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Peter Roos
Overlæge
,
Rigshospitalet
,
Afdeling for Hjerne- og Nervesygdomme
2014
2024
Publikationer pr. år
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Fingeraftryk
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Publikationer
(19)
Lignende profiler
(6)
Fingeraftryk
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Keyphrases
Frontotemporal Dementia
100%
CHMP2B
89%
Cerebrospinal Fluid
33%
Mutation Carriers
29%
Christmas
25%
Novel mutation
25%
Neurofilament Light (NF-L)
17%
Clinical Features
15%
Light Concentration
14%
TMEM106B
14%
Endolysosomal
12%
Stress-related Metabolites
12%
Longitudinal Case
12%
Healthy Controls
12%
Oxidative Stress
12%
Bipolar Disorder
12%
Disorder Control
12%
Lysosomal Proteins
12%
Diagnostic Ratios
12%
Predictive Testing
12%
Dementia Diagnosis
12%
Network Dysfunction
12%
Geographical Variation
12%
Frontoparietal Network
12%
Protein Concentration
12%
Inflammatory Markers
12%
8-oxoguanine
12%
Six Generation
12%
Serum Neurofilament Light
12%
Apolipoprotein E Genotype
12%
Diagnostic Quality
12%
Spinocerebellar Ataxia
12%
Tacrolimus
12%
Neuropsychiatric Symptoms
12%
CYP7B1
12%
Charged multivesicular Body Protein 2b
12%
Muscle Atrophy
12%
Cognitive Examination
12%
Lysosomal Storage Disease
12%
Cerebellar Degeneration
12%
Type I muscle Fiber
12%
AFG3L2
12%
Copenhagen
12%
Allogeneic Hematopoietic Stem Cell Transplantation (allo-HSCT)
12%
Hereditary Spastic Paraplegia
12%
Magnetic Resonance Spectroscopy
12%
Homozygosity
12%
Prion Protein Gene
12%
Variably Protease-sensitive Prionopathy (VPSPr)
12%
Methionine
12%
Biochemistry, Genetics and Molecular Biology
CHMP2B
38%
Neurofilament Light
25%
Protease
16%
Magnetic Resonance Imaging
15%
AFG3L2
12%
Codon
12%
Homozygosity
12%
CYP7B1
12%
Oxidative Stress
12%
Case-Control Study
12%
Metabolite
12%
Tau
12%
Nuclear Magnetic Resonance Spectroscopy
12%
Methionine
12%
Prion Protein
12%
Light Chain
10%
Autosomal Dominant Inheritance
9%
Ubiquitin
7%
Deoxyguanosine
6%
RNA Damage
6%
Metabolic Pathway
6%
Neuroscience
Frontotemporal Dementia
76%
Apolipoprotein E
12%
Cognitive Tests
12%
Spinocerebellar Ataxia
12%
Bipolar Disorder
12%
Neurofilament
12%
Muscle Atrophy
12%
Oxidative Stress
12%
Nuclear Magnetic Resonance Spectroscopy
12%
Hereditary Spastic Paraplegia
12%
Neurodegenerative Disorder
11%
Neurodegeneration
9%
Risk Factor
7%
CCL22
6%
Ubiquitin
6%
CXCL10
6%
Interleukin 15
6%
Cognitive Decline
6%
Ataxia
5%
Magnetic Resonance Imaging
5%
