X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1905) 1905
Book Chapter (13) 13
Magazine Article (5) 5
Dissertation (1) 1
Government Document (1) 1
Newspaper Article (1) 1
Publication (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1445) 1445
sturge-weber syndrome (844) 844
male (726) 726
female (704) 704
child (517) 517
index medicus (462) 462
sturge-weber syndrome - complications (419) 419
sturge-weber syndrome - diagnosis (410) 410
clinical neurology (381) 381
infant (376) 376
child, preschool (372) 372
adolescent (361) 361
adult (348) 348
magnetic resonance imaging (270) 270
pediatrics (267) 267
sturge-weber syndrome - pathology (230) 230
ophthalmology (195) 195
sturge-weber syndrome - diagnostic imaging (192) 192
tomography, x-ray computed (192) 192
epilepsy (191) 191
children (172) 172
diagnosis, differential (171) 171
surgery (166) 166
glaucoma (159) 159
sturge-weber-syndrome (159) 159
infant, newborn (141) 141
sturge-weber syndrome - physiopathology (137) 137
angiomatosis (134) 134
middle aged (132) 132
radiology, nuclear medicine & medical imaging (130) 130
brain - pathology (128) 128
diagnosis (113) 113
sturge-weber syndrome - surgery (109) 109
disease (106) 106
seizures (105) 105
hemangioma (99) 99
follow-up studies (96) 96
treatment outcome (95) 95
electroencephalography (92) 92
neurology (88) 88
retrospective studies (88) 88
sturge–weber syndrome (86) 86
care and treatment (84) 84
brain - diagnostic imaging (82) 82
prognosis (79) 79
neurosciences (77) 77
neuroimaging (76) 76
dermatology (75) 75
syndrome (73) 73
young adult (73) 73
port-wine stains (68) 68
angiomatosis - complications (65) 65
tuberous sclerosis (65) 65
angiomatosis - diagnosis (63) 63
sturge-weber syndrome - therapy (63) 63
brain (62) 62
sturge-weber syndrome - genetics (62) 62
hemangioma - diagnosis (61) 61
glaucoma - etiology (60) 60
glaucoma - surgery (58) 58
port-wine stain (57) 57
sturge weber syndrome (56) 56
hemispherectomy (54) 54
intraocular pressure (54) 54
mutation (54) 54
calcinosis - diagnostic imaging (53) 53
radiography (53) 53
case report (52) 52
seizures - etiology (52) 52
medicine & public health (50) 50
sturge-weber (50) 50
hemangioma - pathology (49) 49
mri (49) 49
sturge-weber syndrome - drug therapy (49) 49
aged (47) 47
magnetic resonance imaging - methods (46) 46
anticonvulsants - therapeutic use (45) 45
research (45) 45
trabeculectomy (45) 45
eye diseases (44) 44
abnormalities (43) 43
angiomatosis - pathology (43) 43
health aspects (43) 43
management (43) 43
visual acuity (43) 43
case studies (41) 41
klippel-trenaunay-weber syndrome - diagnosis (41) 41
risk factors (41) 41
sense organs (41) 41
genetic structures (40) 40
hemangioma - complications (40) 40
angiomatosis - diagnostic imaging (39) 39
sturge‐weber syndrome (39) 39
choroid neoplasms - diagnosis (38) 38
glaucoma - complications (38) 38
epilepsy - surgery (37) 37
nevus (37) 37
usage (37) 37
epilepsy - etiology (36) 36
fluorescein angiography (36) 36
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1516) 1516
French (108) 108
German (73) 73
Spanish (63) 63
Japanese (52) 52
Italian (33) 33
Polish (28) 28
Chinese (16) 16
Russian (16) 16
Korean (13) 13
Portuguese (11) 11
Turkish (11) 11
Czech (7) 7
Hungarian (5) 5
Romanian (5) 5
Croatian (2) 2
Danish (1) 1
Persian (1) 1
Slovak (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Journal Article
Journal Article
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, ISSN 1460-2725, 12/2019, Volume 112, Issue 12, pp. 936 - 936
Journal Article
Indian Journal of Dermatology, Venereology and Leprology, ISSN 0378-6323, 11/2019, Volume 85, Issue 6, pp. 618 - 620
Dermoscopy (DermLite DL3, USA) of the lesions on the face showed red dotted vessels and linear vessels [Figure 5] representing papillary and subpapillary form... 
DERMATOLOGY | Skin Diseases - complications | Humans | Skin Diseases - diagnostic imaging | Dermoscopy | Female | Face | Skin Diseases - congenital | Child | Sturge-Weber Syndrome - complications | Klippel-Trenaunay-Weber Syndrome - complications | Guardians | Nuclear magnetic resonance--NMR | Congenital diseases | Mutation | Pathogenesis
Journal Article
2015, ISBN 0444627022, Volume 132
Sturge–Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis, and impacts approximately 1 in 20000 live births. Sturge... 
epilepsy | port-wine birthmark | Sturge–Weber syndrome | somatic mosaic mutation | glaucoma | GNAQ | Glaucoma | Somatic mosaic mutation | Port-wine birthmark | Sturge-Weber syndrome | Epilepsy | Sturge-Weber Syndrome - physiopathology | GTP-Binding Protein alpha Subunits, Gq-G11 - genetics | Humans | Female | Male | Sturge-Weber Syndrome - genetics | Mutation - genetics
Book Chapter
Clinical Ophthalmology, ISSN 1177-5467, 05/2016, Volume 10, pp. 871 - 878
Sturge-Weber syndrome has been included in the group of phakomatoses that is characterized by hamartomas involving the brain, skin, and eyes... 
Glaucoma | Port-wine stain | Choroidal hemangiomas | Sturge–Weber syndrome | Congenital disease | Glaucoma surgery | Venous pressure | Diagnosis | Cornea | Photodynamic therapy | Medical imaging | Congenital diseases | Tomography | Mutation
Journal Article