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Gema Ariceta

Researcher Next ID · RN-035152

Researcher · Biochemistry, Genetics and Molecular Biology

Hebron University

Hebron, Spain

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Accepting doctoral researchersFunding unknown
Works count
1,126
Citation count
10,995
H-index
57
i10-index
168

Research interests

Biochemistry, Genetics and Molecular Biology
Immunology and Microbiology
Medicine
Biomedical Research and Pathophysiology
Renal Diseases and Glomerulopathies
Complement system in diseases
Parathyroid Disorders and Treatments
Metabolism and Genetic Disorders

Publications

  • The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment

    Kidney International · 2020 · 10.1016/j.kint.2020.01.035

  • FGF23 and its role in X-linked hypophosphatemia-related morbidity

    Orphanet Journal of Rare Diseases · 2019 · 10.1186/s13023-019-1014-8

  • Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome

    Journal of Clinical Investigation · 2018 · 10.1172/jci98688

  • Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome

    Kidney International · 2018 · 10.1016/j.kint.2018.02.029

  • A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases

    Kidney International · 2018 · 10.1016/j.kint.2018.02.027

  • Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

    Kidney International · 2016 · https://doi.org/10.1016/j.kint.2016.10.005

  • Effectiveness of mycophenolate mofetil in C3 glomerulonephritis

    Kidney International · 2015 · 10.1038/ki.2015.227

  • An international consensus approach to the management of atypical hemolytic uremic syndrome in children

    Pediatric Nephrology · 2015 · https://doi.org/10.1007/s00467-015-3076-8

  • Actualización en síndrome hemolítico urémico atípico: diagnóstico y tratamiento. Documento de consenso

    Nefrología · 2015 · 10.1016/j.nefro.2015.07.005

  • Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies

    Nephrology Dialysis Transplantation · 2012 · 10.1093/ndt/gfs493

  • Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome

    Pediatric Nephrology · 2008 · https://doi.org/10.1007/s00467-008-0964-1

  • Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

    The American Journal of Human Genetics · 2006 · 10.1086/508617

Current projects

    No projects listed.