Search Results - "VAQUERIZO, J"
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Catatonia in autism spectrum disorders: A systematic review and meta-analysis
Published in European psychiatry (01-01-2022)“…Catatonic features can appear in autism spectrum disorders (ASDs). There can be overlap in symptoms across catatonia and ASD. The overall aim of this review is…”
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Effect of montelukast added to inhaled budesonide on control of mild to moderate asthma
Published in Thorax (01-03-2003)“…Background: Proinflammatory leukotrienes, which are not completely inhibited by inhaled corticosteroids, may contribute to asthmatic problems. A 16 week…”
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SYNTHESIS AND MAGNETOELECTRIC CHARACTERIZATION OF COBALT FERRITE-BARIUM TITANATE COMPOSITES USING A NEW PULSED MAGNETIC FIELD METHOD
Published in Integrated ferroelectrics (01-11-2006)“…BaTiO 3 -CoFe 2 O 4 composites synthesized by the ceramic method showed a magnetoelectric effect. The CoFe 2 O 4 powders were synthesized by coprecipitation…”
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Magnetoelectric Measurements by Two Different Methods of Cobalt Ferrite-Barium Titanate Composites
Published in Ferroelectrics (01-08-2006)“…The magnetoelectric coefficient, α = dE/dH, of different compositions of BaTiO 3 -CoFe 2 O 4 composites was measured by using the dynamic method and also a new…”
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Journal Article Conference Proceeding -
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Hypersensitivity reaction to azathioprine in a patient with ulcerative colitis. Infrequent manifestations
Published in Inflammatory bowel diseases (01-09-2004)Get full text
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Down-regulation of heart HFABP and UCP2 gene expression in diet-induced (cafeteria) obese rats
Published in Journal of physiology and biochemistry (01-06-2002)“…Long-term exposure to hypercaloric high fat diet induced marked tissue fatty acid accumulation and may influence cell function. Previous results in our…”
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Harlequin Syndrome post-transsphenoidal pituitary macroadenoma surgery
Published in Hormones (Athens, Greece) (01-04-2012)“…A 45-year-old woman, with a history of asymmetric facial flushing, was presented to the Endocrinology Unit after pituitary macroadenoma removal. After other…”
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Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15
Published in Journal of medical genetics (01-02-2002)Get full text
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Transient nonketotic hyperglycinaemia : ultrasound, CT and MRI : case report
Published in Neuroradiology (01-09-1997)“…We report a case of transient nonketotic hyperglycinaemia in which radiography correlated closely with clinical and biochemical findings. Only 5 patients have…”
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Conference Proceeding Journal Article -
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Expression of c-jun, jun B and jun D proto-oncogenes in human peripheral-blood granulocytes
Published in Biochemical journal (15-01-1991)“…We have found that purified human peripheral-blood granulocytes express constitutively significant levels of proto-oncogenes c-jun, jun B and jun D mRNA. Upon…”
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Identification of two new nonsense mutations (Q311X and W326X) in Exon 2 of the adrenoleukodystrophy (ALD) gene
Published in Human mutation (1996)Get full text
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Probability of Transition to Psychosis in Individuals at Clinical High Risk: An Updated Meta-analysis
Published in JAMA psychiatry (Chicago, Ill.) (01-09-2021)“…Estimating the current likelihood of transitioning from a clinical high risk for psychosis (CHR-P) to psychosis holds paramount importance for preventive care…”
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P.0033 The effectiveness of preventive interventions for anxiety features in young people: a systematic review and meta-analysis
Published in European neuropsychopharmacology (01-12-2021)Get full text
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P.0178 Transition to psychosis in adolescents at clinical high risk for psychosis: a meta-analysis
Published in European neuropsychopharmacology (01-12-2021)Get full text
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Primary prevention of depression: An umbrella review of controlled interventions
Published in Journal of affective disorders (01-11-2021)“…•This systematic meta-review provides a comprehensive, evidence-based appraisal of the efficacy of preventive interventions for depression.•87.2% of the…”
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Glutaryl-CoA dehydrogenase deficiency in Spain : Evidence of two groups of patients, genetically, and biochemically distinct
Published in Pediatric research (01-09-2000)“…Glutaryl-CoA dehydrogenase (GCDH) deficiency causes glutaric aciduria type I (GA I), an inborn error of metabolism that is characterized clinically by dystonia…”
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Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15
Published in Journal of medical genetics (01-02-2002)“…[...]a possible explanation for the severe UPD phenotype might be deficiency of both paternal copies. [...]AS patients with a severe phenotype present unusual…”
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18
State of bilateral opercular disorder and pseudobulbar paralysis of late onset in unilateral perisylvian dysplasia
Published in Revista de neurologiá (01-12-1997)“…We come up the case of a six and a half year old girl suffering from right unilateral perisylvian cortical dysplasia who present left spastic hemiparesia,…”
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Clinical assessment of attention deficit hyperactivity disorder, interview model and controversial issues
Published in Revista de neurologiá (2008)“…Attention deficit hyperactivity disorder (ADHD) is one of the most frequent reasons for visits to neuropaediatric services. Although the clinical criteria are…”
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Case report. Transient nonketotic hyperglycinaemia: ultrasound, CT and MRI
Published in Neuroradiology (05-09-1997)Get full text
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