Risk of vascular diseases in patients with dermatitis herpetiformis and coeliac disease: a long-term cohort study von Nilsson, Noora, Leivo, Joonas, Collin, Pekka, Koskinen, Inka, Kaukinen, Katri, Huhtala, Heini, Palmio, Johanna, Reunala, Timo, Hervonen, Kaisa, Salmi, Teea, Pasternack, Camilla

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Risk for hospital-treated infections in dermatitis herpetiformis and coeliac disease von Pasternack, Camilla, Karppelin, Matti, Hervonen, Kaisa, Kaukinen, Katri, Salmi, Teea

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Mortality and causes of death in different celiac disease phenotypes during long-term follow-up von Koskinen, Inka, Hervonen, Kaisa, Huhtala, Heini, Pasternack, Camilla, Salmi, Teea, Reunala, Timo, Collin, Pekka, Kaukinen, Katri

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The risk of renal comorbidities in celiac disease patients depends on the phenotype of celiac disease von Nurmi, Rakel, Pasternack, Camilla, Salmi, Teea, Hervonen, Kaisa, Koskinen, Inka, Järvelin, Jutta, Huhtala, Heini, Collin, Pekka, Mustonen, Jukka, Kaukinen, Katri, Mäkelä, Satu

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Authors' reply: The risk of renal comorbidities in celiac disease patients depends on the phenotype of celiac disease von Nurmi, Rakel, Pasternack, Camilla, Salmi, Teea, Hervonen, Kaisa, Koskinen, Inka, Järvelin, Jutta, Huhtala, Heini, Collin, Pekka, Mustonen, Jukka, Kaukinen, Katri, Mäkelä, Satu

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MO418: The Risk of Renal Co-Morbidities in Celiac Disease Patients Depends on the Phenotype of Celiac Disease von Nurmi, Rakel, Pasternack, Camilla, Salmi, Teea, Hervonen, Kaisa, Koskinen, Inka, Järvelin, Jutta, Huhtala, Heini, Collin, Pekka, Mustonen, Jukka, Kaukinen, Katri, Mäkelä, Satu

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Cancer incidence and factors associated with malignancies in coeliac disease during long‐term follow‐up von Koskinen, Inka, Hervonen, Kaisa, Pukkala, Eero, Reunala, Timo, Kaukinen, Katri, Collin, Pekka

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Risk of vascular diseases in patients with dermatitis herpetiformis and coeliac disease: a long-term cohort study von Nilsson, Noora, Leivo, Joonas, Collin, Pekka, Koskinen, Inka, Kaukinen, Katri, Huhtala, Heini, Palmio, Johanna, Reunala, Timo, Hervonen, Kaisa, Salmi, Teea, Pasternack, Camilla

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Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosis von Gall, Kimberly, Izzo, Emanuela, Seppälä, Eija H, Alakurtti, Kirsi, Koskinen, Lotta, Saarinen, Inka, Singh, Akashdeep, Myllykangas, Samuel, Koskenvuo, Juha, Alastalo, Tero-Pekka

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Genetic Findings from a Multigene Panel for Autoinflammatory Disease von Howell, Victoria, Gall, Kimberly, Scocchia, Alicia, Koskinen, Lotta, Saarinen, Inka, Gentile, Massimiliano, Salmenperä, Pertteli, Paananen, Jussi, Myllykangas, Samuel, Koskenvuo, Juha

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Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 von Gall, Kimberly, Izzo, Emanuela, Seppälä, Eija H, Alakurtti, Kirsi, Koskinen, Lotta, Saarinen, Inka, Singh, Akashdeep, Myllykangas, Samuel, Koskenvuo, Juha, Alastalo, Tero-Pekka

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P622: Genetic results in a cohort of 489 patients with inherited myopathies von Gall, Kim, Hathaway, Julie, Koskinen, Lotta, Alakurtti, Kirsi, Hagström, Äsa, Segura, Monica, Kuisma, Heli, Seppala, Eija, Djupsjöbacka, Janica, Muona, Mikko, Pietila, Tuuli, Salmenperä, Pertteli, Saarinen, Inka, Veeraraghavan, Ray, Myllykangas, Samuel, Koskenvuo, Juha

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PO-01-015 YIELD OF GENETIC TESTING AND RESULT UTILITY IN A COHORT OF 2100 DCM PATIENTS von Heliö, Krista, Hathaway, Julie, Cicerchia, Marcos, Tommiska, Johanna, Huusko, Johanna, Saarinen, Inka, Koskinen, Lotta, Muona, Mikko, Kytölä, Ville, Djupsjobacka, Janica, Gentile, Massimiliano, Salmenperä, Pertteli, Alastalo, Tero-Pekka, Heliö, Tiina, Paananen, Jussi, Myllykangas, Samuel, Koskenvuo, Juha

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P577: Genetic findings in afor cohort of over 1,800 patients tested with a combined cardiomyopathy and arrhythmia panel von Hathaway, Julie, Huusko, Johanna, Cicerchia, Marcos, Ahonen, Saija, Tommiska, Johanna, Gall, Kim, Liaquat, Khalida, Howell, Victoria, Sluyters, Allison, Djupsjöbacka, Janica, Muona, Mikko, Saarinen, Inka, Seppala, Eija, Kangas-Kontio, Tiia, Koskinen, Lotta, Salmenperä, Pertteli, Myllykangas, Samuel, Koskenvuo, Juha

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Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients von Heliö, Krista, Cicerchia, Marcos, Hathaway, Julie, Tommiska, Johanna, Huusko, Johanna, Saarinen, Inka, Koskinen, Lotta, Muona, Mikko, Kytölä, Ville, Djupsjöbacka, Janica, Gentile, Massimiliano, Salmenperä, Pertteli, Alastalo, Tero-Pekka, Steinberg, Christian, Heliö, Tiina, Paananen, Jussi, Myllykangas, Samuel, Koskenvuo, Juha

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Retrospective review of genetic testing for inherited bone marrow failure syndromes von Jacher, Joe, Scocchia, Alicia, Kokkonen, Päivi, Hirvonen, Elina, Mårtensson, Emma, Duzkale, Hatice, Gall, Kim, Powis, Zoe, Saarinen, Inka, Sistonen, Johanna, Koskenvuo, Juha, Koskinen, Lotta, Alastalo, Tero-Pekka

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eP363 - Retrospective review of genetic testing for inherited bone marrow failure syndromes von Jacher, Joe, Scocchia, Alicia, Kokkonen, Päivi, Hirvonen, Elina, Mårtensson, Emma, Duzkale, Hatice, Gall, Kim, Powis, Zoe, Saarinen, Inka, Sistonen, Johanna, Koskenvuo, Juha, Koskinen, Lotta, Alastalo, Tero-Pekka

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P487: Genetic findings from multi-gene panel for primary ciliary dyskinesia von Howell, Victoria, Huusko, Johanna, Bernal, Manuel, Faber, Allison, Valo, Satu, Gall, Kimberly, Koskinen, Lotta, Kangas-Kontio, Tiia, Saarinen, Inka, Kytölä, Ville, Siivonen, Pauli, Djupsjöbacka, Janica, Gentile, Massimiliano, Salmenperä, Pertteli, Paananen, Jussi, Myllykangas, Samuel, Koskenvuo, Juha

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Development of Industrial Internet-Related Asset Management Services with Customers von Ahonen, Toni, Valjakka, Tiina, Lappalainen, Inka, Nuutinen, Maaria

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