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Carola Saloranta

1987 …2019
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International and National Collaboration Publications and projects within past five years.

Publications 1987 2019

SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy

Hakonen, A. H., Polvi, A., Saloranta, C., Paetau, A., Heikkilä, P., Almusa, H., Ellonen, P., Jakkula, E., Saarela, J. & Aittomäki, K., Jul 2019, In : American Journal of Medical Genetics. Part A. 179, 7, p. 1362-1365 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Geneettisen analytiikan mahdollisuudet sikiödiagnostiikassa

Salminen, E., Saloranta, C. & Laivuori, H., 2018, In : Duodecim. 134, 4, p. 383-390 8 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

Open Access
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Fetal left ventricular noncompaction cardiomyopathy and fatal outcome due to complete deficiency of mitochondrial trifunctional protein

Ojala, T., Nupponen, I., Saloranta, C., Sarkola, T., Sekar, P., Breilin, A. & Tyni, T., Dec 2015, In : European journal of pediatrics. 174, 12, p. 1689-1692 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Periderm prevents pathological epithelial adhesions during embryogenesis

Richardson, R. J., Hammond, N. L., Coulombe, P. A., Saloranta, C., Nousiainen, H. O., Salonen, R., Berry, A., Hanley, N., Headon, D., Karikoski, R. & Dixon, M. J., Sep 2014, In : Journal of Clinical Investigation. 124, 9, p. 3891-3900 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Spectrum of Mutations in the Renin-Angiotensin System Genes in Autosomal Recessive Renal Tubular Dysgenesis

Gribouval, O., Moriniere, V., Pawtowski, A., Arrondel, C., Sallinen, S-L., Saloranta, C., Clericuzio, C., Viot, G., Tantau, J., Blesson, S., Cloarec, S., Machet, M. C., Chitayat, D., Thauvin, C., Laurent, N., Sampson, J. R., Bernstein, J. A., Clemenson, A., Prieur, F., Daniel, L. & 35 othersLevy-Mozziconacci, A., Lachlan, K., Alessandri, J. L., Cartault, F., Riviere, J. P., Picard, N., Baumann, C., Delezoide, A. L., Belar Ortega, M., Chassaing, N., Labrune, P., Yu, S., Firth, H., Wellesley, D., Bitzan, M., Alfares, A., Braverman, N., Krogh, L., Tolmie, J., Gaspar, H., Doray, B., Majore, S., Bonneau, D., Triau, S., Loirat, C., David, A., Bartholdi, D., Peleg, A., Brackman, D., Stone, R., DeBerardinis, R., Corvol, P., Michaud, A., Antignac, C. & Gubler, M. C., 2012, In : Human Mutation. 33, 2, p. 316-326 11 p.

Research output: Contribution to journalArticleScientificpeer-review