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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
Journal Article
Neurological Research, ISSN 0161-6412, 06/2010, Volume 32, Issue 5, pp. 472 - 475
Journal Article
FORTSCHRITTE DER NEUROLOGIE PSYCHIATRIE, ISSN 0720-4299, 04/2011, Volume 79, Issue 4, pp. 238 - 241
AGel amyloidosis is an autosomal dominantly inherited systemic amyloidosis which is most commonly observed in Finland. The clinical manifestation is... 
facial palsy | HEREDITARY GELSOLIN AMYLOIDOSIS | CORNEAL LATTICE DYSTROPHY | gelsolin | PSYCHIATRY | polyneuropathy | hereditary amyloidosis | CRANIAL NEUROPATHY | FINNISH TYPE FAF | CLINICAL NEUROLOGY | AGel amyloidosis
Journal Article
Annals of Neurology, ISSN 0364-5134, 03/1999, Volume 45, Issue 3, pp. 305 - 311
Journal Article
Clinical Kidney Journal, ISSN 2048-8505, 04/2013, Volume 6, Issue 2, pp. 189 - 193
Finnish-type familial amyloidosis (FAF) is a rare hereditary systemic amyloidosis that mainly exhibits cranial neuropathy. We describe a Japanese family with... 
Finnish-type familial amyloidosis (FAF) | hereditary renal amyloidosis | gelsolin | nephrotic syndrome | Original Contributions
Journal Article