0000000000674449

AUTHOR

Philipp G. Sämann

showing 2 related works from this author

Automated segmentation of changes in FLAIR-hyperintense white matter lesions in multiple sclerosis on serial magnetic resonance imaging

2019

Longitudinal analysis of white matter lesion changes on serial MRI has become an important parameter to study diseases with white-matter lesions. Here, we build on earlier work on cross-sectional lesion segmentation; we present a fully automatic pipeline for serial analysis of FLAIR-hyperintense white matter lesions. Our algorithm requires three-dimensional gradient echo T1- and FLAIR- weighted images at 3 Tesla as well as available cross-sectional lesion segmentations of both time points. Preprocessing steps include lesion filling and intrasubject registration. For segmentation of lesion changes, initial lesion maps of different time points are fused; herein changes in intensity are analyz…

AdultMaleMultiple SclerosisCognitive Neuroscience610Fluid-attenuated inversion recoverylcsh:Computer applications to medicine. Medical informaticscomputer.software_genrelcsh:RC346-429050105 experimental psychologyCohort StudiesWhite matterLesionYoung Adult03 medical and health sciences0302 clinical medicineSørensen–Dice coefficientVoxelmedicineHumans0501 psychology and cognitive sciencesRadiology Nuclear Medicine and imagingSegmentationLongitudinal Studieslcsh:Neurology. Diseases of the nervous systemmedicine.diagnostic_testbusiness.industry05 social sciencesRegular ArticleMagnetic resonance imagingLesion segmentation; Magnetic resonance imaging; Multiple sclerosis; White matter lesionsMiddle AgedMagnetic Resonance ImagingHyperintensityddc:Cross-Sectional Studiesmedicine.anatomical_structureNeurologylcsh:R858-859.7FemaleNeurology (clinical)medicine.symptombusinessNuclear medicinecomputer030217 neurology & neurosurgeryFollow-Up StudiesNeuroImage: Clinical
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Association of smoking but not HLA-DRB1*15:01, APOE or body mass index with brain atrophy in early multiple sclerosis

2019

Background: The course of multiple sclerosis (MS) shows substantial inter-individual variability. The underlying determinants of disease severity likely involve genetic and environmental factors. Objective: The aim of this study was to assess the impact of APOE and HLA polymorphisms as well as smoking and body mass index (BMI) in the very early MS course. Methods: Untreated patients ( n = 263) with a recent diagnosis of relapsing-remitting (RR) MS or clinically isolated syndrome underwent standardized magnetic resonance imaging (MRI). Genotyping was performed for single-nucleotide polymorphisms (SNPs) rs3135388 tagging the HLA-DRB1*15:01 haplotype and rs7412 (Ɛ2) and rs429358 (Ɛ4) in APOE. …

AdultMaleApolipoprotein EMultiple SclerosisAdolescentPolymorphism Single NucleotideBody Mass IndexYoung Adult03 medical and health sciencesApolipoproteins E0302 clinical medicineAtrophyMedizinische FakultätmedicineHumansSNPGenetic Predisposition to Disease030212 general & internal medicineddc:610Risk factorHLA-DRB1Agedbusiness.industryMultiple sclerosisSmokingNeurodegenerationBrainMiddle Agedmedicine.diseaseNeurologyImmunologyFemaleNeurology (clinical)AtrophybusinessBody mass index030217 neurology & neurosurgeryHLA-DRB1 Chains
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