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Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz, ISSN 1436-9990, 7/2016, Volume 59, Issue 7, pp. 821 - 826
Die Karenz gegenüber Weizen, Gluten und anderen Getreideprodukten ist heute ein zunehmendes Phänomen in industrialisierten Ländern. Die diagnostischen... 
Food allergy | Public Health | General Practice / Family Medicine | Reizdarmsyndrom | Nicht-Zöliakie-Glutensensitivität (NZGS) | Celiac disease | Medicine & Public Health | Zöliakie | Non-celiac disease gluten sensitivity | Wheat | Irritable bowel syndrome (IBS) | Weizen | Nahrungsmittelallergie
Journal Article
Zeitschrift für Epileptologie, ISSN 1617-6782, 11/2019, Volume 32, Issue 4, pp. 326 - 338
Ziel der prospektiven, multizentrischen Studie ist die Erfassung klinischer Charakteristika, des Ressourcenverbrauches sowie der Lebensqualität bei Patienten... 
Anfall | Neurology | Antikonvulsiva | Severe Myoclonic Epilepsy of Infants | Anticonvulsants | Medicine & Public Health | Epilepsie | Epilepsy | Seizure | Status epilepticus
Journal Article
Genetics in Medicine, ISSN 1098-3600, 01/2018, Volume 20, Issue 1, pp. 98 - 108
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 26, pp. 2542 - 2552
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2015, Volume 10, Issue 3, p. e0120075
Capillary leak in severe sepsis involves disruption of endothelial cell tight junctions. We modeled this process by TNF treatment of cultured human dermal... 
ACTIVATION | CELL JUNCTIONS | PERMEABILITY | MYOSIN | PROTEIN-KINASE | MULTIDISCIPLINARY SCIENCES | VASCULAR INTEGRITY | RHO-KINASE | SEPTIC SHOCK | INJURY | LIGHT-CHAIN PHOSPHORYLATION | Endothelium, Vascular - cytology | Tight Junctions - metabolism | RNA, Small Interfering - genetics | Phosphorylation | Dermis - metabolism | Human Umbilical Vein Endothelial Cells - metabolism | Myosin-Light-Chain Kinase - metabolism | Humans | Cells, Cultured | Claudin-5 - metabolism | Cell Membrane Permeability | rho-Associated Kinases - genetics | NF-kappa B - metabolism | rho-Associated Kinases - antagonists & inhibitors | Tumor Necrosis Factor-alpha - pharmacology | Signal Transduction - drug effects | rho-Associated Kinases - metabolism | Endothelium, Vascular - metabolism | Human Umbilical Vein Endothelial Cells - cytology | Myosin Light Chains - metabolism | Dermis - cytology | Microscopy, Fluorescence | Chains | Biology | Kinases | Proteins | Actin | Myosin | Tumor necrosis factor-TNF | Localization | NF-κB protein | Cytokines | Tight junctions | Cloning | Cortex | Electrical resistance | siRNA | Permeability | Substrates | Endothelial cells | Rho-associated kinase | Medicine | Protein kinase | Tumor necrosis factor | Cell death | Sepsis | Skin | Microvasculature | Immunofluorescence | Umbilical vein | Electrical junctions
Journal Article
Journal of Neurosurgery, ISSN 0022-3085, 07/2016, Volume 125, Issue 1, pp. 17 - 23
OBJECTIVE Radiation necrosis (RN), or its imaging equivalent, treatment-related imaging changes (TRIC), is an inflammatory reaction to high-dose radiation in... 
Stereotactic radiosurgery | Oncology | Brain metastases | Immunotherapy | Radiation necrosis | SURGERY | RISK-FACTORS | brain metastases | immunotherapy | INJURY | radiation necrosis | PARAMETERS | TUMORS | oncology | CLINICAL NEUROLOGY | stereotactic radiosurgery
Journal Article
Annals of Clinical and Translational Neurology, ISSN 2328-9503, 04/2019, Volume 6, Issue 4, pp. 655 - 668
Objective FOXG1 syndrome is a rare neurodevelopmental disorder associated with heterozygous FOXG1 variants or chromosomal microaberrations in 14q12. The study... 
MIGRATION | FORNIX | CORPUS-CALLOSUM | TELENCEPHALON | DISORDER | CONGENITAL VARIANT | MUTATIONS | EXPRESSION | ASSOCIATION | NEUROSCIENCES | CLINICAL NEUROLOGY | OLIGODENDROCYTE
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 06/2011, Volume 48, Issue 6, pp. 396 - 406
Journal Article
Human Genetics, ISSN 0340-6717, 04/2017, Volume 136, Issue 4, pp. 463 - 479
Journal Article
Annals of Clinical and Translational Neurology, ISSN 2328-9503, 04/2019, Volume 6, Issue 4, pp. 655 - 668
ObjectiveFOXG1 syndrome is a rare neurodevelopmental disorder associated with heterozygous FOXG1 variants or chromosomal microaberrations in 14q12. The study... 
Datasets | Genotype & phenotype | Pediatrics | Medical imaging | Genes | Mutation | Patients
Journal Article
World Journal of Emergency Surgery, ISSN 1749-7922, 05/2017, Volume 12, Issue 1, pp. 22 - 31
Journal Article