Neuromuscular disorders and 2010: recent advancesSARKOZY, Anna; LOCHMÜLLER, Hanns.Journal of neurology. 2010, Vol 257, Num 12, pp 2117-2121, issn 0340-5354, 5 p.Article

Neurology in sub-Saharan Africa : A challenge for world federation of neurologyAARLI, Johan A; DIOP, Amadou Gallo; LOCHMÜLLER, Hanns et al.Neurology. 2007, Vol 69, Num 17, pp 1715-1718, issn 0028-3878, 4 p.Article

Interventions for muscular dystrophy: molecular medicines entering the clinicBUSHBY, Kate; LOCHMÜLLER, Hanns; LYNN, Stephen et al.Lancet (British edition). 2009, Vol 374, Num 9704, pp 1849-1856, issn 0140-6736, 8 p.Article

Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP)THORNHILL, Paul; BASSETT, David; LOCHMÜLLER, Hanns et al.Brain. 2008, Vol 131, pp 1551-1561, issn 0006-8950, 11 p., 6Article

Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNA^LysHORVATH, Rita; KLEY, Rudolf Andre; LOCHMÜLLER, Hanns et al.Neurology. 2007, Vol 68, Num 1, pp 56-58, issn 0028-3878, 3 p.Article

Gentamicin fails to increase dystrophin expression in dystrophin-deficient muscleDUNANT, Patrick; WALTER, Maggie C; KARPATI, George et al.Muscle & nerve. 2003, Vol 27, Num 5, pp 624-627, issn 0148-639X, 4 p.Article

Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients' primary skeletal myoblastsENDESFELDER, Stefanie; KLICHE, Alexander; LOCHMÜLLER, Hanns et al.Journal of molecular medicine (Berlin. Print). 2005, Vol 83, Num 1, pp 64-71, issn 0946-2716, 8 p.Article

Inclusion Body Myositis: Laser Microdissection Reveals Differential Up-Regulation of IFN-γ Signaling Cascade in Attacked versus Nonattacked MyofibersIVANIDZE, Jana; HOFFMANN, Reinhard; LOCHMÜLLER, Hanns et al.The American journal of pathology. 2011, Vol 179, Num 3, pp 1347-1359, issn 0002-9440, 13 p.Article

Muscle fibres and cultured muscle cells express the B7.1/2-related inducible co-stimulatory molecule, ICOSL: implications for the pathogenesis of inflammatory myopathiesWIENDL, Heinz; MITSDOERFFER, Meike; SCHNEIDER, Dagmar et al.Brain. 2003, Vol 126, pp 1026-1035, issn 0006-8950, 10 p., 5Article

Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA^Val causing MNGIE-like gastrointestinal dysmotility and cachexiaHORVATH, Rita; BENDER, Andreas; ABICHT, Angela et al.Journal of neurology. 2009, Vol 256, Num 5, pp 810-815, issn 0340-5354, 6 p.Article

Human Muscle Cells Express the Costimulatory Molecule B7-H3, Which Modulates Muscle-Immune InteractionsWASCHBISCH, Anne; WINTTERLE, Sabine; LOCHMULLER, Hanns et al.Arthritis and rheumatism. 2008, Vol 58, Num 11, pp 3600-3608, issn 0004-3591, 9 p.Article

The burden of Duchenne muscular dystrophy: An international, cross-sectional studyLANDFELDT, Erik; LINDGREN, Peter; BELL, Christopher F et al.Neurology. 2014, Vol 83, Num 6, pp 529-536, issn 0028-3878, 8 p.Article

Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyWOOD, Alasdair J; MÜLLER, Juliane S; JEPSON, Catherine D et al.Human molecular genetics (Print). 2011, Vol 20, Num 24, pp 4879-4890, issn 0964-6906, 12 p.Article

Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2HSCHOSER, Benedikt G. H; FROSK, Patrick; ENGEL, Andrew G et al.Annals of neurology. 2005, Vol 57, Num 4, pp 591-595, issn 0364-5134, 5 p.Article

Creatine monohydrate in myotonic dystrophy: A double-blind, placebo-controlled clinical studyWALTER, Maggie C; REILICH, Peter; LOCHMÜLLER, Hanns et al.Journal of neurology. 2002, Vol 249, Num 12, pp 1717-1722, issn 0340-5354, 6 p.Article

Ocular features of the congenital cataracts facial dysmorphism neuropathy syndromeMÜLLNER-EIDENBÖCK, Andrea; MOSER, Elisabeth; KLEBERMASS, Nina et al.Ophthalmology (Rochester, MN). 2004, Vol 111, Num 7, pp 1415-1423, issn 0161-6420, 9 p.Article

Myopathy caused by anoctamin 5 mutations and necrotizing vasculitisPENISSON-BESNIER, Isabelle; SAINT-ANDRE, Jean-Paul; HICKS, Debbie et al.Journal of neurology. 2012, Vol 259, Num 9, pp 1988-1990, issn 0340-5354, 3 p.Article

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

Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3HORVATH, Rita; CZERMIN, Birgit; BRODHUN, Michael et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 2, pp 174-178, issn 0022-3050, 5 p.Article

Efficient and Fast Functional Screening of Microdystrophin Constructs In Vivo and In Vitro for Therapy of Duchenne Muscular DystrophyJØRGENSEN, Louise H; LAROCHELLE, Nancy; ORLOPP, Kristian et al.Human gene therapy. 2009, Vol 20, Num 6, pp 641-650, issn 1043-0342, 10 p.Article

Mitochondrial phosphate-carrier deficiency : A novel disorder of oxidative phosphorylationMAYR, Johannes A; MERKEL, Olaf; FREISINGER, Peter et al.American journal of human genetics. 2007, Vol 80, Num 3, pp 478-484, issn 0002-9297, 7 p.Article

Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromesMÜLLER, Juliane S; HERCZEGFALVI, Agnes; POULIN, Chantal et al.Brain. 2007, Vol 130, pp 1497-1506, issn 0006-8950, 10 p., 6Article

Adenovirus vectors based on human adenovirus type 19a have high potential for human muscle-directed gene therapyTHIRION, Christian; LOCHMÜLLER, Hanns; BURGERT, Hans-Gerhard et al.Human gene therapy. 2006, Vol 17, Num 2, pp 193-205, issn 1043-0342, 13 p.Article

Mutations in dynamin 2 cause dominant centronuclear myopathyBITOUN, Marc; MAUGENRE, Svetlana; FARDEAU, Michel et al.Nature genetics. 2005, Vol 37, Num 11, pp 1207-1209, issn 1061-4036, 3 p.Article

Mutation history of the Roma/GypsiesMORAR, Bharti; GRESHAM, David; KALMAR, Lajos et al.American journal of human genetics. 2004, Vol 75, Num 4, pp 596-609, issn 0002-9297, 14 p.Article