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Results 1 to 18 of 18

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Mutational spectra at the hypoxanthine-guanine phosphoribosyltransferase (HPRT) locus in T-lymphocytes of nonsmoking and smoking lung cancer patientsHACKMAN, P; HOU, S.-M; NYBERG, F et al.Mutation research. Genetic toxicology and environmental mutagenesis. 2000, Vol 468, Num 1, pp 45-61, issn 1383-5718Article

Tibial muscular dystrophy in a Belgian familyVAN DEN BERGH, Peter Y. K; BOUQUIAUX, Olivier; VERELLEN, Christine et al.Annals of neurology. 2003, Vol 54, Num 2, pp 248-251, issn 0364-5134, 4 p.Article

Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2JUDD, B; VIHOLA, A; SARPARANTA, J et al.Neurology. 2005, Vol 64, Num 4, pp 636-642, issn 0028-3878, 7 p.Article

Radiation induced chromosomal instability in human T-lymphocytesLAMBERT, B; HOLMBERG, K; HACKMAN, P et al.Mutation research. 1998, Vol 405, Num 2, pp 161-170, issn 0027-5107Conference Paper

Late-onset lower motor neuronopathy: A new autosomal dominant disorderJOKELA, M; PENTTILÄ, S; HUOVINEN, S et al.Neurology. 2011, Vol 77, Num 4, pp 334-340, issn 0028-3878, 7 p.Article

K-ras mutations in human adenocarcinoma of the lung : association with smoking and occupational exposure to absestosHUSGAFVEL-PURIAINEN, K; HACKMAN, P; RIDANPÄÄ, M et al.International journal of cancer. 1993, Vol 53, Num 2, pp 250-256, issn 0020-7136Article

Efficient secretion of Bacillus amyloliquefaciens α-amylase cells by its own signal peptide from Saccharomyces cerevisiae hostRUOHONEN, L; HACKMAN, P; LEHTOVAARA, P et al.Gene (Amsterdam). 1987, Vol 59, Num 2-3, pp 161-170, issn 0378-1119Article

Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by AN05PENTTILÄ, S; PALMIO, J; HACKMAN, P et al.Neurology. 2012, Vol 78, Num 12, pp 897-903, issn 0028-3878, 7 p.Article

MYH7 gene tail mutation causing myopathic profiles beyond Laing distal myopathyMUELAS, N; HACKMAN, P; MILLAN, J. María et al.Neurology. 2010, Vol 75, Num 8, pp 732-741, issn 0028-3878, 10 p.Article

Zaspopathy in a large classic late-onset distal myopathy family. CommentaryGRIGGS, R; VIHOLA, A; CARPEN, O et al.Brain. 2007, Vol 130, issn 0006-8950, 1453-1455, 1477-1484 [11 p.], 6Article

Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patientsMUELAS, N; HACKMAN, P; VILCHEZ, J. J et al.Clinical genetics. 2012, Vol 81, Num 5, pp 491-494, issn 0009-9163, 4 p.Article

Myopathies caused by homozygous titin mutations: limb-girdle muscular dystrophy 2J and variations of phenotypePENISSON-BESNIER, I; HACKMAN, P; SUOMINEN, T et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 11, pp 1200-1202, issn 0022-3050, 3 p.Article

Enrichment of the R77C α-sarcoglycan gene mutation in finnish LGMD2D patientsHACKMAN, P; JUVONEN, V; LÖNNOVIST, T et al.Muscle & nerve. 2005, Vol 31, Num 2, pp 199-204, issn 0148-639X, 6 p.Article

Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophyMAHJNEH, I; LAMMINEN, A. E; UDD, B et al.Acta neurologica scandinavica. 2004, Vol 110, Num 2, pp 87-93, issn 0001-6314, 7 p.Article

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvementVAN GOETHEM, G; LUOMA, P; SUOMALAINEN, A et al.Neurology. 2004, Vol 63, Num 7, pp 1251-1257, issn 0028-3878, 7 p.Article

Missense mutations in hMLH1 associated with colorectal cancerTAO LIU; TANNERGARD, P; HACKMAN, P et al.Human genetics. 1999, Vol 105, Num 5, pp 437-441, issn 0340-6717Article

Genomic characteristics of strains of Itersonilia : taxonomic consequences and life cycleBOEKHOUT, T; POOT, G; HACKMAN, P et al.Canadian journal of microbiology. 1991, Vol 37, Num 3, pp 188-194, issn 0008-4166, 7 p.Article

Mast cells and histamine in adenoid tissue and middle earPALVA, T; TAKINEN, E; LEHTINEN, T et al.Acta oto-laryngologica. 1991, Vol 111, Num 2, pp 349-353, issn 0001-6489, 5 p.Conference Paper

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