[The usefulness of determining basal insulinemia as a cardiovascular risk factor]

Decreased serum selenium concentrations in patients with Parkinson's disease.

European journal of neurology·2013

Human study of ion implantation as a surface treatment for dental implants.

International journal of oral and maxillofacial surgery·2013

[Influence of weight loss in the clinical evolution, metabolic and psychological of the patients with overweight or obesity].

Nutricion hospitalaria·2013

Serum concentrations of osteocalcin, procollagen type 1 N-terminal propeptide and beta-CrossLaps in obese subjects with varying degrees of glucose tolerance.

Clinical endocrinology·2011

Taurine and glucose metabolism: a review.

Nutricion hospitalaria·2011

[Poisonings by oral antidiabetic drugs in Spain. Analysis and evolution during 13 years (1991-2003)].

Revista clinica espanola·2008

[Rockwood Frailty Index as a prognostic classifier in hospital at home: an observational survival study].

Atencion primaria·2026

Gender-related determinants of hypertension self-care behaviours in primary care: Perspectives of patients and healthcare professionals.

Atencion primaria·2026

[Development and validation of Cefalytics: an artificial intelligence-based application for the rapid diagnosis of primary headaches].

Atencion primaria·2026

[Contact with nature and its relationship with perceived stress and health-related quality of life in rural adults served by primary care].

Atencion primaria·2026

Performance of artificial intelligence in the collection of patient history in general practice.

Atencion primaria·2026

[Study on the factors influencing treatment adherence in patients with chronic multimorbidity].

Atencion primaria·2026

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Related Experiment Videos

[The usefulness of determining basal insulinemia as a cardiovascular risk factor]

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Decreased serum selenium concentrations in patients with Parkinson's disease.

Human study of ion implantation as a surface treatment for dental implants.

[Influence of weight loss in the clinical evolution, metabolic and psychological of the patients with overweight or obesity].

Serum concentrations of osteocalcin, procollagen type 1 N-terminal propeptide and beta-CrossLaps in obese subjects with varying degrees of glucose tolerance.

Taurine and glucose metabolism: a review.

[Poisonings by oral antidiabetic drugs in Spain. Analysis and evolution during 13 years (1991-2003)].

[Rockwood Frailty Index as a prognostic classifier in hospital at home: an observational survival study].

Gender-related determinants of hypertension self-care behaviours in primary care: Perspectives of patients and healthcare professionals.

[Development and validation of Cefalytics: an artificial intelligence-based application for the rapid diagnosis of primary headaches].

[Contact with nature and its relationship with perceived stress and health-related quality of life in rural adults served by primary care].

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The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

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