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  1. Article

    Open Access

    A multicenter, matched case–control analysis comparing burden of illness among patients with tuberous sclerosis complex related epilepsy, generalized idiopathic epilepsy, and focal epilepsy in Germany

    Depending on the underlying etiology and epilepsy type, the burden of disease for patients with seizures can vary significantly. This analysis aimed to compare direct and indirect costs and quality of life (Qo...

    Lisa Lappe, Christoph Hertzberg, Susanne Knake in Neurological Research and Practice (2024)

  2. Article

    Open Access

    Trends of mortality rate in patients with congenital heart defects in Germany—analysis of nationwide data of the Federal Statistical Office of Germany

    Congenital heart defects (CHD) are still associated with an increased morbidity and mortality. The aim of this study was to analyze trends of mortality rates in patients with CHD between 1998 and 2018 in Germany.

    Hashim Abdul-Khaliq, Delphina Gomes, Sascha Meyer in Clinical Research in Cardiology (2024)

  3. Article

    Open Access

    Standardized Treatment and Diagnostic Approach to Reduce Disease burden in the early postoperative phase in children with congenital heart defects—STANDARD study: a pilot randomized controlled trial

    To explore the effect of a daily goal checklist on pediatric cardiac intensive care unit (PCICU) length of stay (LOS) after congenital heart surgery. This study is a prospective randomized single-center study....

    Antonia Vogt, Sascha Meyer, Hans-Joachim Schäfers in European Journal of Pediatrics (2023)

  4. Article

    Open Access

    Expression of TRAIL, IP-10, and CRP in children with suspected COVID-19 and real-life impact of a computational signature on clinical decision-making: a prospective cohort study

    We evaluated the host-response marker score “BV” and its components TRAIL, IP-10, and CRP in SARS-CoV-2 positive children, and estimated the potential impact on clinical decision-making.

    Franziska Fröhlich, Benjamin Gronwald, Johannes Bay, Arne Simon, Martin Poryo in Infection (2023)

  5. Article

    Open Access

    Staffing, skill mix, shortage, and survival in the NICU and PICU: pediatrics quo vadis?

    Sascha Meyer, Johannes Pelé Bay, Martin Poryo in European Journal of Pediatrics (2023)

  6. No Access

    Article

    Pseudotumor cerebri bei Kindern und Jugendlichen am Universitätsklinikum des Saarlandes: Eine retrospektive Studie

    Beim Pseudotumor cerebri (PTC) handelt es sich um eine seltene Erkrankung mit intrakranieller Druckerhöhung unbekannter Ätiologie. Ziel der vorliegenden Untersuchung war es, ein einheitliches Diagnose- und The...

    Melanie Freudenberg, Marina Flotats-Bastardas in Wiener Medizinische Wochenschrift (2023)

  7. Article

    Open Access

    Hydrops fetalis with isolated massive ascites in a preterm neonate with rhesus disease

    Significant progress in prenatal care has decreased the incidence of rhesus incompatibility, which may result in hemolytic disease of the fetus and newborn (HDFN). This case report describes an unusual present...

    Nasenien Nourkami-Tutdibi MD, Martina Geipel in Wiener Medizinische Wochenschrift (2022)

  8. Article

    Open Access

    Pott-Puffy-Tumor: die Notwendigkeit einer interdisziplinären Diagnostik und Behandlung

    Der Pott-Puffy-Tumor (PPT) stellt als bakterielle Infektion des Sinus frontalis mit subperiostaler und intrakranieller Abszessbildung eine seltene Erkrankung in der Pädiatrie dar. Nachfolgend präsentieren wir ...

    Dr. med. Jan Philipp Kühn, Stefan Linsler, Nasenien Nourkami-Tutdibi, Sascha Meyer in HNO (2022)

  9. Article

    Open Access

    Pott’s puffy tumor: a need for interdisciplinary diagnosis and treatment

    Pott’s puffy tumor (PPT) is an infection of the frontal sinus with subperiosteal and intracranial abscess formation and one of the rare entities in pediatrics. We present a series of four cases of PPT that occ...

    Dr. med. Jan Philipp Kühn, Stefan Linsler, Nasenien Nourkami-Tutdibi, Sascha Meyer in HNO (2022)

  10. Article

    Open Access

    COVID-19: fighting the foe with Virchow

    Cihan Papan, Katharina Last, Sascha Meyer in Infection (2021)

  11. Article

    Open Access

    Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients’ Perspectives

    The approval of everolimus (EVE) for the treatment of angiomyolipoma (2013), subependymal giant cell astrocytoma (2013) and drug-refractory epilepsy (2017) in patients with tuberous sclerosis complex (TSC) rep...

    Laurent M. Willems, Felix Rosenow, Susanne Schubert-Bast, Gerhard Kurlemann in CNS Drugs (2021)

  12. Article

    Open Access

    Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany

    Tuberous sclerosis complex (TSC) is a monogenetic, multisystemic disease characterised by the formation of benign tumours that can affect almost all organs, caused by pathogenic variations in TSC1 or TSC2. In thi...

    Johann Philipp Zöllner, Nadine Conradi in Neurological Research and Practice (2021)

  13. Article

    Open Access

    Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study

    Tuberous sclerosis complex (TSC), a multisystem genetic disorder, affects many organs and systems, characterized by benign growths. This German multicenter study estimated the disease-specific costs and cost-d...

    Janina Grau, Johann Philipp Zöllner in Orphanet Journal of Rare Diseases (2021)

  14. Article

    Open Access

    Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature

    Tuberous sclerosis complex (TSC) is a monogenetic, multisystem disorder characterized by benign growths due to TSC1 or TSC2 mutations. This German multicenter study estimated the costs and related cost drivers as...

    Johann Philipp Zöllner, Janina Grau, Felix Rosenow in Orphanet Journal of Rare Diseases (2021)

  15. Article

    Hygienestandards auf einer neonatologischen Intensivstation

    In diesem Beitrag werden einige Besonderheiten der Infektionsprävention bei intensivmedizinisch behandelten Früh und Neugeborenen dargestellt. Ergänzend finden sich Hinweise zum krankenhaushygienischen Managem...

    Prof. Dr. Arne Simon, Michael Zemlin, Martina Geipel, Barbara Gärtner in Der Gynäkologe (2021)

  16. Article

    Open Access

    Expertenempfehlung: Therapie nichtgehfähiger Patienten mit Muskeldystrophie Duchenne

    Die Muskeldystrophie Duchenne (DMD) ist die häufigste genetische neuromuskuläre Krankheit im Kindesalter, bei der es meist im Alter von 9 bis 11 Jahren zum Verlust der Gehfähigkeit kommt.

    Guenther Bernert, Andreas Hahn, Cornelia Köhler, Sascha Meyer in Der Nervenarzt (2021)

  17. Article

    Open Access

    Application of two different nasal CPAP levels for the treatment of respiratory distress syndrome in preterm infants—“The OPTTIMMAL-Trial”—Optimizing PEEP To The IMMAture Lungs: study protocol of a randomized controlled trial

    Nasal continuous positive airway pressure (CPAP) applies positive end-expiratory pressure (PEEP) and has been shown to reduce the need for intubation and invasive mechanical ventilation in very low birth weigh...

    Markus Waitz, Corinna Engel, Rolf Schloesser, Ulrich Rochwalsky, Sascha Meyer in Trials (2020)

  18. Article

    Open Access

    Correction to: Incidence of tuberous sclerosis and age at first diagnosis: new data and emerging trends from a national, prospective surveillance study

    .

    Daniel Ebrahimi-Fakhari, Lilian Lisa Mann in Orphanet Journal of Rare Diseases (2019)

  19. Article

    Open Access

    Incidence of tuberous sclerosis and age at first diagnosis: new data and emerging trends from a national, prospective surveillance study

    Tuberous Sclerosis Complex (TSC) is a rare multisystem disorder. In 2012 diagnostic criteria for TSC were revised. However, data on the incidence of TSC are limited.

    Daniel Ebrahimi-Fakhari, Lilian Lisa Mann in Orphanet Journal of Rare Diseases (2018)

  20. No Access

    Article

    An unusual cause of vertigo and headache in childhood

    Spinal perimedullary arteriovenous fistulas (PMAVFs) are rare entities among vascular malformations of the spinal cord. Due to progressive myelopathy, spastic paresis, sensory disturbance, and bowl and bladder...

    Ruben Mühl-Benninghaus, Heiko Körner, Umut Yilmaz in Wiener Medizinische Wochenschrift (2017)

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