| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Maria Martzoukou, Anastasia Nousia, Theodoros Marini. Narrative Abilities of Adults' With Down Syndrome as a Window to Their Morphosyntactic, Socio-Cognitive, and Prosodic Abilities. Frontiers in psychology. vol 11. 2020-10-01. PMID:32982854. |
down syndrome (ds) is the most common developmental disorder characterized by mild to moderate intellectual disability. |
2020-10-01 |
2023-08-13 |
human |
| Osmar Aparecido Cuoghi, Francielle Topolski, Lorraine Perciliano de Faria, Carla Machado Occhiena, Nancy Dos Santos Pinto Ferreira, Camila Ribeiro Ferlin, Marcos Rogério de Mendonç. Prevalence of Dental Anomalies in Permanent Dentition of Brazilian Individuals with Down Syndrome. The open dentistry journal. vol 10. 2020-09-30. PMID:27733874. |
the aim of this study was to evaluate the incidence of dental anomalies in the permanent dentition of individuals with down syndrome (ds) to increase the knowledge on the dental issues in this syndrome. |
2020-09-30 |
2023-08-13 |
Not clear |
| James D Weisfeld-Adams, Amanda K Tkachuk, Kenneth N Maclean, Naomi L Meeks, Stuart A Scot. A NPJ genomic medicine. vol 1. 2020-09-30. PMID:27840696. |
a down syndrome (ds) is the most common genetic cause of intellectual disability (id) and in the majority of cases is the result of complete trisomy 21. |
2020-09-30 |
2023-08-13 |
Not clear |
| Jean-Maurice Delabar, Bernadette Allinquant, Diana Bianchi, Tom Blumenthal, Alain Dekker, Jamie Edgin, John O'Bryan, Mara Dierssen, Marie-Claude Potier, Frances Wiseman, Faycal Guedj, Nicole Créau, Roger Reeves, Katheleen Gardiner, Jorge Buscigli. Changing Paradigms in Down Syndrome: The First International Conference of the Trisomy 21 Research Society. Molecular syndromology. vol 7. issue 5. 2020-09-30. PMID:27867340. |
down syndrome (ds) is the most common genetic cause of intellectual disability (id) in humans with an incidence of ∼1:1,000 live births worldwide. |
2020-09-30 |
2023-08-13 |
human |
| Megan MacDonald, Jennifer Leichtman, Phil Esposito, Nicole Cook, Dale Allen Ulric. The Participation Patterns of Youth with Down Syndrome. Frontiers in public health. vol 4. 2020-09-30. PMID:27891498. |
the purpose of this paper was to investigate the participation patterns of children with down syndrome (ds) using the construct of participation as defined by the international classification of functioning disability and health (icf). |
2020-09-30 |
2023-08-13 |
Not clear |
| Fiorenza Stagni, Andrea Giacomini, Marco Emili, Sandra Guidi, Elisabetta Ciani, Renata Bartesagh. Epigallocatechin gallate: A useful therapy for cognitive disability in Down syndrome? Neurogenesis (Austin, Tex.). vol 4. issue 1. 2020-09-30. PMID:28203607. |
neurodevelopmental alterations and cognitive disability are constant features of down syndrome (ds), a genetic condition due to triplication of chromosome 21. |
2020-09-30 |
2023-08-13 |
Not clear |
| Mark Mims, Prasad John Thottam, Dennis Kitsko, Amber Shaffer, Sukgi Cho. Characterization of Sleep Architecture in Down Syndrome Patients Pre and Post Airway Surgery. Cureus. vol 9. issue 1. 2020-09-30. PMID:28229031. |
to define obstructive sleep architecture patterns in down syndrome (ds) children as well as changes to sleep architecture patterns postoperatively. |
2020-09-30 |
2023-08-13 |
Not clear |
| Régis Pochon, Claire Touchet, Laure Iberno. Emotion Recognition in Adolescents with Down Syndrome: A Nonverbal Approach. Brain sciences. vol 7. issue 6. 2020-09-30. PMID:28545237. |
several studies have reported that persons with down syndrome (ds) have difficulties recognizing emotions; however, there is insufficient research to prove that a deficit of emotional knowledge exists in ds. |
2020-09-30 |
2023-08-13 |
Not clear |
| Susan Helm, Morgan Blayney, Taylor Whited, Mahjabin Noroozi, Sen Lin, Semira Kern, David Green, Ahmad Saleh. Deleterious Effects of Chronic Folate Deficiency in the Ts65Dn Mouse Model of Down Syndrome. Frontiers in cellular neuroscience. vol 11. 2020-09-30. PMID:28649192. |
the most common cause of cognitive dysfunction in children is down syndrome (ds). |
2020-09-30 |
2023-08-13 |
mouse |
| Zheng Fan, Mihye Ahn, Heidi L Roth, Leping Li, Bradley V Vaugh. Sleep Apnea and Hypoventilation in Patients with Down Syndrome: Analysis of 144 Polysomnogram Studies. Children (Basel, Switzerland). vol 4. issue 7. 2020-09-30. PMID:28665356. |
patients with down syndrome (ds) are at risk for both obstructive sleep apnea (osa) and central sleep apnea (csa); however, it is unclear how these components evolve as patients age and whether patients are also at risk for hypoventilation. |
2020-09-30 |
2023-08-13 |
Not clear |
| Ni-Chung Lee, Yin-Hsiu Chien, Wuh-Liang Hw. A Review of Biomarkers for Alzheimer's Disease in Down Syndrome. Neurology and therapy. vol 6. issue Suppl 1. 2020-09-30. PMID:28733957. |
down syndrome (trisomy 21; ds) is a unique disease known to be associated with early-onset alzheimer's disease (ad). |
2020-09-30 |
2023-08-13 |
Not clear |
| Carolina Grego Del Cole, Sheila Cavalcante Caetano, Wagner Ribeiro, Arthur Melo E E Kümmer, Andrea Parolin Jackowsk. Adolescent adaptive behavior profiles in Williams-Beuren syndrome, Down syndrome, and autism spectrum disorder. Child and adolescent psychiatry and mental health. vol 11. 2020-09-30. PMID:28747993. |
our main objective was to verify whether adaptive behavior profiles differ in three conditions-williams beuren syndrome (wbs), down syndrome (ds), and autism spectrum disorder (asd), as compared with healthy controls (hc) and with each other. |
2020-09-30 |
2023-08-13 |
Not clear |
| Momcilo Pavlovic, Karolina Berenji, Marko Bukuro. Screening of celiac disease in Down syndrome - Old and new dilemmas. World journal of clinical cases. vol 5. issue 7. 2020-09-30. PMID:28798921. |
epidemiologic studies confirmed that cd is highly associated with other autoimmune diseases and with down syndrome (ds). |
2020-09-30 |
2023-08-13 |
Not clear |
| Antonella Izzo, Rosanna Manco, Tiziana de Cristofaro, Ferdinando Bonfiglio, Rita Cicatiello, Nunzia Mollo, Marco De Martino, Rita Genesio, Mariastella Zannini, Anna Conti, Lucio Nitsc. Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses. International journal of genomics. vol 2017. 2020-09-30. PMID:29057256. |
dosage-dependent upregulation of most of chromosome 21 (hsa21) genes has been demonstrated in heart tissues of fetuses with down syndrome (ds). |
2020-09-30 |
2023-08-13 |
Not clear |
| Maria Chiara Pelleri, Chiara Cattani, Lorenza Vitale, Francesca Antonaros, Pierluigi Strippoli, Chiara Locatelli, Guido Cocchi, Allison Piovesan, Maria Caracaus. Integrated Quantitative Transcriptome Maps of Human Trisomy 21 Tissues and Cells. Frontiers in genetics. vol 9. 2020-09-30. PMID:29740474. |
down syndrome (ds) is due to the presence of an extra full or partial chromosome 21 (hsa21). |
2020-09-30 |
2023-08-13 |
human |
| Laura Traverso, Martina Fontana, Maria Carmen Usai, Maria C Passolungh. Response Inhibition and Interference Suppression in Individuals With Down Syndrome Compared to Typically Developing Children. Frontiers in psychology. vol 9. 2020-09-30. PMID:29780346. |
three groups took part in the study: 32 individuals with down syndrome (ds) with a mean age of 14 years and 4 months, 35 typically developing children 5 years of age (5td), and 30 typically developing children 6 years of age (6td). |
2020-09-30 |
2023-08-13 |
Not clear |
| Pawan Kumar, Inusha Panigrahi, Naveen Sankhyan, Chirag Ahuja, Prasoon K Goyad. Down Syndrome with Moyamoya Disease: A Case Series. Journal of pediatric neurosciences. vol 13. issue 2. 2020-09-30. PMID:30090136. |
down syndrome (ds), resulting from trisomy 21, is a common cause of mental retardation. |
2020-09-30 |
2023-08-13 |
Not clear |
| Macarena Gómez de Salazar, Cristina Grau, Francisco Ciruela, Xavier Altafa. Phosphoproteomic Alterations of Ionotropic Glutamate Receptors in the Hippocampus of the Ts65Dn Mouse Model of Down Syndrome. Frontiers in molecular neuroscience. vol 11. 2020-09-30. PMID:30140203. |
down syndrome (ds), the main genetic cause of intellectual disability, is associated with an imbalance of excitatory/inhibitory neurotransmitter systems. |
2020-09-30 |
2023-08-13 |
mouse |
| Tomoko Terai, Shohei Eda, Jun Sugasawa, Masahiro Tonari, Junko Matsuo, Hidehiro Oku, Tsunehiko Iked. Ocular findings in Japanese children with Down syndrome: the course of visual acuity and refraction, and systemic and ocular anomalies. Clinical ophthalmology (Auckland, N.Z.). vol 12. 2020-09-30. PMID:30214148. |
to investigate the age-related development of refractive errors and changes of visual acuity (va), and the systemic and ocular anomalies in japanese children and young adults with down syndrome (ds). |
2020-09-30 |
2023-08-13 |
Not clear |
| Laura Del Hoyo Soriano, Angela John Thurman, Leonard Abbedut. Specificity: A Phenotypic Comparison of Communication-Relevant Domains Between Youth With Down Syndrome and Fragile X Syndrome. Frontiers in genetics. vol 9. 2020-09-30. PMID:30327664. |
despite the shared presence of an intellectual disability (id), there is a growing literature documenting important phenotypic differences between down syndrome (ds) and fragile x syndrome (fxs). |
2020-09-30 |
2023-08-13 |
human |