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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
Biochemistry, ISSN 0006-2960, 06/2003, Volume 42, Issue 22, pp. 6656 - 6663
Over 70 transthyretin (TTR) mutations facilitate amyloidosis in tissues other than the central nervous system (CNS). In contrast, the D18G TTR mutation in... 
FIBRIL FORMATION | POLYNEUROPATHY | PHYSIOLOGICAL CONDITIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | L55P | INTERMEDIATE | CHOROID-PLEXUS | SERUM | MENINGOCEREBROVASCULAR AMYLOIDOSIS | VARIANT | HUNGARIAN-TYPE | Central Nervous System Diseases - genetics | Prealbumin - genetics | Humans | Recombinant Proteins - cerebrospinal fluid | Central Nervous System Diseases - blood | Aspartic Acid - genetics | Genetic Variation | Blood-Brain Barrier - physiology | Prealbumin - chemistry | Inclusion Bodies - metabolism | Circular Dichroism | Protein Subunits - genetics | Glycine - genetics | Amino Acid Sequence | Central Nervous System Diseases - cerebrospinal fluid | Amyloid Neuropathies, Familial - genetics | Models, Molecular | Recombinant Proteins - chemistry | Escherichia coli Proteins - metabolism | Recombinant Proteins - genetics | Amyloid Neuropathies, Familial - cerebrospinal fluid | Recombinant Proteins - blood | Prealbumin - metabolism | Escherichia coli Proteins - genetics | Protein Conformation | Centrifugation - methods | Protein Subunits - chemistry | Amyloid Neuropathies, Familial - blood | Escherichia coli Proteins - chemistry | Hydrogen-Ion Concentration | Gene mutations | Central nervous system | Physiological aspects | Causes of | Genetic aspects | Amyloidosis | Cell membranes | Biophysics | Research | Monomers | Index Medicus | Teknik och teknologier | TEKNIKVETENSKAP | Engineering and Technology | TECHNOLOGY
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