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Annals of Neurology|August 2, 2003
Tibial muscular dystrophy in a Belgian familyPeter Y K Van den Bergh, Olivier Bouquiaux, Christine Verellen, et al.Human Genetics|December 22, 1999
Missense mutations in hMLH1 associated with colorectal cancerT Liu, P Tannergård, P Hackman, et al.Environmental Health Perspectives|November 1, 1992
Detection of ras gene mutations in human lung cancer: comparison of two screening assays based on the polymerase chain reactionK Husgafvel-Pursiainen, M Ridanpää, P Hackman, et al.Acta Neurologica Scandinavica|July 10, 2004
Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophyI Mahjneh, A E Lamminen, B Udd, et al.International Journal of Cancer|January 21, 1993
K-ras mutations in human adenocarcinoma of the lung: association with smoking and occupational exposure to asbestosK Husgafvel-Pursiainen, P Hackman, M Ridanpää, et al.European Journal of Neurology|February 25, 2017
Association study reveals novel risk loci for sporadic inclusion body myositisM Johari, M Arumilli, J Palmio, et al.Neuromuscular Disorders : NMD|September 27, 2012
Targeted array comparative genomic hybridization--a new diagnostic tool for the detection of large copy number variations in nemaline myopathy-causing genesK Kiiski, L Laari, V-L Lehtokari, et al.Neuromuscular Disorders : NMD|July 16, 2002
Congenital myasthenic syndrome associated with episodic apnea and sudden infant deathR F Byring, H Pihko, A Tsujino, et al.Brain : a Journal of Neurology|March 6, 2007
Zaspopathy in a large classic late-onset distal myopathy familyR Griggs, A Vihola, P Hackman, et al.Clinical Genetics|March 15, 2011
Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patientsN Muelas, P Hackman, H Luque, et al.Pageof 3