Lewy bodies

Related by string. Lewy Bodies * Lewys : Deena Kastor Magdalena Lewy . Lewy Body Dementia . Magdalena Lewy Boulet . Lewy Boulet . Magda Lewy . Lewy body . Guenter Lewy / BODIES . Bodies . Bodie : badly decomposed bodies . bullet riddled bodies . Bodies Revealed . sanctioning bodies . National Governing Bodies . decomposing bodies upstairs . Governing Bodies * Lewy bodies DLB . Lewy Bodies DLB *

Related by context. All words. (Click for frequent words.) 72 neurofibrillary tangles 70 Amyloid plaques 69 senile plaques 67 amyloid beta plaques 66 pathological hallmark 66 protein tau 65 alpha synuclein protein 65 tau proteins 65 beta amyloid plaques 63 tau protein 62 abnormal clumps 62 frontotemporal dementia 62 tau protein tangles 62 Beta amyloid 62 beta amyloid peptides 62 protein beta amyloid 62 protein alpha synuclein 62 beta amyloid plaque 61 amyloid plaque 61 phosphorylated tau 61 sporadic ALS 61 FXTAS 61 amyloid deposits 61 amyloids 61 protein clumps 61 FTLD 61 PTPN# 61 Abeta# 60 progranulin 60 insoluble protein 60 lipofuscin 60 β amyloid 60 white matter hyperintensities 60 #q#.# [002] 60 amyloid plaques 60 fibrous tangles 60 ataxias 60 abnormal proteins 59 neuritic plaques 59 sCJD 59 amyloid proteins 59 amyloid beta proteins 59 beta amyloid peptide 59 microbleeds 59 Prion diseases 59 Aß# 59 amyloid protein 59 59 Vascular dementia 59 MLH1 59 neurological abnormalities 58 brain lesions 58 Alzheimer disease vascular dementia 58 amyloid plaque deposits 58 beta amyloid fragments 58 MSH2 58 hyperplastic 58 frontotemporal dementia FTD 58 beta amyloid proteins 58 demyelination 58 missense mutations 58 gliosis 58 essential thrombocythemia 58 G#S [002] 58 autopsied brains 58 neuronal cell 58 familial ALS 58 DQB1 * 58 vascular cognitive impairment 58 hyperphosphorylated tau 58 susceptibility gene 58 motor neuron degeneration 58 infarcts 58 pathogenic mutations 58 synuclein 57 SORL1 57 amyloid beta protein 57 neurofibrillary 57 hypermethylation 57 SOD1 57 subcortical 57 ß amyloid 57 underlying vasculopathy 57 amyloid beta peptide 57 hamartomas 57 Lewy body 57 APOE gene 57 insoluble plaques 57 apolipoprotein E APOE 57 microdeletion 57 neuronal dysfunction 57 Amyloid protein 57 synaptic function 57 aggregated Abeta 57 epithelioid 57 cerebrospinal fluid CSF 57 #p#.# [002] 57 circadian genes 57 Alzheimer pathology 57 indels 57 inherited mutations 57 C#Y 57 tau tangles 57 chromosomal rearrangement 57 miRNA genes 57 amyloid beta peptides 57 monogenic 57 cognitively normal 57 hypermethylated 57 chromosome #q#.# [001] 57 DNMT1 57 exocrine 56 beta amyloid 56 TSC1 56 Papillary 56 biochemical abnormalities 56 LIS1 56 HFE gene 56 gene APOE4 56 beta amyloid protein 56 apoE4 56 noncalcified 56 56 hypometabolism 56 systemic amyloidosis 56 ADPKD 56 Amyloid beta 56 Alpha synuclein 56 Clusterin 56 de novo mutations 56 fibrillin 56 antiphospholipid syndrome 56 K ras mutations 56 anterior temporal 56 MGUS 56 drusen 56 astrocytic 56 missense mutation 56 LRRK2 gene 56 sortilin 56 APOE4 56 amyloid deposition 56 Amyloid 56 myeloproliferative neoplasms 56 abnormal prion protein 56 amyloid peptides 56 nucleoli 56 neurofibromas 56 fibrillar 56 somatic mutations 56 microdeletions 56 serine protease 56 Abeta protein 56 amyloid β 56 56 fronto temporal dementia 56 #q# [002] 56 dominantly inherited 56 ADDLs 56 rs# [002] 56 Purkinje cells 56 Aβ# 56 excitatory neurotransmitter glutamate 56 α synuclein 56 medial temporal 56 Abnormalities 56 PTEN mutations 55 behavioral abnormalities 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 progressive neurodegenerative disorder 55 hepatic lipase 55 mucinous 55 Alzheimer disease pathology 55 ApoE4 55 GBA mutations 55 PDGFR 55 p tau 55 carcinoembryonic antigen 55 mesangial 55 KCNH2 55 COL#A# 55 lymphocytic 55 cerebellar 55 Parkinsonian Syndromes 55 Hashimoto thyroiditis 55 mtDNA mutations 55 glucocerebroside 55 soluble beta amyloid 55 oligomers 55 rs# [004] 55 misfolded 55 neurodegenerative disorder 55 naturally occurring neuroprotective 55 alpha synuclein gene 55 APOE e4 55 Beta Amyloid 55 Huntingtin 55 frontotemporal 55 ABCB1 55 constitutively expressed 55 renal cell carcinomas 55 apoE 55 osteosarcomas 55 euthymic patients 55 neoplastic 55 myopathies 55 colorectal carcinoma 55 segmental duplications 55 acyl CoA 55 CDH# 55 Cowden syndrome 55 IgA deficiency 55 chromosome #q# [001] 55 chromosome #q# [002] 55 toxic beta amyloid 55 transgenic mouse models 55 amyloid peptide 55 ependymomas 55 caveolin 55 lactate dehydrogenase LDH 55 basal cell nevus syndrome 55 PHD2 55 parahippocampal gyrus 55 neuropathological 55 glomerular 55 Hutchinson Gilford progeria 55 ApoE gene 55 supratentorial 55 alpha synuclein 55 autonomic dysfunction 55 CALHM1 55 lymphangiogenesis 55 ciliated 55 KIBRA 55 parkinsonism 54 myo inositol 54 cortices 54 subclinical hyperthyroidism 54 #q# [001] 54 unknown etiology 54 sarcomatoid 54 cell adhesion molecule 54 #q#.# [001] 54 extrahepatic 54 neuropathologic 54 periventricular 54 dysbindin 54 gastric carcinoma 54 amyloid ß 54 myelofibrosis polycythemia vera 54 Metastases 54 epithelial tumors 54 arteriosclerotic 54 Brodmann Area 54 missense 54 proximal colon 54 CHD7 54 TCF#L# gene 54 NFTs 54 penetrance 54 caspase activation 54 clusterin 54 akinesia 54 PICALM 54 Amyloid beta protein 54 TMEM#B 54 #p#.# [001] 54 myoclonus 54 renal cortical 54 ptau 54 thyrotropin levels 54 Hurthle cell 54 astrocytomas 54 DLX5 54 KIAA# 54 autophagic 54 atypical hyperplasia 54 Upregulation 54 CDH1 54 adrenocortical cancer 54 nonhereditary 54 hypoperfusion 54 sphingolipid 54 chromosomal instability 54 serous ovarian cancer 54 microvessels 54 perivascular 54 neurofibromatosis type 54 metaplasia 54 TSP1 54 SHANK3 54 Leukemias 54 chromosomal deletions 54 Neuregulin 1 54 hypercoagulable 54 FDDNP 54 misfolded protein 54 immunodeficiencies 54 vimentin 54 fibrous tissues 54 Wnt#b 54 Histologically 54 glycated 54 osteoblastic 54 nondemented 54 chromosome #p# [001] 54 ACh 54 thyrotropin 54 activated microglia 54 amyloid 54 cystatin C 54 ERK2 54 insoluble proteins 54 e4 allele 54 arterial calcification 54 pleomorphic 54 noncoding RNAs 54 calcium oxalate 54 ataxin 54 FMR1 gene 54 DNA methylation patterns 54 chromosomal anomalies 54 electron muon 54 SNCA 54 mRNA expression 54 hippocampal 53 presynaptic 53 Lewy bodies DLB 53 familial aggregation 53 microsatellite instability 53 posterior cingulate 53 Genetic variants 53 S#A# [002] 53 subclinical 53 PrPSc 53 serotonin receptor 53 LRP5 53 autoinflammatory 53 ventricular dilatation 53 pancreatic endocrine 53 NFKBIA 53 LKB1 53 paraneoplastic 53 neurologic abnormalities 53 hepatocellular carcinomas 53 p# mutations 53 genetic polymorphism 53 polyglutamine 53 amyloid fibrils 53 #q# deletion 53 genetic loci 53 inherited neurological disorder 53 toxic amyloid beta 53 amyloid plaque formation 53 benign neoplasms 53 #beta HSD1 53 heterozygosity 53 γ secretase 53 Cystatin C 53 germline mutations 53 chromosomal rearrangements 53 mitochondrial dysfunction 53 pathophysiologic 53 MLL2 53 microcephalin 53 HMGA2 53 chromosome #q#.# [002] 53 raphe 53 hyperphosphorylation 53 microscopic lesions 53 non coding RNA 53 autosomal dominant 53 ccRCC 53 amino acid substitutions 53 papillary 53 Mild Cognitive Impairment 53 ceruloplasmin 53 regulated kinase ERK 53 KCNQ1 53 multinucleated giant cells 53 parkin gene 53 Inherited mutations 53 TGF ß1 53 abnormal tau 53 CYP#A# gene 53 interstitial fibrosis 53 Brugada syndrome 53 histologically 53 Endothelial dysfunction 53 dimeric 53 GPIHBP1 53 microvascular disease 53 huntingtin protein 53 dyskeratosis congenita 53 rCBF 53 acetylcholine receptor 53 tau pathology 53 dysregulation 53 myeloproliferative 53 LDL receptor 53 cytopenias 53 carcinoid 53 FUS1 53 Parkinson Disease PD 53 pRb 53 functional polymorphism 53 ABCA1 53 BRAF gene 53 aMCI precursor 53 neuritic 53 calculi 53 ALK gene 53 epigenetic alterations 53 5 HT1A 53 mental retardation epilepsy 53 Amyloid deposits 53 abnormalities 53 presenilin 53 spinocerebellar ataxia 53 holoprosencephaly 53 Leydig cell 53 vascular endothelial 53 hypomethylation 53 protein tyrosine phosphatase 53 #p# [001] 53 coronary plaques 53 cell adhesion molecules 53 muscular dystrophies 53 tumoral 53 ERK1 2 53 genetic polymorphisms 53 familial pancreatic cancer 53 IL #p# 53 inherited genetic mutations 53 cryptogenic 53 pituitary adenomas 53 Neurofibromatosis type 53 GATA4 53 amyloid protein plaques 53 microRNA expression 53 Dpp 53 fibrillin 1 52 nonischemic 52 hyperinsulinism 52 Purkinje cell 52 sclerosis ALS 52 receptor kinase 52 nonalcoholic steatohepatitis 52 SLC#A# [001] 52 epigenetic markers 52 mice genetically altered 52 Hippocampal 52 metabolic abnormalities 52 underlying pathophysiology 52 3'UTR 52 KRAS oncogene 52 autosomal dominant inheritance 52 histone modifications 52 mitochondrial oxidative 52 FASPS 52 protein fragment 52 synaptogenesis 52 LRRK2 mutation 52 C. pneumoniae 52 GABA receptor 52 FMR1 52 paraganglioma 52 elevated triglycerides 52 Alzheimer's related 52 gene APOE 52 Prion proteins 52 renal fibrosis 52 Gene Linked 52 telomere dysfunction 52 PTEN gene 52 MYCN amplification 52 histone methylation 52 HNPCC 52 SLC#A# [002] 52 mesotheliomas 52 prefrontal cortical 52 SCN5A 52 membranous 52 neuroligins 52 situs inversus 52 Wernicke Korsakoff syndrome 52 klotho 52 BDNF gene 52 hepatic steatosis 52 neovascular AMD 52 BARD1 52 CA1 52 Frontotemporal Dementia 52 pyrimidines 52 granule cells 52 kalirin 52 KLF4 52 PAOD 52 MYH9 gene 52 intermediate filaments 52 apolipoprotein E 52 osteopontin 52 conductance regulator 52 MECP2 gene 52 amyloid pathology 52 BRAF protein 52 Cerebellar 52 neurofibroma 52 tauopathies 52 E selectin 52 familial hypercholesterolemia 52 Haptoglobin 52 alpha helix 52 amyloidogenic 52 amnestic MCI 52 cytokines chemokines 52 neovascular 52 leiomyomas 52 UCP1 52 apoC III 52 amyloid beta plaque 52 paragangliomas 52 microglial activation 52 Cholangiocarcinoma 52 excitotoxicity 52 Prox1 52 autosomal recessive 52 amnestic mild cognitive impairment 52 fibrils 52 #q#.# deletion syndrome 52 eccrine 52 homozygous familial hypercholesterolemia 52 heterozygotes 52 nitric oxide synthase 52 oxidized phospholipids 52 TET2 52 SGPT 52 spontaneous mutations 52 lymphoid 52 Alzheimer Disease AD 52 leiomyoma 52 haematopoietic 52 TP# mutations 52 microRNA molecules 52 Retinitis pigmentosa 52 pancytopenia 52 regulates gene expression 52 atherosclerotic lesion 52 antisense inhibition 52 lymph node enlargement 52 cystatin 52 LRRK2 mutations 52 corticobasal degeneration 52 HGPIN 52 Parkinsonian 52 rs# [003] 52 collagen VI 52 coding exons 52 chromosomal aberrations 52 autosomal dominant disorder 52 CCR5 delta# 52 progressive neurodegenerative 52 opportunistic viral infection 52 Eg5 52 myofibroblasts 52 Asymptomatic 52 adrenal cortex 52 JAK2 enzyme 52 redox active 52 morphogen 52 pathologic diagnosis 52 LQTS 52 hemorrhagic bleeding 52 striatal 52 potent inhibition 52 steatosis 52 eotaxin 52 myoepithelial 52 familial adenomatous polyposis 52 Squamous 52 bullous 52 thymine 52 HLA DR 52 MAPK pathway 52 brain parenchyma 52 miR #a [002] 52 Alu elements 52 oligodendroglial progenitor cells 52 ischemic lesions 52 mitogen activated protein kinase 52 interferon pathway 52 meningiomas 52 hypercoagulability 52 synovial cells 52 abnormal lymphocytes 52 Cathepsin B 52 Smad3 52 PARP inhibition 52 cell nuclei 52 paralogs 52 beta Amyloid 52 intronic 52 bradykinesia 52 troponin T 52 thyrotoxicosis 52 Gaucher cells 52 amyloid fibers 52 Hemorrhagic stroke 52 DARPP 52 MTHFR 52 optic neuropathy 52 neurodegeneration 52 liver metastasis 52 endometrioid 52 Dysregulation 51 NF1 51 gyri 51 serine threonine 51 HG PIN 51 atherosclerotic lesions 51 punctate 51 Chromosomal 51 stress cardiomyopathy 51 APOE ε4 51 chromosome #p#.# 51 normal karyotype 51 neurologic symptoms 51 neuroblastomas 51 familial hypercholesterolemia FH 51 osteochondromas 51 myelination 51 cardiac hypertrophy 51 malignant prostate 51 mild cognitive impairment 51 stellate 51 demyelinating 51 Hyperlipidemia 51 dopaminergic cells 51 epithelial tissues 51 pyrimidine 51 inducible nitric oxide synthase 51 nerve degeneration 51 olivines 51 VCAM 1 51 pituitary adenoma 51 homologues 51 JAK mutations 51 Neurodegenerative diseases 51 APOE 51 seminomas 51 oligomeric 51 arrhythmogenic 51 synovial 51 PGC 1α 51 affective psychoses 51 Alleles 51 MEF2A 51 hematological abnormalities 51 WNK1 51 geographic atrophy 51 Astrocytes 51 methylation patterns 51 HLA DRB1 * 51 BACE1 51 intergenic 51 germline mutation 51 leukoencephalopathy 51 neuropsychiatric diseases 51 transthyretin 51 IL #R 51 hyposmia 51 neurologic disorders 51 TOP2A gene 51 colorectal adenomas 51 glutamic acid decarboxylase 51 PBMCs 51 elevated triglyceride levels 51 autoantibodies 51 CaMKII 51 bullous pemphigoid 51 cerebral infarction 51 demyelinating disease 51 Activating mutations 51 GISTs 51 Sjögren syndrome 51 untranslated regions 51 soluble CD# ligand 51 cardiac fibroblasts 51 colorectal adenoma 51 MEF2D 51 metabolic acidosis 51 ERK signaling 51 glycolipids 51 noncoding 51 myeloproliferative diseases 51 SORL1 gene 51 hereditary nonpolyposis colorectal cancer 51 MC4R gene 51 myoglobinuria rhabdomyolysis 51 apocrine 51 extrapyramidal symptoms 51 dysgenesis 51 airway hyperresponsiveness 51 molecular abnormalities 51 relapsing remitting 51 VHL gene 51 splice junctions 51 tics involuntary 51 neuroimaging studies 51 prothrombotic 51 granzyme B 51 Macrophage 51 progressive neurologic 51 desmin 51 N acetylaspartate 51 ankyrin B 51 monozygotic twins 51 #p# [003] 51 ORMDL3 51 prefrontal regions 51 Prostatitis 51 genetic syndromes 51 affective disorders 51 amyloid precursor protein 51 microRNAs miRNAs 51 uPAR 51 pathologic 51 hyperinsulinemia 51 LV ejection fraction 51 chromosome rearrangements 51 FGFR3 51 Mutational 51 Kufs disease 51 hyaline 51 lipid peroxides 51 rheumatoid arthritis lupus 51 immunoreactive 51 thyroid carcinoma 51 misfolding 51 3' UTR 51 noradrenergic 51 dendritic spines 51 hepatic enzymes 51 IRF6 51 neuropsychological deficits 51 basal forebrain 51 familial clustering 51 sequence homology 51 Brain derived neurotrophic 51 Misfolded proteins 51 Relapsing remitting MS 51 vascular dementia 51 intraepithelial 51 HMGA1 51 insertions deletions 51 adhesion molecule 51 dopamine transporter 51 malignant ovarian 51 sonographic findings 51 predisposing factor 51 fibril 51 hyperhomocysteinemia 51 immunodominant 51 multi infarct dementia 51 inhibitory transmitter 51 CNTNAP2 51 TGF β 51 aneuploidies 51 histiocytes 51 etiologic 51 IGFBP2 51 apolipoprotein E4 51 overactivation 51 PI3K AKT 51 granulomatous 51 OCT4 51 neuron degeneration 51 trigeminal ganglia 51 C1q 51 VIPR2 51 dopamine D4 receptor 51 tubule 51 MLL gene 51 oculomotor 51 tenascin C 51 mutant proteins 51 urinary albumin 51 CAG repeats 51 triiodothyronine 51 Ischemic 51 retinoblastoma Rb 51 hyperplastic polyps 51 FGFs 51 ncRNAs 51 teratoma 51 genetically inherited 51 torsade de pointes 51 WDR# 51 intracranial hemorrhage ICH 51 glucocerebroside primarily 51 protein tangles 51 primary biliary cirrhosis 51 amyloid cascade 51 hepatocellular 51 HER2 HER3 51 coronary stenosis 51 susceptibility genes 51 ectopic expression 51 CXCR2 50 progressive degeneration 50 Amyloid Beta 50 malondialdehyde 50 tremor rigidity 50 Lewy Bodies 50 LRAT 50 angular gyrus 50 homozygous FH 50 activity dependent neuroprotective 50 bronchoalveolar lavage fluid 50 intergenic regions 50 endophenotypes 50 schwannomas 50 connexin 50 MELAS syndrome 50 CYP#C# [002] 50 amnestic 50 APOA5 50 entorhinal cortex 50 artery stenosis 50 Sp1 50 SNPs pronounced snips 50 Telomere length 50 microglial 50 cytochrome oxidase 50 ANCA associated 50 coronary stenoses 50 phenotype 50 proteins misfold 50 Albuminuria 50 Apolipoprotein E 50 podocyte 50 FGF2 50 mitochondrial respiration 50 aggrecan 50 protein tyrosine phosphatase 1B 50 endothelial activation 50 gene polymorphisms 50 ABL1 50 elevated homocysteine 50 INCB# [003] 50 striatal dopamine 50 Glioblastomas 50 nodular lesions 50 cardiolipin 50 CDKN2A 50 susceptibility locus 50 progranulin gene 50 CYP#D# 50 genetic variants associated 50 artery occlusion 50 gastrointestinal stromal tumors GISTs 50 amyloid β peptide 50 neoplasm 50 adenosine receptors 50 neurite outgrowth 50 chromosome #q 50 galanin 50 histologic 50 Igf2 50 neurosensory 50 overt hypothyroidism 50 upregulates 50 MTHFR gene 50 choroidal neovascularization 50 progranulin mutations 50 vascular endothelial cells 50 TGF beta1 50 variant allele 50 protein ADNP 50 endoplasmic reticulum stress 50 arteries atherosclerosis 50 Mouse Model 50 lysosomal storage disease 50 acinar 50 impaired cognition 50 glutamatergic 50 vitamin B# folic acid 50 VLDL C 50 advanced adenomas 50 exons 50 cognitive dysfunctions 50 ribosomal protein 50 chromosome aberrations 50 glaucomatous 50 TRPV1 receptors 50 SPINK1 50 hippocampal function 50 obstructive coronary artery 50 complement inhibitor eculizumab 50 EGFR mutations 50 progressively degenerative 50 prostatic hyperplasia 50 vasogenic edema 50 ubiquitinated 50 MMP2 50 morphologic 50 glial tumors 50 monocytic 50 poorer prognosis 50 lymphoid cells 50 thyroglobulin 50 histologic findings 50 metalloproteases 50 cardiac dysfunction 50 nucleotide sequence 50 urothelial 50 5 lipoxygenase 50 cardioembolic stroke 50 subclinical hypothyroidism 50 aldehyde dehydrogenase 50 COX2 50 chromosomal translocations 50 EoE 50 genomic instability 50 SOD1 gene 50 serum BDNF 50 genes encode proteins 50 disease Chronic Traumatic 50 Autoantibodies 50 COX enzymes 50 haplotypes 50 plexiform 50 CagA 50 von Willebrand factor 50 Pten 50 leukemias lymphomas 50 diabetes mellitus DM 50 micro RNAs 50 constitutively active 50 impaired glucose metabolism 50 glomerulonephritis 50 primary ciliary dyskinesia 50 Neovascularization 50 Insulin resistance 50 atypical hemolytic uremic syndrome 50 cystic fibrosis transmembrane conductance 50 rRNA 50 distinct subtypes 50 dehydrogenases 50 morphological abnormalities 50 myelodysplasia 50 SLITRK1 50 lipoprotein metabolism 50 gene polymorphism 50 factor HGF 50 BDNF protein 50 radiographic findings 50 genomic deletions 50 androgen deficiency 50 Korsakoff syndrome 50 Jhdm2a 50 SMAD4 50 fatty acid oxidation 50 micro RNA 50 disulfide bond 50 generalized epilepsy 50 Ribavirin causes 50 fatal neuromuscular disorder 50 anemias 50 Alzheimer disease cognitive impairment 50 DNA rearrangements 50 Cognitive impairment 50 immunoreactivity 50 cause cardiac channelopathies 50 Adenomas 50 hemolytic anemia 50 endogenous ligands 50 transgenic mice expressing 50 uranophane 50 Parkinson disease PD 50 microalbuminuria 50 ADAMTS# 50 lichen planus 50 apolipoprotein E gene 50 nonalcoholic steatohepatitis NASH 50 Hypercholesterolemia 50 amyloid â 50 peroxisomal 50 TP# gene 50 leukaemias 50 macroalbuminuria 50 autoinflammatory diseases 50 glutamatergic neurons 50 survival motor neuron 50 NPHP 50 proliferative diabetic retinopathy 50 elevated creatine phosphokinase 50 F actin 50 neuropsychiatric disorders

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