X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (319) 319
index medicus (309) 309
corneal dystrophies, hereditary - physiopathology (217) 217
female (213) 213
ophthalmology (208) 208
male (189) 189
adult (162) 162
middle aged (153) 153
aged (110) 110
corneal dystrophies, hereditary - surgery (107) 107
visual acuity - physiology (107) 107
visual acuity (67) 67
cornea (66) 66
retrospective studies (63) 63
corneal dystrophies, hereditary - diagnosis (62) 62
treatment outcome (56) 56
surgery (55) 55
adolescent (54) 54
cornea - physiopathology (49) 49
corneal dystrophies, hereditary - genetics (49) 49
follow-up studies (49) 49
cornea - pathology (47) 47
corneal dystrophies, hereditary - pathology (46) 46
child (45) 45
mutation (39) 39
penetrating keratoplasty (39) 39
abridged index medicus (36) 36
corneal topography (36) 36
aged, 80 and over (35) 35
young adult (34) 34
corneal transplantation (31) 31
eye diseases (31) 31
keratoconus (30) 30
pedigree (30) 30
recurrence (30) 30
tomography, optical coherence (29) 29
endothelium, corneal - pathology (28) 28
corneal dystrophies, hereditary - complications (27) 27
endothelium (27) 27
postoperative complications (27) 27
prospective studies (27) 27
refraction, ocular - physiology (27) 27
child, preschool (25) 25
phototherapeutic keratectomy (25) 25
keratoplasty, penetrating (24) 24
sense organs (23) 23
analysis (22) 22
corneal dystrophy (22) 22
eye (22) 22
genetic structures (22) 22
photorefractive keratectomy (22) 22
transplantation (22) 22
animals (21) 21
fuchs' endothelial dystrophy - physiopathology (21) 21
care and treatment (20) 20
dystrophy (20) 20
corneal diseases (18) 18
corneal diseases - physiopathology (18) 18
corneal dystrophies, hereditary - etiology (18) 18
gene (18) 18
intraocular pressure (18) 18
lasers, excimer - therapeutic use (18) 18
mutations (18) 18
patients (18) 18
cell count (17) 17
corneal transplantation - methods (17) 17
astigmatism - physiopathology (16) 16
cornea - surgery (16) 16
corneal stroma - pathology (16) 16
glaucoma (16) 16
corneal opacity - physiopathology (15) 15
corneal pachymetry (15) 15
descemet stripping endothelial keratoplasty (15) 15
lasers (15) 15
phenotype (15) 15
photorefractive keratectomy - methods (15) 15
biochemistry & molecular biology (14) 14
diagnosis, differential (14) 14
extracellular matrix proteins - genetics (14) 14
fluorescein angiography (14) 14
research (14) 14
age (13) 13
collagen (13) 13
corneal dystrophies, hereditary - metabolism (13) 13
electroretinography (13) 13
intraoperative complications (13) 13
keratoconus - physiopathology (13) 13
medicine & public health (13) 13
microscopy, confocal (13) 13
tissue donors (13) 13
cataracts (12) 12
corneal degeneration (12) 12
corneal diseases - surgery (12) 12
lasers, excimer (12) 12
refraction, ocular (12) 12
transforming growth factor beta - genetics (12) 12
cornea - metabolism (11) 11
corneal stroma - surgery (11) 11
epithelium, corneal - pathology (11) 11
eyes (11) 11
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (298) 298
French (12) 12
German (11) 11
Russian (5) 5
Finnish (1) 1
Hungarian (1) 1
Japanese (1) 1
Polish (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
The British journal of ophthalmology, ISSN 0007-1161, 02/2018, Volume 102, Issue 2, pp. 187 - 194
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