Montse Olive

Montse Olive

UNVERIFIED PROFILE

Are you Montse Olive?   Register this Author

Register author
Montse Olive

Montse Olive

Publications by authors named "Montse Olive"

Are you Montse Olive?   Register this Author

64Publications

1660Reads

46Profile Views

Spanish Pompe registry: Baseline characteristics of first 49 patients with adult onset of Pompe disease.

Med Clin (Barc) 2020 Feb 26;154(3):80-85. Epub 2019 Jun 26.

Unidad de Patología Neuromuscular, Departamento de Neurología, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, España; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER). Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.medcli.2019.03.036DOI Listing
February 2020

Cylindrical spirals in two families: Clinical and genetic investigations.

Neuromuscul Disord 2019 Dec 25. Epub 2019 Dec 25.

Centre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, QEII Medical Centre, Australia. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2019.12.006DOI Listing
December 2019

Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study.

Ann Clin Transl Neurol 2019 Nov 27;6(11):2197-2204. Epub 2019 Sep 27.

Centre for Medical Research, The University of Western Australia and the Harry Perkins Institute for Medical Research, Nedlands, Western Australia, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/acn3.50912DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856620PMC
November 2019

Mutations in the J domain of DNAJB6 cause dominant distal myopathy.

Neuromuscul Disord 2019 Nov 19. Epub 2019 Nov 19.

Neuromuscular Research Center, Tampere University Hospital and Tampere University, P.O. box 100, FIN-33014 Tampere, Finland; Folkhälsan Research Center, Helsinki, Finland and University of Helsinki, Medicum, Helsinki, Finland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2019.11.005DOI Listing
November 2019

Late onset distal myopathy: A new telethoninopathy.

Neuromuscul Disord 2019 01 13;29(1):80-83. Epub 2018 Nov 13.

Unidad de Neuromuscular, Hospital Universitario 12 de Octubre, Instituto i+12 y U-723 del CIBERER, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2018.11.001DOI Listing
January 2019

Muscle imaging in laminopathies: Synthesis study identifies meaningful muscles for follow-up.

Muscle Nerve 2018 12 18;58(6):812-817. Epub 2018 Nov 18.

APHP, Neuromuscular Disorders Unit, Pediatric Department, CHU Paris IdF Ouest - Hôpital Raymond Poincaré, Paris Saclay Universities, UVSQ University of Versailles, UMR 1179 INSERM, Garches, France.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/mus.26312
Publisher Site
http://dx.doi.org/10.1002/mus.26312DOI Listing
December 2018

Different mitochondrial genetic defects exhibit the same protein signature of metabolism in skeletal muscle of PEO and MELAS patients: A role for oxidative stress.

Free Radic Biol Med 2018 10 20;126:235-248. Epub 2018 Aug 20.

Departamento de Biología Molecular, Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Spain; Instituto de Investigación Hospital, 12 de Octubre (i+12), Madrid, Spain. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S08915849183142
Publisher Site
http://dx.doi.org/10.1016/j.freeradbiomed.2018.08.020DOI Listing
October 2018

model of myosin myopathy rescued by overexpression of a TRIM-protein family member.

Proc Natl Acad Sci U S A 2018 07 26;115(28):E6566-E6575. Epub 2018 Jun 26.

Translational Medicine, School of Health and Education, University of Skövde, SE-541 28, Skövde, Sweden

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1073/pnas.1800727115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048496PMC
July 2018

A Roma founder mutation causes a novel phenotype of centronuclear myopathy with rigid spine.

Neurology 2018 07 27;91(4):e339-e348. Epub 2018 Jun 27.

From the Unidad de Enfermedades Neuromusculares, Department of Neurology (M.C.-S., C.P.), Instituto de Biomedicina de Sevilla (IBiS) (M.C.-S., F.M., C.P.), and Department of Pathology, Neuropathology Unit (E.R.), Hospital Universitario Virgen del Rocío, Sevilla, Spain; Laboratoire Diagnostic Génétique (V.B.), Faculté de Médecine-CHRU, Strasbourg; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) (V.B., R.Á., J.L.), Illkirch, France; Harry Perkins Institute of Medical Research and Centre for Medical Research (B.M., N.G.L., L.K.), University of Western Australia, Nedlands; Department of Pathology (Neuropathology) (A.H.-L.), Hospital Universitario 12 de Octubre, Madrid Research Institute; Neuropathology Unit (M.O.), Department of Pathology and Neuromuscular Unit, Department of Neurology, IDIBELL-Hospital de Bellvitge, Hospitalet de Llobregat, Barcelona; Department of Neurology and IIS La Fe (N.M., J.J.V.), Hospital Universitari i Politècnic La Fe, Valencia; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER) (N.M., J.D.-M., J.J.V.); Department of Neurology (E.K.), Consulta de Enfermedades Neuromusculares y Unidad de ELA, Hospital General Universitario Santa Lucía, Cartagena, Murcia; Department of Neurology (A.C.), Hospital Virgen de las Nieves, Granada; Department of Neurology (P.Q.), Hospital Torrecárdenas, Almería; Unidad de Enfermedades Neuromusculares (J.D.-M.), Department of Neurology, Universidad Autónoma de Barcelona, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; Department of Diagnostic Genomics (M.D.), PathWest Laboratory Medicine WA, Perth, Australia; Department of Neurology (C.D.), Hospital 12 de Octubre, Madrid, Spain; Unité de Morphologie Neuromusculaire (N.B.R.), Centre de Référence de Pathologie Neuromusculaire Paris-Est, Institut de Myologie, Groupe Hospitalier Universitaire La Pitié-Salpêtrière, Paris; Université Sorbonne (N.B.R.), UPMC Univ Paris 06, INSERM UMRS974, CNRS FRE3617, Center for Research in Myology, Groupe Hospitalier Universitaire La Pitié-Salpêtrière, Paris, France; Department of Medicine (J.J.V.), Universitat de Valencia; Department of Experimental and Health Sciences (D.C.), Institute of Evolutionary Biology (CSIC-UPF), Universitat Pompeu Fabra, Barcelona, Spain; Centre National de la Recherche Scientifique (J.L.), UMR7104, Illkirch; and Institut National de la Santé et de la Recherche Médicale (J.L.), U964, Illkirch, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000005862DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070382PMC
July 2018

Dilated Cardiomyopathy and Hydroxychloroquine-induced Phospholipidosis: From Curvilinear Bodies to Clinical Suspicion.

Rev Esp Cardiol (Engl Ed) 2018 Jun 18;71(6):491-493. Epub 2017 May 18.

Àrea de Malalties del Cor, IDIBELL, Hospital de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.rec.2017.04.017DOI Listing
June 2018

Targeted Next-Generation Sequencing Reveals Novel TTN Mutations Causing Recessive Distal Titinopathy.

Mol Neurobiol 2017 11 29;54(9):7212-7223. Epub 2016 Oct 29.

Folkhälsan Institute of Genetics, Biomedicum Helsinki and Department of Medical Genetics, Haartman Institute, University of Helsinki, Haartmaninkatu 8, 00290, Helsinki, Finland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12035-016-0242-3DOI Listing
November 2017

Hypoxia triggers IFN-I production in muscle: Implications in dermatomyositis.

Sci Rep 2017 08 17;7(1):8595. Epub 2017 Aug 17.

Neuromuscular Diseases Unit, Neurology Department, Hospital de la Santa Creu I Sant Pau, Universitat Autònoma de Barcelona, Institut de Recerca Sant Pau, (Barcelona) and Biomedical Network Research Centre on Rare Diseases (CIBERER), Sant Pau, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41598-017-09309-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561123PMC
August 2017

Novel mutation in TCAP manifesting with asymmetric calves and early-onset joint retractions.

Neuromuscul Disord 2016 11 16;26(11):749-753. Epub 2016 Jul 16.

Servicio de Neurología, Hospital Universitario 12 de Octubre, Madrid, Spain; Unidad de Neuromuscular, Hospital Universitario 12 de Octubre, Madrid, Spain; Instituto de Investigación I+12, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), grupo U-723, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2016.07.003DOI Listing
November 2016

New aspects of myofibrillar myopathies.

Curr Opin Neurol 2016 10;29(5):628-34

aDepartment of Neurology, Heimer Institute for Muscle Research, University Hospital Bergmannsheil, Ruhr-University Bochum, Bochum, Germany bInstitute of Neuropathology, Department of Pathology and Neuromuscular Unit, IDIBELL-Hospital Universitari de Bellvitge, Barcelona, Spain cInstitute of Neuropathology, University Hospital Erlangen, Erlangen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/WCO.0000000000000357DOI Listing
October 2016

Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes.

Neuromuscul Disord 2016 Jan 22;26(1):33-40. Epub 2015 Oct 22.

Neuromuscular Disorders Unit, Neurology Department, Universitat Autónoma de Barcelona, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2015.10.001DOI Listing
January 2016

New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations.

Hum Mol Genet 2015 Jul 23;24(13):3638-50. Epub 2015 Mar 23.

Department of Pathology, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg SE-413 45, Sweden, Department of Clinical and Medical Genetics, University of Gothenburg, Gothenburg SE-405 30, Sweden and Systems Biology Research Centre, School of Biomedicine, University of Skövde, Skövde SE-541 28, Sweden

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddv108DOI Listing
July 2015

Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations.

Brain 2014 Dec 25;137(Pt 12):3160-70. Epub 2014 Sep 25.

1 IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire), 67404 Illkirch, France 2 Inserm, U964, 67404 Illkirch, France 3 CNRS, UMR7104, 67404 Illkirch, France 4 Université de Strasbourg, 67404 Illkirch, France 5 Collège de France, Chaire de Génétique Humaine, 67404 Illkirch, France

View Article

Download full-text PDF

Source
http://brain.oxfordjournals.org/content/brain/137/12/3160.fu
Web Search
http://www.brain.oxfordjournals.org/cgi/doi/10.1093/brain/aw
Publisher Site
http://dx.doi.org/10.1093/brain/awu272DOI Listing
December 2014

A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failure.

Neuromuscul Disord 2014 Mar 11;24(3):241-4. Epub 2013 Dec 11.

Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle NE1 3BZ, United Kingdom; Department of Neurology, Royal Victoria Infirmary, Queen Victoria Road, Newcastle NE1 4LP, United Kingdom. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2013.12.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988992PMC
March 2014

Myofibrillar myopathies: new developments.

Curr Opin Neurol 2013 Oct;26(5):527-35

Institute of Neuropathology, Department of Pathology, IDIBELL-Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
Publisher Site
http://dx.doi.org/10.1097/WCO.0b013e328364d6b1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127196PMC
October 2013

Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutations.

Autophagy 2013 Mar 13;9(3):422-3. Epub 2012 Dec 13.

Department of Neurology, Neuromuscular Center Ruhrgebiet, University Hospital Bergmannsheil, Ruhr-University, Bochum, Germany.

View Article

Download full-text PDF

Source
http://www.tandfonline.com/doi/abs/10.4161/auto.22921
Publisher Site
http://dx.doi.org/10.4161/auto.22921DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590265PMC
March 2013

Filamin C-related myopathies: pathology and mechanisms.

Acta Neuropathol 2013 Jan 30;125(1):33-46. Epub 2012 Oct 30.

Institute for Cell Biology, University of Bonn, Ulrich-Haberland-Str. 61a, 53121 Bonn, Germany.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s00401-012-1054-9
Publisher Site
http://dx.doi.org/10.1007/s00401-012-1054-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127197PMC
January 2013

Telethonin-deficiency initially presenting as a congenital muscular dystrophy.

Neuromuscul Disord 2011 Jun 6;21(6):433-8. Epub 2011 May 6.

AP-HP, Centre de Référence des Maladies Neuromusculaires Paris-Est, Groupe Hospitalier-Universitaire Pitié-Salpêtrière, Paris F-75013, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2011.03.005DOI Listing
June 2011

Nemaline myopathy type 6: clinical and myopathological features.

Muscle Nerve 2010 Dec;42(6):901-7

Institute of Neuropathology, Pathology Department, IDIBELL-Hospital de Bellvitge and CIBERNED, Hospitalet de Llobregat, Feixa Llarga s/n, Hospitalet de Llobregat, Barcelona 08907, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mus.21788DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3057880PMC
December 2010

Extralysosomal protein degradation in myofibrillar myopathies.

Authors:
Montse Olivé

Brain Pathol 2009 Jul;19(3):507-15

Institut de Neuropatologia, IDIBELL-Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1750-3639.2009.00288.xDOI Listing
July 2009

TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies.

J Neuropathol Exp Neurol 2009 Mar;68(3):262-73

Institut de Neuropatologia, Servei Anatomia Patològica, IDIBELL-Hospital Universitari de Bellvitge, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/NEN.0b013e3181996d8fDOI Listing
March 2009

Intermediate filament diseases: desminopathy.

Adv Exp Med Biol 2008 ;642:131-64

National Institutes of Health, Bethesda, MD 20892-9404, USA.

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776705PMC
http://dx.doi.org/10.1007/978-0-387-84847-1_11DOI Listing
February 2009

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient.

Neuromuscul Disord 2008 Dec 22;18(12):929-33. Epub 2008 Oct 22.

Institut de Neuropatologia, IDIBELL-Hospital de Bellvitge, and Universitat Autónoma de Barcelona, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2008.07.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592511PMC
December 2008

Molecular pathology of myofibrillar myopathies.

Expert Rev Mol Med 2008 Sep 3;10:e25. Epub 2008 Sep 3.

Institut de Neuropatologia, Servei Anatomia Patològica, IDIBELL-Hospital Universitari de Bellvitge, Universitat de Barcelona, Hospitalet de Llobregat, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/S1462399408000793DOI Listing
September 2008

156th ENMC International Workshop: desmin and protein aggregate myopathies, 9-11 November 2007, Naarden, The Netherlands.

Neuromuscul Disord 2008 Jul 1;18(7):583-92. Epub 2008 Jul 1.

Johannes Gutenberg University, Medical Center, Langenbeckstrasse 1, 55131 Mainz, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2008.04.008DOI Listing
July 2008

Oxidative stress in desminopathies and myotilinopathies: a link between oxidative damage and abnormal protein aggregation.

Brain Pathol 2007 Oct 4;17(4):377-88. Epub 2007 Sep 4.

Institut de Neuropatologia, Servei Anatomia Patològica, IDIBELL-Hospital Universitari de Bellvitge CIBERNED, Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1750-3639.2007.00087.xDOI Listing
October 2007

Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy.

Am J Pathol 2007 Oct 6;171(4):1312-23. Epub 2007 Sep 6.

Institut de Neuropatologia, Servei Anatomia Patològica, IDIBELL-Hospital Universitari de Bellvitge, carrer Feixa Llarga sn, 08907 L'Hospitalet de Llobregat, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2353/ajpath.2007.070520DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1988880PMC
October 2007

Desmin is oxidized and nitrated in affected muscles in myotilinopathies and desminopathies.

J Neuropathol Exp Neurol 2007 Aug;66(8):711-23

Institut de Neuropatologia, Servei Anatomia Patològica, Institut d'Investigacio de Bellvitge-Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Plataforma de Proteòmica, Barcelona Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/nen.0b013e3181256b4cDOI Listing
August 2007

Myotilinopathy: refining the clinical and myopathological phenotype.

Brain 2005 Oct 9;128(Pt 10):2315-26. Epub 2005 Jun 9.

Institut de Neuropatologia, IDIBELL-Hospital de Bellvitge, Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
https://brain.oxfordjournals.org/content/brain/128/10/2315.f
Web Search
http://www.brain.oxfordjournals.org/cgi/doi/10.1093/brain/aw
Publisher Site
http://dx.doi.org/10.1093/brain/awh576DOI Listing
October 2005

A novel thymidine phosphorylase mutation in a Spanish MNGIE patient.

J Neurol Sci 2005 Jan 12;228(1):35-9. Epub 2004 Nov 12.

Department of Neurology, Hospital Universitari Vall d' Hebron, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jns.2004.09.034DOI Listing
January 2005

A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia.

Neuromuscul Disord 2004 May;14(5):321-4

Servei de Genètica, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2004.01.006DOI Listing
May 2004

Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis.

J Neuropathol Exp Neurol 2004 May;63(5):484-98

Instituto de Neuropatología, Servicio de Anatomía Patológica, Hospital Universitario de Bellvitge, Hospitalet de Llobregat, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/jnen/63.5.484DOI Listing
May 2004

Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studies.

J Neurol Sci 2004 Apr;219(1-2):125-37

Institut de Neuropatologia, Hospital de Bellvitge, C/Feixa Llarga s/n degrees, 08907 Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jns.2004.01.007DOI Listing
April 2004

Overexpression of semicarbazide-sensitive amine oxidase in human myopathies.

Muscle Nerve 2004 Feb;29(2):261-6

Institut de Neuropatologia, Hospital Universitari de Bellvitge, 08907 Hospitalet de Llobregat, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mus.10550DOI Listing
February 2004

A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.

J Neurol 2004 Feb;251(2):143-9

National Institute of Neurological Disorders and Stroke, National Institutes of Health Bldg 10, Room 4B37, 10 Center Dr., MSC 1361, Bethesda, Maryland 20892-1361, USA.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s00415-004-0289-3
Publisher Site
http://dx.doi.org/10.1007/s00415-004-0289-3DOI Listing
February 2004

Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases.

Acta Neuropathol 2003 Jul 1;106(1):1-7. Epub 2003 Apr 1.

Institut de Neuropatologia, Ciutat Sanitària i Universitària de Bellvitge, C/Feixa Llarga s/n masculine, 08907 Hospitalet de Llobregat, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00401-003-0695-0DOI Listing
July 2003

Pharmaceutical care: pharmacy involvement in prescribing in an acute-care hospital.

Pharm World Sci 2003 Apr;25(2):56-64

Pharmacy Service, Hospital de Barcelona, Avda, Diagonal, 660, 08034 Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1023/a:1023201115649DOI Listing
April 2003