X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1511) 1511
Publication (135) 135
Newsletter (127) 127
Newspaper Article (49) 49
Book Review (28) 28
Book Chapter (24) 24
Magazine Article (16) 16
Conference Proceeding (10) 10
Book / eBook (9) 9
Reference (4) 4
Web Resource (3) 3
Trade Publication Article (2) 2
Transcript (2) 2
Dissertation (1) 1
Video Recording (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1116) 1116
prader-willi syndrome (915) 915
male (627) 627
female (625) 625
index medicus (588) 588
child (518) 518
prader-willi-syndrome (425) 425
adolescent (393) 393
children (366) 366
adult (334) 334
endocrinology & metabolism (332) 332
prader-willi syndrome - drug therapy (331) 331
obesity (319) 319
pediatrics (303) 303
child, preschool (293) 293
prader-willi syndrome - complications (215) 215
human growth hormone - therapeutic use (207) 207
research (196) 196
prader-willi syndrome - physiopathology (193) 193
care and treatment (181) 181
prader-willi syndrome - genetics (181) 181
infant (172) 172
growth hormone (168) 168
body-composition (165) 165
somatotropin (158) 158
therapy (158) 158
medical research (149) 149
body mass index (147) 147
adults (142) 142
animals (141) 141
medicine, experimental (140) 140
genetics & heredity (137) 137
prader-willi syndrome - therapy (129) 129
health aspects (126) 126
prader-willi syndrome - diagnosis (126) 126
body composition (120) 120
diagnosis (112) 112
treatment outcome (104) 104
prader–willi syndrome (103) 103
analysis (99) 99
genetics (98) 98
physiological aspects (98) 98
young adult (95) 95
congenital, hereditary, and neonatal diseases and abnormalities (89) 89
prevalence (89) 89
psychiatry (88) 88
prader-willi syndrome - metabolism (84) 84
abridged index medicus (82) 82
behavior (82) 82
clinical neurology (82) 82
middle aged (82) 82
neurosciences (82) 82
genetic aspects (81) 81
nutritional and metabolic diseases (80) 80
rehabilitation (80) 80
genetic disorders (79) 79
infant, newborn (79) 79
adolescents (77) 77
prader-willi syndrome - psychology (76) 76
autism (74) 74
article (72) 72
drug therapy (72) 72
ghrelin (72) 72
growth-hormone treatment (72) 72
hyperphagia (72) 72
risk factors (72) 72
phenotype (71) 71
prader-willi syndrome - blood (71) 71
age (68) 68
growth hormone - therapeutic use (66) 66
body weight (65) 65
mice (65) 65
infants (63) 63
body-mass index (62) 62
dna methylation (62) 62
genomic imprinting (62) 62
prader-willi (60) 60
body composition - drug effects (59) 59
medicine (59) 59
review (59) 59
growth hormones (58) 58
human growth hormone - adverse effects (57) 57
sleep (52) 52
retrospective studies (51) 51
insulin (50) 50
mental retardation (50) 50
uniparental disomy (50) 50
brain (49) 49
usage (49) 49
disorders (48) 48
education, special (48) 48
gene expression (48) 48
growth (48) 48
obesity - complications (48) 48
obesity - etiology (48) 48
food-intake (47) 47
growth disorders - drug therapy (47) 47
nutrition & dietetics (47) 47
pharmacology & pharmacy (47) 47
scoliosis (47) 47
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1639) 1639
Japanese (19) 19
German (15) 15
Spanish (12) 12
French (11) 11
Polish (10) 10
Chinese (9) 9
Portuguese (5) 5
Danish (4) 4
Italian (4) 4
Korean (4) 4
Dutch (2) 2
Norwegian (2) 2
Swedish (2) 2
Turkish (2) 2
Afrikaans (1) 1
Hebrew (1) 1
Hungarian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Pediatric Neurology, ISSN 0887-8994, 2016, Volume 65, pp. 1 - 13
Abstract Neurogenetic developmental conditions (NDCs) represent a heterogeneous group of rare inherited disorders with neurological manifestation during... 
Pediatrics | Neurology | neurogenetic disorders | genetic diseases | developmental disorders | therapy | fragile X syndrome | RETT-SYNDROME | TREATABLE INBORN-ERRORS | CLINICAL NEUROLOGY | INTELLECTUAL DISABILITY | TUBEROUS SCLEROSIS COMPLEX | PHELAN-MCDERMID SYNDROME | MOUSE MODEL | DOWN-SYNDROME | FRAGILE-X-SYNDROME | PEDIATRICS | PRADER-WILLI-SYNDROME | GROWTH-FACTOR-I | Fragile X Syndrome - therapy | Humans | Autism Spectrum Disorder - therapy | Developmental Disabilities - genetics | Neurodevelopmental Disorders - genetics | Intellectual Disability - genetics | Tuberous Sclerosis - diagnosis | Down Syndrome - diagnosis | Genetic Testing - trends | Child | Developmental Disabilities - diagnosis | Autism Spectrum Disorder - diagnosis | Fragile X Syndrome - genetics | Autism Spectrum Disorder - genetics | Neurodevelopmental Disorders - therapy | Rett Syndrome - diagnosis | Treatment Outcome | Down Syndrome - therapy | Genetic Therapy - trends | Forecasting | Developmental Disabilities - therapy | Intellectual Disability - therapy | Tuberous Sclerosis - genetics | Tuberous Sclerosis - therapy | Enzyme Replacement Therapy - trends | Intellectual Disability - diagnosis | Down Syndrome - genetics | Rett Syndrome - genetics | Fragile X Syndrome - diagnosis | Neurodevelopmental Disorders - diagnosis | Rett Syndrome - therapy
Journal Article
Journal Article
Nature Reviews Endocrinology, ISSN 1759-5029, 02/2017, Volume 13, Issue 2, pp. 105 - 124
Journal Article
Genetics in Medicine, ISSN 1098-3600, 07/2010, Volume 12, Issue 7, pp. 385 - 395
Journal Article
Pediatrics, ISSN 0031-4005, 01/2011, Volume 127, Issue 1, pp. 195 - 204
Journal Article
Journal Article