All Relations between Down Syndrome and ds

Publication Sentence Publish Date Extraction Date Species
Alejandro González-Agüero, Ignacio Ara, Luis A Moreno, Germán Vicente-Rodríguez, José A Casajú. Fat and lean masses in youths with Down syndrome: gender differences. Research in developmental disabilities. vol 32. issue 5. 2011-10-19. PMID:21435834. the present study aimed at comparing fat and lean masses between children and adolescents with and without down syndrome (ds) and evaluating the presence of sexual dimorphism. 2011-10-19 2023-08-12 human
A González-Agüero, G Vicente-Rodríguez, I Ara, L A Moreno, J A Casajú. Accuracy of prediction equations to assess percentage of body fat in children and adolescents with Down syndrome compared to air displacement plethysmography. Research in developmental disabilities. vol 32. issue 5. 2011-10-19. PMID:21458950. from skinfold thickness compared to air displacement plethysmography (adp) in children and adolescents with down syndrome (ds). 2011-10-19 2023-08-12 Not clear
Emiliano Brunamonti, Pierpaolo Pani, Odysseas Papazachariadis, Paolo Onorati, Giorgio Albertini, Stefano Ferrain. Cognitive control of movement in Down syndrome. Research in developmental disabilities. vol 32. issue 5. 2011-10-19. PMID:21482066. inhibition has been poorly investigated in down syndrome (ds) patients. 2011-10-19 2023-08-12 human
Melissa Lamar, Catherine M L Foy, Felix Beacher, Eileen Daly, Michaela Poppe, Nicola Archer, Vee Prasher, Kieran C Murphy, Robin G Morris, Andrew Simmons, Simon Lovestone, Declan G M Murph. Down syndrome with and without dementia: an in vivo proton Magnetic Resonance Spectroscopy study with implications for Alzheimer's disease. NeuroImage. vol 57. issue 1. 2011-10-19. PMID:21504795. it is poorly understood why people with down syndrome (ds) are at extremely high-risk of developing alzheimer's disease (ad) compared to the general population. 2011-10-19 2023-08-12 Not clear
Cintia Perez Duarte, Priscila Covre, Ana Claudia Braga, Elizeu Coutinho de Maced. Visuospatial support for verbal short-term memory in individuals with Down syndrome. Research in developmental disabilities. vol 32. issue 5. 2011-10-19. PMID:21530159. individuals with down syndrome (ds) tend to have impaired verbal short-term memory (stm), which persists even when visual support is provided for carrying out verbal tasks. 2011-10-19 2023-08-12 Not clear
Hannah Nash, James Heat. The role of vocabulary, working memory and inference making ability in reading comprehension in Down syndrome. Research in developmental disabilities. vol 32. issue 5. 2011-10-19. PMID:21536407. thirteen children and young adults with down syndrome (ds) completed tests of language and reading and their performance was compared to that of three control groups. 2011-10-19 2023-08-12 Not clear
Avni Y Joshi, Roshini S Abraham, Melissa R Snyder, Thomas G Boyc. Immune evaluation and vaccine responses in Down syndrome: evidence of immunodeficiency? Vaccine. vol 29. issue 31. 2011-10-18. PMID:21596078. patients with down syndrome (ds) appear to be at a greater risk for serious infections, but it is unclear whether this is due to anatomic variations or intrinsic immune defects. 2011-10-18 2023-08-12 Not clear
Daniela Melis, Rita Genesio, Gerarda Cappuccio, Virginia MariaGinocchio, Roberto Della Casa, Giuseppe Menna, Salvatore Buffardi, Vincenzo Poggi, Anna Leszle, Floriana Imperati, Massimo Carella, Antonella Izzo, Ennio Del Giudice, Lucio Nitsch, Generoso Andri. Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22. American journal of medical genetics. Part A. vol 155A. issue 7. 2011-10-14. PMID:21671372. the region 21q22 is considered crucial for the pathogenesis of both down syndrome (ds) and the partial monosomy 21q syndrome. 2011-10-14 2023-08-12 Not clear
Christina Frøslev-Friis, Karina Hjort-Pedersen, Carsten U Henriques, Lotte Nylandsted Krogh, Ester Garn. Improved prenatal detection of chromosomal anomalies. Danish medical bulletin. vol 58. issue 8. 2011-10-07. PMID:21827720. the aim of this study was to study the trends in prevalence and prenatal detection rates of chromosome anomalies and down syndrome (ds) over a 22-year period. 2011-10-07 2023-08-12 Not clear
Sandra Guidi, Elisabetta Ciani, Paola Bonasoni, Donatella Santini, Renata Bartesagh. Widespread proliferation impairment and hypocellularity in the cerebellum of fetuses with down syndrome. Brain pathology (Zurich, Switzerland). vol 21. issue 4. 2011-10-04. PMID:21040072. evidence in mouse models for down syndrome (ds) and human fetuses with ds clearly shows severe neurogenesis impairment in various telencephalic regions, suggesting that this defect may underlie the cognitive abnormalities of ds. 2011-10-04 2023-08-12 mouse
Laura Regueras, Pablo Prieto, María Teresa Muñoz-Calvo, Jesús Pozo, Lissette Arguinzoniz, Jesús Argent. [Endocrinological abnormalities in 1,105 children and adolescents with Down syndrome]. Medicina clinica. vol 136. issue 9. 2011-09-29. PMID:21306744. children and adolescents with down syndrome (ds) show a greater prevalence of endocrinological abnormalities when compared with the general population. 2011-09-29 2023-08-12 Not clear
L Ricc. Home literacy environments, interest in reading and emergent literacy skills of children with Down syndrome versus typical children. Journal of intellectual disability research : JIDR. vol 55. issue 6. 2011-09-26. PMID:21435070. the present study examined home literacy environments, children's interest in reading and emergent literacy skills of pre-school-aged children with down syndrome (ds; n=20), school-aged children with ds (n=17) and typically developing children (n=18) matched on chronological age with the younger ds group and mental age (ma) with the older ds group. 2011-09-26 2023-08-12 Not clear
Mireia Vilardell, Axel Rasche, Anja Thormann, Elisabeth Maschke-Dutz, Luis A Pérez-Jurado, Hans Lehrach, Ralf Herwi. Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processes. BMC genomics. vol 12. 2011-09-26. PMID:21569303. down syndrome (ds; trisomy 21) is the most common genetic cause of mental retardation in the human population and key molecular networks dysregulated in ds are still unknown. 2011-09-26 2023-08-12 human
Stamatis Agiovlasitis, Robert W Motl, Sushant M Ranadive, Christopher A Fahs, Huimin Yan, George H Echols, Lindy Rossow, Bo Fernhal. Energetic optimization during over-ground walking in people with and without Down syndrome. Gait & posture. vol 33. issue 4. 2011-09-14. PMID:21396824. individuals with down syndrome (ds) show reduced gait stability that may increase the metabolic rate (mr) during over-ground walking and alter their energetic cost per unit distance (ec(transport)) to speed relationship. 2011-09-14 2023-08-12 human
Jason Lockrow, Heather Boger, Heather Bimonte-Nelson, Ann-Charlotte Granhol. Effects of long-term memantine on memory and neuropathology in Ts65Dn mice, a model for Down syndrome. Behavioural brain research. vol 221. issue 2. 2011-09-09. PMID:20363261. the present study assessed the effects of both short- and long-term memantine treatment in a mouse model of down syndrome (ds), the ts65dn mouse. 2011-09-09 2023-08-12 mouse
Jerzy Wegiel, Cheng-Xin Gong, Yu-Wen Hwan. The role of DYRK1A in neurodegenerative diseases. The FEBS journal. vol 278. issue 2. 2011-09-09. PMID:21156028. recent studies indicate that the dual-specificity tyrosine phosphorylation-regulated kinase 1a (dyrk1a) gene, which is located on chromosome 21q22.2 and is overexpressed in down syndrome (ds), may play a significant role in developmental brain defects and in early onset neurodegeneration, neuronal loss and dementia in ds. 2011-09-09 2023-08-12 Not clear
Jennifer Landt, J Carlos D'Abrera, Anthony J Holland, Franklin I Aigbirhio, Tim D Fryer, Roberto Canales, Young T Hong, David K Menon, Jean-Claude Baron, Shahid H Zama. Using positron emission tomography and Carbon 11-labeled Pittsburgh Compound B to image Brain Fibrillar β-amyloid in adults with down syndrome: safety, acceptability, and feasibility. Archives of neurology. vol 68. issue 7. 2011-09-09. PMID:21403005. to investigate the safety, acceptability, and feasibility of positron emission tomography (pet) using carbon 11-labeled pittsburgh compound b ([(11)c]pib) to measure cerebral β-amyloid in adults with down syndrome (ds) and to explore if the technique differentiates between participants with and without alzheimer disease (ad). 2011-09-09 2023-08-12 human
Cao D Nguyen, Alberto C S Costa, Krzysztof J Cios, Katheleen J Gardine. Machine learning methods predict locomotor response to MK-801 in mouse models of down syndrome. Journal of neurogenetics. vol 25. issue 1-2. 2011-09-08. PMID:21391779. down syndrome (ds), caused by trisomy of human chromosome 21 (hsa21), is a common genetic cause of cognitive impairment. 2011-09-08 2023-08-12 mouse
Mara Dierssen, Gloria Arqué, Jerome McDonald, Nuria Andreu, Carmen Martínez-Cué, Jesús Flórez, Cristina Filla. Behavioral characterization of a mouse model overexpressing DSCR1/ RCAN1. PloS one. vol 6. issue 2. 2011-09-01. PMID:21364922. dscr1/ rcan1 is a chromosome 21 gene found to be overexpressed in the brains of down syndrome (ds) and postulated as a good candidate to contribute to mental disability. 2011-09-01 2023-08-12 mouse
Małgorzata Wójcik, Małgorzata Kumorowicz-Czoch, Marta Ciechanowska, Jerzy Starzy. [Autoimmune thyroid disease and type 1 diabetes mellitus in a 2-year-old girl with Down syndrome and congenital hypothyroidism--a case presentation]. Przeglad lekarski. vol 67. issue 11. 2011-08-30. PMID:21442978. autoimmune thyroid disease (aitd) and type 1 diabetes mellitus (dm1) are much more common in down syndrome (ds) in comparison to the general population. 2011-08-30 2023-08-12 Not clear