X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (476) 476
index medicus (467) 467
ophthalmology (275) 275
male (271) 271
female (260) 260
adult (195) 195
middle aged (195) 195
corneal dystrophies, hereditary - genetics (177) 177
aged (158) 158
corneal dystrophies, hereditary - pathology (152) 152
amyloidosis (125) 125
mutation (122) 122
amyloidosis - pathology (109) 109
pedigree (102) 102
cornea (99) 99
amyloidosis - genetics (90) 90
cornea - pathology (88) 88
corneal dystrophies, hereditary - metabolism (66) 66
dna mutational analysis (65) 65
abridged index medicus (63) 63
transforming growth factor beta - genetics (63) 63
corneal dystrophy (59) 59
adolescent (57) 57
corneal dystrophies, hereditary - diagnosis (56) 56
corneal diseases - pathology (54) 54
amyloid - metabolism (52) 52
corneal diseases (51) 51
extracellular matrix proteins - genetics (51) 51
gelsolin (51) 51
eye diseases (50) 50
corneal dystrophies, hereditary - surgery (48) 48
aged, 80 and over (47) 47
gene (46) 46
polymerase chain reaction (46) 46
protein (45) 45
keratoplasty, penetrating (44) 44
biochemistry & molecular biology (43) 43
amyloid (42) 42
corneal transplantation (40) 40
phenotype (40) 40
child (39) 39
amyloidosis - complications (38) 38
familial amyloidosis (37) 37
amyloidosis - metabolism (36) 36
beta-ig-h3 (36) 36
corneal diseases - etiology (36) 36
point mutation (36) 36
amyloidosis - diagnosis (34) 34
corneal dystrophies, hereditary - complications (34) 34
corneal stroma - pathology (34) 34
diagnosis (34) 34
diagnosis, differential (34) 34
lattice corneal dystrophy (34) 34
animals (33) 33
cranial neuropathy (33) 33
dystrophy (33) 33
visual acuity (33) 33
base sequence (32) 32
genetic aspects (32) 32
amyloidosis, familial - genetics (31) 31
gelsolin - genetics (31) 31
growth-factor-beta (31) 31
pathology (31) 31
bigh3 gene (30) 30
sense organs (30) 30
kerato-epithelin mutations (29) 29
molecular sequence data (29) 29
cell adhesion molecules - genetics (28) 28
corneal lattice dystrophy (28) 28
immunohistochemistry (28) 28
microscopy, electron (28) 28
antigens, neoplasm - genetics (27) 27
cornea - metabolism (26) 26
genetics & heredity (26) 26
amyloidosis - etiology (25) 25
recurrence (25) 25
cornea - ultrastructure (24) 24
corneal diseases - metabolism (24) 24
corneal diseases - surgery (24) 24
syndrome (24) 24
amyloid - analysis (23) 23
disease (23) 23
lattice corneal-dystrophy (23) 23
medicine & public health (23) 23
microscopy, confocal (23) 23
research (23) 23
amyloidosis - surgery (22) 22
corneal amyloidosis (22) 22
features (22) 22
research article (22) 22
finland (21) 21
hereditary amyloidosis (21) 21
retrospective studies (21) 21
analysis (20) 20
child, preschool (20) 20
corneal dystrophies, hereditary - physiopathology (20) 20
genes (20) 20
genotype (20) 20
mutation - genetics (20) 20
biopsy (19) 19
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (521) 521
French (27) 27
German (26) 26
Japanese (5) 5
Finnish (4) 4
Korean (4) 4
Chinese (3) 3
Czech (2) 2
Spanish (2) 2
Hungarian (1) 1
Polish (1) 1
Russian (1) 1
more...
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
Kidney International, ISSN 0085-2538, 04/2017, Volume 91, Issue 4, pp. 964 - 971
Journal Article
Amyloid, ISSN 1350-6129, 07/2019, Volume 26, Issue 3, pp. 103 - 111
Timely diagnosis of hereditary variant transthyretin (ATTRv) amyloidosis is critical for appropriate treatment and optimal outcomes. Significant differences... 
follow-up | amyloidosis | transthyretin | progression | hereditary | monitoring | ATTR | MEDICINE, RESEARCH & EXPERIMENTAL | POLYNEUROPATHY | NERVES | BIOCHEMISTRY & MOLECULAR BIOLOGY | VALIDATION | ELECTROCHEMICAL SKIN-CONDUCTANCE | MEDICINE, GENERAL & INTERNAL | NEUROPATHY | TAFAMIDIS | CORNEAL CONFOCAL MICROSCOPY | DYSFUNCTION | Index Medicus
Journal Article
Cornea, ISSN 0277-3740, 06/2011, Volume 30, Issue 6, pp. 716 - 717
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2018, Volume 26, Issue 1, pp. 117 - 123
Journal Article
International Medical Case Reports Journal, ISSN 1179-142X, 2018, Volume 11, pp. 193 - 199
We describe the histological changes in the collagen fibers of a 50-year-old male who presented keratoconus with secondary corneal amyloidosis. Corneal tissue... 
Stroma | Cornea | Lactoferrin | Amyloid | TGFBIp | Viral antibodies | Keratoconus | Collagen | Lactoferrins | Antibodies | Bone morphogenetic proteins | Amyloidosis | Proteins | Edema | Microscopy | Biochemistry | Growth factors | Patients | Polymorphism | lactoferrin | collagen | keratoconus | corneal amyloidosis
Journal Article
The International Journal of Cardiovascular Imaging, ISSN 1569-5794, 2/2019, Volume 35, Issue 2, pp. 351 - 358
Journal Article