Personnel well-being and potentially traumatic COVID-19 pandemic related events (PTES) in the hus helsinki university hospital – baseline results von Laukkala, T., Haravuori, H., Tuisku, K., Junttila, K., Haapa, T., Kujala, A., Pukkala, E., Suvisaari, J., Rosenström, T., Jylhä, P.

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Zaspopathy in a large classic late-onset distal myopathy family von Griggs, R., Vihola, A., Hackman, P., Talvinen, K., Haravuori, H., Faulkner, G., Eymard, B., Richard, I., Selcen, D., Engel, A., Carpen, O., Udd, B.

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Secondary calpain3 deficiency in 2q-linked muscular dystrophy titin is the candidate gene von HARAVUORI, H, VIHOLA, A, BECKMANN, J. S, UDD, B, STRAUB, V, AURANEN, M, RICHARD, I, MARCHAND, S, VOIT, T, LABEIT, S, SOMER, H, PELTONEN, L

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Tibial Muscular Dystrophy Is a Titinopathy Caused by Mutations in TTN, the Gene Encoding the Giant Skeletal-Muscle Protein Titin von Hackman, Peter, Vihola, Anna, Haravuori, Henna, Marchand, Sylvie, Sarparanta, Jaakko, de Seze, Jerome, Labeit, Siegfried, Witt, Christian, Peltonen, Leena, Richard, Isabelle, Udd, Bjarne

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A distinct phenotype of distal myopathy in a large Finnish family von MAHJNEH, I, HARAVUORI, H, PAETAU, A, ANDERSON, L. V. B, SAARINEN, A, UDD, B, SOMER, H

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Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases von Siitonen, H. Annika, Kopra, Outi, Kääriäinen, Helena, Haravuori, Henna, Winter, Robin M., Säämänen, Anna-Marja, Peltonen, Leena, Kestilä, Marjo

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The first European family with tibial muscular dystrophy outside the Finnish population von DE SEZE, J, UDD, B, VERMERSCH, P, HARAVUORI, H, SABLONNIERE, B, MAURAGE, C. A, HURTEVENT, J. F, BOUTRY, N, STOJKOVIC, T, SCHRAEN, S, PETIT, H

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Pharmaceutical industry interactions of psychiatric trainees from 20 European countries von Riese, F, Guloksuz, S, Roventa, C, Fair, J D, Haravuori, H, Rolko, T, Flynn, D, Giacco, D, Banjac, V, Jovanovic, N, Bayat, N, Palumbo, C, Rusaka, M, Kilic, O, Augėnaitė, J, Nawka, A, Zenger, M, Kekin, I, Wuyts, P, Barrett, E, Bausch-Becker, N, Mikaliūnas, J, Del Valle, E, Feffer, K, Lomax, G A, Marques, J G, Jauhar, S

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Assignment of the Tibial Muscular Dystrophy Locus to Chromosome 2q31 von Haravuori, Henna, Mäkelä-Bengs, Päivi, Udd, Bjarne, Partanen, Juhani, Pulkkinen, Leena, Somer, Hannu, Peltonen, Leena

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Zaspopathy in a large classic late-onset distal myopathy family. Commentary von GRIGGS, R, VIHOLA, A, CARPEN, O, UDD, B, LAING, Nigel G, BLOCK, B, HACKMAN, P, TALVINEN, K, HARAVUORI, H, FAULKNER, G, EYMARD, B, RICHARD, I, SELCEN, D, ENGEL, A

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Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3) von Haravuori, Henna, Annika Siitonen, H., Mahjneh, Ibrahim, Hackman, Peter, Lahti, Laura, Somer, Hannu, Peltonen, Leena, Kestilä, Marjo, Udd, Bjarne

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Tibial muscular dystrophy – from clinical description to linkage on chromosome 2q31 von Udd, Bjarne, Haravuori, Henna, Kalimo, Hannu, Partanen, Juhani, Pulkkinen, Leena, Paetau, Anders, Peltonen, Leena, Somer, Hannu

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