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Muscle & Nerve, ISSN 0148-639X, 05/2016, Volume 53, Issue 5, pp. 762 - 769
IntroductionHereditary gelsolin amyloidosis (GA) is a rare condition caused by the gelsolin gene mutation. The diagnostic triad includes corneal lattice... 
cranial neuropathy | amyloidosis | gelsolin | bilateral facial paresis | facial paresis grading | Facial paresis grading | Amyloidosis | Gelsolin | Cranial neuropathy | Bilateral facial paresis | GSN GENE | NEUROSCIENCES | FINNISH TYPE FAF | POLYNEUROPATHY TYPE-IV | CLINICAL NEUROLOGY | LATTICE CORNEAL-DYSTROPHY | HEARING-LOSS | NEUROPATHY | FAMILIAL AMYLOIDOSIS | MERETOJAS SYNDROME | HEREDITARY AMYLOIDOSIS | MUTATION | Vestibulocochlear Nerve Diseases - physiopathology | Cutis Laxa - etiology | Humans | Middle Aged | Vestibulocochlear Nerve Diseases - etiology | Oculomotor Nerve Diseases - etiology | Male | Amyloid Neuropathies, Familial - physiopathology | Facial Nerve Diseases - etiology | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | Facial Paralysis - physiopathology | Aged, 80 and over | Adult | Female | Electromyography | Amyloidosis - complications | Cranial Nerve Diseases - physiopathology | Hypoglossal Nerve Diseases - etiology | Trigeminal Nerve Diseases - physiopathology | Trigeminal Nerve Diseases - etiology | Amyloid Neuropathies, Familial - complications | Amyloidosis - physiopathology | Neural Conduction | Facial Nerve Diseases - physiopathology | Oculomotor Nerve Diseases - physiopathology | Facial Muscles - physiopathology | Cranial Nerve Diseases - etiology | Corneal Dystrophies, Hereditary - complications | Aged | Facial Paralysis - etiology | Development and progression | Paralysis, Facial | Gene mutations | Wood products | Workshops | Index Medicus
Journal Article
American Journal of Neuroradiology, ISSN 0195-6108, 02/2011, Volume 32, Issue 2, pp. 276 - 282
Journal Article
Journal Article
Headache, ISSN 0017-8748, 06/2009, Volume 49, Issue 6, pp. 838 - 850
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 neurosurgery, ISSN 0022-3085, 03/2015, Volume 122, Issue 3, pp. 707 - 720
Journal Article