|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Structural Basis for Neurofibromatosis Type 2显示文摘 | Shimizu T Seto A Malta N | 2002 | J Biol Chem J Biol Chem2002，277，10： | 1 |
| 2 | A meta-analysis of structural brain abnormalities in PTSD显示文摘 | Karl A Schaefer M Malta LS Dorfel D Rohleder N Werner A | 2006 | Neurosci Biobehav Rev2006，30，： | 1 |
| 3 | A combinatorial extracellular matrix platform identifies cell-extracellular matrix inter- actions that correlate with metastasis显示文摘 | Reticker-Flyrm N E Malta D F Winslow M M | 2012 | Nat Commun2012，3，： | 1 |
| 4 | Relationship between bone mineral density and androgen-deprivation therapy in Japanese prostate cancer patients显示文摘 | Yuasa T Malta S Tsuchiya N | 2010 | Urology2010，75，5： | 1 |
| 5 | Genetic activities in micronuclei:Is the DNA entrapped in micronuclei lost for the cell?显示文摘 | Mariona Terradas Malta Martl' n Laura Tusell | 2010 | Mutation Research2010，705，： | 1 |
| 6 | Use of amniotic membrane in trabeculectomy for the treatment of glaucoma: a pilot study 显示文摘 | Eliezer RN Kasahara N Caixeta-Umbelino C Pinheiro RK Mandia C Jr Malta RF | 2006 | Arq Bras Oflalmol2006，69，3： | 1 |
| 7 | Structural and clinical implications of amino acid substitutions in aipha-L-iduronidase: insight into the basis of mucopolysaccharidosis type I 显示文摘 | Saito S Ohno K Malta N | 2014 | Mol Genet Metab2014，111，2： | 1 |
| 8 | Sources and distribution of aliphatie and polyaromatic hydrocarbons in coastal sediments from the Ushuaia Bay(Tierra del Fuego, Patagonia, Argentina)显示文摘 | Malta G C Marina L N Oscar A | 2012 | Marine Envi- ronmental Research2012，74，3： | 1 |
| 9 | The ALSFRS-R: a re- vised ALS functional rating scale that incorporates assessments of respiratory function显示文摘 | Cedarbaum JM Stambler N Malta E | 1999 | J Neurol Sci1999，69，： | 1 |
| 10 | Nano-fibers composite vanadium oxide/polyaniline: synthesis and characterization of an electro-active anisotropic structure显示文摘 | MALTA M LOUARN G ERRIEN N | 2003 | Electrochem Commun2003，5，12： | 1 |
| 11 | Decreased prevalence of celiac disease among Brazilian elderly显示文摘AIM: To evaluate the prevalence of celiac disease in a group of Brazilian individuals over 60 years of age and compare it with the previously known prevalence in a pediatric group living in the same geographical area.METHODS: The research protocol was approved by the Ethics Committee of the University of Brasilia School of Medicine, Brasilia, Brazil. Blood samples from 946 individuals (295 male and 651 female) aged 60 years or older were collected between May 2010 and July 2011. The study subjects' mean and median ages were 68.1 and 67 years, respectively, ranging from 60 to 92 years. That age distribution closely corresponded to the age distribution of the Brazilian population according to the Brazilian 2010 census. The participants were consecutive and unselected outpatients undergoing blood tests at the University of Brasilia Hospital's Clinical Pathology Laboratory. All sera were tested for immunoglobulin A anti-transglutaminase antibodies (IgA-tTG) by enzymelinked immunosorbent assay, and those that were positive were further tested for immunoglobulin A antiendomysium antibodies (IgA-EMA). Human leukocyte antigen (HLA) genotyping was performed for all individuals who exhibited positive serologic results for IgA-tTG and/or IgA-EMA.RESULTS: Out of the 946 studied patients, only one previously diagnosed case of biopsy-proven celiac disease was detected. For the remaining subjects, nine serum samples tested positive for IgA-tTG antibodies; however, none of them tested positive for IgA-EMA antibodies. The HLA genotyping of those nine subjects revealed that one was carrying DQA1*0501 and two were carrying DQB1*0201 alleles. These data showed that, among those 946 elderly individuals, the prevalence of celiac disease (CD) was 0.1% (95%CI: 0.00-0.59). The prevalence of CD for the elderly group was compared with that observed for the group of 2034 children younger than 15 years (age range, 1-14 years; mean age, 8 years) who took part in our previous CD prevalence screening study. All the children came from the same geographical region and shared a similar ethnic and low-income background. As in the elderly group in the current study, the younger group was made up of consecutive outpatients who underwent blood evaluation at the University of Brasilia Hospital's Clinical Laboratory. The prevalence of biopsy-proven CD among those children was 0.54% (95%CI: 0.27-0.57). The comparative analysis between the two groups resulted in the following values: odds ratio = 0.19 (95%CI: 0.01-1.45) Fisher testP = 0.06. CONCLUSION: The prevalence of CD among the children of our previous study was 5.4 times higher than that found in the present elderly group. | Lucas Malta Almeida Luiz Claudio Castro Rosa Harumi Uenishi Fernanda Coutinho de Almeida Patricia Maria Fritsch Lenora Gandolfi Riccardo Pratesi Yanna Karla de Medeiros Nóbrega | 2013 | World Journal of Gastroenterology2013，19，12： | 0 |
| 12 | 镧系离子间无辐射能量传递速率的教程综述显示文摘在本教程综述中,我们重新阐述和表达了镧系离子间无辐射能量传递(ET)速率的理论形式,并且强调了考虑镧系离子本身特异性所引发的与Förster和Dexter理论不同之处。所给出的表达式遵循了Judd-Ofelt的4f-4f跃迁理论框架之下的Kushida方法,并计入了如下电多极机制:偶极-偶极(W_(d-d))、偶极-四极(W_(d-q))和四极-四极(W_(q-q))。更为重要的是,当前的机制也扩展包括了交换(W_(ex))和磁偶极子-磁偶极子(W_(md-md))作用,并经过改进进一步包含了屏蔽效应以及给出了F因子(费米黄金规则中的态密度)的解析表达式。与Kushida的原始方法类似,我们只考虑了强制电偶极子(FED)对Judd-Ofelt强度参数的贡献,并细节性地讨论了磁偶极-磁偶极相互作用的选择定则以及相关矩阵元的计算。此外,我们还以Tb(Ⅲ)-Eu(Ⅲ)和Yb(Ⅲ)-Er(Ⅲ)的能量传递速率计算为例,逐步展示了计算过程、主要的计算支撑信息以及所使用的计算脚本。 | Albano N Carneiro Neto Renaldo T Moura Jr Jorge A A Coelho Mauro E Silva-Junior Janderson L Costa Oscar L Malta Ricardo L Longo | 2022 | 发光学报2022，43，12： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员