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There are 15142 results for: content related to: Fabry disease in children and response to enzyme replacement therapy: results from the Fabry Outcome Survey

  1. Poster abstracts

    Acta Paediatrica

    Volume 94, Issue s447, March 2005, Pages: 95–133,

    Version of Record online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2005.tb02120.x

  2. FABRY DISEASE: GENOTYPE-PHENOTYPE STUDIES; EPIDEMIOLOGY; SCREENING AND MANAGEMENT

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 93–97,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_1.x

  3. FABRY DISEASE

    Acta Paediatrica

    Volume 97, Issue s457, April 2008, Pages: 106–113,

    Version of Record online : 13 MAR 2008, DOI: 10.1111/j.1651-2227.2008.00657_2.x

  4. MUCOPOLYSACCHARIDE DISORDERS AND OTHER LYSOSOMAL STORAGE DISEASES

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 111–112,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_8.x

  5. FABRY DISEASE: EFFICACY OF ENZYME REPLACEMENT THERAPY

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 102–105,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_4.x

  6. MUCOPOLYSACCHARIDOSIS TYPE II

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 109–111,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_7.x

  7. FABRY DISEASE: SKIN MANIFESTATIONS; CARDIAC DISEASE; CASE REPORTS

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 100–102,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_3.x

  8. FABRY DISEASE: SAFETY

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 108–109,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_6.x

  9. FABRY DISEASE: PATHOPHYSIOLOGY; CNS MANIFESTATIONS; ENZYMES FOR REPLACEMENT THERAPY

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 98–99,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_2.x

  10. GAUCHER DISEASE: PATHOPHYSIOLOGY AND TREATMENT

    Acta Paediatrica

    Volume 96, Issue s455, April 2007, Pages: 106–107,

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1651-2227.2006.00219_5.x

  11. The kidney in Fabry's disease

    Clinical Genetics

    Volume 86, Issue 4, October 2014, Pages: 301–309, A. Pisani, B. Visciano, M. Imbriaco, A. Di Nuzzi, A. Mancini, C. Marchetiello and E. Riccio

    Version of Record online : 30 MAY 2014, DOI: 10.1111/cge.12386

  12. Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey

    International Journal of Clinical Practice

    Volume 60, Issue 9, September 2006, Pages: 1053–1059, O. LIDOVE, U. RAMASWAMI, R. JAUSSAUD, F. BARBEY, T. MAISONOBE, C. CAILLAUD, M. BECK, G. SUNDER-PLASSMANN, A. LINHART, A MEHTA and THE FOS EUROPEAN INVESTIGATORS

    Version of Record online : 10 AUG 2006, DOI: 10.1111/j.1742-1241.2006.01061.x

  13. MUCOPOLYSACCHARIDOSIS DISORDERS

    Acta Paediatrica

    Volume 97, Issue s457, April 2008, Pages: 97–105,

    Version of Record online : 13 MAR 2008, DOI: 10.1111/j.1651-2227.2008.00657_1.x

  14. OTHER LYSOSOMAL STORAGE DISEASES

    Acta Paediatrica

    Volume 97, Issue s457, April 2008, Pages: 119–122,

    Version of Record online : 13 MAR 2008, DOI: 10.1111/j.1651-2227.2008.00657_4.x

  15. Fabry disease in children: agalsidase-beta enzyme replacement therapy

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 432–438, L Borgwardt, U Feldt-Rasmussen, AK Rasmussen, M Ballegaard and A Meldgaard Lund

    Version of Record online : 27 SEP 2012, DOI: 10.1111/j.1399-0004.2012.01947.x

  16. Aseptic meningitis and ischaemic stroke in Fabry disease

    International Journal of Clinical Practice

    Volume 63, Issue 11, November 2009, Pages: 1663–1667, O. Lidove, M.-P. Chauveheid, C. Caillaud, R. Froissart, L. Benoist, S. Alamowitch, S. Doan, R. Szalat, N. Baumann, J.-F. Alexandra, P. Lavallée, I. Klein, F. Vuillemet, F. Sedel, K. Sacré, Y. Samson, E. Roullet and T. Papo

    Version of Record online : 9 OCT 2009, DOI: 10.1111/j.1742-1241.2009.02115.x

  17. You have full text access to this OnlineOpen article
    Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications

    Journal of Internal Medicine

    Volume 274, Issue 4, October 2013, Pages: 331–341, F. Weidemann, M. Niemann, S. Störk, F. Breunig, M. Beer, C. Sommer, S. Herrmann, G. Ertl and C. Wanner

    Version of Record online : 6 MAY 2013, DOI: 10.1111/joim.12077

  18. Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey

    European Journal of Clinical Investigation

    Volume 34, Issue 3, March 2004, Pages: 236–242, A. Mehta, R. Ricci, U. Widmer, F. Dehout, A. Garcia de Lorenzo, C. Kampmann, A. Linhart, G. Sunder-Plassmann, M. Ries and M. Beck

    Version of Record online : 15 MAR 2004, DOI: 10.1111/j.1365-2362.2004.01309.x

  19. Does geographical location influence the phenotype of Fabry disease in women in Europe?

    Clinical Genetics

    Volume 77, Issue 2, February 2010, Pages: 131–140, M-Á Barba-Romero, P Deegan, R Giugliani and D Hughes

    Version of Record online : 11 JAN 2010, DOI: 10.1111/j.1399-0004.2009.01345.x

  20. You have free access to this content
    Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women

    European Journal of Heart Failure

    Volume 12, Issue 6, June 2010, Pages: 535–540, Ole Havndrup, Michael Christiansen, Birgitte Stoevring, Morten Jensen, Jakob Hoffman-Bang, Paal Skytt Andersen, Lis Hasholt, Anne Nørremølle, Ulla Feldt-Rasmussen, Lars Køber and Henning Bundgaard

    Version of Record online : 13 JAN 2014, DOI: 10.1093/eurjhf/hfq073