Hasil Pencarian - Ariadna Padró-Miquel

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  1. 1
    Study of common hypertriglyceridaemia genetic variants and subclinical atherosclerosis in a group of women with SLE and a control group

    Study of common hypertriglyceridaemia genetic variants and subclinical atherosclerosis in a group of women with SLE and a control group oleh Beatriz Candás-Estébanez, Marta Fanlo-Maresma, Virginia Esteve-Luque, Xavier Pintó, Ariadna Padró-Miquel, Emili Corbella

    Diterbitkan 2022-07-01
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  2. 2
    Implication between Genetic Variants from APOA5 and ZPR1 and NAFLD Severity in Patients with Hypertriglyceridemia

    Implication between Genetic Variants from APOA5 and ZPR1 and NAFLD Severity in Patients with Hypertriglyceridemia oleh Virginia Esteve-Luque, Ariadna Padró-Miquel, Marta Fanlo-Maresma, Emili Corbella, Xavier Corbella, Xavier Pintó, Beatriz Candás-Estébanez

    Diterbitkan 2021-02-01
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  3. 3
    Polygenic Risk of Hypertriglyceridemia Is Modified by BMI

    Polygenic Risk of Hypertriglyceridemia Is Modified by BMI oleh Virginia Esteve-Luque, Marta Fanlo-Maresma, Ariadna Padró-Miquel, Emili Corbella, Maite Rivas-Regaira, Xavier Pintó, Beatriz Candás-Estébanez

    Diterbitkan 2022-08-01
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  4. 4
    Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?

    Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think? oleh Cinthia Aguilera, Anna Esteve-Garcia, Carlos Casasnovas, Valentina Vélez-Santamaria, Laura Rausell, Pablo Gargallo, Javier Garcia-Planells, Pedro Alía, Núria Llecha, Ariadna Padró-Miquel

    Diterbitkan 2023-12-01
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  5. 5
    KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment.

    KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment. oleh Cristina Ruiz-Iruela, Ariadna Padró-Miquel, Xavier Pintó-Sala, Neus Baena-Díez, Assumpta Caixàs-Pedragós, Roser Güell-Miró, Rosa Navarro-Badal, Xavier Jusmet-Miguel, Pilar Calmarza, José Luis Puzo-Foncilla, Pedro Alía-Ramos, Beatriz Candás-Estébanez

    Diterbitkan 2018-01-01
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  6. 6
    Intermediate Repeat Expansion in the <i>ATXN2</i> Gene as a Risk Factor in the ALS and FTD Spanish Population

    Intermediate Repeat Expansion in the <i>ATXN2</i> Gene as a Risk Factor in the ALS and FTD Spanish Population oleh Daniel Borrego-Hernández, Juan Francisco Vázquez-Costa, Raúl Domínguez-Rubio, Laura Expósito-Blázquez, Elena Aller, Ariadna Padró-Miquel, Pilar García-Casanova, María J. Colomina, Cristina Martín-Arriscado, Rosario Osta, Pilar Cordero-Vázquez, Jesús Esteban-Pérez, Mónica Povedano-Panadés, Alberto García-Redondo

    Diterbitkan 2024-02-01
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  7. 7
    Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype

    Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype oleh Anna Esteve-Garcia, Estefania Cobos, Cristina Sau, Ariadna Padró-Miquel, Jaume Català-Mora, Pilar Barberán-Martínez, Pilar Barberán-Martínez, José M. Millán, José M. Millán, José M. Millán, José M. Millán, Gema García-García, Gema García-García, Gema García-García, Cinthia Aguilera

    Diterbitkan 2024-02-01
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