María Salinas Lacasta

Dr. María Salinas Lacasta

Laboratory Medicine, Clinical Biochemistry, Laboratory Management, University of Miguel Hernandez, Alicante, Spain

Research Focus & Metrics

Academic Career Length

43Years (1984-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2006 in Maternal and Child Health Journal
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Journal Article
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PTPamela L. Thornton
Pamela L. Thornton
EKEdith C. Kieffer
Edith C. Kieffer
YSYamir Salabarría-Peña
Yamir Salabarría-Peña
AOAngela Odoms-Young
Angela Odoms-Young
SWSharla K. Willis
Sharla K. Willis
María Salinas LacastaMaría Salinas Lacasta
María Salinas Lacasta

29 June 2007 in Health Education & Behavior
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Journal Article
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EPEdith A. Parker
Edith A. Parker
BIBarbara A. Israel
Barbara A. Israel
TRThomas G. Robins
Thomas G. Robins
GMGraciela Mentz
Graciela Mentz
XLXihong Lin
Xihong Lin
TLToby C. Lewis
Toby C. Lewis
This article describes the evaluation of a community-based participatory research (CBPR) community health worker (CHW) intervention to improve children's asthma-related health by reducing household environmental triggers for asthma. After randomization to an intervention or control group, 298 households in Detroit, Michigan, with a child, aged 7 to 11, with persistent asthma symptoms participated. The intervention was effective in increasing some of the measures of lung function (daily nadir Forced Expiratory Volume at one second [p = .03] and daily nadir Peak Flow [p = .02]), reducing the frequency of two symptoms (“cough that won't go away,” “coughing with exercise”), reducing the proportion of children requiring unscheduled medical visits and reporting inadequate use of asthma controller medication, reducing caregiver report of depressive symptoms, reducing concentrations of dog allergen in the dust, and increasing some behaviors related to reducing indoor environmental triggers. The results suggest a CHW environmental intervention can improve children's asthma-related health, although the pathway for improvement is complex.

1 January 2007 in Journal of Adolescent Health
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Journal Article
Closed access
ACAlison Chapple
Alison Chapple
María Salinas LacastaMaría Salinas Lacasta
María Salinas Lacasta
SZSue Ziebland
Sue Ziebland
AMAnn McPherson
Ann McPherson
AMAidan Macfarlane
Aidan Macfarlane

23 October 2007 in Psycho-Oncology
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Journal Article
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SHShona Hilton
Shona Hilton
KHKate Hunt
Kate Hunt
CECarol Emslie
Carol Emslie
María Salinas LacastaMaría Salinas Lacasta
María Salinas Lacasta
SZSue Ziebland
Sue Ziebland

7 October 2009 in Cerebral Cortex
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Journal Article
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PBP. Berbel
P. Berbel
DND. Navarro
D. Navarro
EAEva Ausó
Eva Ausó
Emilio VareaEmilio Varea
Emilio Varea
ARA. E. Rodriguez
A. E. Rodriguez
GEG. Morreale de Escobar
G. Morreale de Escobar
Hypothyroxinemia affects 35–50% of neonates born prematurely (12% of births) and increases their risk of suffering neurodevelopmental alterations. We have developed an animal model to study the role of maternal thyroid hormones (THs) at the end of gestation on offspring's cerebral maturation. Pregnant rats were surgically thyroidectomized at embryonic day (E) 16 and infused with calcitonin and parathormone (late maternal hypothyroidism [LMH] rats). After birth, pups were nursed by normal rats. Pups born to LMH dams, thyroxine treated from E17 to postnatal day (P) 0, were also studied. In developing LMH pups, the cortical lamination was abnormal. At P40, heterotopic neurons were found in the subcortical white matter and in the hippocampal stratum oriens and alveus. The Zn-positive area of the stratum oriens of hippocampal CA3 was decreased by 41.5% showing altered mossy fibers’ organization. LMH pups showed delayed learning in parallel to decreased phosphorylated cAMP response element-binding protein (pCREB) and phosphorylated extracellular signal-regulated kinase 1/2 (pERK1/2) expression in the hippocampus. Thyroxine treatment of LMH dams reverted abnormalities. In conclusion, maternal THs are still essential for normal offspring's neurodevelopment even after onset of fetal thyroid function. Our data suggest that thyroxine treatment of premature neonates should be attempted to compensate for the interruption of the maternal supply.

1 October 1997 in Annals of the Rheumatic Diseases
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Journal Article
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María Salinas LacastaMaría Salinas Lacasta
María Salinas Lacasta
JRJosé Rosas
José Rosas
JIJosé Iborra
José Iborra
HMHerminia Manero
Herminia Manero
EPEliseo Pascual
Eliseo Pascual
OBJECTIVE To determine the precision and agreement of synovial fluid (SF) cell counts done manually and with automated counters, and to determine the degree of variability of the counts in SF samples, kept in the tubes used for routine white blood cell (WBC) counts—which use liquid EDTA as anticoagulant—at 24 and 48 hours at 4°C, and at room temperature. METHODS To determine precision, cell counts were repeated 10 times—both manually and by an automated counter—in a SF sample of low, medium, and high cellularity. The variances were calculated to determine the interobserver variation in two manual (M1,M2) and two automated cell counts (C1,C2). The agreement between a manual (M1) and automated counter (C1) results, was analysed by the Bland and Altman method and the difference against the mean of the two methods was plotted. Then, the mean difference between the two methods was estimated and the standard deviation of the difference. To determine the effects of storage, SF samples were kept in a refrigerator at 4°C, and at room temperature; cell counts were done manually (M1) and automatically (C1) at 24 and 48 hours and the changes analysed by the Bland and Altman method. The variances were compared using an F test. RESULTS (1) Precision. With the manual technique, the coefficients of variation were 27.9%, 14%, and 10.7% when used for counting the SF with low (270), medium (6200), and high cellularities (25 000). With the automated technique the coefficients of variation were 20%, 3.4%, and 2.9% in the same SF samples. In the fluids of medium and high cellularity, the variances of the automated cell counts were significatively lower (F test, p<0.002) than those of the manual counts. (2) Interobserver variation. The variance between C1 and C2 (25 SF) was significatively lower (F test, p<0.002) than that of the manual counts (41 SF). (3) Agreement between the two techniques (100 SF). For cellularities above 2000 cells/mm3, the manual method gave results between +10% to −34% of the results obtained by the coulter. For cellularities below 2000 cells/mm3, manual cell counts were between +60 to −1280 cells/mm3 of those obtained by the automated counter. (4) Influence of storage. The coulter counts of SF samples preserved at 4°C showed less variance (F test, p<0.05) than the manual counts. The worst results were obtained in manual counts of SF samples kept at room temperature; these samples at 48 hours showed a variation between −47% to 42% of the initial results. CONCLUSIONS Automated cell count of the SF offers advantages: it gives higher precision and consumes less time. The stability of the samples preserved in the EDTA tubes used for routine WBC counts is of additional interest, because if delay cannot be avoided, the results of the WBC counts are still accurate at 24 and even at 48 hours, at least for clinical purposes.