[Effects of gene localization and its metabolic significance in trisomy 21]

Pembrolizumab in combination with gemcitabine for patients with HER2-negative advanced breast cancer: GEICAM/2015-04 (PANGEA-Breast) study.

BMC cancer·2022

A Review of the EUSO-Balloon Pathfinder for the JEM-EUSO Program.

Space science reviews·2022

GEINOFOTE: efficacy and safety of fotemustine in patients with high-grade recurrent gliomas and poor performance status.

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico·2015

Acute psychosis in propionic acidemia: 2 case reports.

Journal of child neurology·2013

Measurement of the proton-air cross section at √s=57 TeV with the Pierre Auger Observatory.

Physical review letters·2012

Mercury exposure and risks from dental amalgam in the US population, post-2000.

The Science of the total environment·2011

[Advances and perspectives in vascularized composite allotransplantation preservation].

Bulletin de l'Academie nationale de medecine·2025

[COVID-19: Neurological manifestations and complications during the acute phase of the disease].

Bulletin de l'Academie nationale de medecine·2024

[Role of psychological factors in post-COVID-19 condition].

Bulletin de l'Academie nationale de medecine·2023

[Neurological forms of long COVID in adults: Critical approach].

Bulletin de l'Academie nationale de medecine·2023

[Post-COVID-19 syndrome].

Bulletin de l'Academie nationale de medecine·2023

The next psychoactive drugs: From imipramine to ketamine.

Bulletin de l'Academie nationale de medecine·2023

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Neurogenetics·2026

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Vavilovskii zhurnal genetiki i selektsii·2026

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

Frontiers in endocrinology·2026

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Vavilovskii zhurnal genetiki i selektsii·2026

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genome research·2026

Genetic Susceptibility in Relative Maternal Protection From Type 1 Diabetes.

Diabetes care·2026

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Pembrolizumab in combination with gemcitabine for patients with HER2-negative advanced breast cancer: GEICAM/2015-04 (PANGEA-Breast) study.

A Review of the EUSO-Balloon Pathfinder for the JEM-EUSO Program.

GEINOFOTE: efficacy and safety of fotemustine in patients with high-grade recurrent gliomas and poor performance status.

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Measurement of the proton-air cross section at √s=57 TeV with the Pierre Auger Observatory.

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[Advances and perspectives in vascularized composite allotransplantation preservation].

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Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

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