Publikationen in Zusammenarbeit mit Forschern von Hospital Universitario 12 de Octubre (9)

2022

  1. Understanding the ecosystem of patients with lysosomal storage diseases in Spain: a qualitative research with patients and health care professionals

    Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1

2018

  1. Primary constitutional MLH1 epimutations: a focal epigenetic event

    British Journal of Cancer, Vol. 119, Núm. 8, pp. 978-987

  2. What to consider when pseudohypoparathyroidism is ruled out: IPPSD and differential diagnosis

    BMC Medical Genetics, Vol. 19, Núm. 1

2015

  1. Hereditary apolipoprotein AI-associated renal amyloidosis: A diagnostic challenge

    Nefrologia, Vol. 35, Núm. 3, pp. 322-327

  2. Hereditary apolipoprotein AI-associated renal amyloidosis: A diagnostic challenge

    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, Vol. 35, Núm. 3, pp. 322-327

2006

  1. Valor de la determinación del índice tobillo-brazo en pacientes de riesgo vascular sin enfermedad aterotrombótica conocida: Estudio VITAMIN

    Revista Espanola de Cardiologia, Vol. 59, Núm. 7, pp. 662-670

2002

  1. Heterozygous familial hypercholesterolemia in Spain. Description of 819 non related cases

    Medicina Clinica, Vol. 118, Núm. 13, pp. 487-492

1988

  1. Recovery of renal function associated with early use of captopril in scleroderma renal crisis

    Medicina Clinica, Vol. 91, Núm. 15, pp. 586-588

  2. Significance of granulomas in bone marrow: A study of 40 cases

    European Journal of Haematology, Vol. 41, Núm. 1, pp. 12-16