Clínic Barcelona. Hospital Universitari

Teresa Pampols Ros

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Hospital Clínic – Biomedical Diagnostic CenterBiochemistry and Molecular Genetics

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Recent articles

  • Inherited Metabolic Rare Disease
    Pampols T.
    Advances in Experimental Medicine and Biology. Springer. 2010;686:397-431
  • A key role for the peroxisomal Abcd2 transporter in fatty acid homeostasis.
    FOURCADE S, RUIZ M, CAMPS C, SCHLÜTER A, HOUTEN S, MOOYER P, PAMPOLS T, DACREMONT G, WANDERS R, GIROS M, PUJOL A. .
    Am J Physiol Endocrinol Metab. 2008;Oct:1-31
  • X-linked adrenoleukodystrophy (X-ALD) in Spain.Identification of 25 new mutations in the ABCD1
    COLL MJ, PALAU N, CAMPS C, RUIZ M, PAMPOLS T , GIROS M.
    Clin Genet. 2005;67:418-424
  • Functional overlap between ABCD1(ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-Adrenoleukodystrophy
    Pujol A, Ferrer I, Camps C, Metzger E, Hindelang C, Callizot N, Ruiz M, Pampols T, Giros M, Mabdel JL.
    Human Molecular Genetics. 2004;13:2997-3006
  • Newborn Screening in Spain
    Pampols T.
    Orpha News Europe. 2009;April:-

Academic Qualifications

  • (1987)
  • (1968)
  • (1965)

Biomedical Diagnostic Center (CDB)

Villarroel, 170 · 08036 Barcelona
Tel: +34 93 227 54 64 · Fax: +34 93 227 98 75 · · www.hospitalclinic.org