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| 1 | Molecular charac- terization of isoniazid-resist ant Mycobacterium tuberculosis clinical strainsi solated in the Philippines显示文摘 | HERRER AL V AL VERDE A SAIZP | 2004 | Inl J Antimicrob Agents2004，23，6： | 1 |
| 2 | A study of Jacobians in Hardy-Orlicz spaces显示文摘 | IWANIEC T VERDE A | 1999 | Proc Roy Soc Edinburgh Sect1999，3，129： | 1 |
| 3 | Schistosoma mansoni:Characterization of p50,an immunophilin显示文摘 | Osman A Kiang D Verde PTL | 1995 | Exp Parasitol1995，80，： | 1 |
| 4 | Isolated celiac and superior mesenteric artery dissection identified with MDCT: imaging findings and clinical course显示文摘 | Verde F Bleich KB Oshmyansky A | 2012 | J Comput Assist Tomogr2012，36，： | 1 |
| 5 | Genetic linkage mapping in peach using morphological,RFLP and RAPD markers显示文摘 | RAJAPAKSE S BELTHOFF L E HE G ESTAGER A E SCORZA R VERDE I BALLARD R E BAIRD W V CALLAHAN A MONET R ABBOTT A G | 1995 | Theor Appl Genet1995，90，： | 1 |
| 6 | CMOS-MEMS resonators: from devices to applications 显示文摘 | URANGA A VERD J BARNIOL N | 2015 | Mieroelectronic Engineering2015，132，： | 1 |
| 7 | Duode- nal injuries due to trauma:Review of the literature显示文摘 | Garcia Santos E Soto Srnchez A Verde JM | 2015 | Cir Esp2015，93，2： | 1 |
| 8 | Genetic analysis of agronomic traits and genetic linkage mapping in a BC1 peach population using RFLPs and RAPDs显示文摘 | QUARTA R DETTORI M T VERDE I GENTILE A BRODA Z | 1998 | Acta Horticulturae1998，465，： | 1 |
| 9 | Environmental assessment of polycyclic aromatic hydrocarbons (PAHs) in surface sedimentsof file Santander Bay, Northern Spain 显示文摘 | VIGURI J VERDE J IRABIEN A | 2002 | Chemosphere2002，48，2： | 1 |
| 10 | Construction of a saturated linkage map for Prunus using an almondxpeach F2 progeny显示文摘 | JOBEUR T VIRUEL M A DE VICENTE M C JAUREGUI B BALLESTER J DETTORI M T VERDE I TRUCO M J MESSEGUER R BATLLE I QUARTA R DIRLEWANGER E ARUS P | 1998 | Theor Appl Genet1998，97，： | 1 |
| 11 | Assessing the value of an- other cycle in Gaussian process surrogate-based optimization显示文摘 | Queipo N V Verde A Pintos S | 2009 | Structural and Multidisciplinary Optimization2009，39，5： | 1 |
| 12 | Effects of weight loss and exercise training on natural killer cell activity in obese women显示文摘 | SCANGA C B VERDE T J PAOLONE A M | 1995 | Med Sci Sport Exe1995，27，： | 1 |
| 13 | The high-quality draft genome of peach(Prunus persica) identifies unique patterns of genetic diversity,domestication and genome evolution显示文摘 | International Peach Genome Initiative Verde I Abbott A G | 2013 | Nature Genetics2013，45，5： | 1 |
| 14 | 显示文摘 | Verdes C Chantrell R W Satoh A | 2006 | J Magn Magn Mater2006，304，： | 1 |
| 15 | Role of endothel in in the control of peripherd vascular tone in human hypertension显示文摘 | Taddei S Verd is A Chiadoni L | 2001 | Heart FailRev2001，6，4： | 1 |
| 16 | Envrionmental assessmentof polycyclic aromatic hydrocarbons(PAHs)in surfacesediments of the Santander Bay,Northern Spain显示文摘 | Viguri J Verde J Irabien A | 2002 | Chemosphere2002，48，： | 1 |
| 17 | Gluten immunogenic peptide excretion detects dietary transgressions in treated celiac disease patients显示文摘BACKGROUND Life-long removal of gluten from the diet is currently the only way to manage celiac disease(CeD). Until now, no objective test has proven useful to objectively detect ingested gluten in clinical practice. Recently, tests that determine consumption of gluten by assessing excretion of gluten immunogenic peptides(GIP) in stool and urine have been developed. Their utility, in comparison with conventional dietary and analytical follow-up strategies, has not been fully established.AIM To assess the performance of enzyme-linked immunosorbent assay(ELISA) and point-of-care tests(PoCTs) for GIP excretion in CeD patients on gluten-free diet(GFD).METHODS We conducted an observational, prospective, cross-sectional study in patients following a GFD for at least two years. Using the Gastrointestinal Symptom Rating Scale questionnaire, patients were classified at enrollment as asymptomatic or symptomatic. Gluten consumption was assessed twice by 3-d dietary recall and GIP excretion(by ELISA in stool and PoCTs(commercial kits for stool and urine) in two consecutive samples. These samples and dietary reports were obtained 10 day apart one from the other. Patients were encouraged to follow their usual GFD during the study period.RESULTS Forty-four patients were enrolled, of which 19(43.2%) were symptomatic despite being on a GFD. Overall, 83 sets of stool and/or urine samples were collected.Eleven out of 44 patients(25.0%) had at least one positive GIP test. The occurrence of at least one positive test was 32% in asymptomatic patients compared with 15.8% in symptomatic patients. GIP was concordant with dietary reports in 65.9% of cases(Cohen′s kappa: 0.317). PoCT detected dietary indiscretions. Both ELISA and PoCT in stool were concordant(concomitantly positive or negative) in 67 out of 74(90.5%) samples. Excretion of GIP was detected in 7(8.4%) stool and/or urine samples from patients considered to be strictly compliant with the GFD by dietary reports.CONCLUSION GIP detects dietary transgressions in patients on long-term GFD, irrespective of the presence of symptoms. PoCT for GIP detection constitutes a simple homebased method for self-assessment of dietary indiscretions. | Ana Florencia Costa Emilia Sugai María de la Paz Temprano Sonia Isabel Niveloni Horacio Vázquez María Laura Moreno M.Remedios Domínguez-Flores Alba Mu?oz-Suano Edgardo Smecuol Juan Pablo Stefanolo Andrea F González Angel Cebolla-Ramirez Eduardo Mauri?o Elena F Verdú Julio César Bai | 2019 | World Journal of Gastroenterology2019，25，11： | 1 |
| 18 | In vivo study of magnesium plate and screw degradation and bone fracture healing显示文摘 | Chaya A Yoshizawa S Verdelis K | 2015 | Acta biomaterialia2015，18，： | 1 |
| 19 | Environmental assessment of polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Santander Bay,Northern Spain显示文摘 | VERDE J IRABIEN A | 2002 | Chemosphere2002，48，2： | 1 |
| 20 | Investigating the specificity of peptide adsorption on gold using molecular dynamics simulations 显示文摘 | VERDE A V ACRES J M MARAN AS J K | 2009 | Biomacromolecules2009，10，8： | 1 |
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