X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (94) 94
humans (84) 84
male (47) 47
neurosciences (42) 42
female (41) 41
polyneuropathy (41) 41
clinical neurology (35) 35
middle aged (31) 31
adult (30) 30
aged (28) 28
mutation (24) 24
neuropathy (23) 23
polyneuropathies (21) 21
animals (19) 19
biopsy (16) 16
pathology (16) 16
medicine & public health (15) 15
gelsolin (14) 14
immunohistochemistry (14) 14
neurology (14) 14
amyloidosis (13) 13
diabetes (12) 12
medicine, research & experimental (12) 12
cranial neuropathy (11) 11
familial amyloidosis (11) 11
gelsolin - genetics (11) 11
peripheral neuropathy (11) 11
amyloidosis - genetics (10) 10
biochemistry & molecular biology (10) 10
diabetic neuropathy (10) 10
pedigree (10) 10
peripheral nervous system diseases - diagnosis (10) 10
research (10) 10
transthyretin (10) 10
adolescent (9) 9
amyloid (9) 9
collagen (9) 9
corneal lattice dystrophy (9) 9
diabetic polyneuropathy (9) 9
diagnosis (9) 9
gene (9) 9
genetic aspects (9) 9
hereditary amyloidosis (9) 9
medicine, general & internal (9) 9
neural conduction (9) 9
polyneuropathy type-iv (9) 9
amyloid - metabolism (8) 8
disease (8) 8
extracellular-matrix (8) 8
familial amyloid polyneuropathy (8) 8
ophthalmology (8) 8
peripheral nervous system diseases - pathology (8) 8
peripheral-nerve (8) 8
point mutation (8) 8
protein (8) 8
amyloid neuropathies, familial - genetics (7) 7
amyloidosis - pathology (7) 7
analysis (7) 7
diabetic neuropathies - physiopathology (7) 7
familial amyloidotic polyneuropathy (7) 7
inflammatory demyelinating polyneuropathy (7) 7
lattice corneal-dystrophy (7) 7
microscopy, electron (7) 7
prealbumin - genetics (7) 7
sensory neuropathy (7) 7
abridged index medicus (6) 6
amyloid neuropathies, familial - physiopathology (6) 6
amyloidosis, familial - genetics (6) 6
collagen type iv - metabolism (6) 6
diabetic neuropathies (6) 6
expression (6) 6
extracellular matrix (6) 6
finnish type faf (6) 6
marie-tooth-disease (6) 6
medicine (6) 6
mutation - genetics (6) 6
nervous system (6) 6
pain (6) 6
polyneuropathies - diagnosis (6) 6
polyneuropathies - pathology (6) 6
polyneuropathies - physiopathology (6) 6
schwann-cells (6) 6
skin - pathology (6) 6
sural nerve - pathology (6) 6
systemic amyloidosis (6) 6
aged, 80 and over (5) 5
amyloid neuropathies - genetics (5) 5
amyloid neuropathies, familial - pathology (5) 5
care and treatment (5) 5
cells, cultured (5) 5
charcot-marie-tooth disease (5) 5
chemotherapy (5) 5
development and progression (5) 5
diabetes mellitus (5) 5
diabetes-mellitus (5) 5
diagnosis, differential (5) 5
familial amyloid polyneuropathy type iv (5) 5
genetics & heredity (5) 5
health aspects (5) 5
laminin (5) 5
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


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
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 | 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 | 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) | Index Medicus
Journal Article
Experimental Neurology, ISSN 0014-4886, 2010, Volume 224, Issue 1, pp. 318 - 320
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