Related by context. All words. (Click for frequent words.) 75 disease NAFLD 67 alcoholic fatty liver 67 NAFLD 66 hereditary predisposition 66 familial hypercholesterolemia 65 Nonalcoholic fatty liver 65 nonalcoholic steatohepatitis 65 insulin resistance 64 nonalcoholic steatohepatitis NASH 64 basal cell nevus syndrome 63 Fatty liver 63 MYH9 gene 63 Non Alcoholic Steatohepatitis 63 fatty liver disease 63 APOL1 62 diabetes mellitus DM 62 subclinical atherosclerosis 62 Nonalcoholic Fatty Liver Disease 62 familial adenomatous polyposis 62 obesity insulin resistance 62 lipid abnormalities 62 hyperparathyroidism 62 diabetes dyslipidemia 62 insulin resistance syndrome 61 impaired glucose metabolism 61 hyperglycaemia 61 diabetic kidney 61 hyperhomocysteinemia 61 Insulin resistance 61 gallstone disease 61 elevated triglyceride levels 61 narcolepsy cataplexy 61 LRP5 61 hyperinsulinemia 61 progressive neurodegenerative disorder 61 Aortic stenosis 61 elevated triglycerides 60 prediabetes 60 untreated celiac disease 60 Non Alcoholic Fatty 60 homozygous familial hypercholesterolemia 60 ADPKD 60 potentially modifiable 60 metabolic syndrome MetS 60 insulin resistance precursor 60 abnormal lipids 60 dyskeratosis congenita 60 gestational diabetes mellitus 60 Chronic lymphocytic leukemia 60 Vitamin D insufficiency 60 VLDL cholesterol 60 essential thrombocythemia 60 FTLD 60 metabolic disturbances 60 hepatic steatosis 60 atherogenic dyslipidemia 60 colorectal adenoma 60 adrenal function 60 IGFBP2 60 APOE4 60 mitochondrial mutations 60 IDDM 60 glucose intolerance 60 cystic fibrosis chronic pancreatitis 60 Diabetic neuropathy 60 type2 diabetes 60 oesophageal adenocarcinoma 60 Alzheimer Disease AD 59 Haptoglobin 59 chronic granulomatous disease 59 Chronic pancreatitis 59 Proteinuria 59 lactose malabsorption 59 chronic thromboembolic pulmonary 59 carotid atherosclerosis 59 Chronic inflammation 59 Leukemias 59 Hp2 2 59 Epstein Barr virus EBV 59 Lafora disease 59 APOE e4 59 chromium supplementation 59 ABCB1 59 hypovitaminosis D 59 Genetic predisposition 59 membranous nephritis 59 NAT2 59 bronchial hyperresponsiveness 59 leptin deficiency 59 liver scarring 59 cause cardiac channelopathies 59 post transplant lymphoproliferative 59 familial pancreatic cancer 59 folate deficiency 59 gastro oesophageal reflux 59 TGFBR1 * 6A 59 colorectal carcinoma 59 perilipin 59 oxidized cysteine 58 Coronary artery calcification 58 KIF6 gene 58 Hypertriglyceridemia 58 cirrhosis liver failure 58 genetic variants associated 58 T1DM 58 Lymphocytic 58 haemochromatosis 58 systemic inflammation 58 systemic amyloidosis 58 AAT Deficiency 58 subclinical hyperthyroidism 58 STK# gene 58 Ribavirin causes 58 interleukin IL -6 58 Osteoarthritis OA 58 E selectin 58 metabolic abnormalities 58 paraneoplastic 58 GSTP1 58 inherited mutations 58 TTR amyloidosis 58 lupus scleroderma 58 susceptibility gene 58 etiologic 58 SLC#A# [002] 58 Genetic variants 58 diabetes hyperlipidemia 58 hepatic liver 58 hypercoagulable 58 chronic rheumatic 58 serum selenium 58 chorioamnionitis 58 metabolic syndrome 58 familial hypercholesterolemia FH 58 Endothelial dysfunction 58 inflammatory rheumatic 58 Irritable bowel syndrome IBS 58 complement inhibitor eculizumab 58 thyroid deficiency 58 impaired fasting glucose 58 p#INK#a 58 hematopoietic cancers 58 Wernicke Korsakoff syndrome 58 gastric adenocarcinoma 58 psoriatic arthritis PsA 58 myeloproliferative neoplasms 58 Systemic lupus erythematosus 58 Celiac sprue 58 chronic rhinosinusitis CRS 58 leptin receptor 58 prostate carcinogenesis 58 TCF#L# 58 Von Willebrand disease 58 Lupus nephritis 58 Microalbuminuria 58 G6PD deficiency 58 Osteopenia 58 elevated fasting glucose 58 macroalbuminuria 58 cryptogenic 58 multisystem disease 58 glucose homeostasis 58 MTHFR 58 Apolipoprotein E 58 improves insulin sensitivity 58 impaired glucose tolerance 58 proliferative retinopathy 58 inflammatory bowel syndrome 58 recurrent acute pancreatitis 58 hepatic cirrhosis 58 endothelial dysfunction 58 polyp recurrence 58 TCF#L# gene 58 Hypertrophy 58 mixed hyperlipidemia 58 glycated hemoglobin levels 58 hereditary nonpolyposis colorectal cancer 58 de ath 58 central adiposity 58 rs# [002] 58 HNPCC 58 primary biliary cirrhosis 58 monogenic 57 Pulmonary hypertension 57 Venous thromboembolism 57 liver steatosis 57 Sjögren syndrome 57 hepatic fibrosis 57 myelodysplasia 57 Hemolytic Uremic Syndrome HUS 57 squamous cell lung cancer 57 NPHP 57 2 diabetes T2D 57 AAT deficiency 57 progressive neurodegenerative 57 enteroviral infection 57 chronic periodontitis 57 elevated CRP 57 dilated cardiomyopathy DCM 57 autosomal dominant disorder 57 LHON 57 periodontitis 57 serum leptin 57 Colon polyps 57 Hyperphosphatemia 57 prostate cancer CaP 57 hepatorenal syndrome 57 Wwox 57 granulomatous 57 esophageal squamous cell carcinoma 57 hypercholesterolaemia 57 CP CPPS 57 neuritic 57 antiphospholipid syndrome 57 hereditary hemochromatosis 57 systemic autoimmune 57 Hyperlipidemia 57 Bronchiectasis 57 MGUS 57 neuropsychiatric disorder 57 ATTR CM 57 IgA deficiency 57 elevated serum creatinine 57 silent myocardial ischemia 57 hyperinsulinism 57 idiopathic PAH 57 metabolic acidosis 57 Beta thalassemia 57 autosomal dominant polycystic kidney 57 obstructive coronary artery 57 coinfection 57 Lichen planus 57 C Reactive Protein 57 Relapsing remitting MS 57 neuronal dysfunction 57 Prehypertension 57 SHPT 57 pernicious anemia 57 APOE gene 57 subclinical 57 PKCi 57 Heterozygous Familial Hypercholesterolemia 57 thyroid dysfunction 57 Leber Hereditary Optic Neuropathy 57 non alcoholic steatohepatitis 57 sporadic ALS 57 transfusion syndrome 57 susceptibility genes 57 GPC5 57 elevated LDL cholesterol 57 HELLP 57 cholestasis 57 cystatin C 57 Subclinical 57 lysosomal storage disease 57 Leydig cell 57 debilitating complication 57 polymorphic ventricular tachycardia 57 LDL receptor 57 HDL2 57 #q# deletion 57 type 1diabetes 57 fatal myelination disorder 57 diabetes mellitus T2DM 57 GSTM1 gene 57 overt nephropathy 57 precancerous tumors 57 DNA methylation patterns 57 abnormal lipid 57 Hashimoto thyroiditis 57 proliferative diabetic retinopathy 57 progressive dyspnea 57 Alzheimer disease vascular dementia 57 ANCA associated 57 HeFH 57 euthymic patients 57 recurrent wheezing 57 inflammatory demyelinating 57 CMV infection 57 methylenetetrahydrofolate reductase 57 serum parathyroid hormone 57 atypical hemolytic uremic syndrome 57 SLC#A# [001] 57 SIRT1 gene 57 familial ALS 57 juvenile idiopathic arthritis JIA 57 alanine aminotransferase ALT 57 BMPR2 57 chronic myeloid 57 debilitating autoimmune 57 MALT lymphoma 57 pulmonary hypertension PH 57 atopic disorders 57 myeloperoxidase 57 PTPN# 57 haematopoietic 57 H pylori 57 Fatty Liver Disease 57 Vitamin B# deficiency 57 GSTT1 57 HER2 overexpression 57 hyperphenylalaninemia HPA due 57 NOD2 57 Hypoglycaemia 57 neuropathologic 57 Patient Registry 57 abnormal lipid levels 57 Periodontal disease 57 amyloid deposition 56 elevated ALT 56 Stop Hypertension diet 56 1 diabetes T1D 56 neurodegenerative disorder 56 cardiac hypertrophy 56 alcoholic hepatitis 56 Multiethnic Study 56 Diabetes mellitus 56 autonomic dysfunction 56 muscular dystrophies 56 CYT# potent vascular disrupting 56 maintaining cardiorespiratory fitness 56 TMEM#B 56 non cirrhotic portal 56 intestinal biopsy 56 HbF 56 fat malabsorption 56 advanced adenoma 56 renal scarring 56 ApoE4 56 Statin therapy 56 PDGFR 56 Cholangiocarcinoma 56 elevated uric acid 56 prediabetic 56 adenomatous 56 kidney urologic 56 leukaemias 56 fetuin 56 HBeAg 56 Trichomonas vaginalis 56 erythema nodosum 56 persistent pulmonary hypertension 56 impaired insulin secretion 56 neurobehavioral disorder 56 TMS Therapy 56 Radiographic findings 56 channelopathies 56 gastric carcinogenesis 56 NKX2 56 genetic polymorphisms 56 systemic scleroderma 56 onset diabetes mellitus 56 NOMID 56 vitamin B1 deficiency 56 elevated homocysteine 56 familial adenomatous polyposis FAP 56 nondiabetics 56 transthyretin 56 kidney insufficiency 56 dominantly inherited 56 serum lipid levels 56 familial clustering 56 inducible nitric oxide synthase 56 coronary artery atherosclerosis 56 mitochondrial dysfunction 56 Peptide YY 56 Thromboembolism 56 interleukin IL -# 56 diabetic microvascular complications 56 SGPT 56 Arrhythmogenic Right Ventricular Cardiomyopathy 56 congenital adrenal hyperplasia CAH 56 C1 INH deficiency 56 trigylcerides 56 Polycythemia vera 56 #beta HSD1 56 virus XMRV 56 Dental caries 56 CHRNA5 gene 56 Pemphigus 56 transferrin saturation 56 homozygous FH 56 apolipoprotein E4 56 breast endometrial 56 microalbuminuria 56 heterozygous familial 56 bronchopulmonary dysplasia BPD 56 K ras mutations 56 cytomegalovirus infection 56 CaM kinase II 56 arterial calcification 56 Polycystic ovary syndrome PCOS 56 Sleep disordered breathing 56 phosphorylated tau 56 hormone adiponectin 56 neurocognitive deficits 56 COX2 56 chronic obstructive airway 56 AA Amyloidosis 56 alpha1 antitrypsin deficiency 56 TP# mutation 56 Chlamydia pneumoniae 56 chronic eosinophilic leukemia 56 renal cell carcinomas 56 CDH1 56 induced cardiomyopathy 56 Uncontrolled hypertension 56 recessive dystrophic epidermolysis bullosa 56 Idiopathic pulmonary fibrosis 56 Basal Cell 56 aldehyde dehydrogenase 56 overt hypothyroidism 56 abnormal glucose tolerance 56 lipoprotein metabolism 56 autoimmune thyroid 56 obese adolescents 56 Plaque psoriasis 56 Kufs disease 56 E4 variant 56 Leber congenital amaurosis LCA 56 Raynaud syndrome 56 Atypical Hemolytic Uremic Syndrome 56 Subarachnoid hemorrhage 56 predisposing factor 56 SORL1 56 metabolic dysfunction 56 left ventricular hypertrophy 56 Dravet syndrome 56 Homocysteine 56 gluten sensitive enteropathy 56 T2D 56 intestinal polyps 56 Lipodystrophy 56 herpes simplex encephalitis 56 renal fibrosis 56 thyrotoxicosis 56 ApoE 56 Systemic lupus erythematosus SLE 56 Oxidative stress 56 Genetic variation 56 coagulation abnormalities 56 neurologic disorder 56 Epstein Barr Virus EBV 56 apolipoprotein E gene 56 Folate deficiency 56 Parkinson Disease PD 56 LV dysfunction 56 HNSCC 56 albuminuria 56 Philadelphia Chromosome Positive 56 lipid disorders 56 Hyperglycemia 56 Pelvic inflammatory 56 Gestational diabetes 56 ketoacidosis 56 dysglycemia 56 abdominal adiposity 56 HIV HCV coinfected 56 hyperlipidemia hypertension 56 aneuploidies 56 multi infarct dementia 56 Albuminuria 56 subclinical hypothyroidism 56 Papillary 56 ENaC 56 minimally symptomatic 56 GSTM1 56 Brugada syndrome 56 diabetes mellitus hypertension 56 Adiposity 56 nerve degeneration 56 nonmelanoma 56 fat hormone leptin 55 HBeAg negative 55 Irritable bowel syndrome 55 polycystic ovary syndrome PCOS 55 atrophic gastritis 55 Autoimmune disorders 55 giant cell arteritis 55 Hereditary angioedema HAE 55 Dysregulation 55 RIP1 55 bacteraemia 55 humanin 55 proinflammatory cytokines 55 Heterozygous 55 myelofibrosis polycythemia vera 55 c reactive protein 55 IL#R 55 cell adhesion molecule 55 SIADH 55 hamartomas 55 Physical inactivity 55 PTLD 55 transgenic rats 55 SSc 55 exocrine 55 Major depressive disorder 55 Peripheral artery disease 55 Darapladib 55 maldigestion 55 carbohydrate intolerance 55 sCJD 55 vWD 55 chronic hepatitis cirrhosis 55 shorter telomere length 55 congenital hypothyroidism 55 acute leukemias 55 untreated hypothyroidism 55 cerebrospinal fluid CSF 55 atopic asthma 55 LPS induced 55 SRBD 55 Clusterin 55 endometrial hyperplasia 55 Polyneuropathy 55 MSMB 55 autosomal recessive disorder 55 Chronic lymphocytic leukemia CLL 55 fatal neurodegenerative disorder 55 periodontal infection 55 T2DM 55 Ischaemic heart 55 fructose intolerance 55 IL 1ß 55 hyperactivated 55 systolic hypertension 55 preserved ejection fraction 55 GRNCM1 55 Complications Trial 55 nonischemic 55 latent celiac disease 55 autoimmune thyroiditis 55 chronic relapsing 55 liver fibrosis 55 lymphangioleiomyomatosis LAM 55 neurocognitive impairment 55 autosomal recessive genetic 55 Polymorphic Ventricular Tachycardia CPVT 55 haemolytic uraemic syndrome 55 Morquio 55 UGT#A# * 55 PITX2 55 transcranial Doppler ultrasound 55 CLA supplementation 55 multifactorial disease 55 airway hyperresponsiveness 55 triiodothyronine 55 pathophysiological mechanisms 55 colorectal adenomas 55 coronary calcification 55 adenomatous polyps 55 Mycoplasma pneumoniae 55 EoE 55 Calorie restriction 55 breast cancer metastasis 55 mtDNA mutations 55 vascular inflammation 55 Sezary syndrome 55 atherothrombosis 55 haematologic 55 OSAHS 55 MPGN 55 fasting glucose levels 55 Eisenmenger syndrome 55 HGPS 55 UCP2 55 thyrotropin 55 arterial hypertension 55 Parkinson disease PD 55 adiponectin levels 55 Hip dysplasia 55 Leber congenital amaurosis 55 liver dysfunction 55 amino acid homocysteine 55 serum GGT 55 activin 55 autoinflammatory diseases 55 reflux disease 55 HER2 expression 55 Oxidative damage 55 atypical ductal hyperplasia 55 etiologic factors 55 artherosclerosis 55 Heavy snorers 55 H. pylori infection 55 Six3 55 distal colon cancer 55 glycogen metabolism 55 dyslipidaemia 55 nondemented 55 HLA DRB1 55 testicular tumors 55 Brodmann Area 55 Hemolytic Uremic Syndrome 55 motor neuron degeneration 55 MSH2 55 nonfasting triglyceride levels 55 allergic sensitization 55 autosomal recessive 55 serum phosphate 55 cardiolipin 55 lobular carcinoma 55 leiomyomas 55 hippocampal atrophy 55 Chronic HCV 55 unresectable tumors 55 KIBRA 55 osteomalacia 55 Digital Mammographic Imaging 55 atopic disease 55 Peripheral arterial disease 55 DFMO 55 prematurity ROP 55 Hemochromatosis 55 galanin 55 onset diabetes 55 Carcinoid tumors 55 causative genes 55 gene polymorphisms 55 Brugada Syndrome 55 UCP1 55 Cystatin C 55 left ventricular diastolic 55 premalignant 55 choriocarcinoma 55 thromboembolic disease 55 inherited genetic mutations 55 orchitis 55 ALDH2 55 habitual snoring 55 Thiazolidinediones 55 LQTS 55 imatinib resistance 55 reflux disease GERD 55 Helicobacter pylori infection 55 modifiable risk 55 Arch Intern Med 55 bacteriuria 55 metabolic derangements 55 artery stenosis 55 LDLR 55 Atopic eczema 55 Lipoprotein 55 juvenile idiopathic arthritis 55 SNP rs# [001] 55 pancytopenia 55 Alessio Fasano MD 55 leptin resistance 55 systemic lupus erythematosus SLE 55 Loeys Dietz syndrome 55 microangiopathy 55 haptoglobin 55 GH deficiency 55 hydroxyvitamin D levels 55 neoplasias 55 bronchoalveolar lavage 55 microvascular dysfunction 55 HBV infections 55 steatohepatitis 55 primary hyperparathyroidism 55 DGAT1 55 insulin secreting cells 55 tHcy 55 Thyroid hormone 55 sporadic Creutzfeldt Jakob 55 Chronic sinusitis 55 CHD7 55 endocannabinoid signaling 55 EBV infection 55 engineered RAP peptides 55 ORMDL3 55 acetabular dysplasia 55 Inflammatory Markers 55 metastatic malignant 55 polyomavirus nephropathy 55 atherosclerosis 55 paroxysmal nocturnal hemoglobinuria 55 Tardive dyskinesia 55 albumin excretion 55 vascular cognitive impairment 55 hypokalemia hypomagnesemia 55 amnestic MCI 55 galectin 3 55 PAOD 55 PLX STROKE targeting 55 hypoxia inducible factor 55 Peripheral Arterial 55 polycystic ovarian syndrome PCOS 55 Prediabetes 55 biochemical abnormalities 55 Ankylosing spondylitis 55 Iron deficiency anemia 55 diagnose coronary artery 55 Candida infection 55 PTEN gene 55 vascular dysfunction 55 Squamous 55 p# MAPK 55 colorectal cancer CRC 55 Sarcopenia 55 Coeliac disease 55 gastro esophageal reflux 55 pre eclamptic 55 recurrent glioblastoma multiforme 55 neurofibrillary 55 Unsaturated fats 55 malignant lymphoma 55 IPAH 55 familial hypercholesterolaemia 55 Gastroesophageal reflux disease 55 pathophysiological effects 55 Diabetes Mellitus 55 enterocolitis 55 polyarticular 55 enterovirus infection 55 bronchopulmonary dysplasia 55 Barrett Esophagus 54 hyperlipidaemia 54 receptor gene 54 MELAS 54 melatonin receptor 54 hypercalciuria 54 C reactive protein 54 decompensated liver disease 54 metabolic abnormality 54 SCD1 54 Pancreatic 54 B7 H3 54 hypercholesterolemia 54 BCL#A 54 Pancreatic insufficiency 54 Retinopathy 54 GATA4 54 riociguat 54 MCADD 54 polymyalgia rheumatica 54 Binge eating 54 plasma lipid 54 cirrhosis liver cancer 54 acute humoral rejection 54 celiac sprue 54 LKB1 54 lipid levels 54 Acute lymphoblastic leukemia 54 bowel polyps 54 testicular germ cell 54 cardiac dysfunction 54 induced ischemia 54 autosomal dominant 54 myopathies 54 nonfasting triglycerides 54 lichen planus 54 Oxidized LDL 54 Myotonic dystrophy 54 erythematosus 54 idiopathic pulmonary 54 hereditary deafness 54 Singh Manoux 54 TGF ß 54 SGLT2 54 euvolemic 54 serum urate levels 54 MYH9 54 Inflammatory bowel disease 54 phospholipase A2 54 Ischemic 54 autosomal recessive disease 54 glycaemia 54 Hyperuricemia 54 Hypertrophic cardiomyopathy 54 natriuresis 54 plasma lipids 54 cryptogenic cirrhosis 54 leukemia ALL 54 Skin sterol 54 Hyperkalemia 54 pancreatic endocrine 54 lupus erythematosus 54 homozygote 54 aMCI precursor 54 resistin 54 steatosis 54 Von Hippel Lindau 54 Childhood Disorder 54 malignant neoplasm 54 carbohydrate metabolism 54 common disabling neurological 54 Vitamin D supplementation 54 pressure natriuresis 54 bicuspid aortic valves 54 Li Fraumeni 54 Thromboembolic 54 missense mutations 54 electron beam computed tomography 54 Vascular dementia 54 synovial cells 54 leukemia AML 54 childhood disintegrative disorder 54 parathyroid carcinoma 54 oral squamous cell 54 Gastroparesis 54 homocysteine concentrations 54 Retinitis pigmentosa 54 mycosis fungoides 54 acute myeloid 54 systemic juvenile idiopathic 54 Atopic dermatitis 54 nitrotyrosine 54 JAK mutations 54 serum triglyceride levels 54 FLT3 mutations 54 APOE ε4 54 Hyperthyroidism 54 obese postmenopausal 54 Dilated Cardiomyopathy 54 macrovascular disease 54 thrombotic complications 54 bacterial prostatitis 54 plasminogen activator inhibitor 54 untreated sleep apnea 54 chronic renal disease 54 GABRA2 54 chromosomal anomalies 54 low ptau levels 54 iron overload 54 β amyloid 54 hypertension diabetes mellitus 54 aminotransferases 54 cholecystokinin CCK 54 ApoE gene 54 intracranial atherosclerosis 54 Escherichia coli Klebsiella pneumoniae 54 TNFalpha 54 urinary albumin 54 TPMT 54 hyperinsulinemic 54 ductal adenocarcinoma 54 eosinophilic esophagitis 54 cardiovascular disease osteoporosis 54 molecular abnormalities 54 Crohn disease CD 54 eosinophilic pneumonia 54 aminotransferase ALT 54 spermidine 54 biologic pathways 54 myocardial infarction ventricular fibrillation 54 serum triglycerides 54 vascular reactivity 54 Hypophosphatasia 54 gastric cardia 54 cirrhotic liver 54 chromosomal aberrations 54 hemoglobin A1c levels 54 APOE genotype 54 variant angina 54 Ischemic Stroke 54 apoE4 54 silent ischemia 54 idiopathic thrombocytopenic purpura ITP 54 glomerular filtration rate 54 hypervolemic hyponatremia 54 Severe Combined Immunodeficiency 54 Acid reflux disease 54 nonhereditary 54 myofascial pain syndrome 54 Neovascular Age Related Macular 54 vitamin D insufficiency 54 Dilated cardiomyopathy 54 JMML 54 apolipoprotein E 54 Hutchinson Gilford progeria 54 Diabetic retinopathy 54 ARVD 54 bacterium Neisseria meningitidis 54 Impaired glucose tolerance 54 MC4R gene 54 Obstructive sleep apnea OSA 54 hydrops 54 AUDs 54 situ LCIS 54 Enzastaurin 54 cardio respiratory fitness 54 fructose intake 54 comorbid anxiety 54 Viral infections 54 aortic valve stenosis 54 Genetic mutation 54 Pulmonary arterial hypertension 54 HLA B# 54 Myocarditis 54 fatty acid oxidation 54 Adenomas 54 underactive thyroid gland 54 lipid elevations 54 thrombocytosis 54 myositis 54 Diabetes Interventions 54 choline intake 54 IDH1 mutation 54 skeletal muscle mass 54 sortilin 54 PPCM 54 thrombotic thrombocytopenic purpura TTP 54 Hemorrhagic 54 Hurler syndrome 54 obstructive coronary 54 Hemolytic uremic syndrome 54 podocytes 54 Iron Overload 54 PPAR γ 54 Respiratory syncytial virus RSV 54 Acute myeloid leukemia AML 54 genomewide 54 extrapyramidal symptoms 54 folate intake 54 cardiovascular disease hypertension 54 Neurodegenerative 54 Exertional 54 asymptomatic carotid stenosis 54 inherited predisposition 54 neuroinflammation 54 phenylketonuria 54 tau protein tangles 54 journal Arteriosclerosis Thrombosis 54 Uterine cancer 54 triglyceride concentrations 54 ovarian endometrial 54 Cancer Genetic Markers 54 phenotypic expression 54 hepatic lipase 54 cough dyspnea 54 inherited metabolic disorders 54 CYP#C# [001] 54 apolipoprotein E APOE 54 Li Huei Tsai 54 SETDB1 54 Chronic fatigue 54 V Leiden 54 juvenile myelomonocytic leukemia 54 postoperative pulmonary 54 Growth Hormone Deficiency 54 TGF b 54 skeletal fluorosis 54 remyelination 54 nephritis 54 Cholesterol Levels SPARCL 54 leukotriene pathway 54 transaminase levels 54 Entamoeba histolytica 54 Idiopathic 54 transthyretin amyloidosis 54 depressive symptomatology 54 vitamin D deficiency 54 Streptococcus pneumoniae Haemophilus influenzae 54 cAMP signaling 54 S#A# [002] 54 autoantibody positive 54 endotoxemia 54 neurological manifestations 54 murine model 54 abnormal glucose metabolism 54 Myelofibrosis 54 HLA DRB1 * 54 Cancer Incidence Mortality 54 Chronic Heart Failure 54 purpura ITP 54 advanced adenomas 54 lymphoproliferative disorder 54 hypophosphatemia 54 Polymorphisms 54 Hurthle cell 54 p tau 54 familial hypercholesterolaemia FH 54 chronic obstructive lung 54 Familial hypercholesterolemia 54 epithelial tumors 54 Idiopathic Pulmonary Fibrosis 54 diabetic nephropathy 54 candidemia 54 Genetic variations 54 Candidiasis 54 nondiabetic 54 lymphatic cancers 54 Catheter Associated 54 nephrogenic fibrosing dermopathy 54 PEDF 54 prolonged QT interval 54 postoperative AF 54 Acute myeloid leukemia 54 cardiac conduction 54 plasma kallikrein 54 premalignant lesions 54 elevated LDL 54 Valvular heart 54 dietary fructose 54 dyslipidemia abnormal 54 chromosome #p# [001] 54 enteroviral