subclinical

Related by string. Subclinical * * subclinical atherosclerosis . subclinical hypothyroidism . subclinical hyperthyroidism . subclinical mastitis . Subclinical hypothyroidism . subclinical zinc deficiency . subclinical cardiovascular disease . subclinical infection . subclinical disease . subclinical inflammation *

Related by context. All words. (Click for frequent words.) 67 subclinical hyperthyroidism 67 MGUS 67 penetrance 66 asymptomatic 66 neurologic symptoms 66 subclinical atherosclerosis 66 thyroid dysfunction 66 etiologic 66 hyperinsulinemia 66 elevated CRP 65 PCa 65 chronicity 65 chromosomal rearrangement 65 microalbuminuria 65 sCJD 64 APOE e4 64 NNRTI resistance 64 bacteriuria 64 hereditary hemochromatosis 64 autosomal dominant disorder 64 germline mutations 64 subclinical hypothyroidism 64 heterozygotes 64 T2DM 64 hyperplastic 64 subclinical disease 64 neurological abnormalities 64 ischemic lesions 63 ADPKD 63 proliferative diabetic retinopathy 63 neoplasm 63 acetabular dysplasia 63 autonomic dysfunction 63 histologically 63 CP CPPS 63 LV dysfunction 63 HGPIN 63 EBV infection 63 neurocognitive impairment 63 androgen deficiency 63 PAOD 63 prostate cancer CaP 63 neuronal dysfunction 63 airway responsiveness 63 aortic regurgitation 63 thyrotropin 63 anterior uveitis 63 elevated triglyceride levels 63 brain lesions 63 familial aggregation 63 LVNC 63 aminotransferases 63 monoclonal gammopathy 62 NAFLD 62 cryptogenic 62 IgA deficiency 62 neurocognitive deficits 62 pathophysiologic 62 HSV1 62 metabolic abnormalities 62 endotoxemia 62 Chlamydia pneumoniae 62 immunoreactivity 62 ABCB1 62 basal cell nevus syndrome 62 advanced adenoma 62 hematuria 62 microscopic hematuria 62 thyrotropin levels 62 parkinsonism 62 APOE ε4 62 AAT deficiency 62 invasive carcinoma 62 hamartomas 62 Acidosis 62 H pylori 62 NP CRNs 62 amyloid deposits 62 herpesviruses 62 gastric carcinoma 62 amyloid pathology 62 demyelinating 62 untreated celiac disease 62 B7 H3 62 atypical hyperplasia 62 alexithymia 62 missense mutations 62 PrPSc 62 cognitive dysfunction 62 familial ALS 61 albuminuria 61 neoplasias 61 troponin T 61 hepatocellular carcinomas 61 APOE4 61 microvascular disease 61 phenotype 61 hypogonadotropic hypogonadism 61 plasma kallikrein 61 overt hypothyroidism 61 primary aldosteronism 61 immunocompetent 61 amyloid deposition 61 APOE genotype 61 POAG 61 hyperalgesia 61 hepatic steatosis 61 elevated homocysteine 61 coronary calcification 61 seropositivity 61 FTLD 61 microbleeds 61 Asymptomatic 61 microsatellite instability 61 CIN3 61 T1DM 61 atypia 61 leiomyomas 61 obstructive coronary 61 pheochromocytoma 61 Leydig cell 61 angiographically 61 cTnT 61 genetic polymorphisms 61 alpha1 61 HbF 61 sporadic ALS 61 neuropathological 61 Hashimoto thyroiditis 61 nonalcoholic steatohepatitis NASH 61 nonischemic 61 diabetes mellitus DM 61 atopy 61 clinically detectable 61 hypoxemia 61 cerebral infarction 61 CMV infection 61 nephrogenic 61 missense mutation 61 proteinuria 61 epithelial tumors 61 renal dysfunction 61 hypercalciuria 61 coinfection 61 amnestic MCI 61 Vitamin B# deficiency 61 depressive symptomatology 61 adrenal function 61 orchitis 61 macroalbuminuria 61 latent celiac disease 61 GH deficiency 61 airway hyperresponsiveness 61 aminotransferase levels 61 plasma lipid 60 GSTM1 60 alanine aminotransferase ALT 60 MetS 60 haemolysis 60 clinically insignificant 60 premalignant 60 calculi 60 autoimmune thyroid 60 diabetic kidney 60 HBV infection 60 gallstone disease 60 proliferative retinopathy 60 neuropsychological impairments 60 malignant transformation 60 carotid stenosis 60 chronic hepatitis cirrhosis 60 silent myocardial ischemia 60 enteroviral infection 60 neuritic 60 myocardial ischemia 60 GBA mutations 60 TGFBR1 * 6A 60 dopaminergic therapy 60 predisposing factor 60 hydronephrosis 60 situ LCIS 60 glomerular filtration 60 familial pancreatic cancer 60 HER2 overexpression 60 granulomatous 60 Sjögren syndrome 60 rheumatoid factor 60 Subgroup analyzes 60 IGFBP 3 60 cervical carcinoma 60 infarcts 60 rs# [002] 60 germline mutation 60 hematopoietic cancers 60 psychiatric comorbidity 60 prothrombotic 60 lactate dehydrogenase LDH 60 IL 1ß 60 neurologic deficits 60 familial clustering 60 abnormalities 60 thyroglobulin 60 glucose intolerance 60 amenorrhoea 60 myeloproliferative diseases 60 AUDs 60 gastric adenocarcinoma 60 pericardial effusion 60 Hurthle cell 60 Genetic predisposition 60 comorbid disorders 60 mucinous 60 neoplastic 60 MYH9 gene 60 elevated LDH 60 coronary stenosis 60 coagulopathy 60 abnormal lipid 60 MYCN amplification 60 hereditary predisposition 60 chlamydial infection 60 extrapyramidal symptoms 60 heterozygous 60 familial adenomatous polyposis 60 chlamydial 60 lobular carcinoma 60 micrometastases 60 transferrin saturation 60 subsyndromal 60 antibody titer 60 PTPN# 60 neovascular 60 arterial calcification 59 chromosomal aberrations 59 adenoma 59 acidosis 59 neoplasia 59 prostate carcinogenesis 59 presymptomatic 59 XMRV infection 59 endometrial hyperplasia 59 chorioamnionitis 59 eosinophilia 59 periventricular leukomalacia 59 underlying pathophysiology 59 adenomatous polyps 59 colorectal neoplasms 59 serum cortisol 59 Prehypertension 59 histologically proven 59 hippocampal atrophy 59 biochemical markers 59 subthreshold 59 59 prion infection 59 elevated ALT 59 hypoperfusion 59 insulin resistance 59 etiology 59 steatosis 59 hepatitis B infection 59 narcolepsy cataplexy 59 osteocalcin 59 giant cell arteritis 59 cerebellar 59 asymptomatic carriers 59 acute aortic dissection 59 onset diabetes mellitus 59 shorter telomere length 59 Haptoglobin 59 systolic dysfunction 59 G allele 59 mitochondrial dysfunction 59 artery stenosis 59 serum IGF 59 cardiac fibrosis 59 tumoral 59 #q#.# deletion syndrome 59 metabolic acidosis 59 viremia 59 motor neuron degeneration 59 hyperglycaemia 59 renal cell carcinomas 59 atopic 59 prepubertal 59 FDG uptake 59 fasting insulin 59 susceptibility gene 59 BRCA mutation 59 CIN2 + 59 ApoE4 59 IUGR 59 perfusion abnormalities 59 choroidal neovascularization 59 pathologic diagnosis 59 histopathological 59 polyposis 59 hyperplasia 59 lung edema 59 EGFR expression 59 Cowden syndrome 59 white matter hyperintensities 59 pathologic fractures 59 atrophic gastritis 59 alkalosis 59 serum antibodies 59 EoE 59 mtDNA mutations 59 cerebral infarctions 59 elevated triglycerides 59 geographic atrophy 59 prognostic marker 59 histologic 59 E selectin 59 highly heritable 59 atherogenic dyslipidemia 59 autoimmune thyroiditis 59 nephrotoxicity 59 lipid abnormalities 59 GISTs 59 MTHFR 59 developmental abnormalities 59 MLH1 59 C. pneumoniae 59 SGPT 59 olfactory dysfunction 59 predisposing factors 59 chromosomal alterations 59 inducible nitric oxide synthase 59 etiological 59 SLNB 59 adrenalectomy 59 transaminase elevations 59 metabolic disturbances 59 K ras mutations 59 essential thrombocythemia 59 ascites 59 IPAH 59 inherited predisposition 59 systemic inflammation 59 osteopenic 59 corticosterone levels 59 glomerular 59 microglial 59 transaminase levels 59 oxidized phospholipids 59 varicoceles 59 thyroid nodules 59 necrotizing 59 colorectal adenoma 59 serum homocysteine 59 aetiological 59 myeloproliferative 59 SNP rs# [002] 58 hyperacute 58 SRBD 58 androgen excess 58 mIU L 58 sonographic diagnosis 58 nonalcoholic steatohepatitis 58 pathophysiological mechanisms 58 UGT#A# * 58 endothelial activation 58 Chronic pancreatitis 58 lacunar 58 prion disease 58 hyperhomocysteinemia 58 SMAD4 58 PlGF 58 CD#c 58 detrusor 58 homozygotes 58 polypoid lesions 58 osteosarcomas 58 paragangliomas 58 bladder carcinoma 58 biochemical abnormalities 58 precursor lesions 58 scintigraphic 58 #.#ng/ml 58 serum selenium 58 astrocytic 58 microdeletions 58 CC genotype 58 leukocytosis 58 Immunohistochemical analysis 58 amyloid plaque 58 eosinophilic 58 cervical lesions 58 Cognitive impairment 58 coronary artery calcium 58 antiphospholipid antibodies 58 latent tuberculosis infection 58 immunohistochemical 58 ovarian hormones 58 pre malignant lesions 58 LV hypertrophy 58 pathogenetic 58 PTEN mutations 58 obstructive coronary artery 58 atrophic 58 APOE e4 gene 58 bone scintigraphy 58 PTEN gene 58 p# activation 58 pathologic 58 serum folate concentrations 58 LV ejection fraction 58 pyelonephritis 58 MMP# 58 post thrombotic syndrome 58 nephropathy 58 advanced adenomas 58 biochemical recurrence 58 specific antigen PSA 58 autoregulation 58 syndromal 58 C. trachomatis 58 subclinical cardiovascular disease 58 varicocele 58 pathophysiological 58 ovarian carcinoma 58 Barrett esophagus BE 58 inhibin B 58 lymph node involvement 58 thyroid carcinoma 58 serum ferritin 58 CTEPH 58 monogenic 58 metaplasia 58 APOE allele 58 recurrent VTE 58 inherited mutations 58 urothelial carcinoma 58 vesicoureteral reflux 58 folate deficiency 58 Cushing syndrome 58 LTBI 58 BRAF mutation 58 immunodeficiency 58 neurologic complications 58 Proteinuria 58 albumin excretion 58 brain parenchyma 58 de novo mutations 58 viral etiology 58 androgen deprivation 58 mRNA expression 58 familial hypercholesterolemia 58 CSF biomarkers 58 bronchopulmonary dysplasia 58 colorectal polyp 58 hyperparathyroidism 58 aetiology 58 serum cholesterol 58 HeFH 58 periventricular 58 interstitial fibrosis 58 hydroxyvitamin D levels 58 HER2 expression 58 metastatic lesions 58 HIV HCV coinfected 58 hypercalcemia 58 β amyloid 58 PCNSL 58 periodontitis 58 grade cervical intraepithelial 58 autoantibodies 58 parenchymal 58 neurodevelopmental impairment 58 affective psychoses 58 HER2 amplification 58 thromboembolic complications 58 carotid IMT 58 protein tyrosine phosphatase 58 serum testosterone 58 LRRK2 mutations 58 urolithiasis 58 selenium deficiency 58 thyrotoxicosis 58 myocardial dysfunction 58 arrhythmogenic 58 GSTT1 58 mammographically 58 osteochondromas 58 ASCUS 58 antiphospholipid syndrome 58 tryptase 58 HYPP 58 hypertensives 58 colorectal neoplasia 58 CagA 58 IgG antibodies 58 euthymic patients 58 left ventricular dysfunction 58 SSc 58 LRAT 58 prognostic significance 58 nonmelanoma skin cancers 58 cellular prion protein 58 lymphocytic 58 lymphadenopathy 58 intraventricular hemorrhage 58 congenital anomalies 58 intestinal metaplasia 58 lichen planus 58 fetal malformations 58 cardiac dysfunction 58 cognitively normal 58 KCNH2 58 chromosome #q# [001] 58 serum phosphate 58 transgene expression 58 cervical intraepithelial neoplasia 58 NAbs 58 nasal polyposis 58 urate levels 58 Subgroup analysis 58 HNPCC 58 TP# mutations 58 IgA antibodies 58 breast carcinoma 58 epididymitis 58 cardiac troponin T 58 serum urate levels 57 LRP5 57 atherosclerotic lesion 57 nodal metastases 57 paraneoplastic 57 immunohistochemical staining 57 axonal damage 57 CYP #A# 57 Subclinical 57 phenotypic variation 57 pretest probability 57 chest radiograph 57 neoplasms 57 polyp recurrence 57 tHcy 57 lesions 57 BMPR2 57 atherothrombotic 57 bullous 57 renal insufficiency 57 generalized epilepsy 57 pressor response 57 gene polymorphisms 57 pernicious anemia 57 intracranial hemorrhage ICH 57 varicella infection 57 idiopathic PAH 57 serologically 57 recurrent UTI 57 testicular tumors 57 Ischemic 57 myocardial ischaemia 57 superinfection 57 colorectal carcinoma 57 hyperammonemia 57 leukemia AML 57 HRCT 57 hypermethylated 57 mitochondrial mutations 57 lysosomal storage disease 57 cellularity 57 cognitive deficits 57 lymph node metastasis 57 vessel occlusion 57 intact parathyroid hormone 57 deletion 5q 57 genes predisposing 57 lactate dehydrogenase 57 intracerebral 57 incidentalomas 57 CHD7 57 urine NGAL 57 myocardial fibrosis 57 morphological abnormalities 57 polycystic ovary syndrome PCOS 57 nitrotyrosine 57 serum retinol 57 atherosclerotic lesions 57 asymptomatically 57 clinico pathological 57 systemic amyloidosis 57 hypovitaminosis D 57 microglial activation 57 thyroid hormone levels 57 gene polymorphism 57 Multivariate analysis 57 ferritin 57 nonmelanoma skin cancer 57 JAK2 mutation 57 neurological manifestations 57 plasma pharmacokinetics 57 Clusterin 57 beta1 integrin 57 allelic variants 57 nondemented 57 ADAMTS# 57 gene APOE4 57 choroidal 57 sonographically 57 tumorigenicity 57 denervation 57 poorer prognosis 57 arterial thickening 57 endometrial carcinoma 57 microvascular dysfunction 57 thromboembolic 57 comorbid anxiety 57 hepatocellular 57 unknown etiology 57 Rap1 57 thrombophilia 57 p# mutations 57 herpes zoster shingles 57 paroxysmal AF 57 mesotheliomas 57 Logistic regression analysis 57 seminomas 57 mosaicism 57 nanomolar 57 haematopoietic 57 serum aminotransferase levels 57 sonographic findings 57 congenital deficiency 57 neuroimaging studies 57 IGFBP 57 TNF blocker therapy 57 PsA 57 sporadic Creutzfeldt Jakob 57 prodromal 57 COL#A# 57 TT genotype 57 enterovirus infection 57 urinary albumin 57 nonalcoholic fatty liver 57 occlusive disease 57 etiologies 57 serum albumin 57 endocannabinoid signaling 57 colonic mucosa 57 GSTM1 gene 57 neurosensory 57 cardiac troponin 57 cardioembolic stroke 57 carcinoids 57 TNFalpha 57 #q#.# [001] 57 sonographic appearance 57 renal scarring 57 genetic syndromes 57 #q# deletion 57 cytopenias 57 ApoE4 gene 57 enterocolitis 57 obstructive CAD 57 morphologic 57 ACh 57 Vitamin D insufficiency 57 HBeAg negative 57 neurofibromas 57 Non Alcoholic Steatohepatitis 57 herpes simplex encephalitis 57 Orthostatic hypotension 57 disc degeneration 57 eotaxin 57 Multivariate analyzes 57 astrocytomas 57 Genetic variants 57 idiopathic 57 bowel polyps 57 ARVD 57 #q#.# [002] 57 noncardiac 57 rs# [004] 57 M. leprae 57 supratentorial 57 cardiac insufficiency 57 TLR3 57 left ventricular hypertrophy 57 parkinsonian 57 Epidemiologic studies 57 cardioprotective effects 57 radiographic findings 57 recurrent miscarriage 57 elevated IOP 57 fetuin 57 CYP#D# 57 μmol L 57 gliosis 57 MSH2 57 neurosyphilis 57 recurrent wheezing 57 R. equi 57 C#Y 57 β blockers 57 salmeterol HFA MDI 57 atherothrombotic disease 57 advanced neoplasia 57 mitral stenosis 57 chest radiographs 57 extramedullary 57 Squamous 57 APOC3 57 pulmonary dysfunction 57 osteopontin 57 serum BDNF 57 proband 57 seronegative 57 PTLD 57 HBsAg 57 serum concentrations 57 vasogenic edema 57 null mice 57 neurologic disorder 57 LQTS 57 parasitaemia 57 latently infected 57 LPA gene 57 GSTP1 57 asymptomatic carotid stenosis 57 adrenal insufficiency 57 chromosomal anomalies 57 psychiatric comorbidities 57 neuropathologic 57 chromosomal instability 57 pathologic examination 57 fetal chromosomal 57 benign breast 57 aneuploidies 57 soluble CD# ligand 57 dermatomyositis 57 somatic symptoms 57 aortic atherosclerosis 57 prostate carcinoma 57 hemodilution 57 mitochondrial DNA mutations 57 nerve degeneration 57 hyperprolactinemia 57 histopathologic examination 57 Longitudinal studies 57 immunodeficiencies 57 autistic traits 57 eccrine 57 potentially modifiable 57 HFE gene 57 exfoliative glaucoma 57 serologic 57 thrombotic complications 57 detrusor overactivity 57 Endothelial dysfunction 57 clusterin 57 hypovolemia 57 hypercapnia 57 DNMT1 57 malignant lymphoma 57 node metastases 57 urethritis 57 hepatic fibrosis 57 definite stent thrombosis 57 hypopituitarism 57 spirometric 57 toxoplasma 57 T1D 57 asplenia 57 pharmacokinetic interactions 57 chloride secretion 57 serum calcium 57 thrombocytosis 57 infectious mononucleosis 57 Raf MEK ERK 57 fibrocystic 57 cerebrovascular accident 57 abdominal adiposity 57 postoperative morbidity 57 NOMID 57 corticosteroid therapy 57 atherosclerosis 57 rebleeding 57 lymph node metastases 57 Mycoplasma pneumoniae 57 polyhydramnios 57 premorbid 56 carotid atherosclerosis 56 DRD2 56 pharmacologic intervention 56 primary ovarian insufficiency 56 cryptorchidism 56 myeloperoxidase 56 bronchoalveolar lavage 56 thyroid stimulating hormone 56 abnormal lipid levels 56 vascular cognitive impairment 56 cytopathic 56 nonhereditary 56 alanine aminotransferase 56 metabolic syndrome MetS 56 Neovascular AMD 56 MAOA 56 vascular inflammation 56 invasive carcinomas 56 anatomical abnormalities 56 IL 1beta 56 dose ionizing radiation 56 catheter angiography 56 TCF#L# gene 56 serum IgE 56 liver histology 56 deleterious mutations 56 surrogate marker 56 preeclamptic 56 microdeletion 56 SNHL 56 anti JCV antibodies 56 virulence genes 56 antibody titers 56 unmeasured confounding 56 cerebrospinal fluid CSF 56 bullous pemphigoid 56 thiopurine 56 Thrombocytopenia 56 carotid plaque 56 mediastinitis 56 osteochondroma 56 bacteraemia 56 perfusion defects 56 plasma folate 56 cervical lymph nodes 56 coronary artery calcification 56 CD# expression [001] 56 microvascular complications 56 neuroblastomas 56 breast carcinomas 56 cranial irradiation 56 hypophosphatemia 56 arteriography 56 ventricular dilatation 56 BLLs 56 epithelial barrier 56 ataxias 56 psychiatric morbidity 56 grade squamous intraepithelial 56 pg ml 56 postoperative delirium 56 variant alleles 56 comorbidity 56 pT3 56 PDGFR 56 Wernicke Korsakoff syndrome 56 neuropsychological deficits 56 vimentin 56 Leydig cells 56 CD# expression [002] 56 S. neurona 56 activated microglia 56 troponins 56 azoospermia 56 dystrophies 56 carcinoembryonic antigen 56 intestinal permeability 56 euthyroid 56 normotensive 56 autosomal dominant 56 atherosclerotic 56 APOL1 56 MECP2 gene 56 ENaC 56 OSAHS 56 corpus luteum 56 hyperintense lesions 56 heterozygosity 56 hyperbilirubinemia 56 lung lesions 56 curative resection 56 AST ALT 56 hydrops 56 malignant nodules 56 NGAL 56 heritability 56 metastatic prostate 56 biochemical marker 56 HLA DRB1 * 56 dysuria 56 serum PTH 56 MSMB 56 Legg Calvé Perthes disease 56 activin 56 Leukemias 56 experimentally induced 56 elevated serum creatinine 56 demyelination 56 neoplastic lesions 56 ductal breast cancer 56 nephrolithiasis 56 adnexal mass 56 pT2 56 ADPKD patients 56 multivariable analysis 56 cyclin E 56 STAT4 56 MALT lymphoma 56 mammary tumors 56 hypercoagulable 56 cholestasis 56 Wwox 56 BRCA carriers 56 thyroiditis 56 lipid concentrations 56 SHANK3 56 hypoplasia 56 postnatally 56 Fas ligand 56 p#INK#a 56 fibrosis 56 neurofibrillary tangles 56 pCR 56 acute leukemias 56 BRCA1 mutation carriers 56 JAK mutations 56 Alzheimer pathology 56 carotid bruit 56 vitamin D inadequacy 56 TNF antagonist 56 hepatic enzyme 56 ocular toxicity 56 virological response 56 metabolic derangement 56 Helicobacter pylori infection 56 prostatic hyperplasia 56 prognostic indicator 56 Heritability 56 MYH9 56 medial temporal 56 Wegener granulomatosis 56 hypermethylation 56 rCBF 56 Histopathologic examination 56 vitamin D insufficiency 56 inotropic 56 mesangial 56 interstitial pneumonia 56 stratifying patients 56 S#A# [002] 56 basal cell cancers 56 intestinal biopsy 56 subfertility 56 macrophage infiltration 56 IGF2 56 osteogenic differentiation 56 allergic sensitization 56 neurodevelopmental outcome 56 undergoing radical prostatectomy 56 cystatin C 56 urine cytology 56 mesenteric 56 hypercoagulability 56 serum leptin 56 glaucomatous 56 haematological 56 coronary artery atherosclerosis 56 hypertrophic scars 56 adenomatous 56 adiponectin levels 56 rs# [001] 56 HNSCC 56 prognostic factor 56 paresis 56 FGF2 56 ε4 56 pathogenic mechanisms 56 TNFa 56 SNP rs# [001] 56 urinary excretion 56 SE alleles 56 cerebral vasospasm 56 unmeasured confounders 56 overt nephropathy 56 atypical scrapie 56 #F FDG PET 56 alkaline phosphatase ALP 56 lactose maldigestion 56 myopathy 56 infarctions 56 bronchogenic carcinoma 56 cardioprotection 56 familial AF 56 genetic polymorphism 56 hydroxyvitamin D concentrations 56 NMIBC 56 intermittent hypoxia 56 plasminogen activators 56 atherothrombosis 56 macrovascular disease 56 hypogonadal 56 splenic 56 intestinal polyps 56 Fatty liver

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