Related by context. All words. (Click for frequent words.) 68 MYH9 gene 67 MTHFR 66 apolipoprotein E gene 66 UGT#A# * 65 CYP#C# * 65 Von Willebrand 65 MSH2 64 Hashimoto thyroiditis 64 STAT4 64 hereditary hemochromatosis 64 ApoE gene 64 Hemophilia B 64 APOE4 63 HFE gene 63 TCF#L# gene 63 apolipoprotein E4 63 familial hypercholesterolemia 63 mutated BRCA1 63 C#Y 63 thromboembolism 63 PTPN# 63 BRCA1 mutations 63 ApoE4 gene 63 thrombophilia 63 von Willebrand 63 lupus anticoagulant 63 mtDNA mutations 63 G6PD deficiency 63 gestational diabetes mellitus 63 MLH1 62 macrophage migration inhibitory 62 proband 62 CDH1 62 Polycystic ovary syndrome PCOS 62 macrophage colony stimulating 62 ABCB1 62 pre eclamptic 62 postoperative delirium 62 inherited mutations 62 endometrial hyperplasia 62 familial adenomatous polyposis 62 G allele 62 ADPKD 62 idiopathic PAH 62 APOE e4 62 prolonged QT interval 62 narcolepsy cataplexy 62 CYP#C# [002] 62 BRCA2 carriers 62 #q# deletion 62 familial adenomatous polyposis FAP 62 rs# [002] 62 HLA B# 62 APOC3 62 BRCA2 gene mutation 62 K ras mutations 62 BRCA1 BRCA2 62 susceptibility gene 61 elevated triglyceride levels 61 breast cancer genes BRCA1 61 KIF6 gene 61 Vascular Endothelial Growth 61 CHEK2 61 insulin resistance syndrome 61 Genetic variants 61 plasminogen activator inhibitor 61 leiomyomas 61 seropositivity 61 elevated triglycerides 61 cholesteryl ester transfer 61 recurrent UTI 61 diabetic kidney 61 prothrombotic 61 APOE gene 61 LRP5 61 GSTP1 61 persistent pulmonary hypertension 61 abdominal adiposity 61 chorioamnionitis 61 CCR5 delta# 61 heterozygotes 61 apolipoprotein E 61 Non Alcoholic Steatohepatitis 61 AAT deficiency 60 Chlamydia pneumoniae 60 paraneoplastic 60 germline mutation 60 Heterozygous 60 COX2 60 gene BRCA2 60 CC genotype 60 PIGF 60 haptoglobin 60 HNPCC 60 BRIP1 60 subclinical hyperthyroidism 60 methylenetetrahydrofolate reductase 60 Darapladib 60 lichen planus 60 2 diabetes T2D 60 BRCA gene mutation 60 lipid abnormalities 60 discontinued Viread 60 VKORC1 60 fetuin 60 IgA deficiency 60 cardiac insufficiency 60 germline mutations 60 vWD 60 APOL1 60 cell adhesion molecule 60 ApoE 60 Lymphocytic 60 ApoE4 60 TGFBR1 * 6A 60 venous thrombosis 60 BRCA mutation 60 triglyceride concentrations 60 glial derived neurotrophic 60 K#N 60 C. trachomatis 60 homozygotes 60 Fatty Liver Disease 60 familial pancreatic cancer 60 autosomal recessive 60 gastric carcinogenesis 60 H. influenzae 60 chlamydial 60 ApoE4 allele 60 potentially modifiable 60 BRCA2 gene 60 Bucindolol 59 CIN2 + 59 complement inhibitor eculizumab 59 Metal Responsive Transcription 59 congenital toxoplasmosis 59 ertapenem 59 deep vein thromboses 59 granulocyte macrophage colony stimulating 59 CFTR gene 59 Brain derived neurotrophic 59 Proteinuria 59 dopamine receptor gene 59 oesophageal adenocarcinoma 59 Angiotensin II 59 APOE genotype 59 Epidermal Growth Factor Receptor 59 neurologic complications 59 HLA DRB1 * 59 noncarriers 59 Asymptomatic 59 Hypertriglyceridemia 59 colorectal adenoma 59 NKX2 59 breast endometrial 59 oligohydramnios 59 Premature Aging 59 basal cell nevus syndrome 59 TCF#L# 59 BMPR2 59 airway hyperresponsiveness 59 Ad5FGF 4 59 Li Fraumeni 59 Thromboembolism 59 Neurofibromatosis type 59 LQTS 59 genes CYP#C# 59 breast cancer metastasis 59 Familial hypercholesterolemia 59 missense mutation 59 hydrops 59 Fibroblast growth 59 cause cardiac channelopathies 59 nondiabetics 59 COL#A# 59 Aortic stenosis 59 ASCUS 59 mosaicism 59 BRCA2 mutation carriers 59 KRAS oncogene 59 haloperidol Haldol 59 C. pneumoniae 59 autoimmune thyroid 59 TT genotype 59 elevated CRP 59 Hypertrophy 59 alpha1 antitrypsin deficiency 59 nonalcoholic steatohepatitis NASH 59 atypical hyperplasia 59 GSTM1 gene 59 PTEN mutations 59 atrophic gastritis 59 IL#R 59 BRAF V#E 59 nonmelanoma skin cancers 59 CYP#C# gene 59 autosomal recessive disease 59 Subgroup analysis 59 CYP#A# CYP#D# 59 GSTT1 59 von Hippel Lindau 59 Nonalcoholic fatty liver 59 β blockers 59 Platelet Derived Growth 59 advanced adenoma 59 VEGF Vascular Endothelial Growth 59 carotid plaque 59 smoldering myeloma 59 angiotensin converting enzyme 59 BRCA1 mutation carriers 59 underactive thyroid gland 59 nonalcoholic steatohepatitis 59 diuretic hydrochlorothiazide 59 arterial calcification 59 gallstone disease 59 coagulation abnormalities 59 Leydig cell 59 GRK5 59 TNF tumor necrosis 59 procollagen 59 Mg Uk 59 G CSFs 59 Interferon gamma 59 PAOD 59 aneuploidy 59 PDGFR 59 precancerous cervical 59 post transplant lymphoproliferative 59 placental malaria 59 Total Mainline Load 59 testicular tumors 59 Von Willebrand disease 59 APOE e4 gene 58 plasma lipid 58 deep venous thromboses 58 unfavorable prognostic 58 nonischemic 58 Tumor Necrosis Factor 58 mitochondrial toxicity 58 trimethoprim sulfamethoxazole 58 thyroid hormone levels 58 HLA B 58 hyperparathyroidism 58 finasteride Proscar 58 sCJD 58 thrombocytopenic 58 SGPT 58 BRCA2 breast cancer 58 Haptoglobin 58 Endometrial cancer 58 Autoantibodies 58 heterotaxy 58 Gestational 58 HMGA1 58 ACE Inhibitors 58 deletion 5q 58 modifiable cardiovascular 58 herpesviruses 58 hypovitaminosis D 58 familial ALS 58 hereditary predisposition 58 variant alleles 58 TMEM#B 58 CYP#D# gene 58 metaplasia 58 gestational hypertension 58 acarbose 58 colorectal carcinoma 58 chromosomal rearrangement 58 CYP#D# 58 recurrent VTE 58 Invasive Breast Cancer 58 BARD1 58 advanced neoplasia 58 euthyroid 58 Helicobacter pylori infection 58 Respiratory Syncytial Virus RSV 58 induce orthostatic hypotension 58 gene APOE 58 Hutchinson Gilford progeria 58 advanced adenomas 58 CHD7 58 serum potassium 58 Janus kinase 58 ADAMTS# 58 gene locus 58 hereditary nonpolyposis colorectal cancer 58 relapsed ALL 58 isoenzyme 58 sFlt 1 58 severe congenital neutropenia 58 NIDDM 58 ORMDL3 58 gastric carcinoma 58 transferrin saturation 58 Pulmonary hypertension 58 serum triglycerides 58 alpha1 58 HIV HCV coinfected 58 homozygous familial hypercholesterolemia 58 blood clotting protein 58 hypercalciuria 58 APOE ε4 58 neoplasias 58 monozygotic twin 58 thyrotropin 58 Klinefelter syndrome 58 gestational diabetes mellitus GDM 58 progressive neurodegenerative disorder 58 von Willebrand disease 58 TP# mutation 58 genes predisposing 58 CP CPPS 58 Brugada Syndrome 58 hypercholesterolaemia 58 HLA DRB1 58 chloride secretion 58 Trichomonas vaginalis 58 loop diuretics 58 bronchopulmonary dysplasia 58 Serum concentrations 58 MC4R gene 58 G#S mutation 58 fructose intolerance 58 intensive statin therapy 58 nonhereditary 58 Homozygous 58 Leukemias 58 NOTCH1 58 Myocardial infarction 58 spinocerebellar ataxia 58 lupus scleroderma 58 acute humoral rejection 58 Naive Patients 58 fetal chromosomal 58 activin 58 steroid dexamethasone 58 postoperative pulmonary 58 haemochromatosis 58 apoC III 58 Polycystic Ovarian Syndrome PCOS 58 Heavy menstrual bleeding 58 testicular germ cell 58 Lipoprotein 58 Hypotension 58 perioperative complications 58 Hepatitis B Virus 58 DRD2 58 e4 allele 58 polycystic ovary syndrome PCOS 58 TP# mutations 58 Papillary 58 uPA 58 Genetic mutation 58 heterozygous 58 PLX STROKE targeting 58 pneumococci 57 Human papillomavirus 57 inducible nitric oxide synthase 57 HMG CoA reductase inhibitors 57 Parnate 57 HeFH 57 glomerular filtration 57 hypercoagulability 57 IPAH 57 leptin deficiency 57 Adjuvant chemotherapy 57 AAT Deficiency 57 MELAS 57 pancreatic prostate 57 homozygote 57 Genetic predisposition 57 antiphospholipid antibodies 57 Enlarged prostate 57 mutated BRCA 57 Thrombotic 57 adiponectin levels 57 HER2 expression 57 diabetes mellitus DM 57 thromboembolic disease 57 subependymal giant cell 57 Fragile X gene 57 PON1 gene 57 mammographic density 57 Acidosis 57 GBA mutations 57 hyperplasia BPH 57 DQB1 * 57 myeloproliferative neoplasms 57 1 receptor IGF 57 isoprostane 57 microvascular disease 57 Vitamin B# deficiency 57 STK# gene 57 LPA gene 57 interferon pathway 57 fetal malformations 57 genetic polymorphisms 57 Gene Mutation 57 osteocalcin 57 serum IGF 57 Glucocorticoids 57 Severe Combined Immunodeficiency 57 pigment epithelium derived 57 allelic variants 57 HGPIN 57 hepatitis B infection 57 CYP #A# 57 hemochromatosis 57 Bronchopulmonary Dysplasia 57 receptor blocker 57 rs# [001] 57 J. Clin 57 eotaxin 57 external genital lesions 57 monogenic 57 normal karyotype 57 Antihemophilic Factor von Willebrand 57 chromosomal defect 57 apolipoprotein E APOE 57 C#BL/#J 57 ADAM# 57 fibroblast growth 57 Fas ligand 57 Arrhythmogenic 57 Soft Tissue Sarcoma 57 pyelonephritis 57 IUGR 57 cryptorchidism 57 polyp recurrence 57 genetic polymorphism 57 endometritis 57 syngeneic 57 H pylori 57 CDKN2A 57 thromboembolisms 57 Rh positive 57 Epstein Barr virus EBV 57 insulinlike growth 57 untreated celiac disease 57 CXCR2 57 Hp2 2 57 fibroids endometriosis 57 antiphospholipid syndrome 57 thromboembolic 57 elevated LDL cholesterol 57 Thiazolidinediones 57 HBeAg negative 57 Erythropoietic therapies may 57 NOD2 57 hemorrhagic cystitis 57 predisposing factor 57 gene polymorphism 57 microdeletion 57 thyroid deficiency 57 interleukin IL -# 57 urinary calcium 57 #q# deletion syndrome 57 idraparinux 57 diabetes mellitus T2DM 57 obstructive coronary artery 57 hepatotoxicity 57 cystic fibrosis chronic pancreatitis 57 NQO1 57 congenital deficiency 57 nondemented 57 benazepril 57 Lafora disease 57 metastatic neuroendocrine tumors 57 Peptide YY 57 bronchoalveolar 57 primary ovarian insufficiency 57 alpha1 antitrypsin AAT deficiency 57 hepatocellular carcinomas 57 VEGF vascular endothelial 57 Hurthle cell 57 ε4 57 arrhythmogenic right 57 variant allele 57 hypogonadotropic hypogonadism 57 diabetes dyslipidemia 57 chromosomal aberrations 57 gastric adenocarcinoma 57 TNFalpha 57 CVD mortality 57 hepatoma 57 dexrazoxane 57 autosomal dominant disorder 57 paraoxonase 57 JAK2 enzyme 57 Fibrates 57 chronic prostatitis 57 Apolipoprotein E 57 autosomal recessive genetic 57 BRCA2 mutations 57 macrophage migration 57 asymptomatic carriers 57 Epstein Barr Virus EBV 57 hormone receptor negative 57 MEF2A 57 von Willebrand Disease 57 aneuploidies 57 subclinical hypothyroidism 57 osteogenic 57 hypokalemia hypomagnesemia 57 BRAF gene 57 congenital adrenal hyperplasia CAH 57 5 HTTLPR 57 tyrosine phosphorylation 57 hypophosphatemia 57 calcium oxalate stones 57 serum creatinine levels 57 angiotensin receptor blockers ARB 57 autosomal recessive disorder 57 Adiponectin 57 CFH gene 57 Genital Herpes 57 IDDM 57 shorter telomere length 57 neutrophil counts 57 Genetic variation 57 monocyte chemoattractant protein 57 genetic variants associated 57 nonvertebral fracture 57 intestinal polyps 57 ß blockers 57 undescended testicles 57 elevated fasting glucose 57 lobular breast cancer 57 #q#.# deletion syndrome 57 quetiapine Seroquel 57 gene polymorphisms 57 bronchial hyperresponsiveness 57 Li Fraumeni syndrome 57 rs# [004] 57 SHBG levels 57 VHL gene 57 subfertility 57 Thromboembolic 57 thyroxine 57 post thrombotic syndrome 57 chlorthalidone 57 bacterial vaginosis BV 57 Herpes Simplex Virus 57 Avandia Actos 57 undergone radical prostatectomy 57 Univariate analysis 56 pyloric stenosis 56 BRAF V#E mutation 56 grade cervical intraepithelial 56 Autoimmune disorders 56 mutated K ras 56 PIK3CA 56 GSTM1 56 endometriosis ovarian cysts 56 antifibrinolytic 56 bFGF 56 #q#.# [001] 56 intraventricular hemorrhage 56 HELLP 56 NPC1 56 atypical hemolytic uremic syndrome 56 Prostatitis 56 cervical intraepithelial neoplasia 56 MYH9 56 Beta thalassemia 56 Ribavirin causes 56 untreated OSA 56 cardiac hypertrophy 56 blockers angiogenesis inhibitors 56 beta carotene supplementation 56 Non Alcoholic Fatty 56 acute leukemias 56 sonographic diagnosis 56 CYP#A# gene 56 recessive genetic 56 abnormal clotting 56 gonadotropin releasing hormone 56 SNP rs# [001] 56 Ovary removal 56 del 5q MDS 56 Myocarditis 56 nephrosis 56 torsade de pointes 56 SMAD4 56 Bacterial vaginosis 56 gastric cardia 56 dihydrofolate reductase 56 IFNg 56 hepatorenal syndrome 56 Uterine cancer 56 thyrotropin levels 56 airway responsiveness 56 Fibrinogen 56 CYP #D# 56 microdeletions 56 Catheter Associated 56 bacteriuria 56 osteosarcomas 56 thrombotic complications 56 abnormal lipid levels 56 serum BDNF 56 Hyperkalemia 56 homozygosity 56 G6PD 56 Rh factor 56 cardiac channelopathies 56 LPS induced 56 multivariable analysis 56 adipogenic 56 paternally inherited 56 hyperprolactinemia 56 Cytomegalovirus 56 Acute Renal Failure 56 E selectin 56 NFkB 56 Statin therapy 56 Legg Calvé Perthes disease 56 recurrent acute pancreatitis 56 pathophysiological effects 56 Vidaza ® 56 de novo mutations 56 T1c 56 familial dysautonomia 56 microsatellite instability 56 Hemochromatosis 56 histological subtype 56 SCD1 56 thromboembolic complications 56 Peripheral arterial disease 56 missense mutations 56 hydroxyvitamin D levels 56 Clotting 56 clomipramine 56 ectodermal dysplasia 56 thrombocytosis 56 gene MECP2 56 vWF 56 cytomegalovirus infection 56 carotid atherosclerosis 56 triiodothyronine 56 brain derived neurotrophic 56 obesity insulin resistance 56 LRRK2 gene 56 JAK2 mutation 56 sulfonylurea metformin 56 Homocysteine 56 lymphomas leukemias 56 thyroid dysfunction 56 Prolactin 56 coronary calcification 56 myeloproliferative 56 precancerous condition 56 QTc prolongation 56 Moraxella catarrhalis 56 secondary hyperparathyroidism 56 cystic fibrosis muscular dystrophy 56 IgA antibodies 56 Hypertrophic cardiomyopathy 56 heterozygote 56 NNRTI resistance 56 TPMT 56 Primary Hypercholesterolemia 56 Factor XIII 56 bronchogenic carcinoma 56 nondiabetic patients 56 anal cancers 56 IGF1 56 cirrhosis liver failure 56 bacteria Helicobacter pylori 56 IFN beta 56 Polymorphisms 56 epididymitis 56 Basal Cell 56 invasive lobular 56 myelomeningocele 56 thiopurine 56 CMV infection 56 MCAD deficiency 56 dysglycemia 56 ALI ARDS 56 capillary leak 56 Rh negative 56 Ivabradine 56 mild renal insufficiency 56 metabolic acidosis 56 SOD2 gene 56 transgenic rats 56 Brugada syndrome 56 Vascular endothelial growth 56 Systemic lupus erythematosus 56 c KIT 56 artery stenosis 56 #beta 56 H2 blockers 56 lactate dehydrogenase LDH 56 hepatic glucose production 56 chronic myeloid 56 COMT gene 56 fat malabsorption 56 immune thrombocytopenic purpura 56 serum aminotransferase levels 56 nonnucleoside reverse transcriptase inhibitors 56 non polyposis colorectal 56 Deep venous thrombosis 56 soluble tumor necrosis 56 Aprotinin 56 poor metabolizers 56 hereditary nonpolyposis colon cancer 56 shorter telomeres 56 diagnostic biomarker 56 angiotensin receptor blockers ARBs 56 Hypoglycaemia 56 Niemann Pick disease 56 renovascular hypertension 56 oral thrush 56 CYP#A# [002] 56 FGFs 56 Chlamydia psittaci 56 inherited genetic mutation 56 homozygous FH 56 acute rheumatic fever 56 Clusterin 56 APOE allele 56 androgenic alopecia 56 sporadic Creutzfeldt Jakob 56 prolactin levels 56 TNF α 56 Insulin sensitivity 56 Treg cell 56 GH deficiency 56 Magnesium deficiency 56 SSc 56 prolonged QT intervals 56 PON1 56 Mg Usa 56 thrombotic events 56 Hyperlipidemia 56 HIV coinfected 56 radiosensitivity 56 orchitis 56 IGFBP 56 ADH1B * 56 Epstein Barr Virus 56 thrombopoietin TPO 56 AML MDS 56 ELBW infants 56 autonomic dysfunction 56 monocytic 56 BRCA1 mutation 56 confidence interval #.#-#.# 56 extrapyramidal symptoms 56 colorectal neoplasia 56 familial hypercholesterolemia FH 56 5 alpha reductase 56 prostate carcinoma 56 Lipodystrophy 56 Reye Syndrome 56 impaired glucose metabolism 56 endostatin 56 IGFBP 3 56 nitroprusside 56 AT1 receptor 56 VLDL cholesterol 56 IL6 56 Sezary syndrome 56 p# mutations 56 prostate pancreatic 56 abnormal lipids 56 genetic variant 56 D dimer 56 transaminase elevations 56 Cyclooxygenase 2 56 genital ulcer 56 human leukocyte antigen HLA 56 transthyretin 56 ALT elevations 56 intravenous bisphosphonates 56 Fatty liver 56 chromosomal anomalies 56 M. catarrhalis 56 adrenal suppression 55 recurrent miscarriages 55 gastro oesophageal reflux disease 55 HLA DQ2 55 ductal breast cancer 55 GABRA2 55 deoxy 55 LV dysfunction 55 Neutrophil 55 apolipoprotein B 55 tibolone 55 methicillin susceptible Staphylococcus aureus 55 serum phosphate 55 elevated bilirubin 55 SCN5A 55 Hemorrhagic stroke 55 pancreatic endocrine 55 vitamin B# folic acid 55 variceal bleeding 55 receptors EGFR 55 anaplastic lymphoma kinase 55 SLC#A# [002] 55 hypothalamic amenorrhea 55 ACE Inhibitor 55 chlamydial infection 55 DRD4 55 Pulmonary embolism 55 tryptase 55 subclinical 55 triacylglycerol concentrations 55 irregular menstrual cycles 55 Urinary tract 55 PALB2 55 Thrombocytopenia 55 resistin 55 Cushing syndrome 55 Staphylococcus epidermidis 55 serum selenium 55 AMACR 55 murine leukemia virus 55 cisplatin resistant 55 Polycystic Ovary Syndrome 55 erythropoietic 55 airway hyper responsiveness 55 MetS 55 lipoprotein Lp 55 PTLD 55 choriocarcinoma 55 periventricular leukomalacia 55 uterine tumors 55 hypermethylated 55 multivariate adjustment 55 sonographic appearance 55 Vitamin D insufficiency 55 caveolin 55 ticlopidine 55 untreated hypothyroidism 55 hypereosinophilic syndrome 55 induce ovulation 55 BRCA2 mutation 55 indomethacin 55 liver metastasis 55 Roche AmpliChip 55 stratifying patients 55 potassium sparing diuretics 55 S. aureus infection 55 collagen degradation 55 Polycystic ovary syndrome 55 asplenia 55 gene variation 55 amenorrhoea 55 IL#B 55 endometrial cancers 55 polycystic ovary syndrome 55 GPC5 55 SLC#A# [001] 55 GISTs 55 hepatic enzymes 55 Subclinical 55 inherited predisposition 55 NSAID associated 55 lung fibrosis 55 dopamine D4 receptor 55 PPCM 55 chromosome abnormality 55 virus HBV 55 alpha defensin 55 haematopoietic 55 Sulfonylurea 55 Kufs disease 55 serum estradiol 55 myo inositol 55 Cognitive impairment 55 macrovascular events 55 sotalol 55 primary aldosteronism 55 hyperammonemia 55 herpes simplex virus 55 juvenile idiopathic arthritis JIA 55 Glomerular 55 TACI mutations 55 promoter hypermethylation 55 MGUS 55 basal cell carcinoma BCC 55 T2D 55 Non Steroidal Anti Inflammatory 55 von Willebrand factor 55 neuroblastomas 55 variant rs# 55 Lantus insulin 55 Candidiasis 55 Pre eclampsia 55 bacterial prostatitis 55 hyperhomocysteinemia 55 Cholangiocarcinoma 55 de ath 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 genital ulcer disease 55 TNF blocker therapy 55 myopathies 55 homozygous 55 prostate bladder 55 typical antipsychotics 55 Gorlin syndrome 55 Nilotinib 55 Low density lipoprotein 55 monoclonal gammopathy 55 preserved ejection fraction 55 Prostate Cancer Recurrence 55 dominantly inherited 55 HLA DRB1 SE 55 female hormone progesterone 55 Antitumor Activity 55 oncogenic transformation 55 type2 diabetes 55 PEDF 55 cervical vaginal 55 overt nephropathy 55 IL 1Ra 55 microscopic hematuria 55 candidemia 55 Irritable bowel syndrome 55 polycystic ovarian disease 55 Bronchiolitis 55 klotho 55 FGF2 55 unstable detrusor muscle 55 HLA DR4 55 myelofibrosis polycythemia vera 55 Apolipoprotein E4 55 cystatin C 55 Retinopathy 55 onset diabetes mellitus 55 phenothiazines 55 HbF 55 Radiographic findings 55 Procoralan 55 LTB4 55 hepatic toxicity 55 TSC1 55 pyogenes 55 pro angiogenic 55 6 phosphate dehydrogenase 55 Spinal muscular atrophy 55 angiotensin converting enzyme inhibitors 55 NNRTI resistant virus 55 TOMM# 55 aspirin clopidogrel 55 renal toxicity 55 transfusion syndrome 55 abnormal vaginal bleeding 55 squamous cell lung cancer 55 adrenal hormone 55 capillary permeability 55 Estrogen deficiency 55 thromboxane A2 55 tumorigenicity 55 MTHFR gene 55 TNFα 55 galactosemia 55 hyperemesis 55 bone morphogenetic protein 55 LVNC 55 CETP gene 55 MC1R 55 colorectal neoplasms 55 Zollinger Ellison Syndrome 55 latent celiac disease 55 lipohypertrophy 55 untreated sleep apnea 55 Vascular dementia 55 PREMPRO 55 Adjuvant Chemotherapy 55 pulmonary dysfunction 55 intima media thickness 55 Cognitive Impairment 55 polyhydramnios 55 diagnose coronary artery 55 Genital herpes 55 serotonin uptake 55 Venous thromboembolism 55 III EGFRvIII 55 chromosomal instability 55 Rh incompatibility 55 angina chest 55 multivariable adjusted 55 nonsense mutations 55 impair fertility 55 superior mesenteric artery 55 Myostatin 55 systemic amyloidosis 55 hypercoagulable 55 Liver transplantation 55 hyperkalemia 55 T2DM 55 susceptibility alleles 55 Pseudomonas aeruginosa infections 55 adrenal cortex