Related by context. All words. (Click for frequent words.) 70 sporadic Creutzfeldt Jakob 69 MGUS 69 Chlamydia pneumoniae 69 familial pancreatic cancer 69 mtDNA mutations 68 methylation markers 68 herpesviruses 68 GBA mutations 68 CDH1 68 renal cell carcinomas 68 hamartomas 68 IgA deficiency 68 N. gonorrhoeae 68 #q# deletion 68 etiologic agent 67 XMRV infection 67 precursor lesions 67 extramedullary 67 bacteraemia 67 serologically 67 ADPKD 67 serous ovarian cancer 67 pilocytic astrocytomas 67 chromosomal rearrangement 67 gonococcal infection 67 P. knowlesi 67 microsatellite instability 67 MYH9 gene 67 CSF Tf 67 enteroviral 67 etiologic 67 familial ALS 67 LRRK2 mutations 67 mammographically 67 ALK mutations 67 HLA DRB1 67 anti JCV antibodies 67 epithelial tumors 67 EBV infection 67 obstructive coronary artery 67 missense mutations 67 C. trachomatis 66 prion infection 66 seropositivity 66 cardioembolic stroke 66 somatic mutations 66 mesotheliomas 66 Genetic variants 66 Epstein Barr virus EBV 66 PTPN# 66 node metastases 66 supratentorial 66 leiomyomas 66 LPA gene 66 precancerous cervical 66 genetic loci 66 hypermethylated 66 basal cell nevus syndrome 66 mucinous 66 TCF#L# gene 66 HbF 66 ABCB1 66 motor neuron degeneration 66 fluoroquinolone resistance 66 prostate cancer CaP 66 K ras mutations 66 haematological 65 L. pneumophila 65 causal variants 65 chromosomal anomalies 65 chromosomal mutations 65 subclinical hyperthyroidism 65 monogenic 65 Hashimoto thyroiditis 65 TGFBR1 * 6A 65 sporadic ALS 65 gastric carcinoma 65 Trichomonas vaginalis 65 genetic variants associated 65 diabetes mellitus DM 65 germline mutations 65 ataxias 65 SLNB 65 corona virus 65 lobular carcinoma 65 PTEN mutations 65 TMPRSS2 ERG fusion 65 human metapneumovirus 65 de ath 65 molecular abnormalities 65 Mycoplasma pneumoniae 65 Squamous 65 hepatocellular carcinomas 65 HER2 overexpression 65 Hurthle cell 65 neoplasias 65 APOE ε4 65 Cryptococcus neoformans 65 amyloid deposition 65 pathogenic mutations 65 HNPCC 65 lymphocytic 65 penetrance 65 ductal cancer 65 adenomatous polyps 65 susceptibility alleles 65 malignant nodules 65 LQTS 65 inherited mutations 65 distinct subtypes 65 Haptoglobin 65 hematopoietic cancers 65 familial aggregation 65 vivax 65 LRP5 65 carcinoid tumors 65 Chlamydia trachomatis 65 sputum specimens 65 EoE 65 gene APOE4 65 serologic 65 NNRTI resistance 65 nonmelanoma skin cancers 65 prognostic markers 65 subclinical 64 invasive lobular 64 MRSA isolates 64 airway hyperresponsiveness 64 carcinoid 64 autopsied brains 64 HLA B# 64 Trichophyton rubrum 64 virus XMRV 64 causative organism 64 neurologic complications 64 causative mutations 64 chlamydial infection 64 histopathologic examination 64 serologic tests 64 Variant Creutzfeldt Jakob Disease 64 tumoral 64 enterovirus infection 64 APOE e4 64 thyrotropin levels 64 elevated CRP 64 GPC5 64 benign polyps 64 Sporadic CJD 64 #F FDG PET 64 DNA methylation patterns 64 fluoroquinolone resistant 64 IPAH 64 immunodeficiency 64 latent celiac disease 64 bronchogenic carcinoma 64 hereditary predisposition 64 thyroglobulin 64 #q#.# [001] 64 thyroid nodules 64 carcinoids 64 virulence genes 64 ductal breast cancer 64 cardiac troponin 64 syndromic 64 myeloproliferative neoplasms 64 FTLD 64 atypical hyperplasia 64 osteosarcomas 64 nonhereditary 64 pituitary adenomas 64 immunocompetent 64 pancreatic adenocarcinoma 64 BRAF mutation 64 advanced neoplasia 64 Parkinsonian Syndromes 64 LTBI 64 susceptibility loci 64 neuroblastoma tumors 64 toxoplasma 64 hereditary hemochromatosis 64 SSc 64 MYCN amplification 64 Chronic lymphocytic leukemia 64 proband 64 Candida species 64 M. pneumoniae 64 colorectal adenoma 64 systemic amyloidosis 64 Adenomas 64 clade B 64 B7 H3 64 carotid plaques 64 paraneoplastic 64 malignant lesions 64 cTnT 64 SNP rs# [001] 64 UGT#A# * 64 P. malariae 64 de novo mutations 64 chlamydial 64 serologic testing 64 apolipoprotein E gene 64 colorectal carcinoma 64 genetic aberrations 63 Leukemias 63 microdeletions 63 JMML 63 KRAS oncogene 63 sonographic diagnosis 63 liver metastasis 63 squamous cell lung cancer 63 susceptibility gene 63 immunohistochemical 63 PrPSc 63 IL#B 63 intestinal biopsy 63 diffuse gastric 63 childhood leukemias 63 ApoE gene 63 arterial calcification 63 microRNA expression 63 IDH1 mutation 63 modifier genes 63 gene rearrangements 63 spontaneous mutations 63 neuroendocrine cancers 63 lung lesions 63 familial clustering 63 serum antibodies 63 euthymic patients 63 thrombophilia 63 varicella infection 63 bone scintigraphy 63 colorectal neoplasms 63 demyelinating 63 angiographically 63 Cholangiocarcinoma 63 causative genes 63 MSH2 63 Genetic predisposition 63 neurocognitive impairment 63 proteomic analysis 63 hyperplastic 63 CMV infection 63 Circulating tumor cells 63 HIV HCV coinfected 63 genetic heterogeneity 63 MCAD deficiency 63 gallstone disease 63 chromosome #p#.# 63 BCR ABL mutations 63 HSV1 63 brain lesions 63 C. jejuni 63 prion disease 63 elevated triglyceride levels 63 JAK2 mutation 63 cellular prion protein 63 Papillary 63 astrocytomas 63 metaplasia 63 fronto temporal dementia 63 histopathological 63 coinfection 63 presymptomatic 63 chest radiographs 63 clinically detectable 63 advanced adenomas 63 allelic variants 63 enteroviral infection 63 nodal metastasis 63 autonomic dysfunction 63 S. aureus isolates 63 mitochondrial disorders 63 gastric adenocarcinoma 63 recessive inheritance 63 #q#.# [002] 63 chromosomal aberrations 63 GABHS 63 BRAF mutations 63 progressive neurodegenerative disorder 63 genetic polymorphisms 63 S. Typhimurium 63 Plasmodium vivax 63 serological tests 63 Candida infection 63 autosomal dominant polycystic kidney 63 von Willebrand 63 Prion diseases 63 autoimmune thyroid 63 cryptococcal meningitis 63 paragangliomas 63 aneuploidies 63 Salmonella spp 63 Chronic pancreatitis 63 malignant neoplasm 63 viral etiology 63 Hutchinson Gilford progeria 63 intestinal metaplasia 63 HMPV 63 stratifying patients 63 parasitaemia 63 NRTI resistance 63 polymorphic ventricular tachycardia 63 lupus anticoagulant 63 diagnostic modality 63 respiratory viral infections 63 aggregated Abeta 63 colorectal adenocarcinoma 63 rs# [002] 63 neurosyphilis 63 CA MRSA infections 63 G6PD deficiency 63 abnormal prions 63 C. pneumoniae 63 Borrelia 63 monozygotic twins 63 pT2 63 β amyloid 63 CISH 63 nonalcoholic steatohepatitis NASH 62 invasive ductal 62 P. falciparum malaria 62 falciparum 62 Wwox 62 troponin T 62 ADAMTS# 62 KRAS mutations 62 TT genotype 62 mutant allele 62 cerebral microbleeds 62 ANCA associated 62 leukoencephalopathy 62 normal karyotype 62 tubercle bacillus 62 CD# expression [001] 62 incidentalomas 62 diagnostic biomarker 62 neoplasm 62 germline mutation 62 murine leukemia virus 62 familial adenomatous polyposis 62 Cytomegalovirus CMV 62 grade cervical intraepithelial 62 S OIV 62 ARVD 62 colorectal cancer CRC 62 K#R [002] 62 cardiac troponin T 62 cerebrospinal fluid CSF 62 SHANK3 62 Latent TB 62 Vesivirus 62 retrovirus XMRV 62 Variant CJD 62 homozygote 62 disease vCJD 62 Leydig cell 62 APOE genotype 62 gene locus 62 monoclonal gammopathy 62 Nonalcoholic fatty liver 62 cerebral angiography 62 miRs 62 essential thrombocythemia 62 breast carcinomas 62 hypercoagulable 62 transgene expression 62 Radiographic findings 62 telomere lengths 62 etiological factors 62 choriocarcinoma 62 Leptospira 62 chromosomal anomaly 62 BRAF V#E mutation 62 renal carcinoma 62 GISTs 62 Vitamin B# deficiency 62 HG PIN 62 dermatophytes 62 pulmonary metastases 62 holoprosencephaly 62 carcinoid tumor 62 Brugada syndrome 62 skeletal metastases 62 microdeletion 62 hepatoma 62 histopathologic 62 genomewide 62 H pylori 62 ImmuKnow 62 prostate cancer PCa 62 homozygosity 62 microbleeds 62 thymoma 62 herpes infection 62 genetic syndromes 62 ATG#L# 62 Clusterin 62 HHV 6 62 pulmonary TB 62 PTLD 62 Multidrug resistant 62 S. aureus infection 62 EUS FNA 62 lactose malabsorption 62 ischemic lesions 62 autosomal dominant disorder 62 gastrointestinal stromal tumors GISTs 62 cervical carcinoma 62 M. leprae 62 predisposing factor 62 Entamoeba histolytica 62 clinicopathologic 62 S. maltophilia 62 dominantly inherited 62 cystatin C 62 abnormal prion protein 62 MYH9 62 catheter angiography 62 choroidal neovascularization 62 #p#.# [001] 62 infantile hemangioma 62 AAT deficiency 62 metabolomic profiles 62 curable cancers 62 primary hyperparathyroidism 62 genomewide association studies 62 hypermethylation 62 C1q 62 TPMT 62 Sjögren syndrome 62 superinfection 62 haematopoietic 62 subclinical disease 62 enterococcal 62 MLH1 62 HIV seropositive 62 genes predisposing 62 genomic alterations 62 pre malignant lesions 62 CP CPPS 62 histologic subtype 62 TACI mutations 62 Immunohistochemical analysis 62 prion protein gene 62 immunochemical 62 colorectal neoplasia 62 S aureus 62 missense mutation 62 Cystatin C 62 SOD1 gene 62 herpes simplex encephalitis 62 isotypes 62 promoter methylation 62 chromosome #q# [001] 62 gene amplification 62 Endometrial cancer 62 chromosome abnormality 62 neurosensory 62 gene MECP2 62 Gorlin syndrome 62 intracranial hemorrhage ICH 62 pleural mesothelioma 62 LVNC 62 latently infected 62 IDH mutations 62 ductal adenocarcinoma 62 HBeAg negative 62 colonic polyps 62 coagulase negative staphylococci 62 HFE gene 62 PCNSL 62 T. vaginalis 62 atopic disorders 62 myeloproliferative diseases 62 causative gene 62 asymptomatic carriers 62 GSTM1 62 scintigraphic 62 cyclin E 62 bacterium Neisseria meningitidis 62 mutated K ras 62 pheochromocytoma 62 biochemical marker 62 transgenic rats 62 serotype #A 62 ELISpot 62 CIN3 62 aetiological 62 Epstein Barr Virus EBV 62 GBM tumors 62 calculi 62 histologic diagnosis 62 lymphatic tissue 62 S. neurona 62 Wernicke encephalopathy 62 thyroid carcinoma 62 ependymomas 61 CYP#D# gene 61 transgenic mouse models 61 antiphospholipid antibodies 61 pathologic examination 61 transcranial Doppler ultrasound 61 necrotizing pneumonia 61 T2DM 61 Prostatitis 61 classical scrapie 61 percutaneous biopsy 61 P. ovale 61 chlamydial infections 61 prostate adenocarcinoma 61 cytopathic 61 urine cytology 61 causative mutation 61 deCODE BreastCancer TM 61 PCA3 gene 61 eosinophilic 61 STAT4 61 NP CRNs 61 promoter hypermethylation 61 epigenetic markers 61 amnestic MCI 61 prostate carcinoma 61 nonischemic 61 malignant ovarian 61 esophageal squamous cell carcinoma 61 dysglycemia 61 enteroviruses 61 malignant polyps 61 POAG 61 clinico pathological 61 breast endometrial 61 Aspergillus infections 61 NPHP 61 paraganglioma 61 advanced adenoma 61 papillary carcinoma 61 Colon polyps 61 Epstein Barr Virus 61 genes differentially expressed 61 thyroid nodule 61 idiopathic myelofibrosis 61 malignant lymphoma 61 polypoid lesions 61 CHD7 61 Polycythemia vera 61 nondemented 61 biochemical abnormalities 61 PTEN gene 61 NGAL 61 chromosomal alterations 61 chromosome abnormalities 61 chronic hepatitis cirrhosis 61 CC genotype 61 gastric cancers 61 Relapsing remitting MS 61 myeloproliferative 61 neurocysticercosis 61 methicillin susceptible Staphylococcus aureus 61 splice junctions 61 atrophic gastritis 61 TP# gene 61 herpes zoster shingles 61 bladder cancers 61 narcolepsy cataplexy 61 hyperacute 61 glutamic acid decarboxylase 61 tuberculin skin testing 61 exfoliative glaucoma 61 chromosome #q 61 coagulation abnormalities 61 TP# mutation 61 T#I [002] 61 carotid stenosis 61 basal cell carcinoma BCC 61 testicular germ cell 61 Brugada Syndrome 61 acute rheumatic fever 61 urine NGAL 61 TTR amyloidosis 61 ZNF# 61 Neisseria 61 gestational diabetes mellitus 61 Ribavirin causes 61 infarcts 61 neurologic symptoms 61 C#Y 61 obstructive coronary 61 bronchoalveolar 61 chromosome #q#.# [001] 61 mammographic density 61 cholangiocarcinoma 61 congenital disorders 61 sequence homology 61 Serologic 61 atherothrombosis 61 premalignant lesions 61 aneuploid cells 61 liver transplantations 61 molecular subtypes 61 Anaplasma 61 acute aortic dissection 61 paramyxoviruses 61 MIF protein 61 autosomal dominant inheritance 61 chorioamnionitis 61 gonorrhoeae 61 atypical ductal hyperplasia 61 Enterobacteriaceae 61 A. fumigatus 61 thyrotropin 61 Intravenous immunoglobulin 61 Li Fraumeni syndrome 61 nonalcoholic steatohepatitis 61 HRCT 61 neuropathologic 61 ovarian malignancy 61 molecular biomarkers 61 generalized vitiligo 61 idiopathic PAH 61 hydrops 61 adenoma 61 immunodeficient 61 ApoE4 gene 61 methylated DNA 61 GSTP1 61 benign proliferative breast 61 sarcosine 61 transmissible spongiform encephalopathy 61 glaucomatous 61 LRAT 61 APOL1 61 alpha thalassemia 61 antiphospholipid syndrome 61 genomic deletions 61 mycobacterium tuberculosis 61 deletion 5q 61 D dimer 61 clefting 61 NPM1 mutations 61 bladder tumors 61 p tau 61 periodontal pathogens 61 mosaicism 61 oral squamous cell 61 BRCA1 mutation carriers 61 Vascular dementia 61 infecting organism 61 latent tuberculosis TB 61 neurological manifestations 61 HNSCC 61 nucleotide substitutions 61 Aspergillus species 61 HPV genotypes 61 HER2 positive cancers 61 neuropsychiatric disorder 61 immunized mice 61 thyroid dysfunction 61 Creutzfeld Jakob disease 61 lobular carcinomas 61 proliferative retinopathy 61 protein alpha synuclein 61 aberrant methylation 61 neurological abnormalities 61 Serological 61 NPM1 61 familial adenomatous polyposis FAP 61 granulomatous 61 Genetic mutation 61 perfusion abnormalities 61 pancreatic endocrine 61 infectious prion proteins 61 CCR5 delta# 61 NAFLD 61 cytomegalovirus infection 61 HCV infections 61 conserved sequences 61 H#Y 61 atypical scrapie 61 heterozygotes 61 Retinopathy 61 human herpesvirus 61 dengue haemorrhagic fever DHF 61 inherited predisposition 61 ASCUS 61 myelofibrosis polycythemia vera 61 immunohistochemical staining 61 AGHD 61 lymphoid tumors 61 transmissible spongiform encephalopathies TSEs 61 orchitis 61 metastatic prostate 61 Arrhythmogenic Right Ventricular Cardiomyopathy 61 differential gene expression 61 Immunohistochemical staining 61 rs# [001] 61 seminoma 61 tuberculous 61 proton MR spectroscopy 61 Thyroid disorders 61 Balamuthia 61 M#V mutation 61 FISH fluorescence 61 alpha synuclein protein 61 BRAF gene 61 metastatic lymph nodes 61 hyperhomocysteinemia 61 deleterious mutation 61 microalbuminuria 61 malignant growths 61 HIVAN 61 autosomal recessive 61 ORMDL3 61 metastatic neuroendocrine tumors 61 Henoch purpura 61 chromosome aberrations 61 cytogenetic abnormalities 61 neoplastic 61 intracerebral haemorrhage 61 hereditary nonpolyposis colorectal cancer 61 ano genital warts 61 lethal arrhythmias 61 phenotypic variation 60 prognostic indicator 60 Asymptomatic 60 lipid abnormalities 60 Mycobacterium leprae 60 urethritis 60 Campylobacter infections 60 PFGE 60 invasive carcinomas 60 H. influenzae 60 APOE e4 allele 60 Neisseria meningitides 60 Rectal cancer 60 prostate carcinogenesis 60 bacterial prostatitis 60 SCN1A 60 ENPP1 60 FDG PET scans 60 grade serous ovarian 60 overt hypothyroidism 60 pyelonephritis 60 amebiasis 60 transcranial Doppler 60 rotaviruses 60 transfusion transmitted 60 prion strains 60 orthologs 60 Plasmodium species 60 TRAF1 C5 60 MECP2 gene 60 seminomas 60 EGFR mutations 60 GSTT1 60 situ LCIS 60 GIST tumors 60 MMP# 60 microchimerism 60 #q#.# deletion syndrome 60 histocompatibility 60 ESBL producing E. coli 60 CNTNAP2 60 peritoneal carcinomatosis 60 BMPR2 60 Staphylococcus aureus infections 60 causative agent 60 distant metastasis 60 Alzheimer Disease AD 60 metabolic abnormalities 60 breast cancer susceptibility genes 60 adrenocortical cancer 60 #q# [001] 60 neuritic 60 spongiform 60 Aortic stenosis 60 KIF6 gene 60 PBMCs 60 neuro degenerative disease 60 Enterococci 60 congenital CMV infection 60 T1DM 60 conventional coronary angiography 60 ATTR CM 60 C. albicans 60 histologically 60 GNAQ 60 smoldering myeloma 60 p# mutation 60 haematologic 60 P. gingivalis 60 PARP inhibition 60 HCV infection 60 replicase 60 mediastinitis 60 gene BRCA2 60 diagnosing coronary artery 60 cardioembolic 60 allogeneic HSCT 60 chromosomal disorders 60 arrhythmogenic right 60 B. burgdorferi 60 monocytic 60 nephropathy 60 Prox1 60 autosomal dominant 60 plasmodium falciparum 60 Waldenstrom macroglobulinemia 60 polyomavirus nephropathy 60 cryptogenic 60 Cyclin E 60 lymph node metastasis 60 epistasis 60 angiosarcoma 60 LCMV infection 60 renal tumors 60 AUDs 60 bronchopulmonary dysplasia 60 ß amyloid 60 leptin deficiency 60 APOE4 60 Cytogenetic 60 adenocarcinomas 60 P falciparum 60 Mycobacterium bovis 60 prognostic marker 60 neurofibromas 60 CSF biomarkers 60 mycobacterial 60 mitochondrial DNA mtDNA 60 maternally inherited 60 unknown etiology 60 BRCA2 gene mutation 60 1 diabetes T1D 60 underlying pathophysiology 60 Genetic susceptibility 60 Metastases 60 LV dysfunction 60 phylogenetic analyzes 60 p# mutations 60 nonsmall cell lung cancer 60 Genetic mutations 60 MRSA strains 60 Ehrlichiosis 60 squamous intraepithelial lesions 60 metastatic lesion 60 cirrhosis liver failure 60 completely resected 60 oesophageal adenocarcinoma 60 NPM1 mutation 60 cystic fibrosis chronic pancreatitis 60 immunopathology 60 neonatal lupus 60 spongiform encephalopathies 60 sarcomatoid 60 neuropsychological impairments 60 C. neoformans 60 cardiac biomarkers 60 hypovitaminosis D 60 Helicobacter pylori infection 60 extrapulmonary 60 neoplastic diseases 60 somatic mutation 60 T2 lesions 60 micrometastasis 60 pathogenetic 60 endometrial stem cells 60 myelogenous leukemia 60 aetiology 60 lymphovascular invasion 60 WDR# 60 PALB2 60 Ischaemic heart 60 Salmonella Campylobacter 60 seronegative 60 Radical prostatectomy 60 immunostaining 60 gonococcal 60 ALI ARDS 60 candidemia 60 Medullary thyroid cancer 60 serovar 60 preoperative diagnosis 60 Genital herpes 60 MTHFD1L gene 60 heritable variation 60 HCV antibody 60 latent tuberculosis infection 60 ependymoma 60 malignant prostate 60 FDG PET imaging 60 epidemiologically 60 neoplasia 60 deCODE BreastCancer 60 invasive ductal breast cancer 60 subtyped 60 lymph node metastases 60 oxidized phospholipids 60 karyotypes 60 Rh factor 60 autoantibodies 60 abnormal cytology 60 D#N 60 genomic variants 60 KRAS mutation 60 haemochromatosis 60 microvascular disease 60 neuroblastomas 60 chronic pancreatitis 60 BRCA mutation carriers 60 PAOD 60 R#W [002] 60 WNV infections 60 congenital anomalies 60 H#Y mutation 60 latent TB infection 60 genital ulcers 60 aspergillosis 60 HLA DQ2 60 TTR gene 60 A. phagocytophilum 60 qRT PCR 60 R. equi 60 coronary calcification 60 isoenzyme 60 APOE gene 60 PCa 60 MAPK pathway 60 underdiagnosis 60 preeclamptic 60 idiopathic pulmonary 60 anaplastic 60 IgG antibody 60 antemortem 60 genital tract infections 60 adenomatous 60 diagnosed prenatally 60 colorectal carcinomas 60 microcephalin 60 sCD# 60 facial clefts 60 Wegener granulomatosis 60 amyloid beta plaques 60 BRAF V#E 60 HLA genes 60 NMIBC 60 diagnose Alzheimer disease 60 CYT# potent vascular disrupting 60 XMRV virus 60 demyelinating diseases 60 histologic subtypes 60 PNET 60 folate deficiency 60 pathological hallmark 60 retrospective cohort 60 autoimmune pancreatitis 60 autoimmune hemolytic anemia 60 silent myocardial ischemia 60 dyskeratosis congenita 60 NOD mouse 60 ELISPOT 60 p# activation 60 GH deficiency 60 transvaginal sonography 60 microscopic hematuria 60 Kufs disease 60 RAS mutations 60 precancer 60 malignant lymphomas 60 BARD1 60 leiomyoma 60 TSEs 60 murine models 60 urine dipstick 60 splice variants 60 SPECT CT imaging 60 von Hippel Lindau 60 uveal melanoma 60 biomarker identification 60 systemic scleroderma 60 SNP rs# [002] 60 Mendelian disorders 60 serological testing 60 Pseudomonas aeruginosa infections 60 vestibular schwannomas 60 biomarker assay 60 E. coli STEC 60 Tr DNA 60 NAT2 60 previously undescribed 60 thyroid stimulating hormone TSH 60 chromosome translocations 60 bronchoalveolar lavage 60 metastatic lesions 60 T SPOT.TB 60 Pulmonary hypertension 60 VNTR 59 M. bovis