The economics of renewable CaC2 and C2H2 production from biomass and CaO von Pääkkönen, A., Tolvanen, H., Kokko, L.

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Concomitant head or neck injury increases risk of traumatic brain injury in facial fracture patients von Kokko, L., Snäll, J., Puolakkainen, T., Piippo-Karjalainen, A., Suominen, A., Thorén, H.

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The Collagenopathies: Review of Clinical Phenotypes and Molecular Correlations von Jobling, Rebekah, D’Souza, Rohan, Baker, Naomi, Lara-Corrales, Irene, Mendoza-Londono, Roberto, Dupuis, Lucie, Savarirayan, Ravi, Ala-Kokko, L., Kannu, Peter

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Avascular necrosis of the femoral head due to a novel C propeptide mutation in COL2A1 von Kannu, Peter, O'Rielly, D.D., Hyland, J.C., Kokko, L. Ala

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Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis von Taipale, M, Jakkula, E, Kämäräinen, O.-P, Gao, P, Skarp, S, Barral, S, Kiviranta, I, Kröger, H, Ott, J, Wei, G.-H, Ala-Kokko, L, Männikkö, M

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Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis von Noponen-Hietala, N, Kyllönen, E, Männikkö, M, Ilkko, E, Karppinen, J, Ott, J, Ala-Kokko, L

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Genome-wide scan for schizophrenia in the Finnish population : evidence for a locus on chromosome 7q22 von EKELUND, J, LICHTERMANN, D, LÖNNQVIST, J, PELTONEN, L, HOVATTA, I, ELLONEN, P, SUVISAARI, J, TERWILLIGER, J. D, JUVONEN, H, VARILO, T, ARAJÄRVL, R, KOKKO-SAHIN, M.-L

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A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders von Gensure, Robert C, Mäkitie, Outi, Barclay, Catherine, Chan, Catherine, Depalma, Steven R, Bastepe, Murat, Abuzahra, Hilal, Couper, Richard, Mundlos, Stefan, Sillence, David, Ala Kokko, Leena, Seidman, Jonathan G, Cole, William G, Jüppner, Harald

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Phenotypic and population differences in the association between CILP and lumbar disc disease von Virtanen, I M, Song, Y Q, Cheung, K M C, Ala-Kokko, L, Karppinen, J, Ho, D W H, Luk, K D K, Yip, S P, Leong, J C Y, Cheah, K S E, Sham, P, Chan, D

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The role of sequence variations within the genes encoding collagen II, IX and XI in non-syndromic, early-onset osteoarthritis von Jakkula, E., Melkoniemi, M., Kiviranta, I., Lohiniva, J., Räinä, S.S., Perälä, M., Warman, M.L., Ahonen, K., Kröger, H., Göring, H.H.H., Ala-Kokko, L.

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The effect of age and density of the breast on the sensitivity of breast cancer diagnostic by mammography and ultasonography von SAARENMAA, Irma, SALMINEN, Tiina, KÄRKKÄINEN, Alpo, PAKKANEN, Juhani, PELTONEN, Pirkko, PIIRONEN, Anneli, SALO, Anja, TALVIALA, Marja-Liisa, HAKAMA, Matti, GEIGER, Ulla, HEIKKINEN, Pirkko, HYVÄRINEN, Seppo, ISOLA, Jorma, KATAJA, Vesa, KOKKO, Marja-Liisa, KOKKO, Riitta, KUMPULAINEN, Eero

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Clinical assessment of spinal mobility measurements in ankylosing spondylitis: a compact set for follow-up and trials? von Viitanen, J V, Heikkilä, S, Kokko, M L, Kautiainen, H

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Association between sequence variations in genes encoding human zona pellucida glycoproteins and fertilization failure in IVF von Männikkö, M., Törmälä, R.-M., Tuuri, T., Haltia, A., Martikainen, H., Ala-Kokko, L., Tapanainen, J.S., Lakkakorpi, J.T.

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Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions von Körkkö, J, Kaitila, I, Lönnqvist, L, Peltonen, L, Ala-Kokko, L

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Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set von HOVATTA, I, LICHTERMANN, D, JUVONEN, H, SUVISAARI, J, TERWILLIGER, J. D, ARAJÄRVI, R, KOKKO-SAHIN, M.-L, EKELUND, J, LÖNNQVIST, J, PELTONEN, L

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A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci von Hovatta, Iiris, Varilo, Teppo, Suvisaari, Jaana, Terwilliger, Joseph D., Ollikainen, Vesa, Arajärvi, Ritva, Juvonen, Hannu, Kokko-Sahin, Marja-Liisa, Väisänen, Leena, Mannila, Heikki, Lönnqvist, Jouko, Peltonen, Leena

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Aggrecan core protein of a certain length is protective against hand osteoarthritis von Kämäräinen, O.-P., Solovieva, S., Vehmas, T., Luoma, K., Leino-Arjas, P., Riihimäki, H., Ala-Kokko, L., Männikkö, M.

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Genetic risk factors for lumbar disc disease von Ala-Kokko, Leena

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Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen von Di Lullo, Gloria A., Sweeney, Shawn M., Körkkö, Jarmo, Ala-Kokko, Leena, San Antonio, James D.

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Missense mutations in the β strands of the single A-domain of matrilin-3 result in multiple epiphyseal dysplasia von Jackson, G C, Barker, F S, Jakkula, E, Czarny-Ratajczak, M, Mäkitie, O, Cole, W G, Wright, M J, Smithson, S F, Suri, M, Rogala, P, Mortier, G R, Baldock, C, Wallace, A, Elles, R, Ala-Kokko, L, Briggs, M D

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