[Hemophilia "A": genetic and demographic characteristics (author's transl)]

Telemedicine in the management of patients with headache: current situation and recommendations of the Spanish Society of Neurology's Headache Study Group.

Neurologia·2023

[Medical applications of genome discovery].

Revista medica de Chile·2002

[History of the scientific work of Eduardo Cruz-Coke Lassabe].

Revista medica de Chile·2001

[UNESCO's bioethical norms to avoid eugenic practices].

Revista medica de Chile·2000

[The history of genetics in Latin American countries during the twentieth century].

Revista medica de Chile·2000

[Hippocratic philosophy].

Revista medica de Chile·1999

Epidemiology of Obstructive Sleep Apnea in Chile: A Systematic Review and Meta-Analysis.

Revista medica de Chile·2026

Rescue of a Discarded Liver Graft Through Viability Assessment Using Normothermic Ex Vivo Machine Perfusion.

Revista medica de Chile·2026

Diagnosis and Successful Surgical Treatment in a Patient with Takayasu Arteritis: Literature Review and Case Report.

Revista medica de Chile·2026

Self-Reported Sensory and Dental Impairments in Chilean Older Adults with Type 2 Diabetes: Prevalence and Associated Factors.

Revista medica de Chile·2026

Prevalence and Associated Characteristics of Sexual Victimization of Chilean Children and Adolescents in a National Sample: An Update.

Revista medica de Chile·2026

Social Determinants Influencing Cardiovascular Diseases in Adults Aged 60 Years and Older, According to CASEN 2022.

Revista medica de Chile·2026

Adult-Onset Alagille Syndrome Presenting With Recurrent Cholestasis: A Rare Genetic Diagnosis Confirmed by Whole Exome Sequencing.

Cureus·2026

Genomic meta-analyses of binge-eating behavior and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.

Nature. Mental health·2026

The genome sequence of the Bluebell moth, Eana incanana (Stephens, 1852) (Lepidoptera: Tortricidae).

Wellcome open research·2026

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Hemoglobin·2026

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences.

Nature communications·2026

Accelerated Aging Fontan Phenotype Is Associated With Systemic Right Ventricles and Adverse Hemodynamics.

Journal of the American Heart Association·2026

Related Experiment Videos

[Hemophilia "A": genetic and demographic characteristics (author's transl)]

Related Concept Videos

Telemedicine in the management of patients with headache: current situation and recommendations of the Spanish Society of Neurology's Headache Study Group.

[Medical applications of genome discovery].

[History of the scientific work of Eduardo Cruz-Coke Lassabe].

[UNESCO's bioethical norms to avoid eugenic practices].

[The history of genetics in Latin American countries during the twentieth century].

[Hippocratic philosophy].

Epidemiology of Obstructive Sleep Apnea in Chile: A Systematic Review and Meta-Analysis.

Rescue of a Discarded Liver Graft Through Viability Assessment Using Normothermic Ex Vivo Machine Perfusion.

Diagnosis and Successful Surgical Treatment in a Patient with Takayasu Arteritis: Literature Review and Case Report.

Self-Reported Sensory and Dental Impairments in Chilean Older Adults with Type 2 Diabetes: Prevalence and Associated Factors.

Prevalence and Associated Characteristics of Sexual Victimization of Chilean Children and Adolescents in a National Sample: An Update.

Social Determinants Influencing Cardiovascular Diseases in Adults Aged 60 Years and Older, According to CASEN 2022.

Adult-Onset Alagille Syndrome Presenting With Recurrent Cholestasis: A Rare Genetic Diagnosis Confirmed by Whole Exome Sequencing.

Genomic meta-analyses of binge-eating behavior and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.

The genome sequence of the Bluebell moth, Eana incanana (Stephens, 1852) (Lepidoptera: Tortricidae).

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences.

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Related Experiment Videos

[Hemophilia "A": genetic and demographic characteristics (author's transl)]

Related Concept Videos

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