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kw.\*:("Myopathie myotonique proximale")

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Camptocormie révélatrice d'une myopathie myotonique proximale = Camptocornia presenting with a proximal myotonic myopathyRIMBAUX, S; PELLIEUX, S; BERGEMER, A.-M et al.Revue neurologique (Paris). 2003, Vol 159, Num 6-7, pp 678-680, issn 0035-3787, 3 p., CAH1Article

Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: A single shared haplotype indicates an ancestral founder effectBACHINSKI, Linda L; UDD, Bjarne; JURKAT-ROTT, Karin et al.American journal of human genetics. 2003, Vol 73, Num 4, pp 835-848, issn 0002-9297, 14 p.Article

Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2JAKUBICZKA, Sibylle; VIELHABER, Stefan; KRESS, Wolfram et al.Neurogenetics (Oxford. Print). 2004, Vol 5, Num 1, pp 55-59, issn 1364-6745, 5 p.Article

Proximal myotonic myopathy : Clinical, electrophysiological and pathological findings in a familyKOHLER, A; BURKHARD, P; HEFFT, S et al.European neurology. 2000, Vol 43, Num 1, pp 50-53, issn 0014-3022Article

ABSENT, UNRECOGNIZED, AND MINIMAL MYOTONIC DISCHARGES IN MYOTONIC DYSTROPHY TYPE 2YOUNG, Nathan P; DAUBE, Jasper R; SORENSON, Eric J et al.Muscle & nerve. 2010, Vol 41, Num 6, pp 758-762, issn 0148-639X, 5 p.Article

Muscle pathology in 57 patients with myotonic dystrophy type 2SCHOSER, Benedikt G. H; SCHNEIDER-GOLD, Christiane; KRESS, Wolfram et al.Muscle & nerve. 2004, Vol 29, Num 2, pp 275-281, issn 0148-639X, 7 p.Article

Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2VIHOLA, A; BASSEZ, G; MAISONOBE, T et al.Neurology. 2003, Vol 60, Num 11, pp 1854-1857, issn 0028-3878, 4 p.Article

Une cause méconnue de camptocormie : la myopathie myotonique proximale = Proximal myotonic myopathy : an unrecognized cause of camptocormiaSERRATRICE, J; WEILLER, P. J; POUGET, J et al.La Presse médicale (1983). 2000, Vol 29, Num 20, pp 1121-1123, issn 0755-4982Article

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

Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2 : A whole body highfield MRI studyKORNBLUM, Cornelia; LUTTERBEY, Götz; BOGDANOW, Manuela et al.Journal of neurology. 2006, Vol 253, Num 6, pp 753-761, issn 0340-5354, 9 p.Article

A patient with proximal myotonic myopathy and parkinsonismCHU, Kon; CHO, Jin-Whan; SONG, Eun-Chol et al.Canadian journal of neurological sciences. 2002, Vol 29, Num 2, pp 188-190, issn 0317-1671Article

Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging studyKASSUBEK, Jan; JUENGLING, Freimut D; LERCHE, Holger et al.Neuroscience letters. 2003, Vol 348, Num 2, pp 73-76, issn 0304-3940, 4 p.Article

Proximal myotonic myopathy with MRI white matter abnormalities of the brainHUND, E; JANSEN, M. O; KOCH, M. C et al.Neurology. 1997, Vol 48, Num 1, pp 33-37, issn 0028-3878Article

Homozygosity for CCTG mutation in myotonic dystrophy type 2SCHOSER, Benedikt G. H; KRESS, Wolfram; WALTER, Maggie C et al.Brain. 2004, Vol 127, pp 1868-1877, issn 0006-8950, 10 p., 8Article

Proximal myotonic myopathy : Clinical and molecular investigation of a Norwegian family with PROMMSUN, C; HENRIKSEN, O. A; TRANEBJAERG, L et al.Clinical genetics. 1999, Vol 56, Num 6, pp 457-461, issn 0009-9163Article

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

Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutationMASTAGLIA, F. L; HARKER, N; PHILLIPS, B. A et al.Journal of neurology, neurosurgery and psychiatry. 1998, Vol 64, Num 4, pp 543-547, issn 0022-3050Article

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