Related by context. All words. (Click for frequent words.) 71 rheumatoid arthritis lupus 71 muscular dystrophy cystic fibrosis 70 dominantly inherited 70 ANCA associated 70 kidney urologic 69 Sjögren syndrome 68 chronic autoimmune disorder 68 anemias 68 cystic fibrosis muscular dystrophy 68 autosomal recessive genetic 68 TTR amyloidosis 68 Chronic lymphocytic leukemia 68 asplenia 68 cystic fibrosis chronic pancreatitis 67 generalized epilepsy 67 NPHP 67 progressive neurodegenerative 67 Systemic lupus erythematosus SLE 67 genetic syndromes 67 lupus multiple sclerosis 67 protein misfolding diseases 67 hematologic disorders 67 Eisenmenger syndrome 67 biochemical abnormalities 67 neuropsychiatric disorder 67 unknown etiology 67 rheumatoid arthritis inflammatory bowel 67 paraneoplastic 67 Ribavirin causes 67 Relapsing remitting MS 67 immunodeficiency 67 neuro degenerative disorders 67 myopathies 67 dyskeratosis congenita 67 mental retardation epilepsy 67 haematologic 66 neurological disorder affecting 66 lupus scleroderma 66 multisystem disease 66 neutropenia thrombocytopenia 66 coagulopathy 66 meningitis encephalitis 66 mycosis fungoides 66 Magnesium deficiency 66 Aortic stenosis 66 autoimmune thyroid 66 ataxias 66 Systemic lupus erythematosus 66 vascular cognitive impairment 66 Von Willebrand disease 66 lysosomal storage diseases 66 myeloproliferative diseases 66 Hereditary angioedema HAE 66 atypical hemolytic uremic syndrome 66 Myotonic dystrophy 66 Atopic dermatitis 65 hematological disorders 65 myeloproliferative neoplasms 65 de novo mutations 65 Juvenile Idiopathic Arthritis JIA 65 Leukemias 65 cardiovascular cerebrovascular 65 neuro developmental disorders 65 connective tissue disorders 65 Arrhythmogenic Right Ventricular Cardiomyopathy 65 ADPKD 65 muscular dystrophies 65 gastrointestinal dysfunction 65 complement inhibitor eculizumab 65 severe malignant osteopetrosis 65 Hereditary angioedema 65 hemoglobinopathies 65 monogenic 65 chorioamnionitis 65 Hurler syndrome 65 Childhood Disorder 65 neoplastic 65 Severe Primary IGFD 65 included exfoliative dermatitis 65 dysplasias 65 hypokalemia hypomagnesemia 65 collagen vascular 65 Factor XIII 65 Hashimoto thyroiditis 65 hematological diseases 65 inappropriate antidiuretic hormone SIADH 65 vWD 65 hyperinsulinism 65 myeloproliferative 65 rheumatoid arthritis systemic lupus 65 hamartomas 65 primary ciliary dyskinesia 65 Tay Sachs thalassemia 65 neuropsychiatric diseases 65 Polymorphic Ventricular Tachycardia CPVT 65 Osteogenesis imperfecta 65 Psoriatic arthritis 65 progressive neurodegenerative disorder 65 myelodysplasia 65 Inflammatory bowel diseases 65 alpha1 antitrypsin deficiency 65 C1 INH deficiency 65 etiologic 65 degenerative neurological diseases 65 Sezary syndrome 65 neoplastic diseases 65 skeletal muscle weakness 65 multisystemic 65 diabetic microvascular complications 65 inherited neurological disorder 65 Hypertrophic 65 antiphospholipid syndrome 65 multiple sclerosis cerebral palsy 65 autosomal recessive 65 nongenetic 64 #q#.# deletion syndrome 64 untreated celiac disease 64 neutropenia dehydration dyspnea 64 myelofibrosis polycythemia vera 64 neoplasias 64 autism dyslexia 64 chronic metabolic acidosis 64 inherited retinal 64 Dilated cardiomyopathy 64 Leydig cell 64 Chronic sinusitis 64 hormonal abnormalities 64 bronchopulmonary dysplasia BPD 64 pathophysiological effects 64 arterial calcification 64 systemic amyloidosis 64 microdeletion 64 endocrine abnormalities 64 cause cardiac channelopathies 64 cortical dysplasia 64 Diabetic neuropathy 64 IgA deficiency 64 unprovoked seizures 64 erythematosus 64 SSc 64 Myasthenia gravis 64 Endometrial cancer 64 degenerative disorders 64 pathogenetic mechanisms 64 medium chain acyl 64 Pervasive Developmental Disorder 64 lysosomal storage disease 64 nonbacterial prostatitis 64 demyelinating disease 64 Iron deficiency anemia 64 Parkinson disease multiple sclerosis 64 juvenile myelomonocytic leukemia 64 pathophysiologic 64 neurologic disorders 64 thyroid dysfunction 64 Korsakoff syndrome 64 idiopathic PAH 64 Brugada syndrome 64 systemic autoimmune 64 post transplant lymphoproliferative 64 primary hyperparathyroidism 64 sporadic Creutzfeldt Jakob 64 essential thrombocythemia 64 neuropathic pain spasticity 64 gastric carcinoma 64 thalassemia sickle cell 64 autoimmune thyroiditis 64 candidemia 64 genetic lysosomal storage 64 erythema nodosum 64 pancytopenia 64 epilepsies 64 Acute myeloid leukemia 64 neurosensory 64 debilitating neurodegenerative disorder 64 Li Fraumeni syndrome 64 MGUS 64 demyelinating diseases 64 Haptoglobin 64 Acute Bacterial Sinusitis ABS 64 Spinal muscular atrophy 64 bullous 64 pathophysiological mechanisms 64 LRP5 64 Wernicke Korsakoff syndrome 64 immunodeficiency disorder 64 metastatic neuroendocrine tumors 64 Keratitis 64 dystrophies 64 hypereosinophilic syndrome 64 blood coagulation disorders 64 oligodendrogliomas 64 autosomal dominant disorder 64 thyroiditis 64 chromosomal anomalies 64 lupus erythematosus 64 inflammatory demyelinating 64 neurological abnormalities 64 G6PD deficiency 64 lichen planus 64 MELAS syndrome 64 1 diabetes T1D 64 leiomyomas 64 osteosarcomas 64 cystic fibrosis sickle cell 64 predisposing factor 64 paroxysmal nocturnal hemoglobinuria 64 von Willebrand disease 63 chromosomal anomaly 63 fungoides 63 hereditary predisposition 63 Henoch purpura 63 pancreatic endocrine 63 glaucoma ischemia 63 Tourette Syndrome TS 63 inherited retinal degeneration 63 Radiographic findings 63 rheumatologic 63 inherited mutations 63 dissociative disorders 63 esophageal reflux 63 neurofibromas 63 Genetic predisposition 63 comorbid disorders 63 Neurodegenerative diseases 63 autosomal recessive disease 63 undiagnosed celiac disease 63 hyper IgE syndrome 63 immunomodulation 63 HeFH 63 epilepsy multiple sclerosis 63 polymicrobial infections 63 underlying pathophysiology 63 arthritis RA 63 Hurthle cell 63 motor neuron degeneration 63 hematopoietic cancers 63 Systemic lupus 63 neurobehavioral disorders 63 sickle cell cystic fibrosis 63 leukemia lymphomas 63 atopic disorders 63 autoinflammatory diseases 63 convulsive disorders 63 Hutchinson Gilford progeria 63 hyperphenylalaninemia HPA due 63 chronic granulomatous disease 63 CYT# potent vascular disrupting 63 autoinflammatory 63 MELAS 63 psoriasis Crohn disease 63 ceroid lipofuscinosis NCL 63 Dental caries 63 pathological fractures 63 dysmotility 63 neurodevelopmental disorders 63 Niemann Pick disease 63 malignant lymphomas 63 homozygous FH 63 Ankylosing spondylitis 63 Idiopathic 63 etiologies 63 idiopathic pulmonary 63 monoclonal gammopathy 63 adrenocortical cancer 63 Vitamin B# deficiency 63 transfusion syndrome 63 Autoimmune disorders 63 nonalcoholic steatohepatitis 63 chronic obstructive airway 63 neurological manifestations 63 basal cell nevus syndrome 63 neurologic complications 63 bone marrow suppression 63 glomerulonephritis 63 herpes zoster shingles 63 osteoarthritis rheumatoid arthritis 63 cytopenias 63 autosomal recessive disorder 63 constipation OIC 63 Alzheimer disease vascular dementia 63 orchitis 63 dysgenesis 63 neuronal dysfunction 63 endocrine diseases 63 euthymic patients 63 childhood disintegrative disorder 63 epilepsy Parkinson disease 63 endocrine dysfunction 63 fungus Cryptococcus neoformans 63 pulmonary hypertension PH 63 capillary leak 63 arthritis osteoporosis 63 AAT deficiency 63 chronic lymphocytic 63 hepatic renal 63 Medulloblastoma 63 Celiac sprue 63 Chronic ITP 63 diabetic retinopathy DR 63 papillary renal cell carcinoma 63 cutaneous lupus 63 cognitive impairment associated 63 hyperplastic 63 affective psychosis 63 proliferative retinopathy 63 cytomegalovirus infection 63 macular degeneration diabetic retinopathy 62 Nonalcoholic fatty liver 62 Androgenetic alopecia 62 gastrointestinal stromal tumors GISTs 62 autosomal dominant 62 malignant neoplasm 62 chronic eosinophilic leukemia 62 lymphoid tumors 62 coagulation disorders 62 mixed hyperlipidemia 62 clinically heterogeneous 62 demyelinating 62 neurologic abnormalities 62 holoprosencephaly 62 haematopoietic 62 Polycythemia vera 62 myasthenia gravis MG 62 Cockayne syndrome 62 optic neuropathy 62 histologic subtype 62 facioscapulohumeral muscular dystrophy 62 β thalassemia 62 immunodeficiency disorders 62 encephalitis meningitis 62 Vascular dementia 62 fusion enhancers 62 vascular dysfunction 62 Trichophyton rubrum 62 Becker muscular dystrophy 62 myocardial infarction ventricular fibrillation 62 glaucoma macular degeneration 62 VCFS 62 pathological hallmark 62 chronic renal disease 62 neuropathies 62 Papillary 62 deafness neurological 62 neuro degenerative 62 primary generalized tonic 62 Cognitive dysfunction 62 abnormal p# 62 Myelodysplastic syndromes 62 Parkinson disease Alzheimer disease 62 CP CPPS 62 cytogenetic abnormalities 62 Bullous 62 connective tissue diseases 62 nonvascular 62 hypertensive retinopathy 62 epithelioid 62 Neurofibromatosis type 62 Vidaza ® 62 prematurity ROP 62 MYCN amplification 62 spleen enlargement 62 hamartoma 62 inherited neurodegenerative 62 sclerosis ALS 62 NOMID 62 Cowden syndrome 62 cerebral vasospasm 62 Congenital Muscular Dystrophy 62 autosomal dominant polycystic kidney 62 LHON 62 familial hypercholesterolemia 62 multifactorial disease 62 Hp2 2 62 mtDNA mutations 62 Alport syndrome 62 dysthymic disorder 62 abnormal genital 62 Non inferiority 62 NAGS deficiency 62 galactosemia 62 hypercalcaemia 62 systemic juvenile idiopathic 62 rheumatoid arthritis multiple sclerosis 62 recessively inherited 62 aMCI precursor 62 Thyroid nodules 62 fatal hemorrhagic 62 MYH9 gene 62 neurodevelopmental disorder 62 Leber Hereditary Optic Neuropathy 62 Carcinoid tumors 62 channelopathies 62 nonmelanoma skin cancers 62 Polyneuropathy 62 ADAMTS# 62 induce orthostatic hypotension 62 Morquio 62 gene MECP2 62 Pulmonary hypertension 62 hypometabolism 62 thalidomide Thalomid 62 Wegener granulomatosis 62 eosinophilic 62 neurogenic bladder 62 hemolytic anemia 62 neurovascular diseases 62 Retinitis pigmentosa 62 Beta thalassemia 62 Brugada Syndrome 62 Basal Cell 62 nonischemic 62 thrombo embolic 62 Familial hypercholesterolemia 62 headache abdominal pain 62 thrombocytopenia neutropenia 62 spinocerebellar ataxia 62 Pervasive Developmental Disorders 62 metaplasia 62 Enterococcus faecium 62 hypercoagulable 62 mitochondrial disorders 62 renal diseases 62 Inflammatory bowel disease 62 Idiopathic Thrombocytopenic Purpura ITP 62 liver cancers TTR 62 Plaque psoriasis 62 Comorbid 62 chromosome #q#.# [001] 62 nephronophthisis 62 nondemented 62 Sanfilippo Syndrome 62 progressive dyspnea 62 Huntingtons disease 62 enterocolitis 62 lysosomal storage disorder 62 rheumatic disorders 62 renal hepatic 62 multiple sclerosis psoriasis 62 cerebral palsy Down syndrome 62 Lennox Gastaut syndrome 62 eccrine 62 heart palpitations dizziness 62 Leber congenital amaurosis 62 urolithiasis 62 Leber congenital amaurosis LCA 62 fat malabsorption 62 Pemphigus 62 AA Amyloidosis 62 PCNSL 62 CDH1 62 immunopathology 62 neurobehavioral disorder 62 dermatologic reactions 62 T1DM 62 Opportunistic infections 62 mGluR5 antagonist 62 opsoclonus myoclonus syndrome 62 congenital deficiency 62 Acute lymphoblastic leukemia 62 myeloproliferative disorders 62 granulomatous 62 Zinc deficiency 62 smoldering myeloma 62 clefting 62 thrombocytosis 62 rheumatological 62 overt nephropathy 62 metabolic abnormality 62 von Willebrand 61 Malignant mesothelioma 61 AAT Deficiency 61 leptin deficiency 61 hematological abnormalities 61 TEAEs 61 Atypical Hemolytic Uremic Syndrome 61 Lafora disease 61 valvular heart disease 61 rheumatoid arthritis osteoarthritis 61 Idiopathic pulmonary fibrosis IPF 61 carcinoid 61 glutamic acid decarboxylase 61 alpha1 antitrypsin AAT deficiency 61 lactase deficiency 61 rheumatic diseases 61 leukodystrophies 61 Mitochondrial diseases 61 Lou Gehrigs disease 61 fibrosing 61 diabetes mellitus DM 61 debilitating autoimmune 61 genetics immunology 61 Idiopathic Pulmonary Fibrosis IPF 61 anemia thrombocytopenia 61 Entamoeba histolytica 61 colorectal adenoma 61 levodopa induced 61 interstitial pneumonitis 61 epiglottitis 61 Lymphocytic 61 leiomyoma 61 hay fever allergic rhinitis 61 intra abdominal abscess 61 Ischemic 61 hypochondriasis 61 cervicitis 61 ALI ARDS 61 #q#.# [001] 61 autonomic dysfunction 61 interstitial nephritis 61 hyperprolactinemia 61 #q# deletion 61 bacterial prostatitis 61 extrapulmonary 61 Irritable bowel syndrome 61 hemorrhagic colitis 61 spontaneous mutations 61 Bardet Biedl Syndrome 61 renal kidney 61 HNPCC 61 Synovial sarcoma 61 optica 61 hypocalcaemia 61 somatoform disorders 61 Basal cell 61 supratentorial 61 #q# deletion syndrome 61 somatization disorder 61 mediated autoimmune diseases 61 multiple sclerosis Crohn disease 61 extrapulmonary disease 61 Sydenham chorea 61 cytopenia 61 subependymal giant cell 61 Osteoarthritis OA 61 hemophagocytic lymphohistiocytosis 61 chronic GVHD 61 autoimmune encephalitis 61 Myelodysplastic syndrome 61 Intravenous immunoglobulin 61 breast endometrial 61 dyslipidaemia 61 telomere dysfunction 61 Lupus nephritis 61 torsade de pointes 61 Hemangiomas 61 onset diabetes mellitus 61 NASH Huntington 61 hydrops 61 glial tumors 61 cholestasis 61 SGPT 61 lymphocytic 61 lung cancer NSCLC 61 missense mutations 61 Vitamin D insufficiency 61 systemic scleroderma 61 cerebral palsy multiple sclerosis 61 familial hypercholesterolemia FH 61 respiratory gastrointestinal 61 autoimmune inflammatory 61 CTEPH 61 bone marrow mesenchymal stem 61 neurogenetic 61 muscular spasticity 61 nonmelanoma 61 anosognosia 61 inherited genetic mutations 61 pyrexia mucositis sepsis febrile 61 variable immunodeficiency 61 receiving XGEVA 61 dysfunctional voiding 61 astrocytomas 61 aneuploidies 61 multiple sclerosis rheumatoid arthritis 61 endophenotypes 61 neuropathologic 61 Autistic Disorder 61 vestibular dysfunction 61 PLX STROKE targeting 61 chronic thromboembolic pulmonary 61 differential gene expression 61 neuroendocrine cancers 61 neurodevelopment disorder 61 Chronic pancreatitis 61 chronic rhinosinusitis CRS 61 sJIA 61 vascular occlusive diseases 61 prolonged QT interval 61 hereditary emphysema 61 psychiatric comorbidity 61 ectodermal dysplasia 61 neuro developmental disorder 61 paraganglioma 61 neurofibrillary 61 ischemic cardiac 61 blindness deafness 61 Human papillomavirus 61 enteroviral infection 61 cystic fibrosis Duchenne muscular 61 Gliomas 61 CMV infection 61 deCODE Glaucoma TM 61 Rh incompatibility 61 simplex virus 61 microvascular disease 61 CHD7 61 plexiform neurofibromas 61 chromosomal rearrangement 61 ophthalmologic disorders 61 A3 adenosine receptor 61 Hip dysplasia 61 OSAHS 61 leukoencephalopathy 61 Ph + acute lymphoblastic 61 Gorlin syndrome 61 hypertension hypercholesterolemia 61 Chronic lymphocytic leukemia CLL 61 FluCAM arm 61 atopic asthma 61 tic disorders 61 hay fever asthma 61 Wiskott Aldrich syndrome 61 neuro degenerative diseases 61 Legg Calvé Perthes disease 61 allogeneic HSCT 61 hyperreflexia 61 autism Asperger Syndrome 61 AML MDS 61 thiopurine 61 TNF antagonist 61 lymphocytic leukemia 61 cisplatin resistant 61 Prostatitis 61 HHV 6 61 chronic idiopathic urticaria 61 malignant pheochromocytoma 61 velo cardio facial 61 immunocompetent 61 Schizoaffective Disorder 61 microchimerism 61 severe hepatic dysfunction 61 SIADH 61 multiple sclerosis lupus 61 Epstein Barr Virus EBV 61 Bacterial vaginosis 61 Heavy menstrual bleeding 61 thyroid hormone deficiency 61 spinal muscle atrophy 61 mucinous 61 either acutely decompensated 61 neurotology neuropsychology headaches 61 Parnate 61 essential thrombocythemia ET 61 Churg Strauss syndrome 61 fatal neurodegenerative disorder 61 GH deficiency 61 hepatocellular carcinomas 61 Major depressive disorder 61 Myelodysplastic syndromes MDS 61 hemodynamically significant 61 lymph node enlargement 61 atherothrombotic 61 pathophysiological processes 61 immuno deficiency 61 rheumatoid arthritis osteoarthritis ankylosing 61 damage cirrhosis liver 61 Esophagitis 61 nonalcoholic steatohepatitis NASH 61 lymphoproliferative disorders 61 Raynaud syndrome 61 histological subtype 61 mastocytosis 61 PTEN mutations 61 genetic neuromuscular disorder 61 immune thrombocytopenic purpura 61 Adverse effects 61 Hypophosphatasia 61 GERD migraine headaches 61 Leber Congenital Amaurosis LCA 61 macrovascular complications 61 Dysplasia 61 follicular thyroid cancer 61 affective psychoses 61 proliferative disorders 61 Leber hereditary optic neuropathy 61 Meckel Gruber 61 underlying vasculopathy 61 pathogenic mechanisms 61 chromosome abnormality 61 homozygous familial hypercholesterolemia 61 juvenile idiopathic arthritis JIA 61 familial adenomatous polyposis 61 bronchopulmonary dysplasia 61 tardive dyskinesia TD 61 Polycystic kidney disease 61 neovascularisation 61 Medullary thyroid cancer 61 renal cell carcinomas 61 Moraxella catarrhalis 61 dermatitis herpetiformis 61 myelogenous leukemia 61 Atopic eczema 61 psoriatic arthritis PsA 61 hyperalgesia 60 parathyroid carcinoma 60 RhuDex ™ 60 idiopathic generalized epilepsy 60 renal fibrosis 60 diabetes dyslipidemia 60 Lysosomal storage 60 leukemia AML 60 recessive dystrophic epidermolysis bullosa 60 treating neuropathic pain 60 fatal neuromuscular disorder 60 benign paroxysmal positional vertigo 60 Chlamydia pneumoniae 60 Hemorrhagic 60 discoid lupus 60 polymorphic ventricular tachycardia 60 Venous thromboembolism 60 LRAT 60 syndromic 60 cardiomyopathies 60 Angioedema 60 rare autosomal recessive 60 neovascular 60 proliferative diabetic retinopathy 60 developmental abnormalities 60 alpha interferons 60 nonhereditary 60 cardiovascular restenosis cancer 60 Interstitial cystitis 60 Philadelphia Chromosome Positive 60 periodontal tissues 60 deafness blindness 60 Candida infections 60 pancreatic prostate 60 atherothrombotic disease 60 obesity insulin resistance 60 Chronic myeloid leukemia CML 60 APOE genotype 60 2 diabetes T2D 60 familial clustering 60 Pulmonary arterial hypertension 60 Kufs disease 60 dyslexia dyspraxia 60 Arrhythmogenic 60 WAGR syndrome 60 Sudhir Agrawal D.Phil 60 Spasticity 60 glaucoma cataract 60 autoimmune disorder characterized 60 Gastrointestinal disorders 60 juvenile myoclonic epilepsy 60 bacterium Neisseria meningitidis 60 Janus kinase 60 neuritic 60 hereditary deafness 60 behavioral abnormalities 60 thyrotoxicosis 60 Urinary tract 60 Glioblastoma multiforme GBM 60 Suicidal tendencies 60 Chiari malformation 60 chronic periodontitis 60 anatomical abnormalities 60 PKU genetic 60 epilepsy cerebral palsy 60 C. trachomatis 60 nephrogenic fibrosing dermopathy 60 anticholinergic agents 60 uricase 60 MGd 60 familial aggregation 60 thrombophilia 60 Bronchiolitis 60 myotonic muscular dystrophy 60 paralysis blindness 60 proliferative diseases 60 fluconazole resistant 60 Cryptococcus neoformans 60 generalized seizures 60 intra abdominal infections 60 Marfan syndrome connective tissue 60 lymphoma leukemia 60 cell acute lymphoblastic 60 Hodgkin lymphoma HL 60 spina bifida cerebral palsy 60 HbF 60 neuroblastomas 60 Sjogren Syndrome 60 neurodegenerative disorder characterized 60 chromosomal aberrations 60 myoclonus 60 Langerhans cell histiocytosis 60 LHRH receptor positive 60 maple syrup urine 60 Thrombocytopenia 60 aplasia 60 hypercoagulability 60 Retinopathy 60 benign neoplasms 60 Glucocorticoids 60 subarachnoid hemorrhage SAH 60 monocytic 60 lung adenocarcinomas 60 chronic myeloid 60 interferon alpha IFN 60 pheochromocytoma 60 Erythropoietic therapies may 60 optic neuropathy NAION 60 Parathyroid hormone 60 choroidal neovascularization CNV 60 shorter telomere length 60 Parkinsonian Syndromes 60 neurodegenerative disorder 60 polyarticular 60 subsyndromal 60 oncology infectious diseases 60 systemic lupus erythematosus 60 nonarteritic anterior ischemic optic 60 diabetic kidney 60 malabsorptive 60 epithelial tumors 60 Squamous cell 60 hypercholesterolemia liver 60 macrovascular events 60 Premature Ovarian Failure 60 Renal impairment 60 polyglutamine diseases 60 Essential tremor 60 deletion 5q 60 plexiform 60 TRAIL R1 60 familial amyloidotic polyneuropathy FAP 60 esophagitis 60 allergic eczema 60 androgen excess 60 mediastinitis 60 cerebral vascular accident 60 Nonspecific 60 invasive candidiasis 60 rheumatoid arthritis Crohn disease 60 internalizing disorders 60 lysosomal diseases 60 Candidiasis 60 Ischaemic heart 60 Prodarsan R 60 familial ALS 60 skeletal dysplasia 60 Stargardt Macular Dystrophy SMD 60 www.ninds.nih.gov 60 renal failure interstitial lung 60 Hemophilia B 60 recessive inheritance 60 fibrosarcoma 60 myelodysplastic myeloproliferative diseases 60 Chronic Prostatitis 60 Metastases 60 thyrotropin levels 60 K ras mutations 60 ocular inflammatory 60 Autoimmune hepatitis 60 Glioblastoma Multiforme GBM 60 extramedullary 60 coagulation abnormalities 60 Panton Valentine leukocidin PVL 60 Non Alcoholic Steatohepatitis 60 cystic kidney 60 Prion diseases 60 pyelonephritis 60 metastatic malignant 60 Bronchiectasis 60 chronic hepatitis cirrhosis 60 neurological sequelae 60 microsatellite instability 60 Sjogren syndrome 60 pulmonary metastasis 60 HBeAg negative 60 ataxia telangiectasia 60 Aspergillus species 60 arthropathy 60 Research www. elsevier.com 60 motor neuron diseases 60 syndrome OSAS 60 GRNOPC1 contains 60 hippocampal function 60 cardio metabolic diseases 60 retinal blindness 60 predominantly classic subfoveal 60 reproductive endocrine 60 Zollinger Ellison Syndrome 60 small molecule thrombopoietin 60 macular edema secondary 60 Meningiomas 60 Neovascular AMD 60 psychopathological disorders 60 pain syndromes 60 PAOD 60 Kleine Levin 60 gastrointestinal stromal tumor 60 immune dysregulation 60 lymphocyte activation 60 Alzheimer disease cognitive impairment 60 neurocognitive disorder 60 post herpetic 60 severe congenital neutropenia 60 squamous 60 mito 60 aetiological 60 radiochemotherapy 60 acute lymphoid leukemia 60 Myelofibrosis 60 choroidal neovascularization 60 osteopetrosis 60 hereditary nonpolyposis colorectal cancer 60 myalgic encephalomyelitis ME 60 #beta HSD1 60 Fas ligand 60 Borderline personality 60 oral thrush 60 ulcerative colitis Crohn disease 60 pharmacologic treatments 60 post thrombotic syndrome 60 COPD asthma 60 acute myocarditis 60 sequela 60 hypercalciuria 60 Glomerular 60 staphylococcal infections 60 Squamous 60 Schizoaffective disorder 60 neurologic disorder 60 obstructive coronary 60 BH4 deficiency 60 cIAI 60 generalized tonic clonic seizures 60 bacterial parasitic 60 Nephrogenic Systemic Fibrosis NSF 60 Antisocial personality 60 schizophrenia schizoaffective disorder 60 JAK2 mutation 60 acute leukemias 60 Nicotine dependence 60 systemic lupus erythematosus SLE 60 neurocognitive impairment 60 rheumatoid arthritis psoriasis 60 Gastro intestinal 60 Testosterone deficiency 60 commercializes innovative biopharmaceuticals 60 TRIOLEX HE# APOPTONE HE# 60 Subclinical 60 lupus rheumatoid arthritis 60 erythropoietic 60 Oxidative damage 60 comorbid psychiatric 60 gastric carcinomas 60 cerebral palsy muscular dystrophy 60 hereditary disorders 60 lactose malabsorption 60 cerebrovascular disorders 60 von Hippel Lindau 60 NovaBay Aganocide compounds 60 phenotypic expression 60 pancreatic neuroendocrine 60 basal cell carcinoma BCC 60 neurological disorders orphan 60 hepatic enzyme 60 hypertension cardiovascular disease 60 Muscular dystrophies 60 cytomegalovirus CMV 60 polycythemia vera PV 60 Myocarditis 60 syndrome gastroesophageal reflux 60 juvenile idiopathic arthritis 60 Autoimmune diseases 60 nerve degeneration 60 heritable disorders 60 melanocortin receptor 60 NF1 60 infantile onset 60 antimetabolite 60 GBA mutations 60 JAK inhibitors 60 Cognitive impairment 60 hereditary spastic paraplegia 60 osteoid osteoma 60 biologic therapeutics 60 Raynaud disease 60 Torsades de Pointes 60 comorbid anxiety 60 EBV infection 60 cryptococcosis 60 cell adhesion molecule 60 Atherosclerotic 59 urticaria hives 59 autoimmune hemolytic anemia 59 chronicity