein, dystrophin"Dystrophin (2,466 words) [view diff] exact match in snippet view article find links to article
B, Worton RG, Ray PN (1987). "A cDNA clone from the Duchenne/Becker muscular dystrophy gene". Nature. 328 (6129): 434–7. Bibcode:1987Natur.328..434BSNTB2 (1,011 words) [view diff] case mismatch in snippet view article find links to article
Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membraneSNTB1 (1,019 words) [view diff] case mismatch in snippet view article find links to article
Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membranePaul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013 (1,183 words) [view diff] exact match in snippet view article find links to article
Duchenne-Becker muscular dystrophy care considerations for pediatric patients, and (2) develop and disseminate widely Duchenne-Becker muscular dystrophy considerationsMuscular system (1,733 words) [view diff] exact match in snippet view article find links to article
most common types include: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) Myotonic dystrophy Limb-Girdle (LGMD) FacioscapulohumeralEzutromid (1,046 words) [view diff] case mismatch in snippet view article find links to article
Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies". PLOS ONE. 11 (3): e0150818. Bibcode:2016PLoSOSunil Pradhan (2,944 words) [view diff] exact match in snippet view article find links to article
Pradhan, S (June 2004). "Valley sign in Becker muscular dystrophy and outliers of Duchenne and Becker muscular dystrophy". Neurology India. 52 (2): 203–5. PMID 15269471Syntrophin, alpha 1 (1,341 words) [view diff] case mismatch in snippet view article find links to article
Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membraneMultiplex ligation-dependent probe amplification (1,654 words) [view diff] exact match in snippet view article find links to article
diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis". J. Med. Genet. 33 (7): 550–558Cardiomyopathy (2,343 words) [view diff] exact match in snippet view article find links to article
and Genetics. While in Children, Neuromuscular diseases such as Becker muscular dystrophy, including X-linked genetic disorder, are directly linked withDisease registry (1,840 words) [view diff] case mismatch in snippet view article find links to article
DuchenneConnect Patient Registry for patients with Duchenne and Becker Muscular Dystrophy. PatientCrossroads – pan disease patient registries InternationalAerobic conditioning (1,402 words) [view diff] case mismatch in snippet view article find links to article
Ahlke (2018-06-20). "Skeletal Muscle Metabolism in Duchenne and Becker Muscular Dystrophy-Implications for Therapies". Nutrients. 10 (6): 796. doi:10.3390/nu10060796Michel Fardeau (1,212 words) [view diff] exact match in snippet view article find links to article
I study of dystrophin plasmid-based gene therapy in Duchenne-Becker muscular dystrophy », Hum Gene Ther, 2004 15, p. 1065-76 Fardeau, M, Comme vous,Ultraconserved element (4,445 words) [view diff] exact match in snippet view article find links to article
whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients". Human Mutation. 23 (1): 57–66. doi:10.1002/humu.10283List of abbreviations for diseases and disorders (112 words) [view diff] exact match in snippet view article find links to article
Developmental apraxia of speech DBA Diamond–Blackfan anemia DBMD Duchenne–Becker muscular dystrophy DD Developmental disability DEF Deaf DF Dengue fever DH DevelopmentallyMuscle hypertrophy (3,542 words) [view diff] exact match in snippet view article find links to article
infiltration of fat or other tissue). For instance, Duchenne and Becker muscular dystrophy may start as true muscle hypertrophy, but later develop into pseudohypertrophyEteplirsen (1,457 words) [view diff] exact match in snippet view article find links to article
eteplirsen may cause a less severe form of dystrophinopathy, much like Becker muscular dystrophy. Eteplirsen's proposed mechanism of action is to bind to dystrophinList of Nazis (A–E) (3,893 words) [view diff] case mismatch in snippet view article
Daniel Kondziella. "Peter Becker and His Nazi Past The Man Behind Becker Muscular Dystrophy and Becker Myotonia." Journal of Child Neurology (2013). "HeinrichSkeletal muscle (13,834 words) [view diff] case mismatch in snippet view article find links to article
A (20 June 2018). "Skeletal Muscle Metabolism in Duchenne and Becker Muscular Dystrophy-Implications for Therapies". Nutrients. 10 (6): 796. doi:10.3390/nu10060796Sex differences in human physiology (9,645 words) [view diff] exact match in snippet view article find links to article
Muscular Dystrophy X-linked agammaglobulinaemia X-linked ichythyosis Becker muscular dystrophy Non-specific X-linked mental retardation X-linked dominant disorders