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1. Full Text Concerning “Genetic defects of thiamine transport and metabolism: a review of clinical phenotypes, genetics and functional studies” by Marcé‐Grau et al
by Sechi, GianPietro
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 07/2019
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2. Full Text Wernicke's encephalopathy: new clinical settings and recent advances in diagnosis and management
by Sechi, GianPietro, Prof and Serra, Alessandro, MD
Lancet Neurology, The, ISSN 1474-4422, 2007, Volume 6, Issue 5, pp. 442 - 455
Summary Wernicke's encephalopathy is an acute neuropsychiatric syndrome resulting from thiamine deficiency, which is associated with significant morbidity and... 
Neurology | GASTRIC BYPASS | CHRONIC-ALCOHOLICS | KORSAKOFF-SYNDROME | NEUROLOGICAL DISEASE | CROHNS-DISEASE | THIAMINE-DEFICIENT RATS | VITAMIN SUPPLEMENTATION | NONALCOHOLIC PATIENTS | MAGNESIUM-DEFICIENCY | OF-THE-LITERATURE | CLINICAL NEUROLOGY | Diagnosis, Differential | Genetic Predisposition to Disease | Neurology - trends | Wernicke Encephalopathy - diagnosis | Prevalence | Wernicke Encephalopathy - therapy | Humans | Risk Factors | Incidence | Korsakoff Syndrome - complications | Wernicke Encephalopathy - physiopathology | Magnetic Resonance Imaging | Brain - pathology | Thiamine Deficiency - complications | Wernicke Encephalopathy - complications | Care and treatment | Encephalopathy | Diagnosis
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3. Full Text Concerning "Genetic defects of thiamine transport and metabolism: a review of clinical phenotypes, genetics and functional studies" by Marcé-Grau et al
by Sechi, GianPietro
Journal of inherited metabolic disease, 07/2019
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4. Full Text Prognosis and Therapy of Wernicke's Encephalopathy After Obesity Surgery
by Sechi, GianPietro
The American Journal of Gastroenterology, ISSN 0002-9270, 12/2008, Volume 103, Issue 12, pp. 3219 - 3219
GASTROENTEROLOGY & HEPATOLOGY | Obesity - surgery | Wernicke Encephalopathy - diagnosis | Prognosis | Wernicke Encephalopathy - etiology | Humans | Thiamine Deficiency - diagnosis | Vitamin B Complex - administration & dosage | Dose-Response Relationship, Drug | Thiamine Deficiency - etiology | Thiamine Deficiency - drug therapy | Thiamine - administration & dosage | Bariatric Surgery - adverse effects | Wernicke Encephalopathy - drug therapy | Index Medicus
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5. Full Text Thyrotoxicosis-associated Wernicke’s Encephalopathy
by Sechi, GianPietro
Journal of General Internal Medicine, ISSN 0884-8734, 6/2008, Volume 23, Issue 6, pp. 897 - 897
Medicine & Public Health | Internal Medicine | Letter to the Editor
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6. Full Text Dietary Supplements and the Risk of Wernicke's Encephalopathy
by Sechi, GianPietro
Clinical Pharmacology & Therapeutics, ISSN 0009-9236, 08/2010, Volume 88, Issue 2, pp. 164 - 164
PHARMACOLOGY & PHARMACY | Thiamine Deficiency - chemically induced | Hypericum - adverse effects | Humans | Risk | Wernicke Encephalopathy - epidemiology | Diet, Reducing | Ephedra - adverse effects | Drug Interactions | Carotenoids - metabolism | Female | Dietary Supplements - adverse effects | Phytosterols - adverse effects | Wernicke Encephalopathy - chemically induced
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7. Full Text Restless legs syndrome and cerebrovascular disease
by Sechi, GianPietro and Sechi, Elia
Lancet Neurology, The, ISSN 1474-4422, 2013, Volume 12, Issue 8, pp. 734 - 734
Neurology | STROKE | CLINICAL NEUROLOGY | PERIODIC LIMB MOVEMENTS | Movement Disorders - epidemiology | Cerebrovascular Disorders - epidemiology | Animals | Cerebrovascular Disorders - therapy | Movement Disorders - therapy | Humans
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8. Full Text Letter re: Alterations of functional connectivity of the motor cortex in Fabry disease: An RS-fMRI study
by Sechi, GianPietro and Demurtas, Rita and Boadu, William and Ortu, Enzo
Neurology, ISSN 0028-3878, 10/2017, Volume 89, Issue 17, pp. 1842 - 1842
Fabry Disease | Brain Mapping | Magnetic Resonance Imaging | Rest | Motor Cortex | Humans
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9. Full Text Cancer-related Wernicke-Korsakoff syndrome
by Sechi, GianPietro and Batzu, Lucia and Agrò, Luigi and Fois, Chiara
Lancet Oncology, The, ISSN 1470-2045, 2016, Volume 17, Issue 6, pp. e221 - e222
Hematology, Oncology and Palliative Medicine | ONCOLOGY | FEDRATINIB | Korsakoff Syndrome | Humans | Neoplasms
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10. Full Text Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty Clinics
by Favalli, Valentina, PhD and Disabella, Eliana, BD and Molinaro, Mariadelfina, BD and Tagliani, Marilena, BD and Scarabotto, Anna, BD and Serio, Alessandra, MD and Grasso, Maurizia, PhD and Narula, Nupoor, MD and Giorgianni, Carmela, BS and Caspani, Clelia, BD and Concardi, Monica, BS and Agozzino, Manuela, MD and Giordano, Calogero, BD and Smirnova, Alexandra, BD and Kodama, Takahide, MD and Giuliani, Lorenzo, BS and Antoniazzi, Elena, MD and Borroni, Riccardo G., MD and Vassallo, Camilla, MD and Mangione, Filippo, MD and Scelsi, Laura, MD and Ghio, Stefano, MD and Pellegrini, Carlo, MD and Zedde, Marialuisa, MD and Fancellu, Laura, MD and Sechi, GianPietro, MD and Ganau, Antonello, MD and Piga, Stefania, MD and Colucci, Annarita, MD and Concolino, Daniela, MD and Di Mascio, Maria Teresa, MD and Toni, Danilo, MD and Diomedi, Marina, MD and Rapezzi, Claudio, MD and Biagini, Elena, MD and Marini, Massimiliano, MD and Rasura, Maurizia, MD and Melis, Maurizio, MD and Nucera, Antonia, MD and Guidetti, Donata, MD and Mancuso, Michelangelo, MD and Scoditti, Umberto, MD and Cassini, Pamela, BD and Narula, Jagat, MD and Tavazzi, Luigi, MD and Arbustini, Eloisa, MD
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 68, Issue 10, pp. 1037 - 1050
Abstract Background Anderson-Fabry disease (AFD) is a rare X-linked lysosomal storage disease, caused by defects of the alpha-galactosidase A ( GLA ) gene. AFD... 
Cardiovascular | Internal Medicine | family screening | α-Gal | biochemical | GLA | MOGE(S) classification | multidisciplinary evaluation | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | alpha-Gal | PHENOTYPE | SEQUENCE VARIANTS | YOUNG-PATIENTS | PREVALENCE | LYSOSOMAL STORAGE DISORDERS | LEFT-VENTRICULAR HYPERTROPHY | ENZYME REPLACEMENT | MUTATION | ALPHA-GALACTOSIDASE | alpha-Galactosidase - genetics | Genetic Testing | Prospective Studies | Fabry Disease - genetics | Humans | Middle Aged | Male | Medicine | Hospitals | Adolescent | Adult | Female | Mutation | Child | Fabry Disease - diagnosis | Neurosciences | Medical genetics | Skin | Ophthalmology | Medical screening | Cardiology | Genetic screening | Fabry's disease | Pediatrics | Enzymes | Plasma | Stroke | Nephrology | Nuclear magnetic resonance--NMR | Disease | Internal medicine | Dermatology | Cardiomyopathy | Genes | Studies | Celiac disease | Genotype & phenotype | Pain | Genetic counseling | Biopsy | Gastroenterology | Deoxyribonucleic acid--DNA
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11. Full Text Peculiarities of wernicke encephalopathy after bariatric surgery
by Sechi, Gianpietro
Annals of Surgery, ISSN 0003-4932, 06/2009, Volume 249, Issue 6, pp. 1066 - 1066
SURGERY | OBESITY SURGERY | DIAGNOSIS | MANAGEMENT | Wernicke Encephalopathy - diagnosis | Bariatric Surgery - adverse effects | Wernicke Encephalopathy - epidemiology | Wernicke Encephalopathy - therapy | Humans | Index Medicus | Abridged Index Medicus
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12. Full Text Advances in clinical determinants and neurological manifestations of B vitamin deficiency in adults
by Sechi, GianPietro and Sechi, Elia and Fois, Chiara and Kumar, Neeraj
Nutrition Reviews, ISSN 0029-6643, 05/2016, Volume 74, Issue 5, pp. 281 - 300
B vitamin deficiency is a leading cause of neurological impairment and disability throughout the world. Multiple B vitamin deficiencies often coexist, and thus... 
Nervous system | Adults | B vitamins | Deficiency | GASTRIC BYPASS | FOLATE-DEFICIENCY | TRANSIENT ISCHEMIC ATTACK | ALZHEIMERS-DISEASE | adults | COGNITIVE IMPAIRMENT | WERNICKES ENCEPHALOPATHY | FOLIC-ACID | POSTGASTRECTOMY POLYNEUROPATHY | NUTRITION & DIETETICS | nervous system | deficiency | THIAMINE-DEFICIENCY | OXIDE-INDUCED MYELONEUROPATHY | Alzheimer Disease - etiology | Central Nervous System - metabolism | Humans | Central Nervous System - pathology | Vitamin B Deficiency - metabolism | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Nervous System Diseases - etiology | Vitamin B Deficiency - complications | Adult | Nervous System Diseases - metabolism | Parkinson Disease - metabolism | Amyotrophic Lateral Sclerosis - etiology | Vitamin B Complex - metabolism | Parkinson Disease - etiology | Development and progression | Vitamin B deficiency | Degeneration | Risk factors
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13. Full Text Thyrotoxicosis-associated Wernicke's encephalopathy
by Sechi, GianPietro
Journal of General Internal Medicine, ISSN 0884-8734, 06/2008, Volume 23, Issue 6, pp. 897 - 897
MEDICINE, GENERAL & INTERNAL | Thyrotoxicosis - etiology | Thiamine - metabolism | Thiamine Deficiency - complications | Wernicke Encephalopathy - complications | Humans | Starvation - complications | Index Medicus
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14. Full Text Clinical spectrum and IgG subclass analysis of anti-myelin oligodendrocyte glycoprotein antibody-associated syndromes: a multicenter study
by Mariotto, Sara and Ferrari, Sergio and Monaco, Salvatore and Benedetti, Maria Donata and Schanda, Kathrin and Alberti, Daniela and Farinazzo, Alessia and Capra, Ruggero and Mancinelli, Chiara and De Rossi, Nicola and Bombardi, Roberto and Zuliani, Luigi and Zoccarato, Marco and Tanel, Raffaella and Bonora, Adriana and Turatti, Marco and Calabrese, Massimiliano and Polo, Alberto and Pavone, Antonino and Grazian, Luisa and Sechi, GianPietro and Sechi, Elia and Urso, Daniele and Delogu, Rachele and Janes, Francesco and Deotto, Luciano and Cadaldini, Morena and Bianchi, Maria Rachele and Cantalupo, Gaetano and Reindl, Markus and Gajofatto, Alberto
Journal of Neurology, ISSN 0340-5354, 12/2017, Volume 264, Issue 12, pp. 2420 - 2430
Anti-myelin oligodendrocyte glycoprotein antibodies (MOG-Ab) recently emerged as a potential biomarker in patients with inflammatory demyelinating diseases of... 
Neurology | Myelitis | Neurosciences | Medicine & Public Health | Multiple sclerosis (MS) | Optic neuritis | Neuromyelitis optica spectrum disorders (NMOSD) | Acute disseminated encephalomyelitis (ADEM) | Anti-myelin oligodendrocyte glycoprotein (MOG) antibodies | Neuroradiology | NEUROMYELITIS-OPTICA PHENOTYPE | DISORDERS | DISSEMINATED ENCEPHALOMYELITIS | CLINICAL NEUROLOGY | CHILDREN | NMO | NEURITIS | DISEASE | PEDIATRIC MULTIPLE-SCLEROSIS | IMAGING CHARACTERISTICS | MOG ANTIBODIES | Myelin-Oligodendrocyte Glycoprotein - immunology | Brain - diagnostic imaging | Demyelinating Autoimmune Diseases, CNS - diagnostic imaging | Immunoglobulin G - blood | Humans | Middle Aged | Spinal Cord - diagnostic imaging | Male | Immunoglobulin G - classification | Young Adult | Magnetic Resonance Imaging | Image Processing, Computer-Assisted | Adult | Female | Italy | Demyelinating Autoimmune Diseases, CNS - blood | Cohort Studies | Usage | Multiple sclerosis | Encephalomyelitis | Magnetic resonance imaging | Neuromyelitis optica | Research | Aquaporin 4 | Spinal cord | Immunoglobulins | Oligodendrocyte-myelin glycoprotein | Optic nerve | Demyelinating diseases | Laboratories | Myelin | Immunoglobulin G | Central nervous system | Glycoproteins | Demyelination | Immunofluorescence | Original Communication
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15. Full Text Clinical Reasoning: A 58-year-old man with hand tremor and episodes of neck pain
by Urso, Daniele and Monje, Mariana H.G and Piredda, Rosanna and Ortu, Renato and Pineda-Pardo, José A and Martínez-Fernández, Raul and Sechi, GianPietro
Neurology, ISSN 0028-3878, 09/2019, Volume 93, Issue 12, pp. 557 - 561
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16. Full Text Serum and CSF neurofilament light chain levels in antibody-mediated encephalitis
by Mariotto, Sara and Gajofatto, Alberto and Zuliani, Luigi and Zoccarato, Marco and Gastaldi, Matteo and Franciotta, Diego and Cantalupo, Gaetano and Piardi, Francesca and Polo, Alberto and Alberti, Daniela and Sartori, Stefano and Zanusso, Gianluigi and Agrò, Luigi and Demurtas, Rita and Sechi, GianPietro and Sechi, Elia and Monaco, Salvatore and Ferrari, Sergio
Journal of Neurology, ISSN 0340-5354, 7/2019, Volume 266, Issue 7, pp. 1643 - 1648
Circulating and cerebrospinal fluid (CSF) neurofilament light chain (NfL) levels represent a reliable indicator of disease activity and axonal damage in... 
LGI1 | Neurology | Neurosciences | Medicine & Public Health | CASPR2 | NfL | Neurofilament light chain | NMDAR | Neuroradiology | Autoimmune encephalitis | NMDA-RECEPTOR ENCEPHALITIS | BIOMARKER | GLIAL-CELL DAMAGE | CLINICAL NEUROLOGY | DISEASE-ACTIVITY | PROTEINS | CEREBROSPINAL-FLUID MARKERS | PROGRESSION | Diagnosis | Cerebrospinal fluid | Research | Autoimmune diseases | Neurons | Risk factors | Encephalitis | Antigens | Autoantibodies | Surface antigens | Magnetic resonance imaging | Inflammation | Cell surface
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17. Full Text Neurofilament light chain serum levels reflect disease severity in MOG-Ab associated disorders
by Mariotto, Sara and Ferrari, Sergio and Gastaldi, Matteo and Franciotta, Diego and Sechi, Elia and Capra, Ruggero and Mancinelli, Chiara and Schanda, Kathrin and Alberti, Daniela and Orlandi, Riccardo and Bombardi, Roberto and Zuliani, Luigi and Zoccarato, Marco and Benedetti, Maria Donata and Tanel, Raffaella and Calabria, Francesca and Rossi, Francesca and Pavone, Antonino and Grazian, Luisa and Sechi, GianPietro and Batzu, Lucia and Murdeu, Noemi and Janes, Francesco and Fetoni, Vincenza and Fulitano, Daniela and Stenta, Gianola and Federle, Lisa and Cantalupo, Gaetano and Reindl, Markus and Monaco, Salvatore and Gajofatto, Alberto
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 11/2019, Volume 90, Issue 11, pp. 1293 - 1296
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18. Full Text Inflammation, Infectious Triggers, and Parkinson's Disease
by Caggiu, E and Arru, G and Hosseini, S and Niegowska, M and Sechi, G and Zarbo, IR and Sechi, LA
FRONTIERS IN NEUROLOGY, ISSN 1664-2295, 02/2019, Volume 10, p. 122
Parkinson's disease is a neurodegenerative disorder characterized by progressive loss of dopaminergic neurons of the substantia nigra pars compacta with a... 
Parkinson's disease | neurodegenerative disease | MICROGLIAL ACTIVATION | microglia activation | NECROSIS-FACTOR-ALPHA | LYMPHOCYTE POPULATIONS | alpha-synuclein | CEREBROSPINAL-FLUID | SUBSTANTIA-NIGRA | NEUROSCIENCES | CLINICAL NEUROLOGY | autoimmunity | HLA-DR | neuroinflammation | immune system | HERPES-SIMPLEX | CENTRAL-NERVOUS-SYSTEM | autoantibodies | EPSTEIN-BARR-VIRUS | T-CELLS
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19. Full Text Teaching Neuro Images: Subacute encephalopathy in a young woman with THTR2 gene mutation
by Sechi, Elia and Addis, Alberto and Fadda, Giulia and Minafra, Luigi and Bravatà, Valentina and Sechi, GianPietro
Neurology, ISSN 0028-3878, 10/2015, Volume 85, Issue 14, pp. e108 - e109
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20. Old and novel humoral biomarkers of autoimmune myasthenia gravis
by Corda, Davide Giacomo and Deiana, Giovanni Andrea and Arru, Giannina and Masala, Giovanni and Sechi, Gianpietro
01/2018, ISBN 1536138371
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