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Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2004
Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentationNorman Kock, Meike Kasten, Birgitt Schüle, et al.
International Journal of Molecular Sciences|April 25, 2019
The Histone Deacetylase Inhibitor Suberoylanilide Hydroxamic Acid (SAHA) Restores Cardiomyocyte Contractility in a Rat Model of Early DiabetesLeonardo Bocchi, Benedetta M Motta, Monia Savi, et al.
Parkinsonism & Related Disorders|July 19, 2017
Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriersAnne Weissbach, Inke R König, Katja Hückelheim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Nonmotor symptoms in Parkin gene-related parkinsonismGeorg Kägi, Christine Klein, Nicholas W Wood, et al.
International Journal of Molecular Sciences|November 11, 2022
Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in <i>SZT2</i> GeneCecilia Cattelani, Ingrid Battistella, Francesca Di Leva, et al.
Stem Cell Research|September 17, 2018
Derivation of human induced pluripotent stem cell line EURACi004-A from skin fibroblasts of a patient with Arrhythmogenic Cardiomyopathy carrying the heterozygous PKP2 mutation c.2569_3018del50Benedetta Ermon, Claudia B Volpato, Giada Cattelan, et al.
Neurobiology of Disease|May 21, 2010
Structural imaging in the presymptomatic stage of genetically determined parkinsonismKathrin Reetz, Vera Tadic, Meike Kasten, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 11, 2017
Serum iron level and kidney function: a Mendelian randomization studyFabiola Del Greco M, Luisa Foco, Irene Pichler, et al.
Stem Cell Research|July 23, 2021
Generation and characterization of three human induced pluripotent stem cell lines (EURACi007-A, EURACi008-A, EURACi009-A) from three different individuals of the same family with arrhythmogenic cardiomyopathy (ACM) carrying the plakophillin2 p.N346Lfs*12 mutationViviana Meraviglia, Giada Cattelan, Marzia De Bortoli, et al.
BMJ Open|June 8, 2023
Trends and symptoms of SARS-CoV-2 infection: a longitudinal study on an Alpine population representative sampleGiulia Barbieri, Massimo Pizzato, Martin Gögele, et al.
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