X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (68) 68
male (57) 57
index medicus (54) 54
female (53) 53
child (49) 49
adolescent (36) 36
child, preschool (30) 30
life sciences (27) 27
adult (25) 25
clinical neurology (21) 21
genetics & heredity (20) 20
infant (20) 20
young adult (20) 20
analysis (19) 19
children (19) 19
genetics (18) 18
pediatrics (16) 16
duchenne muscular dystrophy (15) 15
phenotype (15) 15
mutation (14) 14
follow-up studies (12) 12
neurology (12) 12
care and treatment (11) 11
muscular dystrophy, duchenne - physiopathology (11) 11
disease (10) 10
france (10) 10
infant, newborn (10) 10
medicine (10) 10
middle aged (9) 9
neurosciences (9) 9
prospective studies (9) 9
clinical trials (8) 8
patients (8) 8
research (8) 8
risk factors (8) 8
treatment outcome (8) 8
chromosome deletion (7) 7
epilepsy (7) 7
human genetics (7) 7
human health and pathology (7) 7
mental-retardation (7) 7
muscular dystrophy (7) 7
muscular dystrophy, duchenne - drug therapy (7) 7
mutations (7) 7
nutrition & dietetics (7) 7
[sdv.gen]life sciences [q-bio]/genetics (6) 6
aged (6) 6
case-control studies (6) 6
cohort studies (6) 6
diagnosis (6) 6
double-blind method (6) 6
dystrophy (6) 6
genomics (6) 6
intellectual disability - genetics (6) 6
magnetic resonance imaging (6) 6
medical research (6) 6
molecular biology (6) 6
multidisciplinary sciences (6) 6
muscular dystrophy, duchenne - complications (6) 6
neuromuscular diseases (6) 6
obesity (6) 6
pedigree (6) 6
physiological aspects (6) 6
proteins (6) 6
spinal muscular atrophy (6) 6
[ sdv.gen ] life sciences [q-bio]/genetics (5) 5
[sdv.gen.gh]life sciences [q-bio]/genetics/human genetics (5) 5
abridged index medicus (5) 5
biochemistry, molecular biology (5) 5
body composition (5) 5
developmental disabilities - genetics (5) 5
dna mutational analysis (5) 5
gene (5) 5
genetic aspects (5) 5
medical education (5) 5
metabolism (5) 5
molecular sequence data (5) 5
mutation - genetics (5) 5
research article (5) 5
retrospective studies (5) 5
science (5) 5
age (4) 4
age factors (4) 4
chromosomes, human, pair 15 - genetics (4) 4
clinical-trials (4) 4
comparative genomic hybridization (4) 4
corticosteroids (4) 4
creatine (4) 4
cytogenetics (4) 4
deletion (4) 4
development and progression (4) 4
dmd gene (4) 4
dystrophin - genetics (4) 4
gene deletion (4) 4
health aspects (4) 4
heterozygote (4) 4
medicine, experimental (4) 4
medicine, research & experimental (4) 4
mental disorders - genetics (4) 4
muscle (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Revue Neurologique, ISSN 0035-3787, 04/2018, Volume 174, pp. S179 - S179
Journal Article
Lancet, The, ISSN 0140-6736, 2015, Volume 385, Issue 9979, pp. 1748 - 1757
Journal Article
Nature Communications, ISSN 2041-1723, 05/2016, Volume 7, Issue 1, p. 11534
Journal Article
by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2017, Volume 16, Issue 7, pp. 513 - 522
Journal Article
Journal Article
by Grimaldi-Bensouda, L and Guillemot, D and Godeau, B and Bénichou, J and Lebrun-Frenay, C and Papeix, C and Labauge, P and Berquin, P and Penfornis, A and Benhamou, P.-Y and Nicolino, M and Simon, A and Viallard, J.-F and Costedoat-Chalumeau, N and Courcoux, M.F and Pondarré, C and Hilliquin, P and Chatelus, E and Foltz, V and Guillaume, S and Rossignol, M and Abenhaim, L and Abdelmoumni, Abdelhakim and Requeda, Elisabeth and Adoue, Daniel and Brassat, David and Aladjidi, Nathalie and Clet, Johanna and Lemasson, Gwendal and Perel, Yves and Vital, Anne and Allain-Launay, Emma and Bru, Marie and Thomas, Caroline and Altman, Jean-Jacques and Amsallem, Daniel and Aras, Nazmiye and Boukari, Latifato and Fain, Olivier and Letellier, Edouard and Lucidarme, Nadine and Arsène Mekinian, Mekinian and Anne-Sophie Morin, Morin and Stirnemann, Jérôme and Atlan, Catherine and Audry, Dominique and Augustin, Jérôme and Bartolucci, Pablo and Chevalier, Xavier and Khellaf, Mehdi and Limal, Nicolas and Mahevas, Matthieu and Méliksetyan, Gayane and Michel, Marc and Bayart, Sophie and Bonnet, Fabrice and Decaux, Olivier and Bekherraz, Amine and Brihaye, Benoit and Daugas, Eric and Hayem, Gilles and Meyer, Olivier and Papo, Thomas and Pasqualoni, Elisa and Sacre, Karim and Travert, Florence and Beltrand, Jacques and François Lefrere, Lefrere and Benveniste, Olivier and Bolgert, Francis and Paz, Raphael De and Demeret, Sophie and Fautrel, Bruno and Jacqueminet, Sophie and Louapre, Céline and Morel, Nathalie and Rigabert, Julie and Berger, Claire and Le Moing, Anne-Gaëlle and Besson, Gérard and Boutte, Célia and Casez, Olivier and Bonnotte, Bernard and Audia, Sylvain and Bossu-Estour, Cécile and Bourgarit, Anne and Dupuy, Alain and Keshmandt, Homa and Brac, Aude and Perrin, Agnès and Pondarré, Corinne and Villar-Fimbel, Sylvie and Bruckert, Isabelle and Cosson, Anne and Magy-Bertrand, Nadine and Tisserand, Guillaume and Camu, William and Carlander, Bertrand and Morales, Raul Juntas and Cances, Claude and ... and PGRx-AID Study Grp and PGRx-AID Study Group and the PGRx-AID Study Group
Journal of Internal Medicine, ISSN 0954-6820, 2014, Volume 275, Issue 4, pp. 398 - 408
Objectives The aim of this study was to investigate whether the quadrivalent human papillomavirus (HPV) vaccine Gardasil is associated with a change in the... 
Vaccine safety | Human papillomavirus | Systematic case-control study | Human papillomavirus vaccine | Autoimmune disorders | Vaccination | autoimmune disorders | SYSTEMIC-LUPUS-ERYTHEMATOSUS | IMMUNE THROMBOCYTOPENIC PURPURA | systematic case-control study | GUILLAIN-BARRE-SYNDROME | CHILDREN | vaccine safety | IMMUNIZATION | MEDICINE, GENERAL & INTERNAL | MULTIPLE-SCLEROSIS | DATABASE | human papillomavirus | SURVEILLANCE | INFLUENZA VACCINATION | human papillomavirus vaccine | DIAGNOSTIC-CRITERIA | vaccination | Autoimmune Diseases - epidemiology | France - epidemiology | Humans | Mass Vaccination - statistics & numerical data | Risk Factors | Autoimmune Diseases - immunology | Autoimmune Diseases - etiology | Case-Control Studies | Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18 | Incidence | Alphapapillomavirus | Young Adult | Connective Tissue Diseases - immunology | Papillomavirus Infections - prevention & control | Purpura, Thrombocytopenic, Idiopathic - immunology | Adolescent | Multiple Sclerosis - immunology | Papillomavirus Infections - immunology | Papillomavirus Vaccines - adverse effects | Adult | Female | Diabetes Mellitus, Type 1 - immunology | Papillomavirus Vaccines - administration & dosage | Papillomaviruses | AIDS vaccines | Guillain-Barre syndrome | Type 1 diabetes | Analysis | Oral contraceptives | Life Sciences
Journal Article
Human mutation, ISSN 1059-7794, 08/2019
Calcium (Ca ) acts as a ubiquitous second messenger, and normal cell and tissue physiology strictly depends on the precise regulation of Ca entry, storage and... 
Journal Article
Brain : a journal of neurology, ISSN 0006-8950, 08/2019, Volume 142, Issue 10, pp. 3009 - 3027
N-methyl d-aspartate receptors are ligand-gated ionotropic receptors mediating a slow, calcium-permeable component of excitatory synaptic transmission in the... 
Journal Article