[Nephrotic syndrome in secondary syphilis]

[Assessment of the antibiotic allergy questionnaire in the medical history].

Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia·2010

[Cerebral toxoplasmosis].

Enfermedades infecciosas y microbiologia clinica·1998

[Drug interactions and their management in patients with human immunodeficiency virus infection].

Anales de medicina interna (Madrid, Spain : 1984)·1998

[Hepatitis C virus antibodies in alcoholic patients].

Revista clinica espanola·1995

[Immunologic prognostic parameters in infection by the human immunodeficiency virus].

Medicina clinica·1992

[Varicella pneumonia in adults. Study of 13 cases].

Revista clinica espanola·1992

Optimising the duration of antimicrobial treatment in the era of Antimicrobial Stewardship Programs.

Medicina clinica·2026

Reduced serum IL-6 as a potential peripheral marker of amnestic mild cognitive impairment: A pilot study.

Medicina clinica·2026

Foundations for the rational prescription of enteral medical nutrition therapy.

Medicina clinica·2026

Ambient AI scribe in pediatric outpatient visits: documentation burden, quality, and scale-up limits.

Medicina clinica·2026

Eating disorders.

Medicina clinica·2026

Tobacco-related and tobacco-attributable cancer mortality in Spain, 1999-2023: trends and gender inequalities.

Medicina clinica·2026

RFC1 Repeat Expansions in Chronic Idiopathic Axonal Polyneuropathy: Prevalence, Phenotype, and Diagnostic Implications.

Journal of the peripheral nervous system : JPNS·2026

Network Analysis in Central Disorders of Hypersomnolence: Insight Into Relationships Between Symptoms, Mental Health, and Quality of Life.

Journal of sleep research·2026

Association between sarcopenia and inflammation in non-geriatric patients with chronic kidney disease: a comparison of hemodialysis and non-hemodialysis patients.

Journal of nephrology·2026

Transmission ratio distortion of NF1 mutant alleles in familial Neurofibromatosis type 1.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Disease-Specific Glycopattern Signatures of Serum Small Extracellular Vesicles in Depression, Schizophrenia, and Glioblastoma.

Proteomics·2026

Blended Hereditary Neuropathy Phenotype Caused by Biallelic PRX and SCN9A Variants: A Case Report.

Molecular syndromology·2026

Related Experiment Videos

[Nephrotic syndrome in secondary syphilis]

Related Concept Videos

[Assessment of the antibiotic allergy questionnaire in the medical history].

[Cerebral toxoplasmosis].

[Drug interactions and their management in patients with human immunodeficiency virus infection].

[Hepatitis C virus antibodies in alcoholic patients].

[Immunologic prognostic parameters in infection by the human immunodeficiency virus].

[Varicella pneumonia in adults. Study of 13 cases].

Optimising the duration of antimicrobial treatment in the era of Antimicrobial Stewardship Programs.

Reduced serum IL-6 as a potential peripheral marker of amnestic mild cognitive impairment: A pilot study.

Foundations for the rational prescription of enteral medical nutrition therapy.

Ambient AI scribe in pediatric outpatient visits: documentation burden, quality, and scale-up limits.

Eating disorders.

Tobacco-related and tobacco-attributable cancer mortality in Spain, 1999-2023: trends and gender inequalities.

RFC1 Repeat Expansions in Chronic Idiopathic Axonal Polyneuropathy: Prevalence, Phenotype, and Diagnostic Implications.

Network Analysis in Central Disorders of Hypersomnolence: Insight Into Relationships Between Symptoms, Mental Health, and Quality of Life.

Association between sarcopenia and inflammation in non-geriatric patients with chronic kidney disease: a comparison of hemodialysis and non-hemodialysis patients.

Transmission ratio distortion of NF1 mutant alleles in familial Neurofibromatosis type 1.

Disease-Specific Glycopattern Signatures of Serum Small Extracellular Vesicles in Depression, Schizophrenia, and Glioblastoma.

Blended Hereditary Neuropathy Phenotype Caused by Biallelic PRX and SCN9A Variants: A Case Report.

Related Experiment Videos

[Nephrotic syndrome in secondary syphilis]

Related Concept Videos

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