[Blastocystis hominis in an HIV-positive homosexual patient]

Strong association of HLA class II sequences in Mexicans with Vogt-Koyanagi-Harada's disease.

Human immunology·1999

Predicting susceptibility of Streptococcus pneumoniae to ceftriaxone and cefotaxime by cefuroxime and ceftizoxime disk diffusion testing.

Journal of clinical microbiology·1999

Single-step PCR amplification and enzyme restriction analysis of the entire Helicobacter pylori cytotoxin vacA gene for genetic variability studies.

FEMS microbiology letters·1999

Mitochondrial DNA damage and altered membrane potential (delta psi) in pancreatic acinar cells induced by reactive oxygen species.

Surgery·1999

Establishment of experimental conditions for the rapid detection of mutations in the von Hippel-Lindau gene by parallel temperature gradient gel electrophoresis.

Electrophoresis·1999

Effects of mild protein prenatal malnutrition and subsequent postnatal nutritional rehabilitation on noradrenaline release and neuronal density in the rat occipital cortex.

Brain research. Developmental brain research·1999

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

Executive summary of the consensus document for recommendations on the treatment of venous thromboembolism in pregnancy: consensus document from the Spanish Society of Internal Medicine, the Spanish Society of Medical Radiology, the Spanish Society of Vascular Interventional Radiology and the Spanish Society of Gynecology and Obstetrics 2026.

Revista clinica espanola·2026

Treatment of osteoporosis in clinical practice: when, whom, how, and for how long.

Revista clinica espanola·2026

Metabolic alkalosis and clinical outcomes in acute heart failure: a systematic review and meta-analysis.

Revista clinica espanola·2026

Proteogenomic Profiling of Idiopathic Pulmonary Arterial Hypertension Identifies Sex-Differential Proteins and Candidate Therapeutic Targets.

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

Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability.

Psychiatric genetics·2026

Leucine-rich glioma inactivated 1 (LGI1) is a ganglioside-binding protein.

FEBS letters·2026

Genetic Heterogeneity of Inborn Errors of Immunity Revealed by Whole-Genome Sequencing: Insights from a Russian Patient Cohort.

International journal of molecular sciences·2026

The genome sequence of the Tufted Button, Acleris cristana (Denis & Schiffermüller, 1775).

Wellcome open research·2026

CYP4F22-Related Autosomal Recessive Congenital Ichthyosis Associated With Hirschsprung Disease and Bartter-Like Renal Manifestations.

Journal of medical cases·2026

Related Experiment Videos

[Blastocystis hominis in an HIV-positive homosexual patient]

Related Concept Videos

Strong association of HLA class II sequences in Mexicans with Vogt-Koyanagi-Harada's disease.

Predicting susceptibility of Streptococcus pneumoniae to ceftriaxone and cefotaxime by cefuroxime and ceftizoxime disk diffusion testing.

Single-step PCR amplification and enzyme restriction analysis of the entire Helicobacter pylori cytotoxin vacA gene for genetic variability studies.

Mitochondrial DNA damage and altered membrane potential (delta psi) in pancreatic acinar cells induced by reactive oxygen species.

Establishment of experimental conditions for the rapid detection of mutations in the von Hippel-Lindau gene by parallel temperature gradient gel electrophoresis.

Effects of mild protein prenatal malnutrition and subsequent postnatal nutritional rehabilitation on noradrenaline release and neuronal density in the rat occipital cortex.

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.

Treatment of osteoporosis in clinical practice: when, whom, how, and for how long.

Metabolic alkalosis and clinical outcomes in acute heart failure: a systematic review and meta-analysis.

Proteogenomic Profiling of Idiopathic Pulmonary Arterial Hypertension Identifies Sex-Differential Proteins and Candidate Therapeutic Targets.

Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability.

Leucine-rich glioma inactivated 1 (LGI1) is a ganglioside-binding protein.

Genetic Heterogeneity of Inborn Errors of Immunity Revealed by Whole-Genome Sequencing: Insights from a Russian Patient Cohort.

The genome sequence of the Tufted Button, Acleris cristana (Denis & Schiffermüller, 1775).

CYP4F22-Related Autosomal Recessive Congenital Ichthyosis Associated With Hirschsprung Disease and Bartter-Like Renal Manifestations.

Related Experiment Videos

[Blastocystis hominis in an HIV-positive homosexual patient]

Related Concept Videos

Related Articles