The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine
暂无分享,去创建一个
Gunadi | D. K. Nurputra | P. Lai | E. Herini | K. Iskandar | A. S. Kalim | E. Dwianingsih | R. Malueka | Sunartini | A. Triono | A. Putranti | L. Pratiwi | Hasna Mardhiah
[1] S. Luchters,et al. Knowledge, perception and practice towards oxytocin stability and quality: A qualitative study of stakeholders in three resource-limited countries , 2018, PloS one.
[2] L. Bastaki,et al. Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine , 2018, PloS one.
[3] S. Pandya,et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management , 2018, The Lancet Neurology.
[4] J. Morgan. Music lives on: fine tuning the memory , 2017, The Lancet Neurology.
[5] E. Mercuri,et al. Development of Exon Skipping Therapies for Duchenne Muscular Dystrophy: A Critical Review and a Perspective on the Outstanding Issues , 2017, Nucleic acid therapeutics.
[6] S. Takeda,et al. Recent advances in innovative therapeutic approaches for Duchenne muscular dystrophy: from discovery to clinical trials. , 2016, American journal of translational research.
[7] Ruth Brassington,et al. Corticosteroids for the treatment of Duchenne muscular dystrophy. , 2016, The Cochrane database of systematic reviews.
[8] A. Manzur,et al. Corticosteroids for the treatment of Duchenne muscular dystrophy. , 2016, The Cochrane database of systematic reviews.
[9] Y. Takeshima,et al. Contributions of Japanese patients to development of antisense therapy for DMD , 2016, Brain and Development.
[10] K. Bushby,et al. The importance of genetic diagnosis for Duchenne muscular dystrophy , 2016, Journal of Medical Genetics.
[11] B. Byrne,et al. Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy , 2015, Annals of neurology.
[12] Jing Liu,et al. Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy , 2014, Molecular Genetics and Genomics.
[13] K. Davies,et al. Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches , 2013, Nature Reviews Genetics.
[14] T. Grimm,et al. Survival in Duchenne muscular dystrophy , 2012, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
[15] Y. Takeshima,et al. P4.03 Mutation spectrum of the dystrophin gene in 456 Duchenne/Becker muscular dystrophy cases from one Japanese referral center , 2010, Neuromuscular Disorders.
[16] R. Finkel,et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management , 2010, The Lancet Neurology.
[17] T. Sura,et al. Sensitivity and Frequencies of Dystrophin Gene Mutations in Thai DMD/BMD Patients As Detected by Multiplex PCR , 2008, Disease markers.
[18] Y. Takeshima,et al. Comparative study on deletions of the dystrophin gene in three Asian populations , 2002, Journal of Human Genetics.
[19] M. A. Khan. Corticosteroid therapy in Duchenne muscular dystrophy , 1993, Journal of the Neurological Sciences.
[20] A. Covone,et al. Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR. , 1992, American journal of human genetics.
[21] F. Hanefeld,et al. Identification of a new DMD gene deletion by ectopic transcript analysis. , 1992, Journal of medical genetics.
[22] A. Emery. Population frequencies of inherited neuromuscular diseases—A world survey , 1991, Neuromuscular Disorders.
[23] C. Mathew,et al. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods. , 1991, Journal of medical genetics.
[24] L. Kunkel,et al. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction , 1990, Human Genetics.
[25] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..
[26] R. Gibbs,et al. 33 – MULTIPLEX PCR FOR THE DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY , 1990 .