87 research outputs found
Deborah Halperin on West Bloomington\u27s Food Desert
Judith Valente, WGLT, spoke to Debra Halperin about the food desert that exists in west Bloomington, and how community organizations are working to make a difference. Debra Haperin is the director of the Action Research Center (ARC) at Illinois Wesleyan University and a member of the West Bloomington Revitalization Project (WBRP)
Daynali Flores-Rodriguez and ISU student Stephanie Rodriguez, January 18, 2018
Judith Valente, from WGLT, interviewed IWU Professor Daynali Flores-Rodriguez and ISU student Stephanie Rodriguez, about the state of Puerto Rico after Hurricane Maria. Both have relatives who live in Puerto Rico
Does phonological overlap of cognate words modulate cognate acquisition and processing in developing and skilled readers?
Very few studies exist on the role of cross-language similarities in cognate word
acquisition. Here we sought to explore, for the first time, the interplay of orthography (O) and
phonology (P) during the early stages of cognate word acquisition, looking at children and
adults with the same level of foreign language proficiency, and by using two variants of the
word-association learning paradigm (auditory learning method vs. auditory + written method).
Eighty participants (forty children and forty adults, native speakers of European Portuguese
[EP]), learned a set of EP-Catalan cognate words and non-cognate words. Among the cognate
words, the degree of orthographic and phonological similarity was manipulated. Half of the
children and adult participants learned the new words via an L2 auditory and written-L1 word
association method, while the other half learned the same words only through an L2 auditoryL1
word association method. Both groups were tested in an auditory recognition task and a
go/no-go lexical decision task. Results revealed a disadvantage for children in comparison to
adults, which was reduced in the auditory learning method. Furthermore, there was an
advantage for cognates relative to non-cognates regardless of the age of participants.
Importantly, there were modulations in cognate word processing as a function of the degree of
O and P overlap which were restricted to children. The findings are discussed in light of the
most relevant bilingual models of word recognition.This research was conducted at the Psychology Research Centre (UID/PSI/01662/2013),
University of Minho, and was funded by the FCT (Foundation for Science and Technology)
through the state budget, with reference IF / 00784/2013 / CP1158 / CT0013. The study has
also been partially supported by the FCT and the EP Ministry of Science, Technology and
Higher Education through national funds, and co-financed by FEDER through
COMPETE2020 under the PT2020 Partnership Agreement (POCI-01-0145-FEDER-007653).
It has also been partially supported by the Spanish Ministry of Economy and Competitiveness
(PCIN-2015-165-C02-02).info:eu-repo/semantics/publishedVersio
Combining gamma with Alpha and Beta power modulation for enhanced cortical mapping in patients with focal epilepsy
About one third of patients with epilepsy have seizures refractory to the medical treatment. Electrical stimulation mapping (ESM) is the gold standard for the identification of "eloquent" areas prior to resection of epileptogenic tissue. However, it is time-consuming and may cause undesired side effects. Broadband gamma activity (55-200 Hz) recorded with extraoperative electrocorticography (ECoG) during cognitive tasks may be an alternative to ESM but until now has not proven of definitive clinical value. Considering their role in cognition, the alpha (8-12 Hz) and beta (15-25 Hz) bands could further improve the identification of eloquent cortex. We compared gamma, alpha and beta activity, and their combinations for the identification of eloquent cortical areas defined by ESM. Ten patients with intractable focal epilepsy (age: 35.9 ± 9.1 years, range: 22-48, 8 females, 9 right handed) participated in a delayed-match-to-sample task, where syllable sounds were compared to visually presented letters. We used a generalized linear model (GLM) approach to find the optimal weighting of each band for predicting ESM-defined categories and estimated the diagnostic ability by calculating the area under the receiver operating characteristic (ROC) curve. Gamma activity increased more in eloquent than in non-eloquent areas, whereas alpha and beta power decreased more in eloquent areas. Diagnostic ability of each band was close to 0.7 for all bands but depended on multiple factors including the time period of the cognitive task, the location of the electrodes and the patient's degree of attention to the stimulus. We show that diagnostic ability can be increased by 3-5% by combining gamma and alpha and by 7.5-11% when gamma and beta were combined. We then show how ECoG power modulation from cognitive testing can be used to map the probability of eloquence in individual patients and how this probability map can be used in clinical settings to optimize ESM planning. We conclude that the combination of gamma and beta power modulation during cognitive testing can contribute to the identification of eloquent areas prior to ESM in patients with refractory focal epilepsy.info:eu-repo/semantics/publishedVersio
Chromosomal evolution trends of the genus Panstrongylus (Hemiptera, Reduviidae), vectors of Chagas disease
Association of Mortality and Risk of Epilepsy With Type of Acute Symptomatic Seizure After Ischemic Stroke and an Updated Prognostic Model
IMPORTANCE: Acute symptomatic seizures occurring within 7 days after ischemic stroke may be associated with an increased mortality and risk of epilepsy. It is unknown whether the type of acute symptomatic seizure influences this risk. OBJECTIVE: To compare mortality and risk of epilepsy following different types of acute symptomatic seizures. DESIGN, SETTING, AND PARTICIPANTS: This cohort study analyzed data acquired from 2002 to 2019 from 9 tertiary referral centers. The derivation cohort included adults from 7 cohorts and 2 case-control studies with neuroimaging-confirmed ischemic stroke and without a history of seizures. Replication in 3 separate cohorts included adults with acute symptomatic status epilepticus after neuroimaging-confirmed ischemic stroke. The final data analysis was performed in July 2022. EXPOSURES: Type of acute symptomatic seizure. MAIN OUTCOMES AND MEASURES: All-cause mortality and epilepsy (at least 1 unprovoked seizure presenting >7 days after stroke). RESULTS: A total of 4552 adults were included in the derivation cohort (2547 male participants [56%]; 2005 female [44%]; median age, 73 years [IQR, 62-81]). Acute symptomatic seizures occurred in 226 individuals (5%), of whom 8 (0.2%) presented with status epilepticus. In patients with acute symptomatic status epilepticus, 10-year mortality was 79% compared with 30% in those with short acute symptomatic seizures and 11% in those without seizures. The 10-year risk of epilepsy in stroke survivors with acute symptomatic status epilepticus was 81%, compared with 40% in survivors with short acute symptomatic seizures and 13% in survivors without seizures. In a replication cohort of 39 individuals with acute symptomatic status epilepticus after ischemic stroke (24 female; median age, 78 years), the 10-year risk of mortality and epilepsy was 76% and 88%, respectively. We updated a previously described prognostic model (SeLECT 2.0) with the type of acute symptomatic seizures as a covariate. SeLECT 2.0 successfully captured cases at high risk of poststroke epilepsy. CONCLUSIONS AND RELEVANCE: In this study, individuals with stroke and acute symptomatic seizures presenting as status epilepticus had a higher mortality and risk of epilepsy compared with those with short acute symptomatic seizures or no seizures. The SeLECT 2.0 prognostic model adequately reflected the risk of epilepsy in high-risk cases and may inform decisions on the continuation of antiseizure medication treatment and the methods and frequency of follow-up
International AIDS Society global scientific strategy: towards an HIV cure 2016
Antiretroviral therapy is not curative. Given the challenges in providing life-long therapy to a global population of over 35 million people living with HIV, there is intense interest in developing a cure for HIV infection. The International AIDS Society convened a group of international experts to develop a scientific strategy for research towards an HIV cure. This Perspective summarizes the group's strategy
Fifteen years of research on oral–facial–digital syndromes: from 1 to 16 causal genes
Oral–facial–digital syndromes (OFDS) gather rare genetic disorders characterised by facial, oral and digital abnormalities associated with a wide range of additional features (polycystic kidney disease, cerebral malformations and several others) to delineate a growing list of OFDS subtypes. The most frequent, OFD type I, is caused by a heterozygous mutation in the OFD1 gene encoding a centrosomal protein. The wide clinical heterogeneity of OFDS suggests the involvement of other ciliary genes. For 15 years, we have aimed to identify the molecular bases of OFDS. This effort has been greatly helped by the recent development of whole-exome sequencing (WES). Here, we present all our published and unpublished results for WES in 24 cases with OFDS. We identified causal variants in five new genes (C2CD3, TMEM107, INTU, KIAA0753 and IFT57) and related the clinical spectrum of four genes in other ciliopathies (C5orf42, TMEM138, TMEM231 and WDPCP) to OFDS. Mutations were also detected in two genes previously implicated in OFDS. Functional studies revealed the involvement of centriole elongation, transition zone and intraflagellar transport defects in OFDS, thus characterising three ciliary protein modules: the complex KIAA0753-FOPNL-OFD1, a regulator of centriole elongation; the Meckel-Gruber syndrome module, a major component of the transition zone; and the CPLANE complex necessary for IFT-A assembly. OFDS now appear to be a distinct subgroup of ciliopathies with wide heterogeneity, which makes the initial classification obsolete. A clinical classification restricted to the three frequent/well-delineated subtypes could be proposed, and for patients who do not fit one of these three main subtypes, a further classification could be based on the genotype
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