[Genetically-based insulin resistance. Mini-review of the literature and personal reports]

[Classification criteria and clinical significance of the metabolic syndrome].

Revista clinica espanola·2006

The glutamine 27 glutamic acid polymorphism of the beta2-adrenoceptor gene is associated with abdominal obesity and greater risk of impaired glucose tolerance in men but not in women: a population-based study in Spain.

Clinical endocrinology·2003

Effect of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor gamma-2 gene on adiposity, insulin sensitivity and lipid profile in the Spanish population.

European journal of endocrinology·2002

Epidemiology of cardiovascular disease in type 2 diabetes.

International journal of clinical practice. Supplement·2001

[Late diagnosis of Turner syndrome: therapeutic implications].

Anales de medicina interna (Madrid, Spain : 1984)·2000

[Tuberculosis as cause of death].

Revista clinica espanola·1998

Trends in the structure, activity, and outcomes of Internal Medicine Services in the National Health System (2007-2024): The RECALMIN Study VI.

Revista clinica espanola·2026

Prognostic value of the Edmonton Obesity Staging System among people hospitalized with obesity.

Revista clinica espanola·2026

Utility of an extended 12-autoantibody panel in systemic sclerosis: Clinical and prognostic implications in a real-life cohort.

Revista clinica espanola·2026

Joint position paper on anterior ischemic optic neuropathy (AION). Vascular Risk Group and Systemic Autoimmune Diseases Group (GEAS) of the Spanish Society of Internal Medicine (SEMI) together with the Spanish Retina and Vitreous Society (SERV).

Revista clinica espanola·2026

Joint pain: a practical guide to the diagnosis of arthritis.

Revista clinica espanola·2026

Stickler syndrome type 1: case series and new genetic variants.

Revista clinica espanola·2026

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

Prenatal diagnosis·2026

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

Experimental biology and medicine (Maywood, N.J.)·2026

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

medRxiv : the preprint server for health sciences·2026

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Molecular genetics and genomics : MGG·2026

Related Experiment Videos

[Genetically-based insulin resistance. Mini-review of the literature and personal reports]

Related Concept Videos

[Classification criteria and clinical significance of the metabolic syndrome].

The glutamine 27 glutamic acid polymorphism of the beta2-adrenoceptor gene is associated with abdominal obesity and greater risk of impaired glucose tolerance in men but not in women: a population-based study in Spain.

Effect of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor gamma-2 gene on adiposity, insulin sensitivity and lipid profile in the Spanish population.

Epidemiology of cardiovascular disease in type 2 diabetes.

[Late diagnosis of Turner syndrome: therapeutic implications].

[Tuberculosis as cause of death].

Trends in the structure, activity, and outcomes of Internal Medicine Services in the National Health System (2007-2024): The RECALMIN Study VI.

Prognostic value of the Edmonton Obesity Staging System among people hospitalized with obesity.

Utility of an extended 12-autoantibody panel in systemic sclerosis: Clinical and prognostic implications in a real-life cohort.

Joint position paper on anterior ischemic optic neuropathy (AION). Vascular Risk Group and Systemic Autoimmune Diseases Group (GEAS) of the Spanish Society of Internal Medicine (SEMI) together with the Spanish Retina and Vitreous Society (SERV).

Joint pain: a practical guide to the diagnosis of arthritis.

Stickler syndrome type 1: case series and new genetic variants.

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Related Experiment Videos

[Genetically-based insulin resistance. Mini-review of the literature and personal reports]

Related Concept Videos

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