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Page 1
The Clinical Outcome Study for dysferlinopathy: An international multicenter study.
Harris E, Bladen CL, Mayhew A, James M, Bettinson K, Moore U, Smith FE, Rufibach L, Cnaan A, Bharucha-Goebel DX, Blamire AM, Bravver E, Carlier PG, Day JW, Díaz-Manera J, Eagle M, Grieben U, Harms M, Jones KJ, Lochmüller H, Mendell JR, Mori-Yoshimura M, Paradas C, Pegoraro E, Pestronk A, Salort-Campana E, Schreiber-Katz O, Semplicini C, Spuler S, Stojkovic T, Straub V, Takeda S, Rocha CT, Walter MC, Bushby K; Jain COS Consortium. Harris E, et al. Among authors: lochmuller h. Neurol Genet. 2016 Aug 4;2(4):e89. doi: 10.1212/NXG.0000000000000089. eCollection 2016 Aug. Neurol Genet. 2016. PMID: 27602406 Free PMC article.
Novel approaches to treat muscular dystrophies.
Walter MC, Lochmüller H. Walter MC, et al. Among authors: lochmuller h. Expert Opin Investig Drugs. 2001 Apr;10(4):695-707. doi: 10.1517/13543784.10.4.695. Expert Opin Investig Drugs. 2001. PMID: 11281819 Review.
Prion codon 129 homozygosity and sporadic inclusion body myositis.
Lampe J, Gossrau G, Reichmann H, Walter MC, Mendel B, Lochmüller H. Lampe J, et al. Among authors: lochmuller h. Neurology. 2001 Jul 24;57(2):368. doi: 10.1212/wnl.57.2.368. Neurology. 2001. PMID: 11468340 No abstract available.
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.
Merlini L, Gooding R, Lochmüller H, Müller-Felber W, Walter MC, Angelicheva D, Talim B, Hallmayer J, Kalaydjieva L. Merlini L, et al. Among authors: lochmuller h. Neurology. 2002 Jan 22;58(2):231-6. doi: 10.1212/wnl.58.2.231. Neurology. 2002. PMID: 11805249
Analysis of HLA class I and II alleles in sporadic inclusion-body myositis.
Lampe JB, Gossrau G, Kempe A, Füssel M, Schwurack K, Schröder R, Krause S, Kohnen R, Walter MC, Reichmann H, Lochmüller H. Lampe JB, et al. Among authors: lochmuller h. J Neurol. 2003 Nov;250(11):1313-7. doi: 10.1007/s00415-003-0204-3. J Neurol. 2003. PMID: 14648147
695 results