Related by context. All words. (Click for frequent words.) 66 tauopathies 66 progressive neurodegenerative disorder 65 tau pathology 64 Chronic lymphocytic leukemia 64 neurodegenerative disorder 63 Systemic lupus erythematosus SLE 63 frontotemporal dementia 63 progressive supranuclear palsy 63 neurodegenerative disorder characterized 63 paraganglioma 62 systemic autoimmune 62 Glioblastoma Multiforme GBM 62 ceroid lipofuscinosis NCL 62 Lewy bodies DLB 62 progressive neurodegenerative 62 neurological manifestations 62 neurological disorder affecting 61 optic neuropathy 61 neuropsychiatric disorder 61 Parkinsonian Syndromes 61 Parkinson Disease PD 61 inherited neurological disorder 61 Brodmann Area 61 multi infarct dementia 61 Alzheimer disease vascular dementia 61 MELAS 61 Vascular dementia 61 ADPKD 60 choroidal neovascularization 60 epithelioid 60 Idiopathic pulmonary fibrosis IPF 60 diabetes mellitus DM 60 myalgic encephalomyelitis ME 60 Alzheimer disease cognitive impairment 60 Alzheimers Disease 60 dementias 60 ANCA associated 60 Myasthenia gravis 60 myeloproliferative 60 fronto temporal dementia 60 Bronchiectasis 59 dominantly inherited 59 Nephrogenic Systemic Fibrosis NSF 59 glioblastoma multiforme GBM 59 transthyretin amyloidosis 59 PCNSL 59 Frontotemporal Dementia 59 leukoencephalopathy 59 kidney urologic 59 subependymal giant cell 59 motor neuron degeneration 59 Papillary 59 Pervasive Developmental Disorder 59 Leukemias 59 inherited neurodegenerative 59 fatal neurodegenerative 59 Alzheimer Disease AD 59 Anaplastic 59 complement inhibitor eculizumab 59 autosomal recessive disorder 59 Lymphocytic 59 apolipoprotein E APOE 59 Major depressive disorder 59 Hutchinson Gilford progeria 59 aMCI precursor 58 Lennox Gastaut syndrome 58 fatal neurodegenerative disorder 58 Prion diseases 58 inherited retinal degeneration 58 euthymic patients 58 FTLD 58 progressive degenerative 58 Hashimoto thyroiditis 58 Glioblastoma 58 Irritable bowel syndrome IBS 58 Lewy bodies 58 glomerulonephritis 58 pathological hallmark 58 Myotonic dystrophy 58 Retinitis pigmentosa 58 polymyalgia rheumatica 58 epilepsies 58 systemic lupus erythematosus SLE 58 Amyotrophic lateral sclerosis ALS 58 de novo mutations 58 BRCA1 BRCA2 58 PsA 58 LHON 58 tics involuntary 58 Meningiomas 58 AA Amyloidosis 58 Lafora disease 58 malignant pancreatic 58 progressive neurodegenerative disease 58 Acute myeloid leukemia 58 autoinflammatory 58 post transplant lymphoproliferative 58 childhood disintegrative disorder 58 myoclonus 58 Philadelphia Chromosome Positive 58 Mild Cognitive Impairment 58 infection progressive multifocal 58 hypereosinophilic syndrome 58 Leber congenital amaurosis LCA 58 congenita 58 motor neuron diseases 58 fatal neuromuscular 58 Neurofibromatosis type 58 myelofibrosis polycythemia vera 58 discoid lupus 58 geographic atrophy 58 sporadic ALS 58 Davunetide 58 hypometabolism 57 systemic amyloidosis 57 hereditary spastic paraplegia 57 TTR amyloidosis 57 Ankylosing spondylitis 57 neuro developmental disorder 57 fatal myelination disorder 57 Alzheimer disease AD 57 Gleevec resistant 57 thymoma 57 squamous cell lung cancer 57 pathologic myopia 57 multisystem disease 57 nonalcoholic steatohepatitis NASH 57 neuro degenerative disorder 57 progressive degenerative neurological 57 NOMID 57 Sezary syndrome 57 Stargardt Macular Dystrophy 57 Ischemic 57 leukoencephalopathy PML 57 Becker muscular dystrophy 57 Huntingtons disease 57 corticobasal degeneration 57 cortical dysplasia 57 Not Otherwise Specified 57 ataxias 57 Research www. elsevier.com 57 Childhood Disorder 57 acute myeloid 57 hematopoietic cancers 57 sclerosis ALS 57 CTEPH 57 incurable degenerative brain 57 Acute lymphoblastic leukemia 57 nondemented 57 dyskeratosis congenita 57 Medulloblastoma 57 mucinous 57 comorbid anxiety 57 Stargardt Macular Dystrophy SMD 57 AAT Deficiency 57 Chronic myeloid leukemia 57 chronic lymphocytic 57 psoriatic arthritis PsA 57 autosomal dominant disorder 57 rheumatoid arthritis psoriatic arthritis 57 neuropathologic 57 PNET 57 chronic myeloid 57 lymphocytic 57 Sjögren syndrome 57 Diabetic neuropathy 57 astrocytomas 57 pleomorphic 57 Maroteaux Lamy syndrome 56 neurologic disorder 56 Squamous 56 1 diabetes T1D 56 gene APOE4 56 cryptogenic 56 predominantly classic subfoveal 56 rare autosomal recessive 56 Glioblastoma multiforme GBM 56 Glioblastoma Multiforme 56 monogenic 56 optic atrophy 56 degenerative neurological diseases 56 essential thrombocythemia 56 primary progressive aphasia 56 facioscapulohumeral muscular dystrophy 56 Pervasive Developmental Disorders 56 polycythemia vera PV 56 debilitating neurodegenerative disorder 56 proliferative retinopathy 56 Geriatric Cognitive Disorders 56 neovascular 56 idiopathic pulmonary 56 choroidal vasculopathy 56 Leber Hereditary Optic Neuropathy 56 supratentorial 56 neuropathic pain spasticity 56 myeloproliferative diseases 56 autosomal dominant 56 lupus erythematosus 56 naturally occurring neuroprotective 56 NPHP 56 anterior ischemic optic neuropathy 56 GBA mutations 56 antiphospholipid syndrome 56 generalized epilepsy 56 neurobiological disorder 56 Von Willebrand disease 56 cause cardiac channelopathies 56 Irritable bowel syndrome 56 Autistic Disorder 56 congenital deficiency 56 familial amyloidotic polyneuropathy FAP 56 malignant ovarian 56 CCR5 delta# 56 meningiomas 56 Polycystic ovary syndrome PCOS 56 lysosomal storage disease 56 Leber Congenital Amaurosis LCA 56 Psoriatic arthritis 56 JAK2 enzyme 56 retinitis pigmentosa RP 56 C1 INH deficiency 56 Aortic stenosis 56 neuronal dysfunction 56 Diabetic nephropathy 56 pathological hallmarks 56 Parkinson disease PD 56 vWD 56 primary Restless Legs 56 Myelofibrosis 56 VaD 56 lateral sclerosis ALS 56 thyrotoxicosis 56 hereditary predisposition 56 MPGN 56 schizotypal 56 Amyloid 56 Wiskott Aldrich Syndrome 56 mitochondrial disorders 56 pulmonary hypertension PH 56 neurofibrillary 56 Atopic dermatitis 56 Nonalcoholic fatty liver 56 gastrointestinal stromal tumor GIST 56 microcephalin 56 holoprosencephaly 56 tuberous sclerosis TS 56 hereditary deafness 55 myeloproliferative neoplasms 55 FXTAS 55 Neovascular AMD 55 oligodendrogliomas 55 susceptibility gene 55 presymptomatic 55 hyperplastic 55 non arteritic anterior ischemic 55 Cerebellar 55 progranulin gene 55 Irritable Bowel Syndrome IBS 55 #q#.# [001] 55 progranulin mutations 55 inherited neurodegenerative disorder 55 cystic fibrosis chronic pancreatitis 55 optic neuropathy NAION 55 Mild cognitive impairment 55 fungoides 55 Myelodysplastic syndrome 55 MALT lymphoma 55 engineered RAP peptides 55 enterocolitis 55 Shy Drager syndrome 55 paragangliomas 55 molecular abnormalities 55 Tardive Dyskinesia 55 protein tau 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 papillary renal cell carcinoma 55 idiopathic Parkinson disease 55 affective psychosis 55 Acute Leukemia 55 giant cell arteritis 55 mood dysregulation 55 mental retardation epilepsy 55 Henoch purpura 55 haematologic 55 paroxysmal nocturnal hemoglobinuria 55 Neurodegenerative diseases 55 MELAS syndrome 55 #q# deletion syndrome 55 SHANK3 55 late infantile neuronal 55 nonalcoholic steatohepatitis 55 smoldering myeloma 55 alpha1 antitrypsin deficiency 55 granulomatous 55 Systemic Sclerosis 55 dysthymic disorder 55 herpes zoster shingles 55 Relapsing remitting MS 55 epilepsy Parkinson disease 55 pancreatic neuroendocrine 55 pheochromocytoma 55 celiac sprue 55 paraneoplastic 55 CDH1 55 abnormal clumps 55 Generalized Anxiety Disorder 55 Hypertrophic 55 Systemic Lupus Erythematosus SLE 55 #q# deletion 55 Systemic lupus 55 neuro degenerative disease 55 Subarachnoid hemorrhage 55 myopathies 55 invasive secretory carcinoma 55 bullous 55 relapsing remitting 55 neovascularisation 55 ischemic optic neuropathy 55 Kufs disease 55 Motor neurone disease 55 leukemia AML 55 KRAS oncogene 55 atypical hemolytic uremic syndrome 55 sarcomatoid 55 associated tremor ataxia 55 TCF#L# gene 55 ductal adenocarcinoma 55 Glioma 55 T#I [002] 55 Enlarged prostate 55 Essential Tremor 55 benign neoplasms 55 myalgic encephalomyelitis 55 myotonic muscular dystrophy 55 Sexsomnia 55 SOD2 gene 55 Metastatic breast cancer 55 ATTR PN 55 recurrent glioblastoma multiforme 55 anemias 55 BRAF V#E 55 hereditary degenerative 55 inflammatory demyelinating 55 membranous nephritis 55 WAGR syndrome 55 Neovascular Age Related Macular 55 anterior temporal 55 demyelinating disease 55 immunodeficiencies 55 Amyotrophic lateral sclerosis 55 common neurovascular complication 55 vascular cognitive impairment 55 erythema nodosum 55 Chronic Fatigue Syndrome CFS 55 juvenile idiopathic arthritis 54 neoplasm 54 Myelodysplastic Syndrome 54 hematologic disorders 54 Leber congenital amaurosis 54 Ménière disease 54 choroidal neovascularization CNV 54 Ribavirin causes 54 Retinitis Pigmentosa RP 54 Autoimmune hepatitis 54 AAT deficiency 54 Neurogenic 54 Wet macular degeneration 54 Chronic pancreatitis 54 hippocampal atrophy 54 metastatic malignant 54 neovascular form 54 sensory neuropathy 54 Cholangiocarcinoma 54 myelogenous leukemia 54 acne vulgaris 54 Pathological gambling 54 metastatic gastric 54 pancreatic ductal adenocarcinoma 54 serous ovarian cancer 54 unknown etiology 54 Creutzfeldt Jacob 54 familial clustering 54 immune thrombocytopenic purpura 54 Acute Myelogenous Leukemia 54 SHANK3 gene 54 CALHM1 54 Non Alcoholic Steatohepatitis 54 Frontotemporal dementia 54 Hurthle cell 54 fibrous tangles 54 Vulvodynia 54 chronic granulomatous disease 54 common disabling neurological 54 Sporadic CJD 54 systemic scleroderma 54 refractory anaplastic astrocytoma 54 transgenic mouse models 54 CYT# potent vascular disrupting 54 Chronic Myelogenous Leukemia 54 Juvenile Idiopathic Arthritis JIA 54 Hypophosphatasia 54 T2 lesions 54 dilated cardiomyopathy DCM 54 Lewy Bodies 54 AMD diabetic retinopathy 54 Chronic Lymphocytic Leukemia CLL 54 anaplastic astrocytoma AA 54 hypogonadotropic hypogonadism 54 inflammatory neuropathy 54 Glioblastoma multiforme 54 recurrent glioblastoma 54 pilocytic astrocytomas 54 malignant lymphomas 54 incurable neurological disorder 54 lupus multiple sclerosis 54 occipital regions 54 Chronic Inflammatory Demyelinating Polyneuropathy 54 Venous thromboembolism 54 Follicular lymphoma 54 renal carcinoma 54 Safinamide 54 homozygous familial hypercholesterolemia 54 gastric cardia 54 essential thrombocythemia ET 54 chronic eosinophilic leukemia 54 chronic thromboembolic pulmonary 54 progressive neurologic 54 Malignant gliomas 54 cardioembolic 54 gene MECP2 54 Peripheral neuropathy 54 Celiac sprue 54 Neuroendocrine tumors 54 Colorectal cancers 54 Idiopathic pulmonary fibrosis 54 Social Anxiety Disorder 54 enteroviral infection 54 basal cell carcinoma BCC 54 patientswith 54 common hematologic malignancy 54 Synovial sarcoma 54 Multiple sclerosis MS 54 endometrioid 54 Sjogren Syndrome 54 Hip dysplasia 54 squamous cell carcinoma SCC 54 Angelman syndrome 54 Mitochondrial dysfunction 54 von Hippel Lindau 54 CPVT 54 biliary tract cancer 54 Gliomas 54 narcolepsy cataplexy 54 Treatment Shows Promise 54 choriocarcinoma 54 Upregulation 54 proliferative diabetic retinopathy 54 inappropriate antidiuretic hormone SIADH 54 osteoid osteoma 54 Maroteaux Lamy Syndrome 54 Acute Renal Failure 54 PAOD 54 Angioedema 54 Wegener granulomatosis 54 degenerative neurological condition 54 Korsakoff syndrome 54 disabling neurological 54 desmoplastic 54 G#S [002] 54 prefrontal regions 54 hypokalemia hypomagnesemia 54 Gene Linked 54 primary hyperparathyroidism 54 prematurity ROP 54 Genetic variants 54 Parkinsons Disease 54 Brugada syndrome 54 Epstein Barr Virus EBV 54 autoimmune hemolytic anemia 54 adrenocortical cancer 54 thyroid carcinoma 54 idiopathic thrombocytopenic purpura ITP 54 recurrent glioblastoma multiforme GBM 54 hemolytic anemia 54 pancreatic endocrine 54 degenerative neurological disease 54 multiple sclerosis lupus 54 HeFH 54 Lewy body 54 bladder ovarian 54 Myelodysplastic syndromes 54 WDR# 54 Chronic Obstructive Pulmonary 54 apolipoprotein E4 54 myeloproliferative disorder 54 underlying vasculopathy 54 Chronic Cerebrospinal Venous Insufficiency 54 severe malignant osteopetrosis 54 veno occlusive disease 54 colorectal carcinoma 54 hepatorenal syndrome 54 Leber hereditary optic neuropathy 54 neurological abnormalities 54 autosomal dominant polycystic kidney 54 APOE genotype 54 underlying pathophysiology 54 Rhabdomyosarcoma 54 CNTNAP2 54 Cell Lymphoma 54 IDH1 mutation 54 atrophic 54 chromosome #q# [002] 54 relapsed leukemia 54 metastatic neuroendocrine tumors 54 Adenocarcinoma 54 microbleeds 54 idiopathic thrombocytopenic purpura 54 sub syndromal 53 autosomal recessive disease 53 Pulmonary hypertension 53 embryonal rhabdomyosarcoma 53 neurofibrillary tangles 53 ABCB1 53 renal fibrosis 53 rheumatic disease 53 MYH9 gene 53 muscular dystrophies 53 chromosome #q#.# [001] 53 excitatory neurotransmitter glutamate 53 Mouse Model 53 mycosis fungoides 53 nasopharyngeal carcinoma 53 nonmelanoma skin cancers 53 exocrine 53 carcinoid tumor 53 autonomic dysfunction 53 blastoma 53 occlusion CRVO 53 neurocognitive impairment 53 demyelinating 53 Cutaneous T 53 Diffuse Large B 53 Eisenmenger syndrome 53 Dysplasia 53 progressively degenerative 53 T1DM 53 ApoE gene 53 LRP5 53 gastrointestinal stromal tumor 53 carcinoid 53 multisystemic 53 alveolar rhabdomyosarcoma 53 Critical limb ischemia 53 Sensory Integration Disorder 53 lymphangioleiomyomatosis LAM 53 gastric adenocarcinoma 53 Hutchinson Gilford Progeria Syndrome 53 SSc 53 white matter hyperintensities 53 Multiple Myeloma MM 53 pancytopenia 53 cerebrovascular accident 53 somatoform disorders 53 inherited mutations 53 lupus scleroderma 53 muscular degeneration 53 fibromyalgia syndrome 53 Adenomas 53 thunderclap headache 53 familial adenomatous polyposis FAP 53 chronic periodontitis 53 Growth Hormone Deficiency 53 premenstrual dysphoric disorder PMDD 53 Acute Myeloid Leukaemia AML 53 androgenetic alopecia 53 causative mutations 53 amnestic 53 Li Fraumeni syndrome 53 Cathepsin B 53 small lymphocytic lymphoma 53 choroidal neovascularisation 53 autosomal recessive 53 neurodegenerative disease 53 rheumatoid arthritis lupus 53 Parkinson disease Alzheimer disease 53 Lateral Sclerosis 53 valvular disease 53 Wet AMD 53 non squamous 53 abnormal genital 53 Acute Stress Disorder 53 Spasticity 53 cytopenias 53 disease NAFLD 53 anterior uveitis 53 neurodevelopmental disorder characterized 53 bladder dysfunction 53 familial ALS 53 Multiple myeloma MM 53 dopamine receptor gene 53 cutaneous lesions 53 ependymomas 53 polyarticular 53 neurobehavioral disorder 53 systemic lupus erythematosus 53 diffuse intrinsic pontine glioma 53 CDKN2A 53 Fas ligand 53 acute leukemias 53 BRAF gene 53 K ras mutations 53 #q#.# [002] 53 prostate adenocarcinoma 53 Chronic lymphocytic leukemia CLL 53 benign paroxysmal positional vertigo 53 pancreatic neuroendocrine tumors 53 opportunistic viral infection 53 Chronic fatigue 53 ocular angiogenesis 53 brain tumor glioblastoma multiforme 53 deCODE Glaucoma TM 53 familial adenomatous polyposis 53 myelodysplastic syndrome MDS 53 primary ciliary dyskinesia 53 GISTs 53 osteosarcomas 53 Tay Sachs thalassemia 53 chronic rheumatic 53 Brugada Syndrome 53 GRNOPC1 contains 53 monoclonal gammopathy 53 Interstitial cystitis 53 alcoholic hepatitis 53 Cystic fibrosis CF 53 clinicopathologic 53 APOE4 53 #:#-#,# CrossRef Medline [001] 53 mastocytosis 53 chronic lymphocytic leukemia CLL 53 refractory anemia RA 53 pancreatic adenocarcinoma 53 nonhereditary 53 autoinflammatory diseases 53 homozygous FH 53 CHD7 53 CYP#A# gene 53 astrocytoma 53 juvenile idiopathic arthritis JIA 53 Diabetes mellitus 53 Lou Gehrigs disease 53 neurological disorder characterized 53 myeloproliferative neoplasms MPNs 53 parkinsonism 53 degenerative disorders 53 pancreatic carcinoma 53 shaking palsy 53 rheumatoid arthritis Crohn disease 53 acquired immunodeficiency syndrome 53 Glycosylation 53 neovascular diseases 53 Crohn disease CD 53 hamartomas 53 paralysis blindness 53 lysosomal storage diseases 53 histologic subtype 53 glaucoma macular degeneration 53 sensorineural hearing loss 53 Retinoblastoma 53 Essential tremor 53 benign prostatic hypertrophy BPH 53 gastrointestinal stromal tumors GISTs 53 CHEK2 53 Autism Asperger Syndrome 53 progressive multifocal PML 53 deafness blindness 53 cardiac dysfunction 53 dysarthria 53 Pulmonary arterial hypertension 53 muscular spasticity 53 acute myelogenous leukemia AML 53 Cognitive Impairment 53 neurosyphilis 53 Glioblastomas 53 Fatty liver 53 histologic findings 53 III EGFRvIII 53 chromosomal rearrangement 53 Autoimmune Disorders 53 Peripheral arterial disease 53 Polycythemia Vera 53 genetic syndromes 53 stress cardiomyopathy 53 Lewy Body 53 disorder ASD 53 posterior cingulate 53 Borderline personality 53 Hemolytic Uremic Syndrome HUS 53 deCODE BreastCancer 53 Aromatase 53 Amyloid plaques 53 atypical Hemolytic Uremic Syndrome 53 variant angina 53 diagnostic biomarker 53 lacunar 53 Basal cell carcinoma 53 disease Chronic Traumatic 53 chronic myocardial ischemia 53 MGUS 53 opioid induced constipation OIC 53 olfactory dysfunction 53 leiomyomas 53 Pulmonary fibrosis 53 APOE gene 53 missense mutations 53 Alzheimer Dementia 53 Macular degeneration 53 epithelial ovarian 53 Juvenile Idiopathic Arthritis 53 leukemia lymphoma multiple myeloma 53 NF1 53 thyroiditis 53 squamous 53 epilepsy multiple sclerosis 53 Uncontrolled hypertension 53 KCNH2 53 Non Hodgkin lymphoma 53 APOE e4 53 susceptibility loci 53 incurable neurodegenerative disease 53 immunocompetent 53 leukaemias 53 Inflammatory bowel disease 53 elevated triglyceride levels 53 #p# [001] 53 glutamic acid decarboxylase 53 Chronic Pelvic Pain 53 Parkinsonism 53 androgen deficiency 53 PLX STROKE targeting 53 papillary 53 cutaneous lupus 53 Epstein Barr Virus 53 Idiopathic 53 HFE gene 53 tau protein tangles 53 vascular abnormalities 53 endophenotypes 53 retinitis 53 amnestic MCI 52 Usher Syndrome 52 myasthenia gravis MG 52 polyneuropathy 52 CSF biomarkers 52 Excessive daytime sleepiness 52 VCFS 52 Alzheimers disease 52 Impaired glucose tolerance 52 Tourette Syndrome TS 52 connective tissue disorders 52 Castration Resistant Prostate Cancer 52 juvenile myoclonic epilepsy 52 gastrin analogue TT 52 Testosterone deficiency 52 Severe Combined Immunodeficiency 52 Prostatitis 52 neurosensory 52 Waldenstrom macroglobulinemia 52 cerebral infarction 52 Autoantibodies 52 polymorphic ventricular tachycardia 52 Polyneuropathy 52 leukemia ALL 52 syndrome OSAS 52 arthritis RA 52 MC4R gene 52 POAG 52 predisposing factor 52 epithelial tumors 52 frontotemporal lobar degeneration 52 Apolipoprotein E 52 polycythemia vera essential thrombocythemia 52 Arrhythmogenic 52 senile plaques 52 infarcts 52 Idiopathic Thrombocytopenic Purpura ITP 52 neurogenic bladder 52 demyelinating diseases 52 dysgenesis 52 TCF#L# 52 chronic idiopathic 52 glaucoma cataract 52 interstitial pneumonia 52 Neurodegenerative 52 myeloproliferative disorders 52 artery stenosis 52 urolithiasis 52 Parkinsons disease 52 Inflammatory Bowel 52 optica 52 pigmented layer 52 generalized tonic clonic seizures 52 parahippocampal gyrus 52 fatal neuromuscular disorder 52 axonal damage 52 malignant brain 52 schizophrenia CIAS 52 Oppositional Defiant Disorder 52 mild cognitive impairments 52 bladder carcinoma 52 Restless Legs Syndrome RLS 52 cervical lymph nodes 52 amyloid deposits 52 Pelizaeus Merzbacher disease 52 Adult Onset 52 cerebral atrophy 52 Wilms tumors 52 Chronic Myeloid Leukemia 52 nerve degeneration 52 pulmonary alveolar 52 lymphoproliferative disorders 52 Tay Sachs Disease 52 experimental autoimmune encephalomyelitis 52 prostate cancer CaP 52 Polycythemia vera 52 periventricular leukomalacia 52 subsyndromal 52 dizziness imbalance 52 unresectable tumors 52 idiopathic generalized epilepsy 52 distinct subtypes 52 Asperger syndrome milder 52 syndrome RLS 52 neuroendocrine tumors 52 Parkinson disease multiple sclerosis 52 medically refractory 52 primary biliary cirrhosis 52 progressive multifocal leukoencephalopathy PML 52 susceptibility alleles 52 Chronic sinusitis 52 Creutzfeldt Jakob 52 thyrotropin levels 52 AA amyloidosis 52 gastro oesophageal reflux 52 sCJD 52 autoimmune encephalitis 52 primary generalized tonic 52 Hereditary angioedema HAE 52 subarachnoid hemorrhage SAH 52 Keratitis 52 Pemphigus 52 Parkinsonian 52 papillary carcinoma 52 metaplasia 52 Non Hodgkin 52 gastric carcinoma 52 Wernicke Korsakoff syndrome 52 cisplatin resistant 52 interstitial cystitis 52 Pancreatic neuroendocrine tumors 52 hepatic lipase 52 spongiform encephalopathies 52 vascular occlusive diseases 52 systemic fungal infections 52 pancreatic prostate 52 Conduct Disorder 52 thyroid dysfunction 52 fatal hemorrhagic 52 psoriasis rheumatoid arthritis 52 polycystic disease 52 incurable neurological 52 TEAEs 52 insulin secreting beta 52 fructose intolerance 52 Sydenham chorea 52 interstitial pulmonary fibrosis 52 subcortical structures 52 pituitary adenomas 52 apolipoprotein E 52 fibrosing 52 somatic mutations 52 JAK STAT signaling 52 Prosopagnosia 52 Magnesium deficiency 52 refractory cutaneous T 52 MLL2 52 Cognitive Deficits 52 cardiac channelopathies 52 Hepatocellular Carcinoma HCC 52 leukemia myeloma 52 Jill Stautner 52 primary immunodeficiency PI 52 1 Antitrypsin Deficiency 52 mania hypomania 52 alpha synuclein protein 52 Coeliac disease 52 lymph node enlargement 52 Carcinoid Syndrome 52 cytopenia 52 prostate carcinoma 52 fibrodysplasia ossificans progressiva 52 agnosia 52 Genetic mutation 52 Non Hodgkins lymphoma 52 lymphomas leukemias 52 glaucoma diabetic retinopathy 52 hypothalamic pituitary adrenal axis 52 akinesia 52 lymphocytic leukemia 52 LRAT 52 chromosome #p#.# 52 kidney insufficiency 52 Dysregulation 52 castrate resistant prostate cancer 52 Endometrial cancer 52 susceptibility locus 52 genetic lysosomal storage 52 Neuroepidemiology 52 INSPIRE Trial Phase III 52 glioblastoma brain tumor 52 inherited genetic mutations 52 familial hypercholesterolemia 52 cerebral infarctions 52 dysphasia 52 debilitating autoimmune 52 Wolf Hirschhorn 52 Malignant Glioma 52 #q#.# deletion syndrome 52 hyperammonemia 52 protein tyrosine phosphatase 1B 52 schizophreniform disorder 52 refractory chronic lymphocytic 52 endogenous ligands 52 chaotic menstrual cycles 52 Nephrotic syndrome 52 hypercalcaemia 52 hyperparathyroidism 52 hormonal abnormalities 52 gene APOE 52 apolipoprotein E gene 52 recurrent acute pancreatitis 52 Hypotension 52 prosopagnosia 52 fibrous dysplasia 52 abdominal abscesses 52 cystic kidney 52 debilitating neurodegenerative 52 SCHIZOPHRENIA DISORDERS SUPPORT GROUP 52 transcranial Doppler ultrasound 52 malignant lymphoma 52 del 5q 52 macular disease 52 Haptoglobin 52 functional polymorphism 52 renovascular hypertension 52 macular edema secondary 52 receptor tyrosine kinase inhibitor 52 juvenile myelomonocytic leukemia 52 neuro endocrine 52 retinal degenerative disease 52 hepatocellular carcinomas 52 lactose malabsorption 52 Peripheral artery disease 52 Obstructive sleep apnea OSA 52 #p#.# [002] 52 herpes simplex encephalitis 52 Kleine Levin 52 SLITRK1 52 generalized seizures 52 Moyamoya disease 52 chronic progressive neurodegenerative 52 Relapsed Refractory 52 Degenerative Disc Disease 52 progressive dyspnea 52 B Cell Lymphoma 52 PKC enzyme 52 SCN5A 52 Uveal melanoma 52 lymphoblastic leukemia 52 prolonged QT interval 52 Major Depressive Disorder 51 autopsied brains 51 Lennox Gastaut Syndrome 51 acute lymphoblastic 51 systemic juvenile idiopathic 51 metastatic bladder 51 de novo AML 51 incurable degenerative 51 nonprogressive 51 chronic autoimmune disorder 51 autoimmune thyroid 51 APOE4 gene 51 SJIA 51 deletion 5q 51 Nonspecific 51 PD LID 51 Von Hippel Lindau 51 migraine aura 51 nonmetastatic 51 uveal melanoma