X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (126) 126
humans (122) 122
gelsolin (92) 92
familial amyloidosis (91) 91
mutation (75) 75
finnish type (61) 61
male (55) 55
amyloidosis (53) 53
female (53) 53
gelsolin - genetics (47) 47
biochemistry & molecular biology (46) 46
middle aged (39) 39
finnish hereditary amyloidosis (38) 38
aged (37) 37
gelsolin - metabolism (35) 35
protein (35) 35
amyloid (34) 34
adult (29) 29
amyloidosis - genetics (27) 27
animals (25) 25
cranial neuropathy (25) 25
gene (23) 23
hereditary amyloidosis (23) 23
polyneuropathy (23) 23
plasma gelsolin (22) 22
point mutation (22) 22
neurosciences (21) 21
pedigree (21) 21
amyloidosis - metabolism (20) 20
amyloidosis, familial - genetics (20) 20
clinical neurology (20) 20
molecular sequence data (20) 20
disease (19) 19
ophthalmology (19) 19
alzheimers-disease (18) 18
amyloid - metabolism (18) 18
gelsolin - chemistry (18) 18
medicine, general & internal (18) 18
pathology (18) 18
amino acid sequence (17) 17
finnish type faf (17) 17
neuropathy (17) 17
corneal lattice dystrophy (16) 16
amyloidosis - pathology (15) 15
cell biology (15) 15
corneal dystrophies, hereditary - genetics (15) 15
genetics & heredity (15) 15
substitution (15) 15
identification (14) 14
medicine, research & experimental (14) 14
actin (13) 13
gelsolin gene (13) 13
immunohistochemistry (13) 13
man (13) 13
dna mutational analysis (12) 12
lattice corneal-dystrophy (12) 12
variant gelsolin (12) 12
aged, 80 and over (11) 11
biophysics (11) 11
finland (11) 11
macromolecular substances (11) 11
proteins (11) 11
variant (11) 11
acid (10) 10
amyloid - chemistry (10) 10
amyloid neuropathies - genetics (10) 10
amyloidogenesis (10) 10
amyloidosis, familial - complications (10) 10
amyloidosis, familial - metabolism (10) 10
article (10) 10
dystrophy (10) 10
familial amyloid polyneuropathy (10) 10
finnish (10) 10
in-vitro (10) 10
mice (10) 10
mutation - genetics (10) 10
abridged index medicus (9) 9
alzheimer's disease (9) 9
amyloid - genetics (9) 9
amyloid neuropathies - pathology (9) 9
amyloidosis, familial - diagnosis (9) 9
amyloidosis, familial - pathology (9) 9
base sequence (9) 9
binding (9) 9
corneal dystrophies, hereditary - pathology (9) 9
furin (9) 9
genes (9) 9
genetic aspects (9) 9
mass spectrometry (9) 9
polymerase chain reaction (9) 9
protein conformation (9) 9
transthyretin (9) 9
activation (8) 8
american family (8) 8
amyloidosis - complications (8) 8
calcium (8) 8
cornea (8) 8
finnish-type (8) 8
microfilament proteins - genetics (8) 8
microscopy, electron (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


BBA - Molecular Basis of Disease, ISSN 0925-4439, 03/2019, Volume 1865, Issue 3, pp. 648 - 660
AGel amyloidosis, formerly known as familial amyloidosis of the Finnish-type, is caused by pathological aggregation of proteolytic fragments of plasma... 
Molecular dynamics | Nanobody | Caenorhabditis elegans | Gelsolin | Familial amyloidosis Finnish-type | Pharmacoperone | DOMAIN 2 | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TO-ORDER TRANSITION | PROTEOLYSIS | BETA OLIGOMERS | CAENORHABDITIS-ELEGANS | RENAL AMYLOIDOSIS | BIOPHYSICS | FAMILIAL AMYLOIDOSIS | DISORDER | SECRETION | Quantitative Biology - Biomolecules
Journal Article
Case Reports in Ophthalmology, ISSN 1663-2699, 05/2017, Volume 8, Issue 2, pp. 446 - 451
Familial amyloidosis of the Finnish type or Meretoja syndrome is a rare autosomic dominant inherited systemic condition. It was first described by Meretoja in... 
Familial amyloidosis | Corneal pathology | Gelsolin | Lattice corneal dystrophy | Meretoja syndrome | Finnish type | Pathology | Genetic counseling | Genetic testing | Mutation | Deoxyribonucleic acid--DNA | Familial amyloidosis, Finnish type
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
Journal Article
Journal Article
Journal Article
FEBS Letters, ISSN 0014-5793, 1993, Volume 335, Issue 1, pp. 119 - 123
Familial amyloidosis, Finnish type is caused by a single base mutation in gelsolin, an actin filament severing and capping protein that is present in most... 
gelsolin | amyloidosis (Finnish familial) | actin-binding protein
Journal Article