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Iranian Journal of Medical Sciences, ISSN 0253-0716, 05/2016, Volume 41, Issue 3, pp. 241 - 244
Familial amyloid polyneuropathy (FAP) type IV (FINNISH) is a rare clinical entity with challenging neuropathy and cosmetic deficits. Amyloidosis can affect... 
Orthostatic | Cranial nerve diseases | Amyloid neuropathies | Familial | Hypotension | Care and treatment | Amyloidosis | Genetic aspects | Diagnosis | Research | Risk factors | Genetic screening
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 1990, Volume 1096, Issue 1, pp. 84 - 86
Amyloid subunit protein was isolated from familial amyloid polyneuropathy type IV (Finnish type) cardiac tissue and purified to homogeneity. N-terminal amino... 
Familial amyloid polyneuropathy type IV | Gelsolin | Amyloid protein | Point mutation
Journal Article
Muscle and Nerve, ISSN 0148-639X, 05/2010, Volume 41, Issue 5, pp. 679 - 684
Hereditary amyloidosis of the Finnish type (HAF, or familial amyloid polyneuropathy type IV) is an autosomal dominant disease that has been described most... 
Corneal lattice dystrophy | Familial amyloid neuropathy | Gelsolin | Facial palsy | Hereditary amyloidosis | facial palsy | SUBSTITUTION | POLYNEUROPATHY | LIVER-TRANSPLANTATION | GELSOLIN AMYLOIDOSIS | gelsolin | familial amyloid neuropathy | corneal lattice dystrophy | FAF | NEUROSCIENCES | CLINICAL NEUROLOGY | GENE | MUTATION | hereditary amyloidosis | EXPERIENCE | Peripheral Nervous System Diseases - diagnosis | Genetic Testing | Cranial Nerve Diseases - genetics | Humans | Middle Aged | Facial Nerve Diseases - metabolism | Male | Peripheral Nervous System Diseases - physiopathology | Amyloid Neuropathies, Familial - physiopathology | Young Adult | Electrodiagnosis | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | DNA Mutational Analysis | Inheritance Patterns - genetics | Adult | Female | Peripheral Nerves - metabolism | Peripheral Nervous System Diseases - genetics | Cranial Nerve Diseases - physiopathology | Disability Evaluation | Amyloid Neuropathies, Familial - genetics | Cranial Nerves - metabolism | Genotype | Oculomotor Nerve Diseases - diagnosis | Corneal Dystrophies, Hereditary - diagnosis | Facial Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - metabolism | Hypoglossal Nerve Diseases - metabolism | Mutation - genetics | Oculomotor Nerve Diseases - physiopathology | Cranial Nerve Diseases - diagnosis | Peripheral Nerves - physiopathology | Neurologic Examination | Genetic Markers - genetics | Adolescent | Finland | Cranial Nerves - physiopathology | Aged | Gelsolin - genetics | Germany | Oculomotor Nerve Diseases - metabolism | Amyloid Neuropathies, Familial - diagnosis | Index Medicus
Journal Article
Journal of Pathology, ISSN 0022-3417, 12/2009, Volume 219, Issue 4, pp. 481 - 490
Familial amyloidotic polyneuropathy (FAP) is characterized by extracellular deposition of amyloid fibrils caused by a point mutation in the transthyretin (TTR)... 
Immunohistochemistry | Collagen IV | Transthyretin | Cardiomyocytes | Amyloidosis | Electron microscopy | Vascular smooth muscle cells | Basement membrane | Familial amyloidotic polyneuropathy | amyloidosis | basement membrane | LIVER-TRANSPLANTATION | WILD-TYPE TRANSTHYRETIN | ENZYME-IMMUNOASSAY | transthyretin | ALZHEIMERS-DISEASE | IV COLLAGEN | PATHOLOGY | cardiomyocytes | PRECURSOR PROTEINS | ONCOLOGY | familial amyloidotic polyneuropathy | electron microscopy | collagen IV | EXTRACELLULAR-MATRIX | immunohistochemistry | HEPARAN-SULFATE PROTEOGLYCANS | SYSTEMIC AMYLOIDOSIS | MONOCLONAL-ANTIBODIES | vascular smooth muscle cells | Amyloidogenesis | Deposits | Cardiac muscle | Fibrils | Data processing | Smooth muscle | beta -Amyloid | Basement membranes | Polyneuropathy | Fibronectin | Serum levels | Fibrillogenesis | Laminin | Autopsy | Point mutation | Amyloid | Collagen (type IV) | Collagen Type IV - metabolism | Cell Line | Basement Membrane - ultrastructure | Muscle, Smooth, Vascular - metabolism | Amyloid Neuropathies, Familial - metabolism | Humans | Middle Aged | Cells, Cultured | Male | Microscopy, Electron | Muscle, Smooth, Vascular - cytology | Basement Membrane - metabolism | Amyloid Neuropathies, Familial - pathology | Disease Progression | Amyloid - metabolism | Myocytes, Cardiac - metabolism | Adult | Female | Aged | Membrane Proteins - metabolism | Myocytes, Cardiac - ultrastructure | Index Medicus
Journal Article
Journal of Neurology, ISSN 0340-5354, 11/2013, Volume 260, Issue 11, pp. 2802 - 2814
Journal Article
The Journal of Pathology, ISSN 0022-3417, 06/2005, Volume 206, Issue 2, pp. 224 - 232
Journal Article
Annals of Neurology, ISSN 0364-5134, 12/2015, Volume 78, Issue 6, pp. 901 - 916
Journal Article