Daniel Ebrahimi-Fakhari1, Lilian Lisa Mann2, Martin Poryo3, Norbert Graf4, Rüdiger von Kries5,6, Beate Heinrich6, Darius Ebrahimi-Fakhari7, Marina Flotats-Bastardas2, Ludwig Gortner2, Michael Zemlin2, Sascha Meyer2. 1. Department of Pediatric Neurology, Saarland University Medical Center, Building 9, Kirrberger Strasse, 66421, Homburg, Saarland, Germany. daniel.ebrahimifakhari@uks.eu. 2. Department of Pediatric Neurology, Saarland University Medical Center, Building 9, Kirrberger Strasse, 66421, Homburg, Saarland, Germany. 3. Department of Pediatric Cardiology, Saarland University Medical Center, Homburg, Germany. 4. Department of Pediatric Oncology and Hematology, Saarland University Medical Center, Homburg, Germany. 5. Division of Epidemiology, Institute of Social Pediatrics and Adolescent Medicine, Ludwig Maximilian's University, Munich, Germany. 6. German Paediatric Surveillance Unit (ESPED), Coordination Center for Clinical Studies, Heinrich Heine University, Düsseldorf, Germany. 7. Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Correction to: Orphanet Journal of Rare Diseases (2018) 13:117https://doi.org/10.1186/s13023-018-0870-yWhen calculating the annual incidence rates in article [1], unfortunately an error occurred. The corrected incidence rates should be the following, and the relevant paragraph of the ‘Results’ should therefore correctly read:IncidenceBased on our findings, the annual incidence rate of TSC (definite or possible TSC) is estimated at a minimum of 1:27.312 live births. However correcting for underreporting using data from previous ESPED analyses, the estimated incidence rate of definite or possible TSC is approximately 1:11.180–1:22.360 live births in Germany.
Authors: Camilla Russo; Anna Nastro; Domenico Cicala; Maria De Liso; Eugenio Maria Covelli; Giuseppe Cinalli Journal: Childs Nerv Syst Date: 2020-06-09 Impact factor: 1.475
Authors: Elena Cristina De Sautu De Borbón; Juan Manuel Guerra Vales; Carlos Lumbreras Bermejo; Felix Guerrero Ramos; María José Buj Padilla; Jesús González de la Aleja; Montserrat Morales Conejo Journal: Orphanet J Rare Dis Date: 2021-05-31 Impact factor: 4.123