2016, First edition., ISBN 9781610396806, xiv, 221 pages
In this exuberant celebration of the world’s museums, great and small, revered writers like Ann Patchett, Julian Barnes, Ali Smith, and more tell us about...
Art criticism | Art appreciation | Museums | Art museums
Art criticism | Art appreciation | Museums | Art museums
Book
2008, ISBN 0300095635, vii, 344
Book
1998, ISBN 2867701074, 231
Book
2008, ISBN 2503524400, viii, 277
Book
2000, ISBN 9781858941127, 288
Book
Conference Proceeding
Speculum, ISSN 0038-7134, 7/2010, Volume 85, Issue 3, pp. 664 - 666
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 3, pp. 292 - 303
Summary In patients presenting with a clinically isolated syndrome, MRI can support and substitute clinical information in the diagnosis of multiple sclerosis...
Neurology | INTRACORTICAL LESIONS | MS LESIONS | PROPOSED MODIFICATION | HIGH-FIELD MRI | SPINAL-CORD | SENSITIVE INVERSION-RECOVERY | OPTIC NEURITIS | CLINICALLY ISOLATED SYNDROMES | CORTICAL-LESIONS | CLINICAL NEUROLOGY | 2010 MCDONALD CRITERIA | Magnetic Resonance Imaging - methods | Multiple Sclerosis - diagnosis | Humans | Consensus | Practice Guidelines as Topic | Multiple sclerosis | Neurosciences | Diagnostic imaging | Diagnosis | Research institutes | Studies | Spinal cord | Funding | Compensation | Clinical trials | Pharmaceutical industry | Revisions | Multiple Sclerosis | Magnetic Resonance Imaging | Criteria
Neurology | INTRACORTICAL LESIONS | MS LESIONS | PROPOSED MODIFICATION | HIGH-FIELD MRI | SPINAL-CORD | SENSITIVE INVERSION-RECOVERY | OPTIC NEURITIS | CLINICALLY ISOLATED SYNDROMES | CORTICAL-LESIONS | CLINICAL NEUROLOGY | 2010 MCDONALD CRITERIA | Magnetic Resonance Imaging - methods | Multiple Sclerosis - diagnosis | Humans | Consensus | Practice Guidelines as Topic | Multiple sclerosis | Neurosciences | Diagnostic imaging | Diagnosis | Research institutes | Studies | Spinal cord | Funding | Compensation | Clinical trials | Pharmaceutical industry | Revisions | Multiple Sclerosis | Magnetic Resonance Imaging | Criteria
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2009, Volume 286, Issue 1, pp. 24 - 27
Abstract The cause of multiple sclerosis is unknown although it is recognised to involve an inflammatory process associated with demyelinating plaques and more...
Neurology | Multiple sclerosis | Mitochondria | Harding's disease | Leber's Hereditary Optic Neuropathy | MITOCHONDRIAL-DNA MUTATIONS | MRI | ITALIAN PATIENTS | ILLNESS | NEUROSCIENCES | CLINICAL NEUROLOGY | DISORDER | WHITE-MATTER DISEASE | BRAIN | Optic Atrophy, Hereditary, Leber - complications | Humans | Optic Atrophy, Hereditary, Leber - epidemiology | Male | Multiple Sclerosis - genetics | Optic Atrophy, Hereditary, Leber - genetics | Optic Atrophy, Hereditary, Leber - therapy | Multiple Sclerosis - epidemiology | Mutation - genetics | Multiple Sclerosis - therapy | Multiple Sclerosis - complications | Magnetic Resonance Imaging | Optic Atrophy, Hereditary, Leber - pathology | Sex Factors | Multiple Sclerosis - pathology | Female | Genetic aspects | Mitochondrial DNA | Optic atrophy | Ophthalmology
Neurology | Multiple sclerosis | Mitochondria | Harding's disease | Leber's Hereditary Optic Neuropathy | MITOCHONDRIAL-DNA MUTATIONS | MRI | ITALIAN PATIENTS | ILLNESS | NEUROSCIENCES | CLINICAL NEUROLOGY | DISORDER | WHITE-MATTER DISEASE | BRAIN | Optic Atrophy, Hereditary, Leber - complications | Humans | Optic Atrophy, Hereditary, Leber - epidemiology | Male | Multiple Sclerosis - genetics | Optic Atrophy, Hereditary, Leber - genetics | Optic Atrophy, Hereditary, Leber - therapy | Multiple Sclerosis - epidemiology | Mutation - genetics | Multiple Sclerosis - therapy | Multiple Sclerosis - complications | Magnetic Resonance Imaging | Optic Atrophy, Hereditary, Leber - pathology | Sex Factors | Multiple Sclerosis - pathology | Female | Genetic aspects | Mitochondrial DNA | Optic atrophy | Ophthalmology
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2013, Volume 335, Issue 1, pp. 5 - 8
Abstract It is not only good medical practice to ensure patients are fully involved in their treatment decisions, but it also improves subsequent compliance,...
Neurology | Multiple sclerosis | Partnership | Treatment choice | Decision aids | Preference sensitive care | Consent | PATIENT INFORMATION | SHARED DECISION-MAKING | KNOWLEDGE | NEUROSCIENCES | CARE | CLINICAL NEUROLOGY | MULTIPLE-SCLEROSIS | AID | Decision Making | Multiple Sclerosis - psychology | Patient Participation - methods | Humans | Patient Participation - psychology | Physician-Patient Relations | Multiple Sclerosis - therapy
Neurology | Multiple sclerosis | Partnership | Treatment choice | Decision aids | Preference sensitive care | Consent | PATIENT INFORMATION | SHARED DECISION-MAKING | KNOWLEDGE | NEUROSCIENCES | CARE | CLINICAL NEUROLOGY | MULTIPLE-SCLEROSIS | AID | Decision Making | Multiple Sclerosis - psychology | Patient Participation - methods | Humans | Patient Participation - psychology | Physician-Patient Relations | Multiple Sclerosis - therapy
Journal Article
Journal of Neurology, ISSN 0340-5354, 04/2016, Volume 263, Issue 4, pp. 826 - 834
Myasthenia gravis (MG) is the archetypic disorder of both the neuromuscular junction and autoantibody-mediated disease. In most patients, IgG1-dominant...
Myasthenia gravis | Thymectomy | MuSK | IgG4 | LRP4 | Cell-based assays | Neuromuscular junction | AUTOANTIBODIES | PROTEIN 4 | INCREASING INCIDENCE | ANTIBODY | ROBOTIC THYMECTOMY | CLINICAL NEUROLOGY | THYMUS CHANGES | TYROSINE KINASE MUSK | DOUBLE-BLIND | NEUROMUSCULAR-JUNCTION | CLUSTERED ACETYLCHOLINE-RECEPTOR | Female | Male | Myasthenia Gravis - epidemiology | Myasthenia Gravis - immunology | Humans | Myasthenia Gravis - therapy | Complications and side effects | Care and treatment | Usage | Analysis | Research | Health aspects | Neurological Update
Myasthenia gravis | Thymectomy | MuSK | IgG4 | LRP4 | Cell-based assays | Neuromuscular junction | AUTOANTIBODIES | PROTEIN 4 | INCREASING INCIDENCE | ANTIBODY | ROBOTIC THYMECTOMY | CLINICAL NEUROLOGY | THYMUS CHANGES | TYROSINE KINASE MUSK | DOUBLE-BLIND | NEUROMUSCULAR-JUNCTION | CLUSTERED ACETYLCHOLINE-RECEPTOR | Female | Male | Myasthenia Gravis - epidemiology | Myasthenia Gravis - immunology | Humans | Myasthenia Gravis - therapy | Complications and side effects | Care and treatment | Usage | Analysis | Research | Health aspects | Neurological Update
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 12/2012, Volume 1275, Issue 1, pp. 49 - 53
Despite being a fairly recent discovery, DOK7 congenital myasthenic syndrome (CMS) is the third most common form of CMS in the United Kingdom. DOK7 is a...
MEDICINE, RESEARCH & EXPERIMENTAL | NEUROMUSCULAR-JUNCTION SYNAPTOPATHY | MUTATIONS | Myasthenic Syndromes, Congenital - genetics | Diagnosis, Differential | Myasthenic Syndromes, Congenital - diagnosis | Humans | Child, Preschool | Infant | Ephedrine - administration & dosage | Muscle Proteins - genetics | Young Adult | Phenotype | Myasthenic Syndromes, Congenital - drug therapy | Adolescent | Albuterol - administration & dosage | Adult | Albuterol - therapeutic use | Drug Therapy, Combination | Child | Infant, Newborn | Ephedrine - therapeutic use | Myasthenic Syndromes, Congenital - physiopathology | Proteins | Limbs | Mutations | Tongue | Pathways | Ephedrine | Eye movements | Clustering
MEDICINE, RESEARCH & EXPERIMENTAL | NEUROMUSCULAR-JUNCTION SYNAPTOPATHY | MUTATIONS | Myasthenic Syndromes, Congenital - genetics | Diagnosis, Differential | Myasthenic Syndromes, Congenital - diagnosis | Humans | Child, Preschool | Infant | Ephedrine - administration & dosage | Muscle Proteins - genetics | Young Adult | Phenotype | Myasthenic Syndromes, Congenital - drug therapy | Adolescent | Albuterol - administration & dosage | Adult | Albuterol - therapeutic use | Drug Therapy, Combination | Child | Infant, Newborn | Ephedrine - therapeutic use | Myasthenic Syndromes, Congenital - physiopathology | Proteins | Limbs | Mutations | Tongue | Pathways | Ephedrine | Eye movements | Clustering
Journal Article
Multiple Sclerosis Journal, ISSN 1352-4585, 5/2015, Volume 21, Issue 6, pp. 689 - 691
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2011, Volume 306, Issue 1, pp. 188 - 191
Abstract The diagnosis of acute inflammatory demyelinating CNS conditions is complex and this is reflected in variations in how cohorts are defined across...
Neurology | Acute disseminated encephalomyelitis | A.D.E.M | Acute inflammatory demyelinating disorders | Classification | PREDICTS | FOLLOW-UP | NEUROMYELITIS-OPTICA-IGG | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | MULTIPLE-SCLEROSIS | ADEM | BRAIN | ACUTE TRANSVERSE MYELITIS | Animals | Encephalomyelitis, Acute Disseminated - diagnosis | Humans | Adolescent | Encephalomyelitis, Acute Disseminated - classification | Male | Central Nervous System Diseases - diagnosis | Child | Encephalomyelitis, Acute Disseminated - etiology | Encephalomyelitis
Neurology | Acute disseminated encephalomyelitis | A.D.E.M | Acute inflammatory demyelinating disorders | Classification | PREDICTS | FOLLOW-UP | NEUROMYELITIS-OPTICA-IGG | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | MULTIPLE-SCLEROSIS | ADEM | BRAIN | ACUTE TRANSVERSE MYELITIS | Animals | Encephalomyelitis, Acute Disseminated - diagnosis | Humans | Adolescent | Encephalomyelitis, Acute Disseminated - classification | Male | Central Nervous System Diseases - diagnosis | Child | Encephalomyelitis, Acute Disseminated - etiology | Encephalomyelitis
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 9, pp. 967 - 981
Summary Atypical inflammatory demyelinating syndromes are rare disorders that differ from multiple sclerosis owing to unusual clinical or MRI findings or poor...
Neurology | FOLLOW-UP OBSERVATIONS | TUMEFACTIVE MULTIPLE-SCLEROSIS | BALOS CONCENTRIC SCLEROSIS | OPTICA SPECTRUM DISORDERS | MYELIN-OLIGODENDROCYTE GLYCOPROTEIN | NEUROMYELITIS-OPTICA | ACUTE DISSEMINATED ENCEPHALOMYELITIS | ENCEPHALITIS PERIAXIALIS DIFFUSA | BRIGHT SPOTTY LESIONS | NERVOUS-SYSTEM LYMPHOMA | CLINICAL NEUROLOGY | Demyelinating Diseases - diagnostic imaging | Magnetic Resonance Imaging | Brain - diagnostic imaging | Aquaporin 4 - immunology | Immunoglobulin G - blood | Central Nervous System Diseases - complications | Central Nervous System Diseases - diagnostic imaging | Humans | Brain - pathology | Demyelinating Diseases - complications | Multiple sclerosis | Nuclear magnetic resonance--NMR | Meetings | Funding | Aquaporins | Patient safety | Pharmaceutical industry
Neurology | FOLLOW-UP OBSERVATIONS | TUMEFACTIVE MULTIPLE-SCLEROSIS | BALOS CONCENTRIC SCLEROSIS | OPTICA SPECTRUM DISORDERS | MYELIN-OLIGODENDROCYTE GLYCOPROTEIN | NEUROMYELITIS-OPTICA | ACUTE DISSEMINATED ENCEPHALOMYELITIS | ENCEPHALITIS PERIAXIALIS DIFFUSA | BRIGHT SPOTTY LESIONS | NERVOUS-SYSTEM LYMPHOMA | CLINICAL NEUROLOGY | Demyelinating Diseases - diagnostic imaging | Magnetic Resonance Imaging | Brain - diagnostic imaging | Aquaporin 4 - immunology | Immunoglobulin G - blood | Central Nervous System Diseases - complications | Central Nervous System Diseases - diagnostic imaging | Humans | Brain - pathology | Demyelinating Diseases - complications | Multiple sclerosis | Nuclear magnetic resonance--NMR | Meetings | Funding | Aquaporins | Patient safety | Pharmaceutical industry
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 01/2018, Volume 1412, Issue 1, pp. 129 - 136
To date, more than 25 genes have been implicated in the etiology of the congenital myasthenic syndromes (CMS), and an ever‐growing phenotypic landscape is now...
congenital myasthenic syndromes | treatment | acetylcholinesterase inhibitors | acetylcholine receptor | neuromuscular junction | Acetylcholinesterase inhibitors | Congenital myasthenic syndromes | Treatment | Neuromuscular junction | Acetylcholine receptor | SALBUTAMOL | MULTIDISCIPLINARY SCIENCES | PLATE ACETYLCHOLINESTERASE DEFICIENCY | PERSISTENT PULMONARY-HYPERTENSION | PHENOTYPES | HEREDITARY MYASTHENIA | EPHEDRINE TREATMENT | NEUROMUSCULAR-TRANSMISSION | 3,4-DIAMINOPYRIDINE | SEROTONIN-REUPTAKE INHIBITORS | MUTATIONS | Health aspects | Enzyme inhibitors | Genetic disorders | Fluoxetine | Immunomodulation | Congenital defects | Medical treatment | Medical services | Disorders | Ephedrine | Pharmacology | Acetylcholinesterase | Pregnancy | Etiology | Quinidine | Neuromuscular junctions | Salbutamol | Pyridostigmine | Myasthenia
congenital myasthenic syndromes | treatment | acetylcholinesterase inhibitors | acetylcholine receptor | neuromuscular junction | Acetylcholinesterase inhibitors | Congenital myasthenic syndromes | Treatment | Neuromuscular junction | Acetylcholine receptor | SALBUTAMOL | MULTIDISCIPLINARY SCIENCES | PLATE ACETYLCHOLINESTERASE DEFICIENCY | PERSISTENT PULMONARY-HYPERTENSION | PHENOTYPES | HEREDITARY MYASTHENIA | EPHEDRINE TREATMENT | NEUROMUSCULAR-TRANSMISSION | 3,4-DIAMINOPYRIDINE | SEROTONIN-REUPTAKE INHIBITORS | MUTATIONS | Health aspects | Enzyme inhibitors | Genetic disorders | Fluoxetine | Immunomodulation | Congenital defects | Medical treatment | Medical services | Disorders | Ephedrine | Pharmacology | Acetylcholinesterase | Pregnancy | Etiology | Quinidine | Neuromuscular junctions | Salbutamol | Pyridostigmine | Myasthenia
Journal Article
Multiple Sclerosis Journal, ISSN 1352-4585, 1/2014, Volume 20, Issue 1, pp. 123 - 123
Journal Article
18.
Full Text
Amazon forests maintain consistent canopy structure and greenness during the dry season
Nature, ISSN 0028-0836, 2014, Volume 506, Issue 7487, pp. 221 - 224
The seasonality of sunlight and rainfall regulates net primary production in tropical forests(1). Previous studies have suggested that light is more limiting...
VARIABILITY | TREES | EMISSIONS | TROPICAL FOREST | MULTIDISCIPLINARY SCIENCES | RAIN-FOREST | DROUGHT | ALLOMETRY | CARBON-DIOXIDE | FLUXES | MODIS | Pigmentation - physiology | Color | Trees - growth & development | Trees - anatomy & histology | Artifacts | Rain | Trees - physiology | Tropical Climate | Droughts | Models, Biological | Plant Leaves - growth & development | Ecosystem | Brazil | Satellite Imagery | Sunlight | Plant Leaves - anatomy & histology | Fresh Water - analysis | Seasons | Photosynthesis | Plant Leaves - physiology | Amazon River region | Forest ecology | Environmental aspects | Research | Rain forests | Ecological research | Geometry | Studies | Rainforests | Forests | Hypotheses | Phenology | Models | Carbon | Estimates | Remote sensing
VARIABILITY | TREES | EMISSIONS | TROPICAL FOREST | MULTIDISCIPLINARY SCIENCES | RAIN-FOREST | DROUGHT | ALLOMETRY | CARBON-DIOXIDE | FLUXES | MODIS | Pigmentation - physiology | Color | Trees - growth & development | Trees - anatomy & histology | Artifacts | Rain | Trees - physiology | Tropical Climate | Droughts | Models, Biological | Plant Leaves - growth & development | Ecosystem | Brazil | Satellite Imagery | Sunlight | Plant Leaves - anatomy & histology | Fresh Water - analysis | Seasons | Photosynthesis | Plant Leaves - physiology | Amazon River region | Forest ecology | Environmental aspects | Research | Rain forests | Ecological research | Geometry | Studies | Rainforests | Forests | Hypotheses | Phenology | Models | Carbon | Estimates | Remote sensing
Journal Article