TUIJA LöPPöNEN

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Publications

• Kaustio, Meri; Nayebzadeh, Naemeh; Hinttala, Reetta; Tapiainen, Terhi; Åström, Pirjo; Mamia, Katariina; Pernaa, Nora; Lehtonen, Johanna; Glumoff, Virpi; Rahikkala, Elisa; Olsén, Päivi; Hassinen, Antti; Polso, Minttu; Sukaiti, Nashat AL.; Alshekaili, Jalila; Al Kindi, Mahmood; Al Hashmi, Nadia; Almusa, Henrikki; Bulanova, Daria; Haapaniemi, Emma et al. [incl. Renko, Marjo; Löppönen, Tuija]. 2021. Loss of DIAPH1 causes SCBMS, combined immunodeficiency and mitochondrial dysfunction Journal of allergy and clinical immunology 148 2: 599-611. 2021
• Karvonen, Marjo; Saari, Antti; Lamidi, Marja-Leena; Selander, Tuomas; Löppönen, Yuija; Lönnqvist, Tuula; Dunkel, Leo; Sankilampi, Ulla. 2020. Screening of hydrocephalus in infants using either WHO or population-based head circumference reference charts Acta paediatrica 2021; 110 3: 881-888. 2020
• Tommiska, V; Lano, A; Kleemola, P; Klenberg, L; Lehtonen, L; Löppönen, T; Olsen, P; Tammela, O; Fellman, V. 2020. Analysis of neurodevelopmental outcomes of preadolescents born with extremely low weight revealed impairments in multiple developmental domains despite absence of cognitive impairment Health science reports 3 3: e180. 2020
• Kröger, L; Löppönen, T; Ala-Kokko, L; Kröger, H; Jauhonen, HM; Lehti, K; Jääskeläinen, J. 2019. A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy Molecular genetics & genomic medicine 7 8: e802. 2019
• Löppönen, Tuija; Mäenpää, Helena; Peltonen, Jari; Ahonen, Matti; Kiviranta, Tuula. 2018. CP-lasten ja -nuorten systemaattinen lonkkaseuranta puuttuu Suomesta Lääkärilehti 73 15: 931-938. 2018