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Kidney International, ISSN 0085-2538, 04/2017, Volume 91, Issue 4, pp. 964 - 971
Journal Article
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
BRITISH JOURNAL OF DERMATOLOGY, ISSN 0007-0963, 02/2005, Volume 152, Issue 2, pp. 250 - 257
Background Hereditary gelsolin amyloidosis (AGel amyloidosis) is an age-associated systemic disease with global distribution, caused by a G6S4A or G654T... 
elastic fibres | P COMPONENT | cutis laxa | gelsolin | FAF | ELASTOSIS | DERMATOLOGY | amyloid | FAMILIAL AMYLOIDOSIS | GENE | SKIN INVOLVEMENT | MUTATION | hereditary amyloidosis | FINNISH TYPE | genodermatosis | SYSTEMIC AMYLOIDOSIS | LAXA
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 02/2005, Volume 152, Issue 2, pp. 250 - 257
Journal Article
BIOCHEMISTRY, ISSN 0006-2960, 06/2011, Volume 50, Issue 22, pp. 4877 - 4889
Finnish type familial amyloidosis (FAF) is a neurodegenerative disease, which involves the deposition of D187N or -Y mutant gelsolin fragments as amyloid in... 
FIBRIL FORMATION | OXIDATIVE STRESS | PROTEIN | HEREDITARY AMYLOIDOSIS | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | X-RAY | ALPHA-SYNUCLEIN | ANTIMICROBIAL PEPTIDES | NEURODEGENERATIVE DISEASES | AGGREGATION
Journal Article
Amyloid, ISSN 1350-6129, 07/2019, Volume 26, Issue 3, pp. 118 - 124
Objectives: Previous clinical studies have shown frequent cardiac symptoms in patients with hereditary gelsolin (AGel) amyloidosis, possibly related to amyloid... 
hereditary amyloidosis | AGel | Meretoja disease | Gelsolin | heart | Index Medicus
Journal Article