41 results match your criteria: "Hospital of the Ludwig- Maximilians-University (LMU) Munich[Affiliation]"

Acute Onset of Impaired Consciousness.

Dtsch Arztebl Int

July 2024

Emergency Department, Hospital of the Ludwig-Maximilians-University (LMU) Munich, Munich; Department of Medicine III, Hospital of the Ludwig-Maximilians-University (LMU) Munich, Munich; Interdisciplinary Emergency Department, University Medical Center Regensburg, Regensburg; Department of Neurology, University Medical Center Freiburg, Freiburg; Kinderklinik und Kinderpoliklinik im Dr von Hauner Children's Hospital, Hospital of the Ludwig-Maximilians-University (LMU) Munich, Munich; Department of Neurology, Hospital of the Ludwig-Maximilians-University (LMU) Munich, Munich.

Article Synopsis
  • Patients with sudden impaired consciousness have a high mortality rate, with 10% not surviving, and multiple underlying causes are often found.
  • Impairment is categorized into quantitative (reduced wakefulness) and qualitative (abnormal content), with about 45-50% linked to neurological issues and 20% to metabolic or infectious origins.
  • Quick recognition of warning signs ("red flags") and immediate treatment in a shock room are crucial for managing these medical emergencies.
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Study Design: Retrospective bicentric Cohort Study.

Objective: Posterior (PLIF) and transforaminal lumbar interbody fusion (TLIF) have been clinically proven for the surgical treatment of degenerative spinal disorders. Despite many retrospective studies, the superiority of either technique has not been proven to date.

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Purpose: Hybrid cervical spine surgery (HS) is a novel surgical strategy wherein an artificial disc replacement is done with a cervical fusion nearby with a stand-alone titanium cage to combine the advantages in both procedures. The aim of this study was to evaluate interactions of these devices within the same patient, and to analyze, if the different goal of each implant is accomplished.

Methods: Thirty-six patients were treated surgically within a non-randomized retrospective study framework with HS.

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Research shows the important role of parents' mental health literacy in detecting depressive symptoms and supporting their children to seek professional help. Improving mental health literacy in parents has recently gained even greater importance due to the negative impact of the COVID-19 pandemic on children and adolescents' mental health. The aim of the present experimental pre-post-follow-up study was to examine knowledge change after the reception of contents from an innovative web-based platform ( www.

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Objective: This study aimed to identify sleep clusters based on objective multidimensional sleep characteristics and test their associations with adolescent cardiometabolic health.

Methods: The authors included 1090 participants aged 14.3 to 16.

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Background: Adolescent major depression (MD) is characterized by deficits in emotion regulation (ER). Little is known about the neurophysiological correlates that are associated with these deficits. Moreover, the additional examination of visual attention during ER would allow a more in-depth understanding of ER deficits but has not yet been applied simultaneously.

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Evaluation of an information booklet for adolescents on depression: evidence from a randomized controlled study.

Child Adolesc Psychiatry Ment Health

May 2023

Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Hospital of the Ludwig- Maximilians-University (LMU) Munich, Nussbaumstrasse 5, D-80336, Munich, Germany.

Background: Adolescents with depression often show barriers to seek treatment offers due to various reasons, including limited knowledge about the manifestation of the disorder, its treatment options, or fear of stigmatization. Psychoeducational approaches might reduce these barriers by increasing depression literacy. The aim of the present randomized controlled study was to evaluate whether an innovative and age-appropriate evidence-based information booklet about youth depression increases depression-specific knowledge in adolescents with depression and is also appealing to the target group.

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The role of syllables and morphemes in silent reading: An eye-tracking study.

Q J Exp Psychol (Hove)

November 2023

School of Psychological Sciences and Macquarie Centre for Reading, Macquarie University, Sydney, NSW, Australia.

Article Synopsis
  • German skilled readers use both morphological and syllable processing when recognizing words, but the importance of each is unclear.
  • A study using eye-tracking technology examined whether readers preferred syllables or morphemes by visually marking words with color changes or hyphens at different boundaries.
  • Results showed no change in eye movements with color alternation, but hyphens that disrupted syllables slowed reading more than those disrupting morphemes, indicating a greater reliance on syllable structure in reading.
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Background: Molecular measurements of the genome, the transcriptome, and the epigenome, often termed multi-omics data, provide an in-depth view on biological systems and their integration is crucial for gaining insights in complex regulatory processes. These data can be used to explain disease related genetic variants by linking them to intermediate molecular traits (quantitative trait loci, QTL). Molecular networks regulating cellular processes leave footprints in QTL results as so-called trans-QTL hotspots.

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Evaluation of a Web-based Information Platform for Youths on Mental Health During the COVID-19 Pandemic.

Child Psychiatry Hum Dev

June 2024

Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Hospital of the Ludwig-Maximilians-University (LMU) Munich, Nußbaumstr. 5, D-80336, Munich, Germany.

During the corona pandemic, youths were confronted with substantial challenges and in urgent need of information on how to prevent mental health problems. This experimental pre-post-follow-up study examined the efficacy and reception of an innovative website ( www.corona-und-du.

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Background: Variants in genes of the nucleotide excision repair (NER) pathway have been associated with heterogeneous clinical presentations ranging from xeroderma pigmentosum to Cockayne syndrome and trichothiodystrophy. NER deficiencies manifest with photosensitivity and skin cancer, but also developmental delay and early-onset neurological degeneration. Adult-onset neurological features have been reported in only a few xeroderma pigmentosum cases, all showing at least mild skin manifestations.

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Potential uses of assistive robotic systems in acute inpatient care were defined based on the Framework for Complex Interventions developed by the Medical Research Council (MRC). This process of definition requires the consideration of personal-related and contextual factors.

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Objectives: To assess the clinical and radiological outcomes after ACDF with 3D printed cellular titanium cages filled with bone marrow and to compare the clinical and radiological results with the current scientific literature.

Methods: ACDF was performed monosegmentally under standardized conditions. X-rays were analyzed to determine the range of motion, fusion rates, and subsidence preoperatively and 3 and 12 months postoperatively.

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ExomeChip-based rare variant association study in restless legs syndrome.

Sleep Med

June 2022

Institute of Neurogenomics, Helmholtz Zentrum München - German Research Centre for Environmental Health, Neuherberg, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany; Institute of Human Genetics, School of Medicine, Technische Universität München, Munich, Germany. Electronic address:

Restless legs syndrome (RLS) is a common sleep-related movement disorder in populations of European descent and disease risk is strongly influenced by genetic factors. Common variants have been assessed extensively in several genome-wide association studies, but the contribution of rarer genetic variation has not been investigated at this scale. We therefore genotyped a case-control set of 9246 individuals for mainly rare and low frequency exonic variants using the Illumina ExomeChip.

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Adolescent major depression (MD) is associated with impaired emotion regulation. However, results on cognitive reappraisal (CR) are mixed. Investigation of gaze behavior during CR allows a more thorough understanding of intact and deviant CR processes in MD.

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Introduction: Depressive symptoms are highly prevalent in adolescence, highlighting the need for early identification of precursors. Research into psychopathological symptoms predicting depressive psychopathology in adolescents is therefore of great relevance. Moreover, given that the prevalence of depressive symptomatology in adolescence shows marked differences between girls and boys, insight into potential sex-specific differences in precursors is important.

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In adolescence, both major depression (MD) and anorexia nervosa (AN) are associated with deficits in emotion regulation (ER). However, studies have yet to compare ER profiles within the disorders and the effect of comorbid MD+AN is unclear. This study examined the habitual use of ER in 229 girls, aged 12-18 years, with MD (n = 84), AN (n = 37), comorbid MD+AN (n = 25), and healthy girls (n = 83).

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Article Synopsis
  • Brugada syndrome (BrS) is a serious heart condition linked to sudden death in young adults, with few known genetic factors beyond the SCN5A gene.
  • A large study involving 2,820 BrS cases and 10,001 controls revealed 21 genetic signals across 12 locations, suggesting a strong genetic component to the disorder.
  • Key findings highlight the importance of transcription regulation in BrS development and introduce microtubule-related mechanisms that affect the expression of a key cardiac protein, shedding light on the disorder's genetic and molecular basis.
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CD4 T cells play an important role in the immune response against cancer and infectious diseases. However, mechanistic details of their helper function in hepatitis B virus (HBV) infection in particular, or their advantage for adoptive T cell therapy remain poorly understood as experimental and therapeutic tools are missing. Therefore, we identified, cloned, and characterized a comprehensive library of 20 MHC class II-restricted HBV-specific T cell receptors (TCRs) from donors with acute or resolved HBV infection.

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It is still unclear how genetic information, provided as single-nucleotide polymorphisms (SNPs), can be most effectively integrated into risk prediction models for coronary heart disease (CHD) to add significant predictive value beyond clinical risk models. For the present study, a population-based case-cohort was used as a trainingset (451 incident cases, 1488 noncases) and an independent cohort as testset (160 incident cases, 2749 noncases). The following strategies to quantify genetic information were compared: A weighted genetic risk score including Metabochip SNPs associated with CHD in the literature (GRS ); selection of the most predictive SNPs among these literature-confirmed variants using priority-Lasso (PL ); validation of two comprehensive polygenic risk scores: GRS based on Metabochip data, and GRS (available in the testset only) based on cross-validated genome-wide genotyping data.

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A scoping review was prepared in the first study phase of the REsPonSe project. The objective was to gain an overview of existing literature and available evidence on the subject of service robotics in nursing care. The systematic literature search took place using the following databases: PubMed, CINAHL, Cochrane, Web of Science and IEEE Xplore.

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This scoping review gives an overview of current research activities in the field of very early mobilization with robotic devices of intensive care patients. It presents the effect of very early, robot-assisted mobilization on intensive care patients based on their outcomes.

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Upon activation, neutrophils release neutrophil extracellular traps (NETs), which contribute to circulating DNA burden and thrombosis, including ST-segment elevation myocardial infarction (STEMI). Deoxyribonuclease (DNase) 1 degrades circulating DNA and NETs. Lower DNase activity correlates with NET burden and infarct size.

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Cis-epistasis at the LPA locus and risk of cardiovascular diseases.

Cardiovasc Res

March 2022

Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen, Technische Universität München, 80636 Munich, Germany.

Aims: Coronary artery disease (CAD) has a strong genetic predisposition. However, despite substantial discoveries made by genome-wide association studies (GWAS), a large proportion of heritability awaits identification. Non-additive genetic effects might be responsible for part of the unaccounted genetic variance.

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