X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (56) 56
index medicus (54) 54
male (40) 40
female (32) 32
child, preschool (31) 31
clinical neurology (24) 24
infant (24) 24
child (23) 23
mutation (22) 22
pediatrics (22) 22
mutations (20) 20
autoimmune diseases of the nervous system - genetics (17) 17
genetics & heredity (17) 17
nervous system malformations - genetics (17) 17
infant, newborn (15) 15
adolescent (14) 14
article (14) 14
adult (13) 13
aicardi-goutieres syndrome (11) 11
aicardi-goutières syndrome (11) 11
children (11) 11
magnetic resonance imaging (11) 11
risk factors (11) 11
leukodystrophy (10) 10
samhd1 (10) 10
genetic aspects (9) 9
leukoencephalopathy (9) 9
phenotype (9) 9
aicardi–goutières syndrome (8) 8
basal ganglia (8) 8
interferon (8) 8
interferon-alpha (8) 8
young adult (8) 8
autoimmune diseases of the nervous system - immunology (7) 7
brain (7) 7
disorders (7) 7
gene (7) 7
genetics (7) 7
infants (7) 7
infection (7) 7
nervous system malformations - immunology (7) 7
neurology (7) 7
neurosciences (7) 7
research (7) 7
systemic-lupus-erythematosus (7) 7
age (6) 6
autoimmune diseases of the nervous system - diagnosis (6) 6
calcification (6) 6
congenital infection (6) 6
disease (6) 6
follow-up studies (6) 6
gene mutations (6) 6
genes (6) 6
nervous system malformations - diagnosis (6) 6
pregnancy (6) 6
ribonuclease h - genetics (6) 6
trex1 (6) 6
adenosine deaminase - genetics (5) 5
biological response modifiers (5) 5
birth weight (5) 5
brain - pathology (5) 5
calcinosis - genetics (5) 5
case-control studies (5) 5
dna mutational analysis (5) 5
exodeoxyribonucleases - genetics (5) 5
genotype (5) 5
genotype & phenotype (5) 5
gestational age (5) 5
obstetrics & gynecology (5) 5
progressive familial encephalopathy (5) 5
prospective studies (5) 5
surveys and questionnaires (5) 5
analysis (4) 4
atrophy (4) 4
autoimmune diseases of the nervous system - pathology (4) 4
autoimmunity (4) 4
basal ganglia diseases - genetics (4) 4
biomarkers (4) 4
cerebral calcification (4) 4
cerebral-palsy (4) 4
child development - physiology (4) 4
diagnosis (4) 4
duchenne muscular dystrophy (4) 4
genetic association studies (4) 4
hereditary central nervous system demyelinating diseases - genetics (4) 4
interferonopathy (4) 4
intracranial calcification (4) 4
involvement (4) 4
logistic models (4) 4
lupus (4) 4
medical research (4) 4
mutation - genetics (4) 4
nervous system malformations - pathology (4) 4
phosphoproteins - genetics (4) 4
preterm infants (4) 4
proteins (4) 4
rna-binding proteins (4) 4
studies (4) 4
abridged index medicus (3) 3
adar1 (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Lancet Neurology, The, ISSN 1474-4422, 2013, Volume 12, Issue 12, pp. 1159 - 1169
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 5, pp. 503 - 509
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2012, Volume 44, Issue 11, pp. 1243 - 1248
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2009, Volume 41, Issue 7, pp. 829 - U89
Journal Article
by Crow, Y.J and Chase, D.S and Schmidt, J.L and Szynkiewicz, M and Forte, G.M.A and Gornall, H.L and Oojageer, A and Anderson, B and Pizzino, A and Helman, G and Abdel-Hamid, M.S and Abdel-Salam, G.M and Ackroyd, S and Aeby, A and Agosta, G and Albin, C and Allon-Shalev, S and Arellano, M and Ariaudo, G and Aswani, V and Babul-Hirji, R and Baildam, E.M and Bahi-Buisson, N and Bailey, K.M and Barnerias, C and Barth, M and Battini, R and Beresford, M.W and Bernard, G and Bianchi, M and de Villemeur, T.B and Blair, E.M and Bloom, M and Burlina, A.B and Carpanelli, M.L and Carvalho, D.R and Castro-Gago, M and Cavallini, A and Cereda, C and Chandler, K.E and Chitayat, D.A and Collins, A.E and Corcoles, C.S and Cordeiro, N.J.V and Crichiutti, G and Dabydeen, L and Dale, R.C and D'Arrigo, S and De Goede, C.G.E.L and de Laet, C and De Waele, L.M.H and Denzler, I and Desguerre, I and Devriendt, K and Di Rocco, M and Fahey, M.C and Fazzi, E and Ferrie, C.D and Figueiredo, A and Gener, B and Goizet, C and Gowrinathan, N.R and Gowrishankar, K and Hanrahan, D and Isidor, B and Kara, L and Khan, N and King, M.D and Kirk, E.P and Kumar, R and Lagae, L and Lanieu, P and Lauffer, H and Laugel, V and La Piana, R and Lim, M.J and Lin, J.P.S.M and Linnankivi, T and Mackay, M.T and Marom, D.R and Lourenco, C.M and McKee, S.A and Moroni, I and Morton, J.E.V and Moutard, M.L and Murray, K and Nabbout, R and Nampoothiri, S and Nunez-Enamorado, N and Oades, P.J and Olivieri, I and Ostergaard, J.R and Perez-Duenas, B and Prendiville, J.S and Ramesh, V and Rasmussen, M and Regal, L and Ricci, F and Rio, M and Knaap, M and ...
American Journal of Medical Genetics Part A, ISSN 1552-4825, 2015, Volume 167, Issue 2, pp. 296 - 312
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 5/2017, Volume 47, Issue 5, pp. 1490 - 1495
The aim of this retrospective study, with prospective data collection, was to correlate congenital cytomegalovirus (CMV) infection with autism spectrum... 
Pediatrics | Child and School Psychology | Neurosciences | Public Health | Neonate | Prevalence | Psychology | Congenital Cytomegalovirus | Autism spectrum disorder | DIAGNOSIS | PSYCHOLOGY, DEVELOPMENTAL | PREVENTION | SCALES | DISABILITIES | CMV | CHILDREN | Autism | Correlation | Congenital Impairments | Referral | Etiology | Pervasive Developmental Disorders | Special Health Problems | Infants | Foreign Countries | Communicable Diseases | Clinical Diagnosis | Incidence | Prospective Studies | Humans | Autism Spectrum Disorder - virology | Child, Preschool | Infant | Male | Cytomegalovirus Infections - complications | Cytomegalovirus Infections - psychology | Autism Spectrum Disorder - epidemiology | Female | Italy - epidemiology | Retrospective Studies | Cytomegalovirus Infections - congenital | Infant, Newborn | Psychological aspects | Complications and side effects | Demographic aspects | Pervasive developmental disorders | Cytomegalovirus infections | Research | Risk factors | Urine | Cytomegalovirus | Intensive care | Nuclear magnetic resonance--NMR | Congenital diseases | Fetuses | Autistic spectrum disorders | Infections | Hearing impairment | Autistic children | Virology | Infection | Preschool children | Diagnosis | Children | Health risk assessment | Age | Viral infections | Apoptosis | Child & adolescent psychiatry
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2016, Volume 20, Issue 4, pp. 604 - 610
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 10/2015, Volume 74, Issue 10, pp. 1931 - 1939
Journal Article