X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
slc2a1 (75) 75
index medicus (65) 65
humans (51) 51
glucose transporter type 1 - genetics (44) 44
clinical neurology (43) 43
epilepsy (43) 43
male (36) 36
female (35) 35
ketogenic diet (33) 33
slc2a1 gene (30) 30
glucose (29) 29
glut1 (29) 29
mutations (26) 26
seizures (25) 25
child (22) 22
neurology (22) 22
glut1 deficiency syndrome (20) 20
mutation (20) 20
adolescent (18) 18
dextrose (18) 18
blood-brain-barrier (17) 17
spectrum (17) 17
child, preschool (16) 16
adult (15) 15
glucose transporter type 1 - deficiency (15) 15
monosaccharide transport proteins - deficiency (15) 15
movement disorders (15) 15
analysis (14) 14
carbohydrate metabolism, inborn errors - genetics (14) 14
genetic aspects (14) 14
neurosciences (14) 14
expression (13) 13
monosaccharide transport proteins - genetics (13) 13
pediatrics (13) 13
middle aged (12) 12
mutation - genetics (12) 12
glucose metabolism (11) 11
young adult (11) 11
animals (10) 10
dna mutational analysis (10) 10
glucose-transporter-1 deficiency (10) 10
glut1 deficiency (10) 10
phenotype (10) 10
absence epilepsy (9) 9
carbohydrate metabolism, inborn errors - diagnosis (9) 9
gene (9) 9
genes (9) 9
research (9) 9
aged (8) 8
children (8) 8
electroencephalography (8) 8
genetics & heredity (8) 8
glucose transporter type 1 - metabolism (8) 8
glucose-transport (8) 8
infant (8) 8
metabolism (8) 8
movement disorder (8) 8
oncology (8) 8
onset (8) 8
ataxia (7) 7
brain (7) 7
chorea - genetics (7) 7
developmental delay (7) 7
diet, ketogenic (7) 7
glucose - metabolism (7) 7
glucose transporter (7) 7
glucose-transporter glut1 (7) 7
glut-1 deficiency syndrome (7) 7
microcephaly (7) 7
paroxysmal exercise-induced dyskinesia (7) 7
article (6) 6
biochemistry & molecular biology (6) 6
case report (6) 6
cells (6) 6
diet, ketogenic - methods (6) 6
epilepsy - genetics (6) 6
glucose transporter 1 deficiency syndrome (6) 6
hypoglycorrhachia (6) 6
medicine (6) 6
paroxysmal dyskinesia (6) 6
proteins (6) 6
syndrome (6) 6
age of onset (5) 5
association (5) 5
behavioral sciences (5) 5
biology (5) 5
deficiency syndrome (5) 5
gene expression (5) 5
gene mutations (5) 5
genetic research (5) 5
genetics (5) 5
glucose transporter type 1 deficiency syndrome (5) 5
glycolysis (5) 5
ketogenic-diet (5) 5
medical research (5) 5
original (5) 5
patients (5) 5
pedigree (5) 5
psychiatry (5) 5
risk (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Journal of Gene Medicine, ISSN 1099-498X, 04/2018, Volume 20, Issue 4, pp. e3013 - n/a
Journal Article
Journal Article
FRONTIERS IN IMMUNOLOGY, ISSN 1664-3224, 05/2018, Volume 9
Untreated HIV infection is associated with progressive CD4+ T cell depletion, which is generally recovered with combination antiretroviral therapy (cART).... 
SURVIVAL | ACTIVATION | immune activation | SLC2A1 | immune reconstitution | AKT | IMMUNOLOGY | PATHOGENESIS | CD4+T cells | Glutl | HIV | immunometabolism | GLUCOSE-METABOLISM | IMMUNODEFICIENCY-VIRUS TYPE-1 | INFECTION | LEUKEMIA | EXPRESSION | T-CELLS
Journal Article
Frontiers in Immunology, ISSN 1664-3224, 05/2018, Volume 9, Issue MAY, p. 900
Untreated HIV infection is associated with progressive CD4+ T cell depletion, which is generally recovered with combination antiretroviral therapy (cART).... 
Immunometabolism | HIV | Glut1 | Immune reconstitution | SLC2A1 | AKT | Immune activation | CD4+ T cells | Antiviral agents | Dosage and administration | Genetic aspects | Single nucleotide polymorphisms | Research | Drug therapy | HIV infection | immune reconstitution | immunometabolism
Journal Article
by Lee, DH and Won, GW and Lee, YH and Ku, EJ and Oh, TK and Jeon, HJ
JOURNAL OF KOREAN MEDICAL SCIENCE, ISSN 1011-8934, 06/2019, Volume 34, Issue 24, pp. e171 - 10
Background: Diabetic nephropathy (DN) is the most serious microvascular complication of diabetes mellitus and is one of the leading causes of end stage renal... 
MORTALITY | GLUT1 | Diabetic Nephropathies | SLC2A1 | RISK | GLUCOSE-TRANSPORT | Diabetes Mellitus | MEDICINE, GENERAL & INTERNAL | Type 2 | CARDIOVASCULAR-DISEASE | COMPLICATIONS | AFRICAN-AMERICANS | EXPRESSION | Polymorphism | HaeIII | 의학일반
Journal Article
Journal of pediatric neurosciences, ISSN 1817-1745, 10/2018, Volume 13, Issue 4, pp. 496 - 499
Glucose transporter type 1 deficiency syndrome (GLUT1-DS) was first described by De Vivo in 1991, and the classic clinical manifestations include infantile... 
Ataxia | Genetic aspects | Research | Gene mutations | Pediatric research | Biological transport | Genes | Epilepsy | Physiological aspects | Glucose | Dextrose | Genotype & phenotype | Convulsions & seizures | Gait | Biomarkers | Electroencephalography | Mutation | Microcephaly | Patients | SLC2A1 gene | movement disorder | ketogenic diet | Glucose transporter type 1 deficiency syndrome | Case Report
Journal Article
Molecular Genetics and Metabolism Reports, ISSN 2214-4269, 03/2017, Volume 10, Issue C, pp. 67 - 74
We generated an adeno-associated virus (AAV) vector in which the human gene was expressed under the synapsin I promoter (AAV-h ) and examined if AAV-h... 
Adeno-associated virus (AAV) | SLC2A1 | GLUT1 | Glucose transporter I deficiency syndrome (GLUT1DS) | Gene therapy | NONHUMAN-PRIMATES | GLUT1 DEFICIENCY | TRANSDUCTION | CEREBROSPINAL-FLUID | KETOGENIC DIET | METABOLISM | GENETICS & HEREDITY | NEURONS | GLUCOSE-TRANSPORTER PROTEINS | NATIONWIDE SURVEY | BRAIN DELIVERY
Journal Article