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David González Jiménez

Biographic Data

ID7611089
NAMEDavid González Jiménez
GIVEN NAMESDavid González
FAMILY NAMEJiménez
SIGNATUREJIMÉNEZ D G
AFFILIATIONSHospital Universitario Central de Asturias
ORCID0000-0001-8696-9194
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2024
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Impact on Body Composition After Two Years of Elexacaftor–Tezacaftor–Ivacaftor Therapy in Children with Cystic Fibrosis

    Open Access•María Álvarez Merino, Concepción Marina López Cárdenes et al.•ARTICLE•Children•2025

    Background: Triple therapy with cystic fibrosis transmembrane conductance regulator (CFTR) modulators in patients with cystic fibrosis (CF) has led to a shift in the nutritional management of the disease. Correct assessment of nutritional status is crucial due to its significant impact in pulmonary function and overall patient survival. This study aims to provide mid-term data on anthropometric and body composition changes in pediatric patients t…

  • Plasma Citrulline in the Diagnosis and Follow-Up of Celiac Disease

    Open Access•Alicia Isabel Pascual Pérez, Elene Larrea tamayo et al.•ARTICLE•Children•2024

    Plasma citrulline could serve as a valuable marker for mucosal recovery in the follow-up of diagnosed celiac patients adhering to a GFD

No prominent works on this page.

  • Plasma Citrulline in the Diagnosis and Follow-Up of Celiac Disease

    Open Access•Alicia Isabel Pascual Pérez, Elene Larrea tamayo et al.•ARTICLE•Children•2024

    Plasma citrulline could serve as a valuable marker for mucosal recovery in the follow-up of diagnosed celiac patients adhering to a GFD

  • Impact on Body Composition After Two Years of Elexacaftor–Tezacaftor–Ivacaftor Therapy in Children with Cystic Fibrosis

    Open Access•María Álvarez Merino, Concepción Marina López Cárdenes et al.•ARTICLE•Children•2025

    Background: Triple therapy with cystic fibrosis transmembrane conductance regulator (CFTR) modulators in patients with cystic fibrosis (CF) has led to a shift in the nutritional management of the disease. Correct assessment of nutritional status is crucial due to its significant impact in pulmonary function and overall patient survival. This study aims to provide mid-term data on anthropometric and body composition changes in pediatric patients t…

Amino acid (1 work) · Anthropometry (1 work) · Antibody (1 work) · Arginine (1 work) · Biochemistry (1 work) · Bioelectrical impedance analysis (1 work) · Body Composition Measurement Techniques (1 work) · Body mass index (1 work) · Body water (1 work) · Celiac Disease Research and Management (1 work)

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