Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Lindvall, Björn"'
Autor:
Lindvall, Björn
Publikováno v:
Sammanfattning på engelska (spikblad).
Diss. (sammanfattning) Linköping : Univ., 2002.
Härtill 4 uppsatser.
Härtill 4 uppsatser.
Externí odkaz:
http://www.bibl.liu.se/liupubl/disp/disp2002/med760s.pdf
Autor:
Nordin, Sofia, Stelmaszuk, M. Natalia, MacCulloch, Alasdair, Graham, Ryan, Ekström, Anne-Berit, Lindvall, Björn, Freilich, Jonatan
Publikováno v:
In Molecular Genetics and Metabolism February 2023 138(2)
Publikováno v:
In Neuromuscular Disorders 2009 19(6):412-417
Autor:
Niemelä, Valter, Salih, Ammar, Solea, Daniela, Lindvall, Björn, Weinberg, Jan, Miltenberger, Gabriel, Granberg, Tobias, Tzovla, Aikaterini, Nordin, Love, Danfors, Torsten, Savitcheva, Irina, Dahl, Niklas, Paucar, Martin
Publikováno v:
Neurology: Genetics
Objective To perform a comprehensive characterization of a cohort of patients with chorea-acanthocytosis (ChAc) in Sweden. Methods Clinical assessments, targeted genetic studies, neuroimaging with MRI, [18F]-fluorodeoxyglucose (FDG) PET, and dopamine
Autor:
Danielsson, Olof1,2 olof.danielsson@regionostergotland.se, Lindvall, Björn3, Hallert, Claes4,5, Vrethem, Magnus1,2,6, Dahle, Charlotte2,7
Publikováno v:
Brain & Behavior. Oct2017, Vol. 7 Issue 10, pn/a-N.PAG. 7p.
Publikováno v:
In Journal of Electromyography and Kinesiology 2006 16(3):281-290
Akademický článek
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Autor:
Bladen, Catherine, Rafferty, Karen, Straub, Volker, Monges, Soledad, Moresco, Angélica, Dawkins, Hugh, Roy, Anna, Chamova, Teodora, Guergueltcheva, Velina, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Barišić, Nina, Kos, Tea, Brabec, Petr, Rahbek, Jes, Lahdetie, Jaana, Tuffery-Giraud, Sylvie, Claustres, Mireille, Leturcq, France, Ben Yaou, Rabah, Walter, Maggie C, Schreiber, Olivia, Karcagi, Veronika, Herczegfalvi, Agnes, Viswanathan, Venkatarman, Bayat, Farhad, de La Caridad Guerrero Sarmiento, Isis, Ambrosini, Anna, Ceradini, Francesc, Kimura, En, van den Bergen, Jan, Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Oliveira, Jorge, Santos, Rosário, Neagu, Elena, Butoianu, Niculina, Artemieva, Svetlana, Rasic, Vedrana Milic, Posada, Manuel, Palau, Francesc, Lindvall, Björn, Bloetzer, Clemens, Karaduman, Ayşe, Topaloğlu, Haluk, Inal, Serap, Oflazer, Piraye, Stringer, Angela, Shatillo, Andriy V, Martin, Ann S, Peay, Holly, Flanigan, Kevin M, Salgado, David, von Rekowski, Brigitta, Lynn, Stephen, Heslop, Emma, Gainotti, Sabina, Taruscio, Domenica, Kirschner, Jan, Verschuuren, Jan, Bushby, Kate, Béroud, Christophe, Lochmuller, Hanns, Roy, Hugh, Tuffery-Giraud, France, Claustres, France, Walter, Maggie C., Shatillo, Andriy V., Martin, Ann S., Flanigan, Kevin M.
Publikováno v:
Human Mutation, 34(11), 1449-1457
HUMAN MUTATION
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Human Mutation
Human Mutation, 2013, 34 (11), pp.1449-1457. ⟨10.1002/humu.22390⟩
Human Mutation, Wiley, 2013, 34 (11), pp.1449-1457. ⟨10.1002/humu.22390⟩
HUMAN MUTATION
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Human Mutation
Human Mutation, 2013, 34 (11), pp.1449-1457. ⟨10.1002/humu.22390⟩
Human Mutation, Wiley, 2013, 34 (11), pp.1449-1457. ⟨10.1002/humu.22390⟩
International audience; Duchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by the absence of the dystrophin protein. Although many novel therapies are under development for DMD, there is currently no cure and affected individual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c2647260e6ae2f3061809a1dc3d0113
http://hdl.handle.net/1887/100815
http://hdl.handle.net/1887/100815