المؤلفون: K. Bushby, R. Finkel, B. Wong, R. Barohn, C. Campbell, A. M. Connolly, J. W. Day, K. M. Flanigan, N. Goemans, K. J. Jones, E. Mercuri, R. Quinlivan, J. B. Renfroe, B. Russman, M. M. Ryan, M. Tulinius, T. Voit, S. A. Moore, H. Lee Sweeney, R. T. Abresch, K. L. Coleman, M. Eagle, J. Florence, E. Gappmaier, A. M. Glanzman, E. Henricson, J. Barth, G. L. Elfring, A. Reha, R. J. Spiegel, M. W. O'Donnell, S. W. Peltz, C. M. Mcdonald, G.P. Comi

المساهمون: K. Bushby, R. Finkel, B. Wong, R. Barohn, C. Campbell, G.P. Comi, A.M. Connolly, J.W. Day, K.M. Flanigan, N. Goeman, K.J. Jone, E. Mercuri, R. Quinlivan, J.B. Renfroe, B. Russman, M.M. Ryan, M. Tuliniu, T. Voit, S.A. Moore, H. Lee Sweeney, R.T. Abresch, K.L. Coleman, M. Eagle, J. Florence, E. Gappmaier, A.M. Glanzman, E. Henricson, J. Barth, G.L. Elfring, A. Reha, R.J. Spiegel, M.W. O'Donnell, S.W. Peltz, C.M. Mcdonald

مصطلحات موضوعية: Duchenne muscular dystrophy, genetic, pediatric, nonsense mutation, orphan, Settore MED/26 - Neurologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/25042182; info:eu-repo/semantics/altIdentifier/wos/WOS:000342634100002; volume:50; issue:4; firstpage:477; lastpage:487; numberofpages:11; journal:MUSCLE & NERVE; http://hdl.handle.net/2434/424651; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84927669185

الاتاحة: http://hdl.handle.net/2434/424651
https://doi.org/10.1002/mus.24332

المؤلفون: L E, Taylor, Y J, Kaminoh, C K, Rodesch, K M, Flanigan

المصدر: Neuropathology and applied neurobiology. 38(6)

مصطلحات موضوعية: Adult, Dystrophin, Muscular Dystrophy, Duchenne, Image Processing, Computer-Assisted, Fluorescent Antibody Technique, Humans, Spectrin, Muscle, Skeletal

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::1bba68483a6d33d3896597cdcbfdfb24
https://pubmed.ncbi.nlm.nih.gov/22243335

المؤلفون: K. M. Flanigan, D. M. Dunn, A. von Niederhausern, M. T. Howard, J. Mendell, A. Connolly, C. Saunders, A. Modrcin, M. Dasouki, A. Pickart, R. Jacobson, R. Finkel, L. Medne, R. B. Weiss, G.P. Comi, R. Del Bo

المساهمون: K.M. Flanigan, D.M. Dunn, A. von Niederhausern, M.T. Howard, J. Mendell, A. Connolly, C. Saunder, A. Modrcin, M. Dasouki, G.P. Comi, R. Del Bo, A. Pickart, R. Jacobson, R. Finkel, L. Medne, R.B. Weiss

مصطلحات موضوعية: Becker muscular dystrophy, DMD, Duchenne muscular dystrophy, Founder allele, Settore MED/26 - Neurologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/19793655; info:eu-repo/semantics/altIdentifier/wos/WOS:000272020400001; volume:19; issue:11; firstpage:743; lastpage:748; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/2434/72157; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-70350182211

الاتاحة: http://hdl.handle.net/2434/72157
https://doi.org/10.1016/j.nmd.2009.08.010

المؤلفون: K M, Flanigan, L, Kerr, M B, Bromberg, C, Leonard, J, Tsuruda, P, Zhang, I, Gonzalez-Gomez, R, Cohn, K P, Campbell, M, Leppert

المصدر: Annals of neurology. 47(2)

مصطلحات موضوعية: Male, Adolescent, Genotype, Genetic Linkage, Homozygote, Chromosome Mapping, Syndrome, Magnetic Resonance Imaging, Muscular Dystrophies, Phenotype, Humans, Female, Spinal Diseases, Lod Score, Child, Muscle, Skeletal, Alleles

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::820a9cc5d7b68dab1ec9e92aff10108b
https://pubmed.ncbi.nlm.nih.gov/10665483

المؤلفون: C C, Meltzer, S W, Wells, M W, Becher, K M, Flanigan, G A, Oyler, R R, Lee

المصدر: AJNR Am J Neuroradiol

مصطلحات موضوعية: Adult, Male, AIDS Dementia Complex, Cocaine, Substance-Related Disorders, Journal Article, Humans, Female, Magnetic Resonance Imaging, Basal Ganglia, Retrospective Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::00d0a41eeaa971e725f3a5732b1fc678
https://pubmed.ncbi.nlm.nih.gov/9432162

المؤلفون: K M, Flanigan, T O, Crawford, J W, Griffin, H H, Goebel, A, Kohlschütter, J, Ranells, P R, Camfield, L J, Ptácek

المصدر: Annals of neurology. 43(1)

مصطلحات موضوعية: Consanguinity, Genotype, Genetic Linkage, Genome, Human, Homozygote, Chromosome Mapping, Humans, Lod Score, Nervous System Diseases, Axons, Chromosomes, Human, Pair 16, Pedigree

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::849b1c50c2d41f8a1176e5ba831a20ae
https://pubmed.ncbi.nlm.nih.gov/9450783

المؤلفون: K M, Flanigan, D R, Johns

المصدر: Neurology. 43(12)

مصطلحات موضوعية: Adult, Male, Optic Atrophies, Hereditary, Mutation, Humans, Female, DNA, Mitochondrial, Demyelinating Diseases

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d180963fc1eedad2b74a8b8b71aa9ac6
https://pubmed.ncbi.nlm.nih.gov/8255489