Related by context. All words. (Click for frequent words.) 49 muscular dystrophy cystic fibrosis 47 Fanconi anemia FA 46 CDH1 46 autosomal recessive disease 46 progressive retinal degenerative 45 BRAF V#E 45 non syndromic 45 G6PD deficiency 44 Spinal muscular atrophy 44 Bishop Erwin Kraeutler 44 chronic obstructive airway 44 Beta Thalassemia 44 Uterine cancer 44 Colorectal cancer CRC 44 Beta thalassemia 44 actor Elio Germano 44 Porphyria 44 autosomal recessive 44 retinal dysfunction 44 congenital hypothyroidism 44 perinatal morbidity 44 gynecologic malignancy 44 craniofacial abnormalities 44 commonest cause 44 neurological abnormalities 44 disabling neurological 44 cleft lip cleft palate 44 familial hypercholesterolemia FH 43 dyskeratosis congenita 43 reproductive endocrine 43 bronchial airway 43 Cx# [002] 43 JAK mutations 43 leukemia lymphomas 43 Myocardial infarction 43 ptau 43 papillary thyroid cancer 43 plexiform 43 Hedgehog agonist 43 testicular germ cell 43 mitochondrial mutations 43 hypertension cardiovascular disease 43 Folate deficiency 43 Oxidative damage 42 clinically heterogeneous 42 whooping cough vaccines 42 Premature Ovarian Failure 42 LRRK2 mutations 42 Male pattern baldness 42 cervical uterine 42 cause cardiac channelopathies 42 chromosomal anomaly 42 LHRH receptor positive 42 Rosa Sgorbati 42 Androgenetic Alopecia 42 Lafora disease 42 reproductive abnormalities 42 INAF 42 neurological disorder affecting 42 autism Asperger Syndrome 42 hyperphenylalaninemia HPA due 42 neurobehavioral disorder 42 POMC gene 42 cirrhosis liver failure 42 testicular tumors 42 gestational diabetes mellitus GDM 42 cleft lip palate 42 biochemical abnormalities 42 fibrosing 42 choriocarcinoma 42 familial hypercholesterolaemia 42 acute lymphoblastic 42 immunodeficiencies 42 Apert syndrome 42 gastrointestinal stromal tumors GISTs 42 Hereditary angioedema 42 multisystem disease 42 vaso occlusive crisis 42 Endometrial cancer 42 Cerebral malaria 41 HeFH 41 androgenetic alopecia 41 acute lymphoid leukemia 41 AIDs epidemic 41 Bazedoxifene 41 medullary thyroid 41 Hutchinson Gilford progeria 41 neuro degenerative disorders 41 MELAS 41 LRRK2 mutation 41 Hemolytic uremic syndrome 41 congenital toxoplasmosis 41 Abano Terme 41 glucokinase activators 41 parkin gene 41 Chronic lymphocytic leukemia 41 prevent invasive pneumococcal 41 teratogen 41 cholestasis 41 leukodystrophies 41 atrophic gastritis 41 Meckel Gruber 41 Prodarsan R 41 THALOMID ® 41 multicentric 41 Polymorphic Ventricular Tachycardia CPVT 41 Dr. Alois Alzheimer 41 Kufs disease 41 NPM1 gene 41 hereditary predisposition 41 mito 41 Duchenne muscular dystrophy DMD 41 Foetal 41 Hurler syndrome 41 Osteogenesis imperfecta 41 Variant Creutzfeldt Jakob Disease 41 hereditary deafness 41 neuropsychiatric disorder 41 genital tracts 41 5a RIs 41 Leber congenital amaurosis 41 disorder FASD 41 SSc 41 PCA3 gene 41 Becker muscular dystrophy 41 PDGFR 41 alopecia sufferers 41 antimetabolites 41 ADPKD 41 cardio metabolic diseases 41 PCOD 41 Retinitis Pigmentosa RP 41 epithelial tissues 41 Arrhythmogenic Right Ventricular Cardiomyopathy 41 facial clefts 41 melanocortin receptor 41 phenothiazines 41 embryonal 41 primary hyperparathyroidism 41 Acute myeloid leukemia 41 opsoclonus myoclonus syndrome 41 disorder thalassemia 41 lipodystrophy syndrome 41 alpha synuclein protein 41 SNT MC# 41 euthymic patients 41 Milan Bicocca 41 Alois Alzheimer 41 Pierre Fabre Laboratories 41 disease epidermolysis bullosa 41 ankyrin repeat 41 glia cells 41 familial ALS 41 genetic lysosomal storage 41 Etna Biotech 41 Epstein Barr Virus EBV 41 Leukemias 41 cytomegalovirus CMV infections 41 Induced pluripotent stem cells 41 endocrine dysfunction 40 Atopic dermatitis 40 myeloproliferative neoplasms 40 γ secretase 40 renal diseases 40 LHON 40 neuronal nitric oxide synthase 40 Gervain 40 cervix uteri 40 IMiDs ® 40 infertility miscarriage 40 congenital cataract 40 uterus womb 40 Aviptadil 40 molar pregnancy 40 mycosis fungoides 40 tricolored battles 40 ocular albinism 40 Severe Primary IGFD 40 chromosomal defect 40 Alport syndrome 40 universalis 40 diseases fat malabsorption 40 pAkt 40 Leber congenital amaurosis LCA 40 Phenylketonuria 40 hemoglobinopathies 40 epilepsy Parkinson disease 40 Ospedale di 40 neuroendocrine cells 40 Genetic mutation 40 ADAMTS# 40 malignant brain 40 survival motor neuron 40 inherited mutations 40 Iodine deficiency 40 severe dehydrating diarrhea 40 lung carcinomas 40 prematurity ROP 40 stylishly crafted 40 chronic myeloid 40 Alopecia Areata 40 antiphospholipid antibodies 40 Crouzon syndrome 40 Li Fraumeni syndrome 40 Italian Rosa Venerini 40 Wiskott Aldrich syndrome 40 inherited metabolic disorders 40 pancreatic endocrine 40 TP# mutation 40 familial hypercholesterolaemia FH 40 genital abnormalities 40 familial polyposis 40 childhood acute lymphoblastic 40 subclinical atherosclerosis 40 neoplastic diseases 40 congenital deafness 40 vesicoureteral reflux VUR 40 Ivanhoe Newswire Patients 40 Retinopathy 40 renal carcinoma 40 Cockayne Syndrome 40 lupus anticoagulant 40 teratogens 40 cystic kidney 40 Genetic variation 40 SCN9A 40 fatal neurodegenerative disorder 40 breast endometrial 40 medium chain acyl 40 leukemia lymphoma myeloma 40 maturational 40 acute leukemias 40 Squamous Cell 40 developmental abnormalities 40 hereditary pancreatitis 40 Lafora 40 Chronic myeloid leukemia CML 40 hemolytic uremic syndrome HUS 40 antenatal screening 40 nonalcoholic steatohepatitis NASH 40 inborn errors 40 Kinase inhibitors 40 psoriatic disease 40 INF2 40 autoimmune cardiovascular 40 MELAS syndrome 40 Brugada syndrome 40 familial pancreatic cancer 40 Erythropoietic 40 basal cell carcinoma BCC 40 Myotonic dystrophy 40 autosomal dominant inheritance 40 biologies 40 CHEK2 gene 40 hypophosphatasia 40 National Birth Cohort 40 prostate cancer benign prostatic 40 alpha thalassemia 40 Chronic lymphocytic leukemia CLL 40 idiopathic PAH 40 Carlo Besta 40 congenital blindness 40 essential thrombocythemia 40 neuro developmental disorder 40 renovascular hypertension 40 Tay Sachs genetic 40 embryoid body 40 Ectopic pregnancy 40 Dental caries 40 thalassemic 40 Eclampsia 40 alopecia totalis 40 limb girdle muscular dystrophy 40 NF1 40 metabolomic profiles 40 progressive neurodegenerative disorders 40 severe congenital neutropenia 40 Magnesium deficiency 39 chromosome #p# [001] 39 progressive neurodegenerative 39 hyperlipidaemia 39 acute myeloid 39 limb malformations 39 autosomal recessive disorder 39 Friedreich ataxia 39 endocrine disorder 39 uncontrolled epilepsy 39 infertility miscarriages 39 pathophysiological effects 39 consanguineous 39 leiomyomas 39 Axxam 39 Hor irw 39 Lipodystrophy 39 familial adenomatous polyposis FAP 39 genetically inherited 39 Neuroendocrine 39 urolithiasis 39 Congenital Adrenal Hyperplasia 39 latent celiac disease 39 neuro sciences 39 neurological manifestations 39 Genetic profiling 39 MLL2 39 dementia praecox 39 Fetal alcohol 39 Epstein Barr virus EBV 39 ovary uterus 39 Giulia Salzano 39 multifactorial disease 39 Bardet Biedl syndrome 39 PTPN# 39 recurrent miscarriage 39 defeated Andreas Seppi 39 enlarged prostate BPH 39 Dwarfism 39 Adiponectin 39 familial hypercholesterolemia 39 CRTAP 39 Genetic mutations 39 malignant myeloma 39 Chronic inflammation 39 dominantly inherited 39 Pulmonary fibrosis 39 Myelodysplastic syndromes MDS 39 congenital birth defects 39 Fatebenefratelli hospital 39 Hypertrophic cardiomyopathy 39 Cystic fibrosis affects 39 genomic rearrangement 39 infantile autism 39 mitochondrial disorders 39 Pope baptizes 39 bladder ovarian 39 PNET 39 Diabetic nephropathy 39 leukemia ALL 39 NPHP 39 Alopecia areata 39 robs sufferers 39 SLC#A# gene [001] 39 idiopathic pulmonary arterial hypertension 39 Basal Cell 39 progressive neurodegenerative disorder 39 chromosomal aberrations 39 alpha1 antitrypsin deficiency 39 thetreatment 39 chromosomal disorders 39 de ath 39 nonmetastatic 39 elevated serum ALT 39 Bone marrow transplant 39 P. falciparum malaria 39 leukaemias 39 colorectal gastric 39 Tyrosine Kinase Inhibitors 39 Wilms tumors 39 atopic sensitization 39 debilitating neurological disorder 39 oligodendrocyte progenitor cells 39 incurable neurological disorder 39 diffuse gastric 39 adrenal hormones 39 lymphoma myeloma 39 T2D 39 neurogenerative diseases 39 Acute Respiratory Failure 39 histone deacetylase 39 myeloid leukemia 39 Langerhans cell histiocytosis 39 cardiac channelopathies 39 Basal cell carcinoma 39 chromosome deletion 39 TLE3 39 Sclerosing 39 Seveso 39 vascular lesion 39 plaque buildup restricts 39 malignant lymphomas 39 confers susceptibility 39 grade serous ovarian 39 puerperal psychosis 39 molecular chaperones 39 androgenic alopecia 39 PAH afflicts approximately 39 adipose derived regenerative 39 telogen effluvium 39 deletion 5q 39 Systemic lupus erythematosus SLE 39 enterocolitis 39 Gestational Diabetes Mellitus 39 Toxicogenomics 39 perinatal outcomes 39 fatal myelination disorder 39 Alagille syndrome 39 congenital malformations 39 consanguineous marriages 39 Peutz Jeghers syndrome 39 DeveloGen 39 prenatally diagnosed 39 leptin deficiency 39 recessive inheritance 39 reproductive tract infections 39 hitherto unrecognized 39 motor neuron degeneration 39 Gene Mutation Linked 39 biliary cancer 39 autoinflammatory 39 lyase 39 containing bioactive nutrients 39 NF kB signaling 39 Prognostic factors 39 causative genes 39 ESKD 39 scarring alopecia 39 postpartum depression PPD 39 Coronary artery calcification 39 TTR amyloidosis 39 Alzheimer Disease AD 39 skeletal dysplasia 39 cryptoxanthin 39 proband 39 PKU genetic 39 Ph + acute lymphoblastic 39 bony metastases 39 La Sapienza Rome 39 IL#R 39 genetically reprogrammed 39 debilitating neurodegenerative 39 smoldering myeloma 39 Human papillomavirus 39 predisposing factor 39 cortical cataract 39 CHDs 39 PCNSL 39 FSHR 39 pathophysiological processes 39 Epidermal Growth Factor 39 colorectal cancer CRC 39 lung ovary 39 focal segmental glomerulosclerosis FSGS 39 induced cardiomyopathy 39 Atoh1 39 Hereditary angioedema HAE 39 CINtec R 39 ovarian carcinomas 39 presymptomatic 39 astressin B 39 cardiovascular disease osteoporosis 39 Oxidative stress 39 leukemia Hodgkin 39 diabetic microvascular complications 39 GPC5 39 thalassemic patients 39 multiply uncontrollably 39 pseudotumor 39 CSF biomarkers 39 complement inhibitor eculizumab 39 cervical breast 39 Duchene muscular dystrophy 39 ovarian breast 39 Susanna Maiolo Swiss 39 Vitamin B# deficiency 39 Bardet Biedl Syndrome 39 HNPCC 39 cataracts clouding 39 thymosin beta 4 39 RNA antagonists 39 pluripotent embryonic 39 Casa della 39 ORMDL3 39 HDAC enzymes 39 sickle cell cystic fibrosis 39 Benign Prostatic Hypertrophy 39 relapsing remitting MS RRMS 39 facial disfiguration 39 utero exposure 39 umbilical hernias 39 amyloid beta plaques 39 autosomal dominant 39 Associated Adipose Redistribution 39 Sjögren syndrome 39 optic neuropathy 39 molecular abnormalities 39 recessive disorders 39 dystrophies 39 chronic hemodialysis 39 Aicardi syndrome 39 Retinal vein occlusion 39 subtype selective 39 Progressive Multifocal Leukoencephalopathy 39 hydrops 39 CP CPPS 39 pancreatic prostate 38 congenital disorders 38 P#X# 38 placental malaria 38 undiagnosed celiac disease 38 Legg Calvé Perthes disease 38 idiopathic myelofibrosis 38 secretory diarrhea 38 breast pancreatic 38 pseudotumor cerebri 38 craniofacial defects 38 MYH9 gene 38 neurocognitive dysfunction 38 disorders FASD 38 osteoporotic vertebral fractures 38 Down syndrome spina bifida 38 hormone FSH 38 congenital adrenal hyperplasia CAH 38 gastric carcinoma 38 nonhereditary 38 cardio vascular diseases 38 Nephrotic Syndrome 38 Neurological disorders 38 Chlamydia trachomatis infection 38 endocrinological 38 pregnancy lactation 38 Androgenetic alopecia 38 ROME JTA 38 polycystic kidneys 38 Takayasu arteritis 38 Cognitive Neurology 38 HuMax Inflam 38 Preimplantation Genetic Diagnosis PGD 38 genetic variants associated 38 hepatic lipase 38 legend Roberto Baggio 38 immuno modulatory 38 neuronal dysfunction 38 deCODE BreastCancer 38 Gluten intolerance 38 amyloid toxicity 38 LPA receptors 38 TNF alpha selectively neutralizing 38 FTLD 38 Medulloblastoma 38 familial clustering 38 emphysema bronchitis 38 Enzo Bearzot 38 Acne vulgaris 38 filaggrin gene 38 cranial irradiation 38 HER2 neu 38 spermidine 38 Peanut allergy 38 Insulin Sensitivity 38 inherited neurodegenerative 38 metabolic dysfunction 38 Clusterin 38 Adenomas 38 degenerative neuromuscular disease 38 urologic diseases 38 nonalcoholic steatohepatitis 38 Middelheim Hospital 38 Familial hypercholesterolemia 38 Alport Syndrome 38 Moyamoya disease 38 Hypoglycaemia 38 hippocampal sclerosis 38 Activating mutations 38 Acute lymphoblastic leukemia 38 L Ergothioneine 38 neuritic 38 STK# gene 38 Lysosomal storage 38 colon pancreatic 38 APOE genotype 38 type 1diabetes 38 myasthenia gravis MG 38 motor neuron diseases 38 enteropathy 38 tissue fibrosis 38 nicotine metabolite 38 Polyneuropathy 38 vascular birthmarks 38 Paris Institut d' 38 psychosomatic medicine 38 skeletal abnormalities 38 cystic fibrosis muscular dystrophy 38 metastatic bladder 38 molecular etiology 38 Carcinoid tumors 38 Waldenstrom macroglobulinemia 38 neurogenic inflammation 38 Novartis Afinitor 38 maternally transmitted 38 gastric carcinomas 38 DNA methylation patterns 38 monocytic 38 Medullary thyroid cancer 38 University Vita Salute 38 leukemias lymphomas 38 thalassemia sickle cell 38 CHARGE syndrome 38 Cojocaru correspondent 38 peptide YY PYY 38 MEF2A 38 Kit CD# positive 38 cell nuclei 38 Human papillomavirus HPV 38 therapeutical 38 Infertility affects 38 nasopharyngeal carcinoma 38 lowest birthrates 38 autism spectrum disorders ASD 38 familial adenomatous polyposis 38 neurovascular diseases 38 alpha#beta# 38 ovarian endometrial 38 dysgenesis 38 neurocysticercosis 38 Cytomegalovirus CMV 38 Siena Biotech 38 syndrome FAS 38 imexon 38 treating sarcoma testicular 38 Tay Sachs thalassemia 38 oncological diseases 38 neurodevelopment disorder 38 LRAT 38 chromosomal alterations 38 Ribavirin causes 38 corticotrophin releasing factor 38 tuberous sclerosis TS 38 Imatinib Mesylate 38 IDDM 38 dei Tumori 38 micronutrient supplementation 38 neurofibroma 38 sensorineural hearing loss 38 cervical lymph nodes 38 Tourette Syndrome TS 38 T1DM 38 hereditary retinal 38 Autoimmune hepatitis 38 HIV HCV coinfected 38 de novo mutations 38 generalized vitiligo 38 CYT# potent vascular disrupting 38 Sydenham chorea 38 SOCS2 38 Phenylketonuria PKU 38 cervical prostate 38 Preimplantation Factor 38 inhibit metastasis 38 Sezary syndrome 38 degenerative nerve disorder 38 Dr. Domenico Corrado 38 choroidal neovascularisation 38 nulliparous 38 gastric adenocarcinoma 38 Mitochondrial dysfunction 38 IPSOGEN 38 deafness meningitis 38 MPS VI 38 deficiency syndrome 38 nasopharyngeal cancer 38 precancerous cervical 38 intracerebral hemorrhage ICH 38 Inflammatory Bowel 38 HLA DQ2 38 Streptococcus pneumoniae pneumococcus 38 CCR5 delta# 38 functional polymorphism 38 budding yeast Saccharomyces 38 gastroesophageal reflux GERD 38 DNA rearrangements 38 Related Dementia 38 ovarian malignancy 38 By Raza Mumtaz 38 Cord Blood Stem Cells 38 MC1R 38 hypercalcaemia 38 CRP concentrations 38 MAPT 38 dysfunctional voiding 38 miscarriages premature births 38 undergoing radical prostatectomy 38 DBMD 38 AVIANO AIR BASE 38 node metastasis 38 thyroid dysfunction 38 #beta hydroxysteroid dehydrogenase 38 Troponin T 38 muscle degeneration 38 neuro degenerative disease 38 polyglutamine diseases 38 β thalassemia 38 leiomyoma 38 bladder carcinoma 38 GSTP1 38 Cell Lymphoma CTCL 38 bacterial pathogenesis 38 Anaplastic 38 Unintentional injuries 38 Cancer Res 38 Folic acid deficiency 38 Papillary 38 Malignant Melanoma 38 Upregulation 38 diabetes dyslipidemia 38 Li Fraumeni 38 thyroid deficiency 38 Rotavirus causes 38 Idiopathic pulmonary fibrosis 38 non polyposis colorectal 38 homozygous FH 38 PDGFRA 38 distinct subtypes 38 Bab al Azaziya 38 trachea transplant 38 polymorphic ventricular tachycardia 38 Meningioma 38 glucocorticoid induced 38 metabolic abnormality 38 Marc Weisskopf 38 Preterm infants 38 Hemorrhagic 38 uncurable 38 pancreatic adenocarcinoma 38 Perthes disease 38 abnormal uterine bleeding 38 Proteus syndrome 38 seminoma 38 gene APOE 38 BH4 deficiency 38 B streptococcal 38 Multiple myeloma MM 38 breast cancer metastasis 38 colorectal cancer therapeutics 38 rheumatic disease 38 atypical hemolytic uremic syndrome 38 Viral Genetics discovers 38 extradites Noriega 38 colorectal carcinoma 38 trophoblastic 38 nonmelanoma 38 epigenetic changes 38 picornavirus 38 paraneoplastic 38 pulmonary metastasis 38 PARP inhibition 38 Oesophageal cancer 38 cardiomyopathies 38 cardiac repolarization 38 Behavior Disorder 38 Misfolded proteins 38 homochirality 38 uterine cervix 38 overt hepatic encephalopathy 38 curry spice 38 Hutchinson Gilford Progeria Syndrome 38 extramedullary 38 neuro developmental disorders 38 Variant CJD 38 abnormal glucose metabolism 38 Mootha 38 tryptase 38 Hypertriglyceridemia 38 angiosarcoma 38 interstitial nephritis 38 Alpha lipoic acid 38 SMN protein 38 NMDA N 38 Depressive disorders 38 Thromboembolism 38 Christine Van Broeckhoven 38 Gestational diabetes 38 gastric cancers 38 SCN5A 38 Progeria 38 homocystinuria 38 onco 38 fungus Fusarium 38 astrocytomas 38 nodal metastasis 38 chronic granulomatous disease 38 Istituto Nazionale di Astrofisica 38 Pneumococcal disease 38 Laura Mezzetti 38 Leber Hereditary Optic Neuropathy 38 Policlinico San 38 immunotoxin 38 tau protein tangles 37 aciduria 37 epigenetic alterations 37 autosomal dominant polycystic kidney 37 MAXY VII 37 Neural stem cells 37 breast uterine 37 adenomatous polyps 37 mutated K ras 37 Theramex 37 neuronal precursor 37 glucocorticoid receptors 37 underlying pathophysiology 37 immuno deficiency 37 obesity insulin resistance 37 cutaneous lupus 37 alcoholic hepatitis 37 Smecta ® 37 ovarian colon 37 post natally 37 neovascular age 37 pediatric acute lymphoblastic 37 Baldness 37 ovarian cervical 37 ovarian germ 37 neurobehavioral disorders 37 Karl Unterkircher 37 leukoencephalopathy 37 #q# [001] 37 PICALM 37 Théramex 37 inherited retinal 37 parthenolide 37 hypercoagulable 37 Chronic Prostatitis 37 MYH9 37 Exon Skipping 37 fibrosarcoma 37 lymphomas leukemias 37 hyper IgE syndrome 37 neovasculature 37 breat cancer 37 masculinizing 37 mastocytosis 37 GRNOPC1 contains 37 genetic mutation 37 MYBPC3 37 Chronic Myeloid Leukemia CML 37 neural tube defect 37 transfusion syndrome 37 metabolizer 37 disregulation 37 prolonged immobilization 37 Personal Hygiene Personal 37 oxidized cysteine 37 spice turmeric 37 IRCCS 37 Myocarditis 37 progressive multifocal PML 37 node metastases 37 malignant pheochromocytoma 37 cleft lips cleft palates 37 Helicobacter pylori infection 37 inherited metabolic diseases 37 axonal damage 37 mesenchyme 37 circadian genes 37 monoclonal gammopathy 37 www.niams.nih.gov 37 neurocognitive disorders 37 epigenetic markers 37 HER2 positivity 37 FABIO CANNAVARO 37 primitive neuroectodermal tumors 37 CCR9 antagonist 37 C EBP alpha 37 dermatologic diseases 37 achromatopsia 37 cycle kinase inhibition 37 Niacinamide 37 premenstrual syndrome PMS 37 Fibroblast Growth Factor Receptor 37 rRNA gene 37 opioid tolerant adult 37 neural crest 37 confer susceptibility 37 acadesine 37 premature graying 37 gene MECP2 37 combination antiretroviral therapy 37 elevated creatinine 37 malignant pancreatic 37 Cholestagel 37 chromosomal anomalies 37 esophagus bladder 37 myelination disorders 37 Goalkeepers Gianluigi Buffon 37 pediatric neuroblastoma 37 spontaneous miscarriages 37 born preterm 37 unprovoked seizures 37 pigment melanin 37 obstructive pulmonary disease 37 Alfa Wassermann 37 hepatic insulin resistance 37 Polycystic kidney disease 37 congenital malformation 37 cervical precancers 37 HMGA1 37 systemic lupus erythematosus 37 heritable diseases 37 Von Willebrand Disease 37 hemolytic disease 37 grows grayer 37 spina bifida cerebral palsy 37 Melasma 37 VCFS 37 nephrosis 37 p# mutations 37 precocious puberty 37 Parasitic worms 37 Oral Hygiene 37 heritable component 37 Politecnico di Torino 37 deafness blindness 37 hormonal disorder 37 antithyroid 37 Vascular Inflammation 37 chloracne 37 Huntington Chorea 37 non hodgkin lymphoma 37 metaplasia 37 pelvic malignancies 37 HER signaling pathway 37 haematological malignancies 37 microRNA profiling 37 MCADD 37 deleterious mutation 37 pathophysiologic 37 histone deacetylases HDAC 37 unexplained mental retardation 37 perinatal transmission 37 CFTR gene 37 recessive trait 37 hepatic liver 37 enkephalin 37 lymphatic leukemia 37 transplantation HCT 37 Jill Stautner 37 penetrance 37 Uveal melanoma 37 common neurovascular complication 37 BRAF V#E mutation 37 Genetic Disorders 37 immunodeficiency diseases 37 deCODE BreastCancer TM 37 Polycystic Ovary Syndrome 37 radiotherapy induced 37 Respiratory Distress 37 chronic inflammatory bowel 37 myofascial pain syndrome 37 Amyotrophic lateral sclerosis ALS 37 esophageal squamous cell carcinoma 37 postpartum hemorrhage 37 Ischaemic heart 37 oligodendrogliomas 37 small RNAs encoded 37 #q#.# deletion syndrome 37 Leber Congenital Amaurosis LCA 37 Acute Intermittent Porphyria 37 Oncogenic 37 Chronic hepatitis B 37 OncoVAX ® 37 Angelman syndrome 37 Primary Immune Deficiency 37 La Vecchia 37 von Hippel Lindau 37 lymphatic cancers 37 spinal metastases 37 Krabbe Leukodystrophy 37 consanguineous marriage 37 soluble fms 37 progressive degeneration 37 hepatorenal syndrome 37 Coeliac disease 37 kidney urologic 37 Wernicke Korsakoff syndrome 37 Adrenoleukodystrophy 37 Hemochromatosis 37 skeletal metastases 37 neovascularisation 37 retinitis pigmentosa RP 37 Joubert syndromes 37 prostate carcinomas 37 Cleft lip 37 Crohns disease 37 BRAF gene mutations 37 hyperinsulinemic 37 GRK5 37 pathological hallmark 37 suppresses tumor 37 allogeneic HSCT 37 neurodevelopmental disorder 37 protein tyrosine phosphatase 1B 37 Topoisomerase II 37 post herpetic 37 genetics immunology 37 B7 H4 37 Polycystic Ovarian Syndrome PCOS 37 Aneuploidy 37 Levi Montalcini 37 mitochondrial DNA mtDNA 37 sporadic ALS 37 blindness paralysis