X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1551) 1551
Publication (147) 147
Newspaper Article (35) 35
Book Chapter (15) 15
Book Review (11) 11
Magazine Article (4) 4
Dissertation (2) 2
Book / eBook (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1291) 1291
female (957) 957
microcephaly (684) 684
index medicus (639) 639
male (636) 636
pregnancy (492) 492
microcephaly - etiology (484) 484
infant, newborn (425) 425
infant (395) 395
child, preschool (348) 348
child (342) 342
microcephaly - genetics (340) 340
genetics & heredity (298) 298
pediatrics (275) 275
adult (240) 240
mutation (230) 230
zika virus (217) 217
animals (212) 212
adolescent (197) 197
microcephaly - complications (193) 193
clinical neurology (189) 189
syndrome (186) 186
microcephaly - pathology (163) 163
intellectual disability - genetics (161) 161
microcephaly - diagnosis (160) 160
phenotype (150) 150
intellectual disability - etiology (149) 149
magnetic resonance imaging (135) 135
microencephaly (132) 132
research (129) 129
brain (128) 128
genetic aspects (118) 118
microcephaly - epidemiology (115) 115
neurosciences (115) 115
infections (114) 114
zika virus infection - complications (113) 113
epilepsy (111) 111
brain - pathology (109) 109
zika virus infection - epidemiology (108) 108
genetics (104) 104
mutations (99) 99
analysis (98) 98
abnormalities, multiple - genetics (96) 96
pedigree (96) 96
children (90) 90
infants (89) 89
genes (88) 88
health aspects (88) 88
article (86) 86
congenital diseases (86) 86
diagnosis (85) 85
mice (84) 84
microcephaly - virology (83) 83
genetic disorders (81) 81
proteins (81) 81
brazil (80) 80
mental retardation (77) 77
intellectual disability (75) 75
risk factors (75) 75
medicine (73) 73
brain - abnormalities (72) 72
abridged index medicus (70) 70
epidemiology (70) 70
mental-retardation (67) 67
public health (67) 67
infection (66) 66
viruses (66) 66
birth defects (65) 65
diagnosis, differential (65) 65
growth (64) 64
microcephaly - physiopathology (64) 64
seizures (64) 64
age (63) 63
gene (63) 63
young adult (62) 62
microcephaly - diagnostic imaging (61) 61
retrospective studies (61) 61
fetuses (60) 60
facies (59) 59
medicine, general & internal (55) 55
consanguinity (54) 54
electroencephalography (54) 54
follow-up studies (54) 54
intellectual disability - diagnosis (54) 54
zika virus infection - virology (54) 54
epidemics (53) 53
gestational age (53) 53
zika virus infection - transmission (53) 53
disease (52) 52
chromosome deletion (51) 51
medical research (51) 51
patients (51) 51
brazil - epidemiology (50) 50
developmental disabilities - genetics (50) 50
guillain-barre syndrome (50) 50
intellectual disabilities (50) 50
infectious diseases (49) 49
neurology (48) 48
intellectual disability - complications (47) 47
tomography, x-ray computed (47) 47
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1444) 1444
French (33) 33
German (33) 33
Spanish (20) 20
Russian (15) 15
Italian (12) 12
Polish (12) 12
Japanese (9) 9
Chinese (5) 5
Portuguese (4) 4
Hungarian (3) 3
Czech (2) 2
Romanian (2) 2
Turkish (2) 2
Croatian (1) 1
Danish (1) 1
Dutch (1) 1
Finnish (1) 1
Hebrew (1) 1
Swedish (1) 1
Urdu (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
JAMA Neurology, ISSN 2168-6149, 12/2016, Volume 73, Issue 12, pp. 1407 - 1416
Journal Article
Archives of Disease in Childhood, ISSN 0003-9888, 06/2019, Volume 104, Issue Suppl 3, p. A350
Microcephaly is a developmental disorder in which the head circumference, measured as an occipitofrontal, is below the third circumferential, or at least 2... 
Journal Article
Journal Article
Best Practice & Research: Clinical Obstetrics & Gynaecology, ISSN 1521-6934, 2016, Volume 38, pp. 97 - 107
Cytomegalovirus (CMV) congenital infection affects 0.7% of live births worldwide and is the leading cause of congenital neurological handicap of infectious... 
Obstetrics and Gynecology | hyperimmune globulin | valaciclovir | cytomegalovirus | imaging | fetus | serology | TIME PCR QUANTIFICATION | MATERNAL INFECTION | OBSTETRICS & GYNECOLOGY | HEARING-LOSS | RISK-FACTOR | IGG AVIDITY | AMNIOTIC-FLUID SAMPLES | PREGNANT-WOMEN | 1ST TRIMESTER | CONGENITAL CYTOMEGALOVIRUS | PRENATAL-DIAGNOSIS | Oligohydramnios - diagnostic imaging | Porencephaly - etiology | Acyclovir - therapeutic use | Immunoglobulin G - blood | Humans | DNA, Viral - analysis | Cytomegalovirus Infections - complications | Lissencephaly - etiology | Antibodies, Viral - blood | Lissencephaly - diagnostic imaging | Hydrocephalus - diagnostic imaging | Female | Porencephaly - diagnostic imaging | Cytomegalovirus Infections - congenital | Amniotic Fluid - virology | Hydrops Fetalis - etiology | Pregnancy Complications, Infectious - diagnosis | Fetal Diseases - drug therapy | Ascites - etiology | Fetal Diseases - diagnosis | Acyclovir - analogs & derivatives | Antiviral Agents - therapeutic use | Valine - analogs & derivatives | Hydrops Fetalis - diagnostic imaging | Ascites - diagnostic imaging | Polyhydramnios - diagnostic imaging | Hydrocephalus - etiology | Microcephaly - diagnostic imaging | Cytomegalovirus Infections - diagnosis | Oligohydramnios - etiology | Seroconversion | Pregnancy | Polyhydramnios - etiology | Immunoglobulin M - blood | Cytomegalovirus Infections - drug therapy | Ultrasonography, Prenatal | Microcephaly - etiology | Pregnancy Complications, Infectious - drug therapy | Immunization, Passive | Valine - therapeutic use | Infectious Disease Transmission, Vertical - prevention & control | Cytomegalovirus infections | Pregnant women | Epidemiology | Health aspects
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2017, Volume 12, Issue 8, p. e0181791
The CASK gene (Xp11.4) is highly expressed in the mammalian nervous system and plays several roles in neural development and synaptic function.... 
CAUSE PONTOCEREBELLAR HYPOPLASIA | CYTOPLASMIC DYNEIN | SYNAPTIC FUNCTION | MENTAL-RETARDATION | REELIN | ARRAY-CGH | MULTIDISCIPLINARY SCIENCES | BRAIN-DEVELOPMENT | PHENOTYPE | NEURONS | DELETION | Guanylate Kinases - genetics | Microcephaly - genetics | Myristoylated Alanine-Rich C Kinase Substrate | Humans | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Cerebellum - abnormalities | Intellectual Disability - genetics | Point Mutation - genetics | Swine | Female | Nervous System Malformations - genetics | Child | Intracellular Signaling Peptides and Proteins - genetics | Dynactin Complex - genetics | Nervous System Malformations - etiology | Histone Deacetylase 2 - genetics | Genetic Predisposition to Disease - genetics | Membrane Proteins - genetics | Developmental Disabilities - etiology | Cytoplasmic Dyneins - genetics | Mutation - genetics | Animals | Adolescent | Microcephaly - etiology | Intellectual Disability - etiology | Inositol 1,4,5-Trisphosphate Receptors - genetics | Usage | Genetic disorders | Gene mutations | Exome sequencing | Research | Causes and theories of causation | Diseases | Cerebellum | Pediatrics | Histone deacetylase | Neurosciences | Nuclear magnetic resonance--NMR | Synaptogenesis | Intellectual disabilities | Genes | Nervous system | Genomes | Single-nucleotide polymorphism | Microcephaly | Kinases | Gene sequencing | Etiology | CASK gene | HDAC2 protein | Uncertainty analysis | Chromosomes | Transfer RNA | Hypoplasia | Pathogens | Medical research | Sex differences | Patients | Pathogenicity | Screening | Brain research | Microencephaly | Cytogenetics | Low density lipoprotein receptors | MARCKS protein | Mutation | Aberration | Females | Nuclear magnetic resonance | NMR
Journal Article
Current Neurology and Neuroscience Reports, ISSN 1528-4042, 8/2013, Volume 13, Issue 8, pp. 1 - 10
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 5/2017, Volume 32, Issue 6, pp. 543 - 549
Serine biosynthesis defects can present in a broad phenotypic spectrum ranging from Neu-Laxova syndrome, a lethal disease with multiple congenital anomalies at... 
microcephaly | seizures | spasticity | Neu-Laxova syndrome | PGDH | INTELLECTUAL DISABILITY | DISORDERS | PEDIATRICS | NEU-LAXOVA-SYNDROME | 3-PHOSPHOGLYCERATE | CHILD | CLINICAL NEUROLOGY | Limb Deformities, Congenital - genetics | Abnormalities, Multiple - etiology | Fetal Growth Retardation - diagnostic imaging | Microcephaly - genetics | Seizures - genetics | Ichthyosis - etiology | Humans | Brain Diseases - genetics | Carbohydrate Metabolism, Inborn Errors - complications | Child, Preschool | Limb Deformities, Congenital - therapy | Family Health | Fetal Growth Retardation - genetics | Infant | Male | Psychomotor Disorders - complications | Serine - biosynthesis | Carbohydrate Metabolism, Inborn Errors - genetics | Seizures - complications | Seizures - diagnostic imaging | Young Adult | Psychomotor Disorders - genetics | Ichthyosis - diagnostic imaging | Brain Diseases - therapy | Fetal Growth Retardation - etiology | Ichthyosis - genetics | Female | Microcephaly - therapy | Brain Diseases - etiology | Carbohydrate Metabolism, Inborn Errors - diagnostic imaging | Psychomotor Disorders - diagnostic imaging | Abnormalities, Multiple - genetics | Microcephaly - complications | Abnormalities, Multiple - diagnostic imaging | Brain Diseases - diagnostic imaging | Microcephaly - diagnostic imaging | Mutation - genetics | Fetal Growth Retardation - therapy | Phosphoglycerate Dehydrogenase - genetics | Phenotype | Abnormalities, Multiple - therapy | Limb Deformities, Congenital - etiology | Adolescent | Limb Deformities, Congenital - diagnostic imaging | Microcephaly - etiology | Phosphoglycerate Dehydrogenase - deficiency | Ichthyosis - therapy
Journal Article
PLoS Genetics, ISSN 1553-7390, 08/2013, Volume 9, Issue 8, p. e1003695
Journal Article
Brain, ISSN 0006-8950, 08/2016, Volume 139, Issue 8, pp. 2122 - 2130
Journal Article
Journal Article