Related by context. All words. (Click for frequent words.) 62 smoldering myeloma 62 lysosomal storage diseases 61 Severe Primary IGFD 61 MYH9 gene 61 Magnesium deficiency 60 Kufs disease 60 Chronic lymphocytic leukemia 60 ADPKD 60 Myelodysplastic syndromes MDS 60 imatinib resistance 60 Beta thalassemia 60 Becker muscular dystrophy 59 Haptoglobin 59 hypophosphatasia 59 dyskeratosis congenita 59 alveolar rhabdomyosarcoma 59 narcolepsy cataplexy 58 myotonic muscular dystrophy 58 Niemann Pick disease 58 muscular dystrophy cystic fibrosis 58 carbohydrate intolerance 58 Lafora disease 58 1 diabetes T1D 58 immunodeficiencies 58 recessive genetic 58 chronic granulomatous disease 58 mitochondrial disorders 58 autosomal recessive genetic 58 Myelodysplastic syndrome 58 nonalcoholic steatohepatitis 58 Duchenne muscular dystrophy DMD 57 progressive neurodegenerative disorder 57 fatal neuromuscular disorder 57 Aortic stenosis 57 kidney urologic 57 MELAS 57 myositis 57 APOL1 57 myasthenia gravis MG 57 clinically heterogeneous 57 Myotonic dystrophy 57 Nonalcoholic fatty liver 57 Myasthenia gravis 57 allogeneic HSCT 57 Acute myeloid leukemia 57 neuroendocrine cancers 57 myeloproliferative neoplasms MPNs 57 2 diabetes T2D 57 pulmonary hypertension PH 57 spinal muscular atrophy SMA 57 Morquio 57 Juvenile Idiopathic Arthritis JIA 57 nonalcoholic steatohepatitis NASH 57 Genetic predisposition 56 Parkinson disease neurodegenerative disorder 56 EBV infection 56 PCNSL 56 pemphigus vulgaris 56 Vitamin B# deficiency 56 degenerative neurological diseases 56 GBA mutations 56 insulin resistance syndrome 56 Autoimmune diseases 56 Primary IGFD 56 SOD2 gene 56 primary immunodeficiency 56 heritable diseases 56 HNPCC 56 hereditary spastic paraplegia 56 Myelodysplastic syndromes 56 lysosomal storage disease 56 Chronic myeloid leukemia 56 Fabry Disease 56 Glioblastoma multiforme GBM 56 elevated triglyceride levels 56 Celiac sprue 56 Niemann Pick 56 familial ALS 56 Pulmonary arterial hypertension 56 BRAF V#E 56 neuropsychiatric disorder 56 glutamic acid decarboxylase 56 epilepsies 56 Inflammatory bowel diseases 56 Vitamin D insufficiency 56 systemic mastocytosis 56 debilitating autoimmune 56 Fanconi syndrome 56 Glioblastoma Multiforme GBM 56 chronic myeloid 56 TTR amyloidosis 56 hereditary predisposition 56 Sjögren syndrome 56 CFH gene 56 GH deficiency 56 Aplastic anemia 56 myelogenous leukemia 56 Leukemias 56 Hp2 2 56 autoinflammatory diseases 56 human metapneumovirus 56 ectodermal dysplasia 55 MPS VI 55 hereditary deafness 55 Coeliac disease 55 AAT deficiency 55 subclinical disease 55 Spinal muscular atrophy 55 Endometrial cancer 55 T1DM 55 Fatty liver 55 autosomal recessive disease 55 immunodeficient 55 Gorlin syndrome 55 SNT-MC#/idebenone 55 Postnatal depression 55 autosomal recessive disorder 55 squamous cell lung cancer 55 homozygous FH 55 mutated K ras 55 Klinefelter Syndrome 55 Hurler syndrome 55 Nicotine dependence 55 bronchopulmonary dysplasia BPD 55 induced anemia 55 HER2 positivity 55 Genetic variants 55 lymphoproliferative disease 55 Von Willebrand disease 55 NPHP 55 Dr. Bezprozvanny 55 Leber Congenital Amaurosis LCA 55 progressive neurodegenerative 55 chronic periodontitis 55 neuroblastoma tumor 55 chronic hepatitis cirrhosis 55 K ras mutations 55 HBeAg negative 55 hematological malignancy 55 Congenital Muscular Dystrophy 55 isolated systolic hypertension 55 Cognitive impairment 55 immunosuppressed patients 55 metastatic neuroendocrine tumors 55 GRNOPC1 contains 55 benign thyroid nodules 55 Diabetic nephropathy 55 genetic lysosomal storage 55 basal cell nevus syndrome 55 transthyretin amyloidosis 55 smoldering multiple myeloma 55 Premature Ovarian Failure 55 progressive degenerative neurological 55 pediatric bipolar disorder 55 disease NAFLD 55 familial clustering 55 relapsed leukemia 55 Prolastin A1PI 55 protein misfolding diseases 55 leukodystrophies 55 oligodendrogliomas 55 HLA B# 55 multisystem disease 55 acute myelogenous leukemia AML 55 herpes zoster shingles 55 polycystic ovarian syndrome PCOS 55 T. vaginalis 55 monogenic 55 thrombophilia 55 lactose malabsorption 55 spastic diplegia 54 untreated celiac disease 54 juvenile idiopathic arthritis JIA 54 Atopic dermatitis 54 HER2 overexpression 54 Duchenne Muscular Dystrophy DMD 54 Gleevec resistant 54 chromosome abnormality 54 Hereditary angioedema HAE 54 Synovial sarcoma 54 familial pancreatic cancer 54 chromosomal anomaly 54 coronary calcification 54 Opportunistic infections 54 Hemophilia B 54 Langerhans cell histiocytosis 54 generalized epilepsy 54 lysosomal diseases 54 AA Amyloidosis 54 LHON 54 T2DM 54 Fanconi Anemia 54 Pulmonary fibrosis 54 CALHM1 54 KRAS oncogene 54 Hutchinson Gilford progeria 54 varicella infection 54 Anal cancer 54 neurologic disorder 54 vWD 54 herpesviruses 54 nonmelanoma skin cancers 54 1 Antitrypsin Deficiency 54 muscular dystrophies 54 spinocerebellar ataxia 54 embryonal rhabdomyosarcoma 54 Li Fraumeni 54 autoimmune thyroid 54 Ribavirin causes 54 neuro degenerative disorders 54 AChE inhibitors 54 neuro developmental disorder 54 autism spectrum disorders ASDs 54 CTAP# Capsules 54 atypical hemolytic uremic syndrome 54 thiopurine 54 Factor XIII 54 circulating endothelial cells 54 Chronic pancreatitis 54 Zinc deficiency 54 VCFS 54 acute rheumatic fever 54 hereditary degenerative 54 undiagnosed celiac disease 54 paraneoplastic 54 de novo AML 54 minimally symptomatic 54 hypertrophic cardiomyopathy HCM 54 systemic lupus erythematosus SLE 54 Alport syndrome 54 rheumatologic 54 fatal neurodegenerative disorder 54 Malignant glioma 54 primary immunodeficiency PI 54 Hashimoto thyroiditis 54 haematological cancers 54 sporadic ALS 54 retinal degenerative disease 54 APOE ε4 54 neurological manifestations 54 IgA deficiency 54 Acute Myelogenous Leukemia 54 Myelodysplastic Syndrome MDS 54 Spinal Muscular Atrophy SMA 54 immunodeficiency diseases 54 lung cancer NSCLC 54 fructose intolerance 54 CC genotype 54 acute lymphoid leukemia 54 p# biomarker 54 HGPS 54 sJIA 54 inherited neurodegenerative disorder 54 Friedreich Ataxia 54 chlamydial infections 54 SRBD 54 metabolic abnormality 54 neurobehavioral disorder 54 HLA DR4 54 hematologic disorders 54 TCF#L# gene 54 Valproic acid 54 Idiopathic Thrombocytopenic Purpura ITP 54 pilocytic astrocytomas 54 Lou Gehrigs disease 54 Muscular dystrophy 54 hematopoietic cancers 54 Belimumab 54 rheumatic disorders 54 Sporadic CJD 54 haematologic malignancies 54 monoclonal gammopathy 54 transgenic rats 54 Dilated cardiomyopathy 54 genetically inherited 54 Bronchiolitis 54 Alzheimer Disease AD 53 histiocytosis 53 IPAH 53 apolipoprotein E4 53 Crohns disease 53 SSc 53 herpes zoster virus 53 Inflammatory bowel disease 53 late onset Pompe 53 cardio metabolic diseases 53 Lung transplantation 53 nonseminoma 53 Genital herpes 53 Peutz Jeghers syndrome 53 neuroblastoma tumors 53 CP CPPS 53 JAK2 mutation 53 Idiopathic pulmonary fibrosis 53 Aviptadil 53 myeloproliferative neoplasms 53 Osteosarcoma 53 neuroblastomas 53 efalizumab 53 APOE genotype 53 inherited neurodegenerative 53 Hereditary angioedema 53 severe malignant osteopetrosis 53 prion disease 53 cancer cachexia 53 streptococcal infections 53 LRRK2 gene 53 underlying pathophysiology 53 Pompe Disease 53 FLT3 mutations 53 Soft tissue sarcomas 53 Moyamoya 53 Pulmonary hypertension 53 Thyroid nodules 53 lupus nephritis 53 latent TB infection 53 Chronic Fatigue Syndrome CFS 53 medulloblastoma tumors 53 PKU genetic 53 PLX MS 53 von Willebrand Disease 53 diabetic kidney 53 gastrointestinal dysfunction 53 HLA DQ2 53 ALI ARDS 53 candidemia 53 MELAS syndrome 53 Velculescu 53 bladder carcinoma 53 gastrointestinal stromal tumors GISTs 53 lupus sufferers 53 MCAD deficiency 53 idiopathic pulmonary arterial hypertension 53 eosinophilic asthma 53 Dravet syndrome 53 haemolytic anemia 53 NNRTI resistant virus 53 Carcinoid tumors 53 Medulloblastoma 53 mutated KRAS gene 53 CB2 receptor 53 Cryptococcus neoformans 53 primary hyperparathyroidism 53 heterozygous FH 53 FSAD 53 HIV HCV coinfected 53 GBMs 53 inflammatory demyelinating 53 Histiocytosis 53 familial dysautonomia 53 transfusion syndrome 53 NOMID 53 decompensated cirrhosis 53 dexpramipexole 53 Myopathy 53 fronto temporal dementia 53 M. pneumoniae 53 hepatitis C genotype 53 hereditary hemochromatosis 53 immunodeficiency disorder 53 dasatinib Sprycel 53 post transplant lymphoproliferative 53 congenital toxoplasmosis 53 acute promyelocytic leukemia 53 HeFH 53 Gluten intolerance 53 cystic fibrosis chronic pancreatitis 53 MYCN amplification 53 Noonan Syndrome 53 immunocompetent 53 IGFD 53 recessively inherited 53 Iron deficiency anemia 53 endocrine dysfunction 53 differentiated thyroid 53 Neurofibromatosis type 53 refractory Hodgkin 53 Crigler Najjar syndrome 53 congenital muscular dystrophy 53 G6PD deficiency 53 homozygous familial hypercholesterolemia 53 molecular mimicry 53 neurogenetic 53 genetic syndromes 53 TGFBR1 * 6A 53 chronic rheumatic 53 fatal myelination disorder 53 Zavesca 53 juvenile idiopathic arthritis 53 immunodeficiency disorders 53 serous ovarian cancer 53 childhood disintegrative disorder 53 autoimmune encephalitis 53 Leydig cell 53 AAT Deficiency 53 rheumatic disease 53 juvenile myelomonocytic leukemia 53 Hutchinson Gilford Progeria 53 Wiskott Aldrich syndrome 53 breast endometrial 53 fatal neurodegenerative 53 Systemic lupus erythematosus SLE 53 Colon polyps 53 autosomal dominant polycystic kidney 53 Chlamydia psittaci 53 nonhereditary 53 Generalized anxiety disorder 53 CFS ME 53 lymphoid tumors 53 Chronic Lyme disease 53 Acute Myelogenous Leukemia AML 53 immunodeficiency 53 huntingtin gene 53 R. equi 53 elevated CRP 53 Epstein Barr virus EBV 53 arterial thickening 53 MGUS 53 chronic HBV infection 53 acute leukemias 53 myopathies 53 inherited retinal 53 Hemiplegia 53 neurological disorder affecting 53 chronic autoimmune disorder 53 nephrosis 53 Celiac disease affects 53 OnDose TM 53 clade B 53 causative gene 52 atherothrombosis 52 anticancer therapy 52 lymphocytic leukemia 52 RSV infections 52 motor neuron diseases 52 Zolinza 52 chronic prostatitis 52 Pervasive Developmental Disorder 52 Atypical Hemolytic Uremic Syndrome 52 Osteoarthritis OA 52 CHD7 52 autoimmune thyroiditis 52 Alport Syndrome 52 Inflammatory Bowel Disease 52 Arranon 52 hypereosinophilic syndrome 52 T#I [002] 52 thalidomide Thalomid 52 Hemolytic uremic syndrome 52 congenital hyperinsulinism 52 obesity insulin resistance 52 debilitating neurological disorder 52 nonsmall cell lung cancer 52 BRAF V#E mutation 52 galactosemia 52 Rilonacept 52 fibrosarcoma 52 demyelinating 52 Irritable bowel syndrome IBS 52 sickle cell hemoglobin 52 Porphyria 52 diffuse gastric 52 ABCB1 52 ceroid lipofuscinosis NCL 52 nongenetic 52 hepatorenal syndrome 52 leukaemias 52 pharmacologic intervention 52 Irritable bowel syndrome 52 Bronchiectasis 52 Waldenstrom macroglobulinemia 52 precancerous condition 52 Leukemia lymphoma 52 beta carotene supplementation 52 debilitating neurological disease 52 progressive neurodegenerative disorders 52 deletion 5q 52 LRP5 52 Pancreatic neuroendocrine tumors 52 immunosuppressive therapies 52 Chronic Myeloid Leukaemia 52 GIST tumors 52 prostate cancer CaP 52 Ulcerative colitis 52 AA amyloidosis 52 Chronic fatigue 52 spastic paraplegia 52 alpha thalassemia 52 convulsive disorders 52 histological subtype 52 NAFLD 52 Chronic hepatitis B 52 Pemphigus 52 Uncontrolled hypertension 52 carcinoid cancer 52 APOE4 52 nasopharyngeal carcinoma 52 Sanfilippo Syndrome 52 primary IGFD 52 incidentalomas 52 Cockayne Syndrome 52 Ankylosing spondylitis 52 discoid lupus 52 FLT3 52 mGluR4 activation 52 neurodegenerative disorder 52 Rotavirus infection 52 HER2 expression 52 Bone marrow transplant 52 mtDNA mutations 52 CMV infection 52 allogeneic bone marrow 52 mitochondrial mutations 52 Chiari malformation 52 PIDD 52 Diamyd ® 52 immunopathology 52 progressive neuromuscular 52 Fanconi anemia 52 investigational therapies 52 Arrhythmogenic Right Ventricular Cardiomyopathy 52 ADA SCID 52 subclinical atherosclerosis 52 familial hypercholesterolemia FH 52 chronic renal disease 52 multiple sclerosis lupus 52 Fibromyalgia syndrome 52 FTLD 52 BARD1 52 kidney insufficiency 52 rheumatic diseases 52 Acute Myeloid Leukaemia AML 52 Eisenmenger syndrome 52 primary biliary cirrhosis 52 metastatic gastric 52 Niemann Pick Disease 52 cause cardiac channelopathies 52 Canavan Disease 52 Malignant mesothelioma 52 indolent lymphomas 52 mitochondrial diseases 52 receptor inhibitor 52 Behcet disease 52 invasive fungal 52 HbF 52 lichen planus 52 TMEM#B 52 sargramostim 52 Follicular lymphoma 52 ataxias 52 periodontal tissues 52 EoE 52 Henoch purpura 52 orchitis 52 Diabetic neuropathy 52 SNT MC# 52 gastrointestinal stromal tumor GIST 52 CETP gene 52 maternally inherited 52 non alcoholic steatohepatitis 52 Fragile X gene 52 congenital deafness 52 incurable neurological disorder 52 ARVD 52 canakinumab 52 polymyalgia rheumatica 52 Venous thromboembolism 52 limb girdle muscular dystrophy 52 Parkinson Disease PD 52 parkinsonian symptoms 52 HNSCC 52 INSPIRE Trial Phase III 52 dysglycemia 52 chlamydial infection 52 lumiliximab 52 CMV infections 52 Fc gamma receptor 52 myeloid leukemia 52 Alequel 52 autoantibody positive 52 chronic Hepatitis B 52 multi factorial disease 52 bronchopulmonary dysplasia 52 Acute myelogenous leukemia 52 Marfan mice 52 systemic scleroderma 52 presymptomatic 52 cystic fibrosis CF 52 GBM tumors 52 JMML 52 Hervé Hoppenot President 52 neuro degenerative disease 52 dominantly inherited 52 LQTS 52 genotypic resistance 52 metabonomics 52 vitamin B# deficiency 52 MODY 52 acute psychosis 52 epithelial tumors 52 atopic eczema 52 Klinefelter syndrome 52 neurocognitive disorders 52 familial adenomatous polyposis FAP 52 hematopoietic cell 52 diabetic retinopathy DR 52 progranulin mutations 52 molecularly defined 52 Autoimmune disorders 52 ENPP1 52 kidney allograft 52 Gaucher Disease 52 herpes encephalitis 52 Helicobacter pylori infection 52 T1c 52 degenerative retinal diseases 52 autonomic dysfunction 52 Cystinosis 52 Childhood Disorder 52 systemic lupus erythematosus 52 constipation predominant irritable bowel 52 Marfan 51 mGluR5 antagonist 51 Cockayne syndrome 51 intractable epilepsy 51 sarcoid 51 lupus 51 secondary hyperparathyroidism 51 Acute lymphoblastic leukemia 51 Leber congenital amaurosis LCA 51 Avandia Actos 51 Ets2 51 cancerdefine 51 T2D 51 LRRK2 mutations 51 autoimmune pancreatitis 51 carcinoid 51 respiratory viral infections 51 Phenoptin 51 HMGCR 51 Difficulty swallowing 51 debilitating neurodegenerative disorder 51 Epstein Barr Virus 51 hypovitaminosis D 51 malignant lymphomas 51 PTPN# 51 skeletal dysplasia 51 malignant pleural mesothelioma 51 histologic subtype 51 Peanut allergy 51 chronic rhinosinusitis CRS 51 testicular germ cell 51 hematological diseases 51 ErbB2 positive 51 type 1diabetes 51 misfolded SOD1 51 achondroplasia 51 BioNumerik 51 hypokalemia hypomagnesemia 51 chromosomal disorders 51 inherited retinal degeneration 51 Duchene Muscular Dystrophy 51 Eosinophilic esophagitis 51 de novo mutations 51 lupus scleroderma 51 Male pattern baldness 51 KIBRA 51 gallstone disease 51 ANCA associated 51 cystic fibrosis Duchenne muscular 51 hyperinsulinism 51 GISTs 51 KRAS mutation 51 melanocortin receptor 51 Proteus syndrome 51 anemia neutropenia 51 XMRV retrovirus 51 Umbilical cord stem cells 51 castrate resistant prostate cancer 51 lymphoma leukemia 51 Treg cell 51 limiting generalizability 51 recurrent glioblastoma multiforme 51 Sjogren Syndrome 51 autism spectrum diagnoses 51 CSF biomarkers 51 anemias 51 cardiomyopathy weakening 51 Prostrate cancer 51 Lennox Gastaut syndrome 51 neurodevelopment disorder 51 cholangiocarcinoma 51 Testicular cancer 51 skeletal muscle weakness 51 multifactorial disease 51 invasive secretory carcinoma 51 Glioblastoma Multiforme 51 genetic variants associated 51 simplex virus 51 modifier genes 51 Velcade bortezomib 51 nasopharyngeal cancer 51 cirrhosis liver failure 51 neuro degenerative disorder 51 inverse agonist 51 neurodevelopmental disorder 51 cytomegalovirus retinitis 51 familial predisposition 51 Enzyme Replacement Therapy 51 dermatomyositis 51 beta interferons 51 Arcalyst 51 Usher Syndrome 51 leptin deficiency 51 NF1 51 Down syndrome chromosomal disorder 51 interstitial cystitis IC 51 subclinical hyperthyroidism 51 familial hypercholesterolemia 51 MPGN 51 Hypoparathyroidism 51 EC Cysteamine 51 severe Primary IGFD 51 acute myeloid 51 androgenetic alopecia 51 hyperphenylalaninemia HPA due 51 Cytomegalovirus 51 Pelizaeus Merzbacher disease 51 gastric lymphoma 51 cisplatin chemotherapy 51 blood clotting disorder 51 Staphylococcus aureus infections 51 cystic fibrosis muscular dystrophy 51 diabetes mellitus T2DM 51 coinfected patients 51 HYPP 51 hormone deprivation 51 Uterine cancer 51 chronic eosinophilic leukemia 51 Interstitial cystitis 51 rhinovirus infection 51 primary immunodeficiencies 51 Acute leukemia 51 Systemic lupus 51 idiopathic pulmonary fibrosis IPF 51 FMRP protein 51 myeloproliferative diseases 51 BMPR2 51 immunotherapeutic approaches 51 Lateral Sclerosis 51 cystinosis 51 Glioblastoma 51 thromboembolic disease 51 CYT# potent vascular disrupting 51 outgrow peanut allergy 51 plasma kallikrein 51 JAK mutations 51 genetic determinants 51 APOE e4 allele 51 S. maltophilia 51 autistic traits 51 VKORC1 51 Myocarditis 51 progressive neurodegenerative disease 51 Dravet Syndrome 51 leukemia AML 51 Osteopenia 51 Campath alemtuzumab 51 Maroteaux Lamy syndrome 51 atherothrombotic 51 shorter telomere length 51 diabetes mellitus DM 51 biologic therapeutics 51 IL#R 51 ADAM# 51 Plaque psoriasis 51 dermatologic reactions 51 SGS# 51 holoprosencephaly 51 lupus multiple sclerosis 51 glioblastoma tumors 51 FASPS 51 diabetic gastroparesis 51 comorbid anxiety 51 euthymic patients 51 nondemented 51 tuberous sclerosis complex 51 gastric carcinoma 51 mTOR inhibitors 51 RNAi therapeutic targeting 51 chromosomal alterations 51 alpha1 antitrypsin deficiency 51 Leber Hereditary Optic Neuropathy 51 lipid abnormalities 51 seminomas 51 PTEN mutations 51 G#D 51 interferon beta therapy 51 genetic abnormality 51 Temsirolimus 51 diagnose coronary artery 51 Acute Promyelocytic Leukemia 51 null responder 51 Chronic constipation 51 idiopathic thrombocytopenic purpura 51 Tesmilifene 51 NASH Huntington 51 nonhuman primate model 51 remyelination 51 SJIA 51 Polycystic Kidney Disease 51 neurodegenerative disorder characterized 51 microscopic colitis 51 blood clotting disorders 51 Vertebral compression fractures 51 Hypophosphatasia 51 INF2 51 congenital hemophilia 51 Alessandro Riva 51 Autism Spectrum Disorders ASD 51 Idiopathic Pulmonary Fibrosis IPF 51 hepatic liver 51 curative therapy 51 celiac sprue 51 enteroviral infection 51 cutaneous lupus 51 Pseudomonas aeruginosa infections 51 BCR ABL inhibitor 51 phthalate syndrome 51 Malignant gliomas 51 proliferative retinopathy 51 LVNC 51 selective modulator 51 Cholangiocarcinoma 51 Alopecia Areata 51 Neurofibromatosis 51 Acute lymphocytic leukemia 51 XMRV infection 51 anosognosia 51 Dasatinib 51 amnestic mild cognitive impairment 51 roseola 51 retinal dystrophies 51 etiologic factors 51 Lactose intolerance 51 gluten sensitive enteropathy 51 neurological illnesses 51 Cryopyrin Associated Periodic Syndromes 51 inherited metabolic disorders 51 hypogonadotropic hypogonadism 51 chronic GVHD 51 Clinical Trials Consortium 51 Chronic Myelogenous Leukemia 51 congenita 51 fragility fractures 51 hypercoagulable 51 antiproliferative effects 51 Leber congenital amaurosis 51 hemoglobinopathies 51 neuropsychiatric diseases 51 multigene 51 ependymoma 51 hemophagocytic lymphohistiocytosis 51 HPV subtypes 51 antenatal depression 51 ciliopathies 51 Glioma 51 mastocytosis 51 hormone receptor negative 51 myelofibrosis polycythemia vera 51 YONDELIS 51 HER2 positive cancers 51 persistent pulmonary hypertension 51 Dwarfism 51 neurodevelopmental disorders 51 immuno deficiency 51 alexithymia 51 androgenic alopecia 51 lymphoproliferative disorder 51 commercialize deforolimus 51 Hurler Syndrome 51 faulty BRCA2 gene 51 posaconazole 51 human leukocyte antigens 50 diagnostic biomarker 50 CA MRSA infections 50 osteosarcomas 50 Heritability 50 F#del 50 recurrent miscarriage 50 Levy Lahad 50 DQB1 * 50 opioid dependent 50 relapsing remitting 50 Loeys Dietz syndrome 50 sporadic Creutzfeldt Jakob 50 murine models 50 Moyamoya disease 50 clinicopathological 50 medulloblastomas 50 Li Fraumeni syndrome 50 nephritis 50 Cognitive Deficits 50 neurologic symptoms 50 basiliximab 50 neurodevelopmental impairment 50 degenerative neurological condition 50 nonsense mutations 50 Evoltra ® 50 Respiratory Virus 50 malarial anemia 50 BCR ABL protein 50 susceptibility loci 50 TOMM# 50 chronic myocardial ischemia 50 DEB# 50 polycystic ovary syndrome 50 arteritis 50 pouchitis 50 amyloid cascade 50 nephrogenic fibrosing dermopathy 50 uricase 50 NSCLC tumors 50 muscle degeneration 50 Opioid induced bowel dysfunction 50 hepatitis C HCV 50 Alessio Fasano MD 50 combination antiretroviral therapy 50 tumor histology 50 EGFR tyrosine kinase inhibitors 50 neurobiological disorder 50 Hypertensive heart 50 pheochromocytoma 50 specific chemokine receptors 50 Hemolytic Uremic Syndrome 50 Alzheimers disease 50 Human Leukocyte Antigen 50 Oral mucositis 50 DIPG 50 carotid plaques 50 biologic pathways 50 Genetic variation 50 HELLP 50 LV dysfunction 50 chromosomal defect 50 Intravenous immunoglobulin 50 bacterial prostatitis 50 Congenital Emphysema 50 Amyotrophic lateral sclerosis ALS 50 NPM1 50 Wegener granulomatosis 50 Darapladib 50 anticholinergic agents 50 Symadex 50 immunodeficiency disease 50 basal cell carcinoma BCC 50 VaD 50 Cushing Syndrome 50 5q deletion 50 PARP inhibition 50 vaso occlusive crisis 50 Raynaud syndrome 50 neurocognitive dysfunction 50 exome sequencing 50 demyelinating diseases 50 Nilotinib 50 Febrile neutropenia 50 pharmacokinetic interactions 50 #q#.# deletion syndrome 50 neurofibrillary 50 TNF blocker therapy 50 Renal Cell Carcinoma RCC 50 microsatellite instability 50 Rhabdomyosarcoma 50 pretreatment serum 50 familial adenomatous polyposis 50 sarcopenia 50 ZNF# 50 A1PI 50 CDH1 50 colorectal carcinoma 50 proteasome inhibitor 50 Myelodysplastic Syndrome 50 membranous nephropathy 50 prognostically 50 Guillain Barré 50 autoimmune reactions 50 histone deacetylases 50 invasive ductal breast cancer 50 pancreatic endocrine 50 eosinophilic esophagitis 50 stratifying patients 50 fat malabsorption 50 EGFR mutation positive 50 autoinflammatory 50 variant rs# 50 Retinitis pigmentosa 50 Marfan Syndrome 50 hypoparathyroidism