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European Journal of Neurology, ISSN 1351-5101, 11/2003, Volume 10, Issue 6, pp. 763 - 765
Parkinson's disease | viral meningitis | psychiatry | galantamine | acetylcholine receptor antibodies | paradoxical activity | 18F‐FDG‐PET | intracerebral haemorrhage | video electroencephalographic monitoring | outcomes | camptocormia | paired transcranial magnetic stimulation | sensory perineuritis | non‐epileptic seizures | thymoma | Alzheimer's disease | prevention | atherosclerosis | pituitary | trauma | motor neuron disease | cerebrovascular disease | familial Parkinson's disease | migraine without aura | bradykinin | sympathetic dysfunction | freezing of gait | bitemporal epilepsy | stereotactic | dementia | dysarthria‐clumsy hand | central conduction | histamine | care of | vascular dementia | titin antibodies | uncertainty | cognitive rehabilitation | interferon‐alpha | transcranial Doppler | polyglandular autoimmune disorders | autoimmune thyroiditis | health resource allocation | demyelinating neuropathy | point mutation | mind | warning clinical criteria | migraine | β‐amyloid | cerebral venous thrombosis | vigabatrin | jaw opening | HAM/TSP | protein S‐100B | botulinum toxin type A | Hospital Anxiety and Depression Scale | amnesia | Charcot–Marie–Tooth neuropathy type 1B | familial hemiplegic migraine | 5‐hydroxytryptamine | unilateral neglect | clinical scores | malignancy | arterio‐arterial embolism | lacunar infarction | language | peripheral nervous system | myokymia | event‐related potentials | atrial fibrillation | antibodies | rubella | neuropathology | dopamine receptor agonists | mild head injury | presence of plaque | intracortical facilitation | carotid arteries | study design | presenilin‐1 mutation | subacute rhombencephalitis | optic neuritis | anxiety | re‐certification | cerebrospinal fluid | Italy | arterial occlusion | electrophysiological study | white matter diseases | peripheral nerve disorders | structural brain lesions | cognitive disorders | semen | cadaveric dura mater graft | neurocognitive disorders | southern Taiwan | spectroscopy | HLA genes | human | health care | hemangiosarcoma | cerebral arteries | interferon beta | QALYs | refractory epilepsy | transitory ischemic attacks | tuition | stroke | striato‐capsular region | neuro‐Behcet disease | cerebellar damage | respiratory failure | cost‐effectiveness analysis | movement disorders | positron emission tomography | apraxia | hypertension | Rathke's cyst | coronary artery disease | education | occupational disease | focus | hepatic form | intractable epilepsy | micrographia | transcranial magnetic stimulation | chemotherapy | encephalopathy | multivariate analysis | rehabilitation | axonal polyneuropathy | demyelination | electrophysiological tests | acute disseminate encephalomyelitis | botulinum toxin | suramin | praxis | carpal tunnel release | Tau protein | primary progressive multiple sclerosis | specialization | anterior communicating artery | caudate nucleus | eosinophilic myositis | mixed dementia | volumetry | CNS | protein S | laparotomy | prevalence | acute stroke | inflammation | monoclonal gammopathy | ryanodine receptor antibodies | carotid stenosis | giant aneurysm | protein C | alpha B‐crystallin | outcome | cyclosporine | obstructive sleep apnea | PK11195 | endarterectomy | focal myopathy | interferon β‐1a | spinothalamic tract | interferon β‐1b | neuroscience funding | systematic review | varicella | comorbidity | meralgia paresthetica | circle of Willis | post‐polio syndrome | epilepsy | residency | lewy body disease | Bickerstaff's brainstem encephalitis GQ1b and GM1 antibodies | Brueghel's syndrome | Chlamydia pneumoniae | hereditary PD | ultrasonography | ictal dystonia | intracortical inhibition | intracranial lesion | interleukin‐5 | adult onset myopathy | mononuclear cells | hypothyroid | carotid artery diseases | Creutzfeldt–Jakob disease | health economy | Europe | relapsing–remitting multiple sclerosis | fronto‐subcortical circuits | peroneal nerve palsy | middle cerebral artery | valproate | brain diseases | functional independence measure | survey | magnetic resonance imaging | basal ganglia | intrathecal fraction | trigemino‐cervical reflex | anticoagulation | progression | cutaneous stimulation | peripheral neuropathy | olanzapine | lifestyle‐associated risk factors | levodopa | smoking | oxaliplatin | tibial nerve stimulation | cisplatin | oligoclonal antibody | motor polyneuropathy | stimulation | cavum septi pellucidi | cerebral vasculitis | ageing | motor cortex | intravenous immunoglobulin (IVIG) | somatosensory‐evoked potential | traffic accidents | meta‐analysis | anti‐glutamic acid decarboxylase antibodies | hyponatremia | post‐infectious | teaching of neurology | economic evaluation | neurosurgery | aseptic meningitis | electrophysiological disorders | cognitive processing | hemicrania | jaw‐opening dystonia | Mycoplasma pneumoniae | paradoxical cerebral embolism | human experimental model | transient epileptic amnesia | intrathecal humoral immune response | muscular dystrophy | right‐to‐left shunt | intracranial aneurysm | writer's cramp | executive functions | brain mapping | aphasia | cost of secondary prevention of stroke | parkin | steroid‐responsive encephalopathy | inhibitory control | aneurysm surgery | CD4+CD25+ regulatory T cells | cranial computed tomography | CVA | specialist registry | subcortical | pathogenesis | cerebral infarction | Lhermitte's sign | intrathecal antibody production | locked‐in state | cost of stroke | vagal nerve stimulation | Topiramate | seizure | SCA3 | hepatitis C | SCA2 | intima‐media thickness | myasthenia gravis | α‐synuclein | trigeminal system | multiple risk factors | muscle computed tomography | expectations | posterior circulation | atropine | ischemic stroke | Lyme Neuroborreliosis | paroxysmal gait disturbances | complications | vertebral artery | chronic diseases | invasive EEG | multiple sclerosis | comorbility | hypophonia | migraine with typical aura | prognosis | status epilepticus | prednisolone | disease susceptibility | dystonia | acetazolamide | atrophy | cardiac surgery | myasthenia gravis severity | progress | gammopathy | monoclonal gammopathy of unknown significance | familial PD | magnetoencephalography | hypertensive encephalopathy | experimental headache | frontal‐subcortical circuit | transcranial | duplex | bradykinesia | amyotrophic lateral sclerosis | intoxication | continua | functional improvement | neuroscience curriculum | T. b. gambiense | syndrome of inappropriate antidiuretic hormone | prostaglandin E2 | myelin protein zero | cardiopathy | lateral femoral cutaneous nerve | familial Mediterranean fever | α‐synuclein Parkinson's disease | dorsal column | temporal lobe epilepsy | single photon emission computed tomography | plasticity | cerebral hemodynamic studies | hemiplegia | seizure worsening | IL‐10 | neuroborreliosis | autonomic dysfunction | brain stem | cross sign | GABA | yawning | CD45 | Doppler | choreoathetosis | memory | IgG | etiological subtypes | IgM | stereotyped and disinhibited behavior | thigh muscle weakness | T‐cell lines | organomegaly | epidemiology | thrombosis | CXCR3 | hepatitis C virus | masticatory muscles | immunoglobulin therapy | thalamus | lumbar puncture | pain | hippocampal sclerosis | relapse rate | associated movements | anomia | first‐ever stroke | intracerebral hemorrhage | family history | subarachnoid hemorrhage | cerebral palsy | M139V | stroke treatment | Tripterugium wilfordii multiglucoside | palatal tremor | tension‐type headache | specialty development | Miller Fisher syndrome | whiplash | binding | Guillain–Barré syndrome | IVIg | Streptococcus infection | lithium intoxication | healthcare systems | Devic's Disease | cerebrovascular accidents | population relative risk | children | anticoagulants | cardiopulmonary bypass | young‐onset parkinsonism | cerebral hemorrhage | glyceryl trinitrate | wheelchair‐dependency | clementia | risk perception | nitric oxide | risk factors | SUNCT | traumatic brain injury | coma | carbamazepine | central nervous system | long‐time consequences | internal carotid artery dissection | emotional motor system | musculoskeletal | autosomal recessive inheritance | DRB1 gene of HLA class II | secondary adrenal hypofunction | stroke outcome | stroke management | east–west differences | yes/no reversals | glatiramer acetate | clinical phenotype | indomethacin | acetylcholinesterase inhibitors | poliomyelitis | bilateral | human leucocyte antigen DR | financing | neutralizing | eosinophilic major basic protein | Sardinia | long‐term experience | focally folded myelin | CIDP | body weight loss | electromyography | organization | anomia for people's names | incidence | magnetic resonance angiography | antibody index | vasomotor reactivity | enterovirus | injuries | disability | pallidum | entacapone | expanded disability status scale | cervical problems | HTLV‐1 | putamen | magnetization transfer | brain imaging | plaques | ptosis | attentional disorders | acute aseptic meningitis | anterior thalamic peduncle | history | mental impairment | post‐concussion symptoms | gait | essential tremor | peripheral benzodiazepine receptor | human African trypanosomiasis | Hashimoto's encephalopathy | nerve conduction | blink reflex | intravenous immunoglobulins | Datura stramonium | carpal tunnel syndrome follow‐up | gender difference | grasp reflex | quadriceps weakness | paraventricular white matter | computed tomography scan | corticosteroids | oromandibular dystonia | quadriceps myopathy | microglia | Wilson's disease | neurology | drug therapy | cognition | sleep‐disordered breathing | therapy | polyneuropathy | Tr cells | lymphoproliferative | FIM | Stroke Registry | thrombolysis | spasticity | depression | headache | cerebrovascular reactivity and reserve capacity | Verga's ventricle
Journal Article
Revista Brasileira de Hematologia e Hemoterapia, ISSN 1516-8484, 10/2017, Volume 39, Issue 4, pp. 349 - 353
The term ‘economy class syndrome’ refers to the occurrence of thrombotic events during long-haul flights that mainly occur in passengers in the economy class... 
Pregnancy | Economy class syndrome | Air travel | Thromboembolism | Review
Journal Article
British Journal of Haematology, ISSN 0007-1048, 03/2003, Volume 120, Issue 6, pp. 1100 - 1103
androgens | ABO incompatibility | graft‐versus ‐plasma cell effect | telomere | Z deficiency | t(14;18) | acutemyeloid leukaemia | α‐thalassaemia | childhoodAPL | plateletshape change | T‐cell lymphoma | UMPH deficiency | karyotype | prognosticmodel | stomatocytosis | cyclophosphamide | eosinophilia | cobalamin deficiency | doxorubicin | Factor VIIa | leukaemogenesis | Burkitt'slymphoma | antifactor VIII antibody | 52Fe | PML/RARα | non‐homologous recombination | endocytic vesiculation | cardiolipin | bFGF | Aiolos | autoimmunethrombocytopenic purpura | irondeficiencyanaemia | chelation | proteinS | monoclonal gammopathy ofunknown significance | CD2 expression | acute lymphoblastic leukaemia | CD45isoforms | drug resistance | NUP98 | adult | childhoodcancer | treatment | plasmaexchange | recombinant | multicentric Castleman's disease | myelomaanimal model | NF‐κB inhibitor | venous | myeloma | haemostasis | bloodsubstitutes | enoxaparin | autoimmune idiopathic thrombocytopenic purpura | point mutation | fluorescence in situ hybridization | catheter‐relatedthrombosis | long haul flights | TCR‐γ | vasculitis | cytotoxic CD8 | TCR‐β | sex | blood | congenital bleeding disorder | bone marrow | skin rash | idiopathic myelofibrosis | MALT lymphoma | genetichaemochromatosis | autologous | monoclonal gammopathy ofundetermined significance | severe | solubleurokinase‐type plasminogen activator  receptor (suPAR) | translocation4;14 | resorption | clinical features | beta2‐glycoprotein I | gemcitabine | plasma | long‐term follow‐up | real‐time quantitativereverse‐transcription polymerase chain reaction | Danny Thomas | immunohaematological reconstitution | ironpolymaltose | screening | type 2M VWF | polycythaemia vera | T‐cellreceptor | autologous stem cell transplantation | immunosuppressive drugs | APC resistance | bonedensity | IL‐8/CXCL8 | aplastic anaemia | l‐arginine | sialoadhesin | thalidomide | chromosome 13 | recombinant ADAMTS13 | childhoodAML | protein C | autoimmune | STI571 | factorVII | chromosomes | Rituximab | primary progressive | soluble | RTK class III | Ikaros | guideline | transplantation | acutepromyelocytic leukaemia | economy class syndrome | P‐selectin | ferritin | Meningococcal sepsis | methionine synthase | ADP receptors | standardization | training | allogeneicstem cell transplantation | HOXD11 | RT‐PCR | fibrinogen Aα chain | prognosticindicators | Giovanni Di Guglielmo | integrin beta‐1 | β2m‐free HLA class I heavy chain | HHV‐8‐encoded viral homologues of cellular genes | human | bone marrowtransplantation | bcr‐abltranscript | haemochromatosis | translocation | graft‐versus ‐host disease | lymphoma | breast cancer | Gleevec | stroke | real‐time quantitative | FLT3 internal tandem duplication | idiotype | p38 MAP kinase | management | treatment‐related toxicity | PEL | synthase | iron | platelet | cancer | age | killing inhibitory receptor | factor IX gene | monocytic leukaemia zinc finger protein‐related factor gene | transferrinsaturation | C282Y mutation | CLL | in vivo imaging | perforin | bleeding | sickle | therapy‐relatedmyelodysplastic syndrome | B lymphocytes | transferrin | CD40/CD40L | stem celltransplantation | chemotherapy | fluorescencemicroscopy | severe aplastic anaemia | reactive T cells | SLL | normalization | stemcells | hairy cell leukaemia | spectratype | guidelines | activatedprotein C | CMK | granulocyte colony‐stimulating factorreceptor | osteolytic bone destructions | CML | angiogenesis | activated factor VII | polycythaemia veramanagement | quantitative real‐time PCR | antiphospholipid antibodies | deferiprone | mutation | haplotypes | hypogonadism | megakaryoblastic cell line | HS‐40 | obligate heterozygotes | tumourantigen | leukaemia | Hodgkin's disease | T‐LGL | real‐time quantitativereverse transcription polymerase chain reaction (PCR) | imatinib mesylate | basophilic leukaemia | dysfunction | myelodysplasia | haemolytic anaemia | SCID mouse | sicklecell disease | tumour | venousthromboembolism | Ca2+ ionophore | c‐fms | haemophilia | blood stem cells | transplant | outcome | lipopolysaccharide (LPS) | plateletglycoprotein Ib | orthopaedic surgery | leucocytes | high‐dose therapy | interleukin 2 2 (IL‐2) | hydroxyurea | BCL6 | plateletsize heterogeneity | lymphoproliferativedisorder | BCL2 | hypercoagulable state | granulocyte‐macrophage colony stimulating factor (GM‐CSF) | rhodamine | Donald Pinkel | ALL | granzyme B | FLT3 | adultALL | polymorphism | transfusion | immunocompromised | LSP1 | non‐Hodgkin's lymphoma | amino‐terminal telopeptide of collagen type I | dendritic cell (DC) | mast cells | CD11c | E‐cadherin | t(1;19) translocation | imatinib mesylate (Glivec, Gleevec) | paediatrics | haematological malignancies | mutations | OHK | fluorescence | von Willebranddisease | T‐LGLleukaemia | NOD/SCID mice | puberty | erythropoiesis | single nucleotide polymorphisms | chronic | desmopressin | haemoglobin ‐based oxygen carrier Hemolink | AML | peripheral | multiple myeloma | endogenouserythroid colony growth | signal transduction | therapy‐related | beta‐2 glycoprotein 1 | diagnosis | Cos‐7 cells | t(2;11)(q31;p15) | VWF‐cleaving protease | acutemyelomonocytic leukaemia | clinical | lead poisoning | methylenetetrahydrofolate reductase | target antigens | erythroblasts | unstable angina | ATRA | paroxysmal nocturnal haemoglobinuria | E2A–PBX1 | intracellular Ca2 | chemokine | differentiation | GVHD prophylaxis | PRCA | elderly | leucocyte | anticoagulation | apoptosis | HLA molecules | Burkitt‐like | GATA‐1 | von Willebrand | Di Guglielmo's syndrome | triathlon | TTP | oxidative burst | telomerase | Bernard–Soulier syndrome | leucopenia | nitric oxidemetabolites | cisplatin | N‐glycosylation | erythropoietin | endothelium | p‐glycoprotein | proteindegradation | follicular lymphoma | sports | CNS infiltration | DDAVP | miscarriage | air travel | control | acutemyeloid leukaemia (AML) | myeloidproliferative disease | first remission | prothrombin deficiency | Beta‐2‐glycoprotein I | NK cell | Fanconi's anaemia | mu class isoforms | ataxia‐telangiectasia | CTL | irondepletion | autoimmunelymphoproliferative syndrome | activated | haemophiliaB | megaloblastic anaemia | myeloproliferativedisorders | photosensitivity | ironoverload | PNH | cytogenetics | M3 variant | ischaemic stroke | Japanese cord blood bank network | twin study | pregnancycomplications | catheter‐related | protein | glutathione S‐transferases | homing | monoclonal gammopathy of uncertain significance | bloodmononuclear cells | cord blood transplantation | tamoxifen | Helios | short isoform | peptide | relapse | pregnancy | molecular response | prognostic factor | platelets | LGL | vaso‐occlusive crisis | lymph nodes | t(3;14) | erythema nodosum | pyruvate kinase deficiency | stem cell collection | plateletactivation and function | dendritic cell | essential thrombocythaemia | lymphoproliferative disease of granular lymphocytes | CD20 | endogenous | immune deficiency | refractory anaemia | Fcγ receptors | haemolytic | cell activation | chest crisis | irondeficiency | genetic associations | recombinantprotein | imatinib mesylate(Glivec | TCR/CD3 protein | diversity | dendritic celldepigmentation | vinblastine | allogeneic | haematological malignancy | mantle cell lymphoma | monoclonal gammopathy of | MTFHR MTHFR | severecongenital neutropenia | prognosticfeatures | genetic | CD30 | adultT‐cell leukaemia | childhood | complications | trisomy 21 | prognosis | haematopoiesis | cation leak | catheter‐related infection | erythrocytosis | desferrioxamine | haemoglobinraffimer | t(11;18) | immunoglobulin variable region genes | FISH | dysprothrombinaemia | myelodysplastic syndrome | somatic mutation | standard therapy | centralnervous system relapse | pharmacokinetic study | transient leukaemia | T‐celllarge granular lymphocyte leukaemia | tissue factor | centralvenous catheter | brachydactyly type C | haematopoietic | CD27–CD70 interaction | CD38 | antisickling agents | 59Fe | CD35 | CD34 | chroniclymphocytic leukaemia | IL‐4 | antithymocyte globulin | endogenousthrombin potential | neutropenia | haemolyticuraemic syndrome | NOS inhibitor | chronicmyeloid leukaemia (CML) | nucleotidase | IL‐15 | systemic mast cell disease | genotype | folate | T‐prolymphocytic leukaemia (T‐PLL) | serine/threonine phosphorylation | hypoprothrombinaemia | TNF‐α transcription | instability | cardiolipinbinding | plateletfunction | haematopoietic cell transplantation | CD45 | CD43 | DNA sequencing | gestational thrombotic miroangiopathic anaemia | α‐globin gene | clopidogrel | chronic graft‐versus‐host disease | clinicalmanagement | T‐cellacute lymphoblastic leukaemia (T‐ALL) | haematopoieticstem cell transplantation | adults | T‐cell | thrombus precursor protein | modified CHOP chemotherapy | gag | cutaneous T‐cell lymphoma (CTCL) | therapy‐related acute myeloid leukaemia/myelodysplasia | epidemiology | minimal | central | thrombosis | CXCR1 | BNLI | CD59 | cytopenia | factor | isotype switching | MTHFRC677T | PFA‐100 | harvest | pain | risk factor | bonepain | P5 N deficiency | high‐grade transformation | genotypes | SLVL | bone | p15 methylation | polymorphisms | parvovirus B19 | neurological dysfunction | flt3‐ligand | G‐CSF | deep vein thrombosis | deficiency | haemolysis | T‐ALL | immunophenotype | myeloproliferative | tumournecrosis factor‐alpha (TNF‐α) | morphological dysplasia | MIP‐1α | risk | cell–cell interaction | extramedullary relapse | mean platelet volume | CD86 | minimalresidual disease (MRD) | Philadelphia‐chromosome‐positive acute lymphoblastic leukaemia | CD80 | HFE | analgesia | anti‐thymocyte globulin | graft‐versus ‐leukaemia effect | adultT‐cell leukaemia/lymphoma | p53 | paediatric | humanherpesvirus 6 | large‐volume leukapheresis | haemoglobin | high‐risk febrile neutropenia | myeloid leukaemia | children | deletion | menstruation | manganese superoxide dismutase | 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venousthrombosis | Burkitt's | childhoodITP | red cell utilization | positron emission tomography (PET) | bone marrowmicroenvironment | Siva | myocardial infarction | gene expression | microangiopathic haemolytic anaemia | innate immunity | menopause | interleukin 2 | genetransfer | activatedprotein C(APC) resistance | conditioning regimens | cone and plate(let) analyser | crisis | graft‐versus ‐lymphoma effect | hyaluronan | survival | CREB binding protein gene | blood coagulation | c‐kit | prognostic | CD45 (LCA) | thrombophilia | myeloproliferative disorder | complete remission | fludarabine | von Willebrandfactor | neuropathy | malignant lymphoma | acute | bcr‐abl | GPIb | pathology | thalassaemia | thrombocytopenia | allogeneichaematopoietic stem‐cell transplantation | idiotypevaccination | case report | INR | TFPI | β‐thalassaemia | Hashimoto's thyroiditis | low leucocyte count | integrins | MUC1 | respiratory symptoms | autologoustransplantation | GPI anchor | Helicobacter pylori | myeloid | plateletperoxidase | stem cell | immunotherapy | allogeneicbone marrow transplantation | glucocorticoids | immunohistochemistry | plasma cell purification | tyrosine phosphorylation | interleukin | α thalassaemia | peripheral blood mononuclear cells | HHV‐6 | bonelesions | ζ chain | anaemia | interleukin8 | endothelial cell | riskfactors | human herpesvirus‐8 | lymphoproliferative | myeloperoxidase | thrombotic thrombocytopenic purpura | intracranial haemorrhage | MEGO1 | extra‐gastric | erythroleukaemia | granulocyte colony‐stimulating factor | high‐resolution computerized tomography | investigation | leukaemic pulmonary infiltrates | SCL
Journal Article
Health Expectations, ISSN 1369-6513, 09/2013, Volume 16, Issue 3, pp. e24 - e35
Journal Article
Clinical Neurology, ISSN 0009-918X, 08/2004, Volume 44, Issue 8, pp. 503 - 507
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