Plasma C24:0- and C26:0-lysophosphatidylcholines are reliable biomarkers for the diagnosis of peroxisomal β-oxidation disorders.

Autor: Morales-Romero B; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain; Biomedical Research Institute August Pi i Sunyer (IDIBAPS), Barcelona, Spain; Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain., González de Aledo-Castillo JM; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., Fernández Sierra C; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., Martínez Carreira C; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., Zaragoza Bonet C; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., Fernández Bonifacio R; CORE Laboratory, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., Caro Miró MA; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., Argudo-Ramírez A; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain., López Galera RM; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain; Biomedical Research Institute August Pi i Sunyer (IDIBAPS), Barcelona, Spain; Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain., García-Villoria J; Section of Inborn Errors of Metabolism-IBC, Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain; Biomedical Research Institute August Pi i Sunyer (IDIBAPS), Barcelona, Spain; Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain. Electronic address: jugarcia@clinic.cat.

Publikováno v: Journal of lipid research [J Lipid Res] 2024 Mar; Vol. 65 (3), pp. 100516. Date of Electronic Publication: 2024 Feb 04.

Clinically isolated syndrome: diagnosis and risk of developing clinically definite multiple sclerosis.

Autor: López-Gómez J; Unidad de Proteínas, Servicio de Análisis Clínicos, Hospital Universitario de Badajoz, Badajoz, España. Electronic address: lopezhospi@gmail.com., Sacristán-Enciso B; Sección de Proteínas y Autoinmunidad, Servicio de Análisis Clínicos, Hospital de Mérida, Badajoz, España., Caro-Miró MA; Servicio de Análisis Clínicos, Hospital Universitario de Badajoz, Badajoz, España., Querol Pascual MR; Servicio de Neurología. Hospital Universitario de Badajoz, Badajoz, España.

Publikováno v: Neurologia [Neurologia (Engl Ed)] 2021 Mar 21. Date of Electronic Publication: 2021 Mar 21.

Síndrome clínico aislado: diagnóstico y riesgo de desarrollar esclerosis múltiple clínicamente definida

Autor: López-Gómez, J., Sacristán Enciso, B., Caro Miró, MA.

Publikováno v: Neurología; 20210101, Issue: Preprints

Precision Medicine in Neurodegenerative Disorders : Part II

Autor: Alberto J. Espay

Precision Medicine in Neurodegenerative Disorders, Part Two, Volume 193 in the Handbook of Clinical Neurology deals with the'How'in the reconfiguration of our approach to slow accelerated brain aging. The book rethinks animal models on which therapie