| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sara Laura Vimercati, Manuela Galli, Chiara Rigoldi, Andrea Ancillao, Giorgio Albertin. Feedback reliance during an arm-tapping task with obstacle avoidance in adults with Down syndrome. Experimental brain research. vol 226. issue 4. 2013-11-05. PMID:23529511. |
in subjects with down syndrome (ds), the study of the wrist's trajectory during an arm-tapping task revealed feedback-based corrections designed to reduce the degree of discrepancy between the position of the limb and the target, leading to the assumption that performers with ds have problems with movement planning and feedforward control. |
2013-11-05 |
2023-08-12 |
human |
| Donna M Wilcock, W Sue T Griffi. Down's syndrome, neuroinflammation, and Alzheimer neuropathogenesis. Journal of neuroinflammation. vol 10. 2013-11-05. PMID:23866266. |
down syndrome (ds) is the result of triplication of chromosome 21 (trisomy 21) and is the prevailing cause of mental retardation. |
2013-11-05 |
2023-08-12 |
Not clear |
| b' Noem\\xc3\\xad Rueda, Jes\\xc3\\xbas Fl\\xc3\\xb3rez, Carmen Mart\\xc3\\xadnez-Cu\\xc3\\xa. Apoptosis in Down\'s syndrome: lessons from studies of human and mouse models. Apoptosis : an international journal on programmed cell death. vol 18. issue 2. 2013-10-29. PMID:23224708.' |
down syndrome (ds) is the most common chromosomal abnormality in humans. |
2013-10-29 |
2023-08-12 |
mouse |
| Mehran Ahmadlou, Masoud Gharib, Sahel Hemmati, Roshanak Vameghi, Firoozeh Sajed. Disrupted small-world brain network in children with Down Syndrome. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 124. issue 9. 2013-10-29. PMID:23583023. |
to explore how the global organization or topology of the functional brain connectivity (fbc) is affected in down syndrome (ds). |
2013-10-29 |
2023-08-12 |
Not clear |
| Alejandro González-Agüero, Angel Matute-Llorente, Alba Gómez-Cabello, José A Casajús, Germán Vicente-Rodrígue. Effects of whole body vibration training on body composition in adolescents with Down syndrome. Research in developmental disabilities. vol 34. issue 5. 2013-10-22. PMID:23474995. |
the present study aimed to determine the effect of 20 weeks of whole body vibration (wbv) on the body composition of adolescents with down syndrome (ds). |
2013-10-22 |
2023-08-12 |
Not clear |
| Anna Ashworth, Catherine M Hill, Annette Karmiloff-Smith, Dagmara Dimitrio. Cross syndrome comparison of sleep problems in children with Down syndrome and Williams syndrome. Research in developmental disabilities. vol 34. issue 5. 2013-10-22. PMID:23475007. |
based on previous findings of frequent sleep problems in children with down syndrome (ds) and williams syndrome (ws), the present study aimed to expand our knowledge by using parent report and actigraphy to define sleep problems more precisely in these groups. |
2013-10-22 |
2023-08-12 |
Not clear |
| Yannick Courbois, Emily K Farran, Axelle Lemahieu, Mark Blades, Hursula Mengue-Topio, Pascal Sockee. Wayfinding behaviour in Down syndrome: a study with virtual environments. Research in developmental disabilities. vol 34. issue 5. 2013-10-22. PMID:23528440. |
the aim of this study was to assess wayfinding abilities in individuals with down syndrome (ds). |
2013-10-22 |
2023-08-12 |
human |
| Susan M Gribble, Frances K Wiseman, Stephen Clayton, Elena Prigmore, Elizabeth Langley, Fengtang Yang, Sean Maguire, Beiyuan Fu, Diana Rajan, Olivia Sheppard, Carol Scott, Heidi Hauser, Philip J Stephens, Lucy A Stebbings, Bee Ling Ng, Tomas Fitzgerald, Michael A Quail, Ruby Banerjee, Kai Rothkamm, Victor L J Tybulewicz, Elizabeth M C Fisher, Nigel P Carte. Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome. PloS one. vol 8. issue 4. 2013-10-22. PMID:23596509. |
down syndrome (ds) is caused by trisomy of chromosome 21 (hsa21) and presents a complex phenotype that arises from abnormal dosage of genes on this chromosome. |
2013-10-22 |
2023-08-12 |
mouse |
| Sergey I Nikolaev, Federico Santoni, Anne Vannier, Emilie Falconnet, Emanuela Giarin, Giuseppe Basso, Alexander Hoischen, Joris A Veltman, Jurgen Groet, Dean Nizetic, Stylianos E Antonaraki. Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome. Blood. vol 122. issue 4. 2013-10-22. PMID:23733339. |
some neonates with down syndrome (ds) are diagnosed with self-regressing transient myeloproliferative disorder (tmd), and 20% to 30% of those progress to acute megakaryoblastic leukemia (amkl). |
2013-10-22 |
2023-08-12 |
Not clear |
| Cristina Claret, Albert Goday, David Benaiges, Juan J Chillarón, Juana A Flores, Elisa Hernandez, Josep M Corretger, Juan F Can. Subclinical hypothyroidism in the first years of life in patients with Down syndrome. Pediatric research. vol 73. issue 5. 2013-10-18. PMID:23403803. |
subclinical hypothyroidism (sh), defined as mild thyroid-stimulating hormone (tsh) elevation with normal free thyroxine (ft4) levels and no symptoms, is common during the first few years of life in down syndrome (ds) and can be self-limiting. |
2013-10-18 |
2023-08-12 |
Not clear |
| I Acikbas, A G Tomatir, B Akdag, A Koksa. Retrospective analysis of live birth prevalence of children with Down syndrome in Denizli, Turkey. Genetics and molecular research : GMR. vol 11. issue 4. 2013-10-17. PMID:23079965. |
down syndrome (ds) is the most frequent chromosome abnormality among live births. |
2013-10-17 |
2023-08-12 |
Not clear |
| T Patterson, C M Rapsey, P Glu. Systematic review of cognitive development across childhood in Down syndrome: implications for treatment interventions. Journal of intellectual disability research : JIDR. vol 57. issue 4. 2013-10-17. PMID:23506141. |
there is conjecture regarding the profile of cognitive development over time in children with down syndrome (ds). |
2013-10-17 |
2023-08-12 |
Not clear |
| Jeffrey P Solzak, Yun Liang, Feng C Zhou, Randall J Rope. Commonality in Down and fetal alcohol syndromes. Birth defects research. Part A, Clinical and molecular teratology. vol 97. issue 4. 2013-10-17. PMID:23554291. |
down syndrome (ds) and fetal alcohol syndrome (fas) are two leading causes of birth defects with phenotypes ranging from craniofacial abnormalities to cognitive impairment. |
2013-10-17 |
2023-08-12 |
Not clear |
| Ann Steele, Gaia Scerif, Kim Cornish, Annette Karmiloff-Smit. Learning to read in Williams syndrome and Down syndrome: syndrome-specific precursors and developmental trajectories. Journal of child psychology and psychiatry, and allied disciplines. vol 54. issue 7. 2013-10-17. PMID:23718731. |
less is understood about how early reading develops in children with neurodevelopmental disorders who display specific profiles of linguistic strengths and weaknesses, such as down syndrome (ds) and williams syndrome (ws). |
2013-10-17 |
2023-08-12 |
Not clear |
| Michele Salemi, Concetta Barone, Carmelo Romano, Federico Ridolfo, Cataldo Scavuzzo, Rita Anna Cantarella, Maria Grazia Salluzzo, Aldo E Calogero, Corrado Romano, Paolo Bosc. KIF21A mRNA expression in patients with Down syndrome. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 34. issue 4. 2013-09-26. PMID:22968744. |
down syndrome (ds) is a chromosomal disorder caused by chromosome 21 trisomy and is the most frequent genetic cause of intellectual disability. |
2013-09-26 |
2023-08-12 |
human |
| Márcia R Amorim, Marcelo A Costa Lim. MTRR 66A>G polymorphism as maternal risk factor for Down syndrome: a meta-analysis. Genetic testing and molecular biomarkers. vol 17. issue 1. 2013-09-25. PMID:23094987. |
down syndrome (ds) is the most common cause of mental retardation. |
2013-09-25 |
2023-08-12 |
Not clear |
| R L Silva-Grecco, G C Navarro, R M Cruz, M A S Balari. Micronucleated lymphocytes in parents of Down syndrome children. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas. vol 45. issue 7. 2013-09-24. PMID:22527126. |
down syndrome (ds) is the most common disease due to an autosomal aneuploidy in live born children and also the major known genetic cause of mental retardation. |
2013-09-24 |
2023-08-12 |
human |
| Nancy Miodrag, Sophie E Silverberg, Richard C Urbano, Robert M Hodap. Deaths among children, adolescents, and young adults with Down syndrome. Journal of applied research in intellectual disabilities : JARID. vol 26. issue 3. 2013-09-24. PMID:23580207. |
although life expectancies in down syndrome (ds) have doubled over the past 3-4 decades, there continue to be many early deaths. |
2013-09-24 |
2023-08-12 |
Not clear |
| Jeroen C Vis, Marielle G Duffels, Pepijn Mulder, Rianne H A C M de Bruin-Bon, Berto J Bouma, Rolf M F Berger, Elke S Hoendermis, Arie P J van Dijk, Barbara J M Mulde. Prolonged beneficial effect of bosentan treatment and 4-year survival rates in adult patients with pulmonary arterial hypertension associated with congenital heart disease. International journal of cardiology. vol 164. issue 1. 2013-09-23. PMID:21723630. |
in this study we evaluated 4 years treatment effect of bosentan on exercise capacity and quality of life and survival rates in 64 adult patients with pah associated with chd, including patients with down syndrome (ds). |
2013-09-23 |
2023-08-12 |
Not clear |
| Flávia Aline Silva Jesuino, José Valladares-Net. Craniofacial morphological differences between Down syndrome and maxillary deficiency children. European journal of orthodontics. vol 35. issue 1. 2013-09-23. PMID:21911842. |
maxillary deficiency is one of the facial features of down syndrome (ds). |
2013-09-23 |
2023-08-12 |
human |