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au.\*:("KOSKELA, S")

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FIRST ISOLATIONS OF KPC-2-CARRYING ST258 KLEBSIELLA PNEUMONIAE STRAINS IN FINLAND, JUNE AND AUGUST 2009ÖSTERBLAD, M; KIRVESKARI, J; KOSKELA, S et al.Euro surveillance. 2009, Vol 14, Num OCTDEC, pp 657-658, issn 1025-496X, 2 p.Article

Variant Bernard-Soulier syndrome due to homozygous Asn45Ser mutation in the platelet glycoprotein (GP) IX in seven patients of five unrelated finnish familiesKOSKELA, S; JAVELA, K; JOUPPILA, J et al.European journal of haematology. 1999, Vol 62, Num 4, pp 256-264, issn 0902-4441Article

Expression of CYP2A genes in human liver and extrahepatic tissuesKOSKELA, S; HAKKOLA, J; HUKKANEN, J et al.Biochemical pharmacology. 1999, Vol 57, Num 12, pp 1407-1413, issn 0006-2952Article

Difficulty in making contact with others and social withdrawal as early signs of psychosis in adolescents - the Northern Finland Birth Cohort 1986MÄKI, P; KOSKELA, S; MURRAY, G. K et al.European psychiatry. 2014, Vol 29, Num 6, pp 345-351, issn 0924-9338, 7 p.Article

Adapting spa typing for national laboratory-based surveillance of methicillin-resistant Staphylococcus aureusVAINIO, A; KOSKELA, S; VIROLAINEN, A et al.European journal of clinical microbiology & infectious diseases (Print). 2011, Vol 30, Num 6, pp 789-797, issn 0934-9723, 9 p.Article

Molecular characterization of two mutations in platelet glycoprotein (GP) Ibα in two Finnish Bernard-Soulier syndrome familiesKOSKELA, S; PARTANEN, J; SALMI, T. T et al.European journal of haematology. 1999, Vol 62, Num 3, pp 160-168, issn 0902-4441Article

Screening of inherited oligosaccharidurias among mentally retarded patients in Northern FinlandAULA, P; RENLUND, M; RAIVIO, K. O et al.Journal of mental deficiency research. 1986, Vol 30, Num 4, pp 365-368, issn 0022-264XArticle

The incidence of Down syndrome in northern Finland with special reference to maternal ageLEISTI, J; VAHTOLA, L; LINNA, S.-L et al.Clinical genetics. 1985, Vol 27, Num 3, pp 252-257, issn 0009-9163Article

Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyprolineNÄNTÖ-SALONEN, K; AUTIO, S; NÄRÖ, E et al.Journal of inherited metabolic disease. 1984, Vol 7, Num 3, pp 117-121, issn 0141-8955Article

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