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Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 08/2014, Volume 86, Issue 2, pp. 159 - 167
Objectives Since liver transplant (LT) was introduced to treat patients with familial amyloid polyneuropathy carrying the V30M mutation (ATTR-V30M), ocular and... 
SURGERY | POLYNEUROPATHY | URBAN NORTHERN PORTUGAL | LIVER-TRANSPLANTATION | HEMORRHAGE | PSYCHIATRY | LEPTOMENINGEAL AMYLOIDOSIS | VARIANT | TRANSIENT ISCHEMIC ATTACKS | VAL30MET | CLINICAL NEUROLOGY | ANGIOPATHY | SPECTRUM | Prealbumin - genetics | Brain - diagnostic imaging | Amyloid Neuropathies, Familial - metabolism | Humans | Middle Aged | Symptom Assessment | Male | Electroencephalography | Case-Control Studies | Brain - metabolism | Amyloid - metabolism | Adult | Female | Nervous System Diseases - metabolism | Nervous System Diseases - physiopathology | Retrospective Studies | Nervous System Diseases - pathology | Amyloid - genetics | Prealbumin - cerebrospinal fluid | Amyloid Neuropathies, Familial - genetics | Brain - physiopathology | Kaplan-Meier Estimate | Amyloid Neuropathies, Familial - complications | Liver Transplantation - mortality | Amyloid - blood | Nervous System Diseases - complications | Amyloid Neuropathies, Familial - pathology | Disease Progression | Amyloid - cerebrospinal fluid | Amyloid Neuropathies, Familial - cerebrospinal fluid | Radiography | Liver Transplantation - statistics & numerical data | Prealbumin - metabolism | Brain - pathology | Amyloid Neuropathies, Familial - blood | Amyloid Neuropathies, Familial - diagnosis | CT imaging | Care and treatment | Usage | Central nervous system | Amyloidosis | Risk factors | Index Medicus
Journal Article
World Neurosurgery, ISSN 1878-8750, 03/2018, Volume 111, pp. 190 - 193
Oculoleptomeningeal amyloidosis (OLMA) represents a rare subtype of familial transthyretin ( ) amyloidosis, characterized by deposition of amyloid in cranial... 
Familial amyloidosis | Oculoleptomeningeal amyloidosis | Transthyretin | SURGERY | HOMOCYSTEINE | POLYNEUROPATHY | GENE MUTATION | LEPTOMENINGEAL AMYLOIDOSIS | VARIANT | CLINICAL NEUROLOGY | ALA25THR | DISEASE | SPECTRUM | Genetic research | Nervous system | Amyloidosis | Genetic aspects | Surgery | Resveratrol | Index Medicus
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 04/2014, Volume 9, Issue 1, pp. 61 - 61
Background: Transthyretin amyloidosis is a systemic disorder caused by amyloid deposits formed by misfolded transthyretin monomers. Two main forms exist:... 
Functional | Secondary | Transthyretin | Cardiomyopathies | Amyloid | Amyloidosis | Gastrointestinal disorders | Hereditary | Amyloid neuropathies | Nutritional status | Quality of life | MEDICINE, RESEARCH & EXPERIMENTAL | FECAL INCONTINENCE | POLYNEUROPATHY | LIVER-TRANSPLANTATION | OCULOLEPTOMENINGEAL AMYLOIDOSIS | CLINICAL-FEATURES | LEPTOMENINGEAL AMYLOIDOSIS | ATTR VAL30MET | FAMILIAL AMYLOIDOSIS | GENETICS & HEREDITY | LATE-ONSET | ENDOCRINE-CELLS | Prealbumin - genetics | Gastrointestinal Diseases - physiopathology | Humans | Amyloid Neuropathies, Familial - complications | Quality of Life | Female | Gastrointestinal Diseases - complications | Male | Nutritional Status | Mutation | Amyloid Neuropathies, Familial - physiopathology | Complications and side effects | Care and treatment | Gene mutations | Gastrointestinal diseases | Cardiac patients | Development and progression | Research | Health aspects | Risk factors | Surveys | Albumin | Medicine, Experimental | Medical research | Pharmaceutical industry | Analysis | Transplants & implants | Review boards | Cardiomyopathy | Mortality | Clinical trials | Diarrhea | Nausea | Proteins | Studies | Confidence intervals | Body mass index | Biopsy | Vomiting | Drug therapy | Constipation | Age | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap | Gastroenterologi | Klinisk medicin | Clinical Medicine | Gastroenterology and Hepatology
Journal Article
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 2014, Volume 22, Issue 4, pp. 769 - 771
Journal Article
Cell Death and Disease, ISSN 2041-4889, 09/2013, Volume 4, Issue 9, pp. e789 - e789
Oculoleptomeningeal amyloidosis (OA) is a fatal and untreatable hereditary disease characterized by the accumulation of transthyretin (TTR) amyloid within the... 
Amyloid fibril | Neurodegeneration | Transthyretin | Microglia | POLYNEUROPATHY | LIVER-TRANSPLANTATION | transthyretin | ALZHEIMERS-DISEASE | neurodegeneration | RECEPTOR | GENE MUTATION | LEPTOMENINGEAL AMYLOIDOSIS | VARIANT | NEUROTOXICITY | BETA | CELL BIOLOGY | CEREBRAL-HEMORRHAGE | amyloid fibril | microglia | Tumor Necrosis Factor-alpha - metabolism | Memory Disorders - physiopathology | Microglia - metabolism | Phosphorylation | Minocycline - pharmacology | Culture Media, Conditioned - pharmacology | Glycogen Synthase Kinase 3 beta | NF-kappa B - metabolism | Memory Disorders - complications | Amyloid Neuropathies, Familial - physiopathology | Brain - metabolism | Endocytosis | Cell Nucleus - metabolism | Synapses - metabolism | Inflammation Mediators - metabolism | Microglia - pathology | Amyloid | Neurons - metabolism | Cell Death - drug effects | Neurons - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Interleukin-6 - metabolism | Memory Disorders - pathology | Disease Models, Animal | Synapses - drug effects | Microglia - drug effects | Cells, Cultured | Amyloid Neuropathies, Familial - complications | Memory, Short-Term - drug effects | Glycogen Synthase Kinase 3 - metabolism | Mutation - genetics | Amyloid Neuropathies, Familial - pathology | Protein Transport | Animals | Prealbumin - metabolism | Mice | Index Medicus | Original
Journal Article
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 08/2013, Volume 1832, Issue 8, pp. 1183 - 1193
Journal Article