au.\*:("MOXLEY, R. T")
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The myotonias : Their diagnosis and treatmentMOXLEY, R. T.Comprehensive therapy. 1996, Vol 22, Num 1, pp 8-21, issn 0098-8243Article
Early predictors of poor outcome in congenital fiber-type disproportion myopathyTORRES, C. F; MOXLEY, R. T.Archives of neurology (Chicago). 1992, Vol 49, Num 8, pp 855-856, issn 0003-9942Article
Rippling muscle diseaseRICKER, K; MOXLEY, R. T; ROHKAMM, R et al.Archives of neurology (Chicago). 1989, Vol 46, Num 4, pp 405-408, issn 0003-9942Article
Hypertrophy of the calf with S-1 radiculopathyRICKER, K; ROHKAMM, R; MOXLEY, R. T. III et al.Archives of neurology (Chicago). 1988, Vol 45, Num 6, pp 660-664, issn 0003-9942Article
American experience with low-dose thalidomide therapy for severe cutaneous lupus erythematosusDAIHUNG JAY DUONG; SPIGEL, G. T; MOXLEY, R. T et al.Archives of dermatology (1960). 1999, Vol 135, Num 9, pp 1079-1087, issn 0003-987XArticle
Deletion and conversion in spinal muscular atrophy patients : Is there a relationship to severity ?DIDONATO, C. J; INGRAHAM, S. E; MENDELL, J. R et al.Annals of neurology. 1997, Vol 41, Num 2, pp 230-237, issn 0364-5134Article
Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophyWINNARD, A. V; KLEIN, C. J; MOXLEY, R. T et al.Human molecular genetics (Print). 1993, Vol 2, Num 6, pp 737-744, issn 0964-6906Article
Duchenne dystrophy : randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)GRIGGS, R. C; MOXLEY, R. T; KING, W et al.Neurology. 1993, Vol 43, Num 3, pp 520-527, issn 0028-3878, 1Article
Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1LOGIGIAN, E. L; MOXLEY, R. T; BLOOD, C. L et al.MOXLEY, R. T; Neurology. 2004, Vol 62, Num 7, pp 1081-1089, issn 0028-3878, 9 p.Article
Proximal myotonic myopathy: a syndrome with a favourable prognosis?MEOLA, G; SANSONE, V; MARINOU, K et al.Journal of the neurological sciences. 2002, Vol 193, Num 2, pp 89-96, issn 0022-510XArticle
Proximal myotonic myopathy : a new dominant disorder with myotonia, muscle weakness, and cataractsRICKER, K; KOCH, M. C; LEHMANN-HORN, F et al.Neurology. 1994, Vol 44, Num 8, pp 1448-1452, issn 0028-3878Article
Managed care and the survival of neurology referral centers A commitment to centers of excellenceMENKEN, M; GOLDBLATT, D; MOXLEY, R. T et al.Archives of neurology (Chicago). 1997, Vol 54, Num 11, pp 1349-1350, issn 0003-9942Article
Abnormal regulation of venous alanine after glucose ingestion in myotonic dystrophyMOXLEY, R. T. III; KINGSTON, W; GRIGGS, R. C et al.Clinical science (1979). 1985, Vol 68, Num 2, pp 151-157, issn 0143-5221Article
Dissociation of glucose and potassium arterial-venous differences across the forearm by acetazolamide: a possible relationship to acetazolamidés beneficial effect in hypokalemic periodic paralysisRIGGS, J. E; GRIGGS, R. C; MOXLEY, R. T. III et al.Archives of neurology (Chicago). 1984, Vol 41, Num 1, pp 35-38, issn 0003-9942Article
Myotonia fluctuans : a third type of muscle sodium channel diseaseRICKER, K; MOXLEY, R. T; HEINE, R et al.Archives of neurology (Chicago). 1994, Vol 51, Num 11, pp 1095-1102, issn 0003-9942Article
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathyMEOLA, G; SANSONE, V; PERANI, D et al.Neurology. 1999, Vol 53, Num 5, pp 1042-1050, issn 0028-3878Article
Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP geneTHORNTON, C. A; WYMER, J. P; SIMMONS, Z et al.Nature genetics. 1997, Vol 16, Num 4, pp 407-409, issn 1061-4036Article
Mononuclear cell analysis of muscle biopsies in prednisone- and azathioprine-treated Duchenne muscular dystrophyKISSEL, J. T; LYNN, D. J; RAMMOHAN, K. W et al.Neurology. 1993, Vol 43, Num 3, pp 532-536, issn 0028-3878, 1Article
Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophyMENDELL, J. R; MOXLEY, R. T; SCHIERBECKER, J et al.The New England journal of medicine. 1989, Vol 120, Num 24, pp 1592-1597, issn 0028-4793Article
Quantitative analysis of the warm-up phenomenon in myotonic dystrophy type 1LOGIGIAN, E. L; BLOOD, C. L; DILEK, N et al.Muscle & nerve. 2005, Vol 32, Num 1, pp 35-42, issn 0148-639X, 8 p.Article
Proximal myotonic myopathy : clinical features of a multisystem disorder similar to myotonic dystrophyRICKER, K; KOCH, M; LEHMANN-HORN et al.Archives of neurology (Chicago). 1995, Vol 52, Num 1, pp 25-31, issn 0003-9942Article
Linkage mapping of the spinal muscular atrophy geneBURGHES, A. H. M; INGRAHAM, S. E; MOXLEY, R. T et al.Human genetics. 1994, Vol 93, Num 3, pp 305-312, issn 0340-6717Article
Location of phosphotyrosine-containing proteins by immunocytochemistry in the rat forebrain corresponds to the distribution of the insulin receptorMOSS, A. M; UNGER, J. W; MOXLEY, R. T et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 12, pp 4453-4457, issn 0027-8424, 5 p.Article
Randomized, double-blind trial of mazindol in Duchenne dystrophyGRIGGS, R. C; MOXLEY, R. T; KING, W et al.Muscle & nerve. 1990, Vol 13, Num 12, pp 1169-1173, issn 0148-639X, 5 p.Article
Mitochondrial encephalomyopathy with decreased succinate-cytochrome c reductase activityRIGGS, J. E; SCHOCHET, S. S; FAKADEJ, A. V et al.Neurology. 1984, Vol 34, Num 1, pp 48-53, issn 0028-3878Article