| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Romain Favre, Grégoire Moutel, Nathalie Duchange, Christophe Vayssière, Monique Kohler, Nicole Bouffet, Marie-Christine Hunsinger, Anne Kohler, Cécile Mager, Muriel Neumann, Christine Vayssière, Brigitte Viville, Christian Hervé, Israel Nisan. What about informed consent in first-trimester ultrasound screening for Down syndrome? Fetal diagnosis and therapy. vol 23. issue 3. 2008-06-04. PMID:18417975. |
we evaluate the level of information and informed consent given for the screening of down syndrome (ds) before the first-trimester ultrasound scan. |
2008-06-04 |
2023-08-12 |
Not clear |
| George P Henry, David W Britt, Mark I Evan. Screening advances and diagnostic choice: the problem of residual risk. Fetal diagnosis and therapy. vol 23. issue 4. 2008-06-04. PMID:18417998. |
data on down syndrome (ds) births for colorado from 1989 to 2005 were used to examine the implications of a decreasing use of amniocentesis. |
2008-06-04 |
2023-08-12 |
Not clear |
| Barbara Hämmerle, Carina Elizalde, Francisco J Tejedo. The spatio-temporal and subcellular expression of the candidate Down syndrome gene Mnb/Dyrk1A in the developing mouse brain suggests distinct sequential roles in neuronal development. The European journal of neuroscience. vol 27. issue 5. 2008-06-03. PMID:18364031. |
it is widely accepted that the neurological alterations in down syndrome (ds) are principally due to modifications in developmental processes. |
2008-06-03 |
2023-08-12 |
mouse |
| Bradley McPherson, Sandy Pui-Shan Lai, Kevin Kwong-Ki Leung, Iris Hoi-Yee N. Hearing loss in Chinese school children with Down syndrome. International journal of pediatric otorhinolaryngology. vol 71. issue 12. 2008-05-30. PMID:17936369. |
there is well-documented evidence in the literature concerning a high prevalence of deafness in children with down syndrome (ds). |
2008-05-30 |
2023-08-12 |
Not clear |
| Shirley Ramos da Rosa Utiyama, Renato Mitsunori Nisihara, Flávia Raphaela Nass, Nanci P Oliveira, Patrícia T Fiedler, Iara Taborda de Messias-Reaso. Autoantibodies in patients with Down syndrome: early senescence of the immune system or precocious markers for immunological diseases? Journal of paediatrics and child health. vol 44. issue 4. 2008-05-27. PMID:17927730. |
down syndrome (ds) patients present several immunological disturbances, with high rates of infections, malignancies and autoimmune phenomena. |
2008-05-27 |
2023-08-12 |
Not clear |
| Juan J Alio, Jose Lorenzo, Carmen Iglesia. Cranial base growth in patients with Down syndrome: a longitudinal study. American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics. vol 133. issue 5. 2008-05-27. PMID:18456147. |
the purpose of this study was to assess the growth of the cranial base in a sample of patients diagnosed with down syndrome (ds). |
2008-05-27 |
2023-08-12 |
Not clear |
| Jacques M Lignon, Zoë Bichler, Bruno Hivert, François E Gannier, Pierre Cosnay, José A del Rio, Danièle Migliore-Samour, Claire O Maléco. Altered heart rate control in transgenic mice carrying the KCNJ6 gene of the human chromosome 21. Physiological genomics. vol 33. issue 2. 2008-05-22. PMID:18303085. |
congenital heart defects (chd) are common in down syndrome (ds, trisomy 21). |
2008-05-22 |
2023-08-12 |
mouse |
| Donald E Kuhn, Gerard J Nuovo, Mickey M Martin, Geraldine E Malana, Adam P Pleister, Jinmai Jiang, Thomas D Schmittgen, Alvin V Terry, Katheleen Gardiner, Elizabeth Head, David S Feldman, Terry S Elto. Human chromosome 21-derived miRNAs are overexpressed in down syndrome brains and hearts. Biochemical and biophysical research communications. vol 370. issue 3. 2008-05-22. PMID:18387358. |
down syndrome (ds), or trisomy 21, is the most common genetic cause of cognitive impairment and congenital heart defects in the human population. |
2008-05-22 |
2023-08-12 |
human |
| Fabian Fernandez, Craig C Garne. Episodic-like memory in Ts65Dn, a mouse model of Down syndrome. Behavioural brain research. vol 188. issue 1. 2008-05-19. PMID:17950473. |
ts65dn mice, like individuals with down syndrome (ds), demonstrate a functional dissociation between explicit and implicit forms of memory, showing selective impairment in explicit or declarative learning tasks. |
2008-05-19 |
2023-08-12 |
mouse |
| Rubén López-Pérez, S Aida Borges-Yáñez, Patricia López-Morale. Anterior open bite and speech disorders in children with Down syndrome. The Angle orthodontist. vol 78. issue 2. 2008-05-14. PMID:18251613. |
to estimate the prevalence and to determine if there is an association between anterior open bite and the presence of speech disorders in a group of mexican children with down syndrome (ds). |
2008-05-14 |
2023-08-12 |
Not clear |
| Sonia Palminiello, Elizabeth Kida, Kulbir Kaur, Marius Walus, Krystyna E Wisniewski, Teresa Wierzba-Bobrowicz, Ausma Rabe, Giorgio Albertini, Adam A Golabe. Increased levels of carbonic anhydrase II in the developing Down syndrome brain. Brain research. vol 1190. 2008-05-06. PMID:18083150. |
by using a proteomic approach, we found increased levels of carbonic anhydrase ii (ca ii) in the brain of ts65dn mice, a mouse model for down syndrome (ds). |
2008-05-06 |
2023-08-12 |
mouse |
| Maria Cristina Caselli, Laura Monaco, Manuela Trasciani, Stefano Vicar. Language in Italian children with Down syndrome and with specific language impairment. Neuropsychology. vol 22. issue 1. 2008-05-02. PMID:18211153. |
this article compares lexical and grammatical abilities of a mental-age-matched sample of italian preschoolers with down syndrome (ds), specific language impairment (sli), or typical development. |
2008-05-02 |
2023-08-12 |
Not clear |
| Disha Banerjee, Krishnadas Nandagopa. Potential interaction between the GARS-AIRS-GART Gene and CP2/LBP-1c/LSF transcription factor in Down syndrome-related Alzheimer disease. Cellular and molecular neurobiology. vol 27. issue 8. 2008-05-01. PMID:17902044. |
(1) gars-airs-gart is an important candidate gene in studies of down syndrome (ds)-related alzheimer's disease (ad), due to its chromosomal localization (21q22.1) in the down syndrome critical region, involvement in de novo purine biosynthesis, and over-expression in ds brain. |
2008-05-01 |
2023-08-12 |
human |
| Sharon Knoll, Malvin Janal, Ahmed Khoch. Radiographic assessment of periodontitis in African-Americans with Down syndrome. Journal of the International Academy of Periodontology. vol 10. issue 1. 2008-04-28. PMID:18333596. |
down syndrome (ds) is a neurodevelopmental genetic disorder affecting millions of americans. |
2008-04-28 |
2023-08-12 |
Not clear |
| Ana Cristina Borges Oliveira, Saul Martins Paiva, Mônica Rodrigues Campos, Dina Czeresni. Factors associated with malocclusions in children and adolescents with Down syndrome. American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics. vol 133. issue 4. 2008-04-28. PMID:18405808. |
our aims in this study were to determine the prevalence of malocclusion stemming from vertical or transversal occlusal alterations in subjects with down syndrome (ds) and the associations with individual, socioeconomic, and behavioral factors. |
2008-04-28 |
2023-08-12 |
human |
| David P Black, Beth A Smith, Jianhua Wu, Beverly D Ulric. Uncontrolled manifold analysis of segmental angle variability during walking: preadolescents with and without Down syndrome. Experimental brain research. vol 183. issue 4. 2008-04-25. PMID:17717659. |
in this study we applied the ucm analysis to gait and to a population known for exhibiting high levels of performance variability, down syndrome (ds). |
2008-04-25 |
2023-08-12 |
Not clear |
| Jan-Henning Klusmann, Ursula Creutzig, Martin Zimmermann, Michael Dworzak, Norbert Jorch, Claudia Langebrake, Arnulf Pekrun, Katarina Macakova-Reinhardt, Dirk Reinhard. Treatment and prognostic impact of transient leukemia in neonates with Down syndrome. Blood. vol 111. issue 6. 2008-04-25. PMID:18182574. |
approximately 10% of the neonates with down syndrome (ds) exhibit a unique transient leukemia (tl). |
2008-04-25 |
2023-08-12 |
Not clear |
| Damien J Keating, Daphne Dubach, Mark P Zanin, Yong Yu, Katherine Martin, Yu-Feng Zhao, Chen Chen, Sílvia Porta, Maria L Arbonés, Laureane Mittaz, Melanie A Pritchar. DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease. Human molecular genetics. vol 17. issue 7. 2008-04-17. PMID:18180251. |
genes located on chromosome 21, over-expressed in down syndrome (ds) and alzheimer's disease (ad) and which regulate vesicle trafficking, are strong candidates for involvement in ad neuropathology. |
2008-04-17 |
2023-08-12 |
mouse |
| Sheng-Wen Shaw, Chih-Ping Chen, Po-Jen Cheng, Tzu-Hao Wang, Jia-Woei Hou, Cheng-Tao Lin, Shuenn-Dhy Chang, Hsiao-Lin Hwa, Ju-Li Lin, An-Shine Chao, Yung-Kuei Soong, Fon-Jou Hsie. Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome. Journal of human genetics. vol 53. issue 2. 2008-04-15. PMID:18074101. |
only 4% of down syndrome (ds) cases have a robertsonian translocation (rob). |
2008-04-15 |
2023-08-12 |
Not clear |
| David Keinan, Patricia Smith, Uri Zilberma. Prenatal growth acceleration in maxillary deciduous canines of children with Down syndrome: histological and chemical composition study. Archives of oral biology. vol 52. issue 10. 2008-04-14. PMID:17570340. |
the study was carried out on exfoliated or extracted maxillary primary canines of children with down syndrome (ds) and cerebral palsy (cp) and they were compared to a control group of children with no adverse medical history. |
2008-04-14 |
2023-08-12 |
Not clear |