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Search Results - Anderson, L.V.B.
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Calpainopathy—A Survey of Mutations and Polymorphisms
by
Richard, I.
,
Roudaut, C.
,
Saenz, A.
,
Pogue, R.
,
Grimbergen, J.E.M.A.
,
Anderson, L.V.B.
,
Beley, C.
,
Cobo, A-M
,
de Diego, C.
,
Eymard, B.
,
Gallano, P.
,
Ginjaar, H.B.
,
Lasa, A.
,
Pollitt, C.
,
Topaloglu, H.
,
Urtizberea, J.A.
,
de Visser, M.
,
van der Kooi, A.
,
Bushby, K.
,
Bakker, E.
,
Lopez de Munain, A.
,
Fardeau, M.
,
Beckmann, J.S.
Published in
American journal of human genetics
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The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach
by
Pollitt, C.
,
Anderson, L.V.B.
,
Pogue, R.
,
Davison, K.
,
Pyle, A.
,
Bushby, K.M.D.
Published in
Neuromuscular disorders : NMD
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Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice
by
Leriche-Guérin, K
,
Anderson, L.V.B
,
Wrogemann, K
,
Roy, B
,
Goulet, M
,
Tremblay, J.P
Published in
Neuromuscular disorders : NMD
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Dystrophin and the dystrophin-associated glycoprotein, β-dystroglycan, co-localize in photoreceptor synaptic complexes of the human retina
by
Drenckhahn, D.
,
Holbach, M.
,
Ness, W.
,
Schmitz, F.
,
Anderson, L.V.B.
Published in
Neuroscience
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Abnormalities in α-, β- and γ-sarcoglycan in patients with limb-girdle muscular dystrophy
by
Sewry, C.A.
,
Taylor, J.
,
Anderson, L.V.B.
,
Ozawa, E.
,
Pogue, R.
,
Piccolo, F.
,
Bushby, K.
,
Dubowitz, V.
,
Muntoni, F.
Published in
Neuromuscular disorders : NMD
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Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease
by
Auranen, M
,
Rapola, J
,
Pihko, H
,
Haltia, M
,
Leivo, I
,
Soinila, S
,
Virtanen, I
,
Kalimo, H
,
Anderson, L V
,
Santavuori, P
,
Somer, H
Published in
Neuromuscular disorders : NMD
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Dystrophinopathy or sarcoglycanopathy: the importance of a full diagnostic assessment in suspected manifesting carriers of Duchenne and Becker muscular dystrophy
by
Bushby, K.
,
Anderson, L.V.B.
,
Sewry, C.A.
,
Pogue, R.
,
Taylor, J.
,
Pollitt, C.
,
Muntoni, F.
Published in
Neuromuscular disorders : NMD
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Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy
by
Ginjaar, H.B.
,
vd Kooi, A.
,
Ceelie, H.
,
Kneppers, A.L.J.
,
Barth, P.G.
,
Busch, H.F.M.
,
Wokke, J.H.J.
,
Kerkhoff, H.
,
Broere, D.
,
Anderson, L.V.B.
,
Bönnemann, C.G.
,
Jeanpierre, M.
,
Bakker, E.
,
de Visser, M.
,
v Ommen, G.J.B.
Published in
Neuromuscular disorders : NMD
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Research database for dystrophin gene and protein expression 35th ENMC Workshop, 6–8 October 1995, Naarden, The Netherlands
by
Anderson, L.V.B.
Published in
Neuromuscular disorders : NMD
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