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38 Possible Causes for lavrijsen

  • Invasive Pulmonary Aspergillosis

    Infection 2008; 36: 533–538 Crossref Web of Science Google Scholar [22] Heykants J, van Peer A, van de Velde V, van Rooy P, Meuldermans W, Lavrijsen K.[degruyter.com]

  • Congenital Ichthyosis

    Huber M, Rettler I, Bernasconi K, Frenk E, Lavrijsen SP, Ponec M, et al. Mutations of keratinocyte transglutaminase in lamellar ichthyosis.[ijp.tums.pub]

  • Lamellar Ichthyosis

    Reports M Huber , I Rettler , K Bernasconi , E Frenk , SP Lavrijsen , M Ponec , A Bon , S Lautenschlager , DF Schorderet , D Hohl Department of Dermatology, Centre Hospitalier[science.sciencemag.org] Huber M, Rettler I, Bernasconi K, Frenk E, Lavrijsen SP, Ponec M, Bon A, Lautenschlager S, Schorderet DF, Hohl D (1995) Mutations of keratinocyte transglutaminase in lamellar[link.springer.com] (eds), Rook/Wilkinson/Ebling: Textbook of Dematology , Blackwell Science, Oxford, pp. 1483 –1530. 4 Lavrijsen, A.P., Bouwstra, J.A., Gooris, G.S., Weerheim, A., Bodde, H.E[hmg.oxfordjournals.org]

  • Itraconazole

    Lavrijsen A, Balmus K, Nugteren-Huying W, et al "Hepatic injury associated with itraconazole." Lancet 340 (1992): 251-2 11.[drugs.com]

  • Foreign-Body Reaction

    Related publications Rothuizen TC, Damanik FF, Lavrijsen T, Visser MJ, Hamming JF, Lalai RA, Duijs JM, van Zonneveld AJ, Hoefer IE, van Blitterswijk CA, Rabelink TJ, Moroni[moronilab.org]

  • Heart Valve Prosthesis

    Tom Lavrijsen MSc Biomedical Engineering Principal R&D Engineer Xeltis open / download factsheet Depending on your Internet browser and the settings for the PDF reader program[lifetecgroup.com]

  • Rapp-Hodgkin Syndrome

    Breslau-Siderius EJ, Lavrijsen APM, Otten FWA, et al. The Rapp-Hodgkin syndrome. Am J Med Genet. 1991;38: 107-10. View abstract Moerman P, Fryns J-P.[health24.com] Breslau-Siderius EJ , Lavrijsen APM , Otten FWA , van der Schroeff JG , Swart JGN : The Rapp–Hodgkin syndrome . Am J Med Genet 1991; 38 : 107–110. 7.[nature.com]

  • Hypomagnesemia

    Ferrè S, de Baaij JH, Ferreira P, Germann R, de Klerk JB, Lavrijsen M, van Zeeland F, Venselaar H, Kluijtmans LA, Hoenderop JG, Bindels RJ: Mutations in PCBD1 cause hypomagnesemia[karger.com]

  • Carney Complex Type 1

    Paes EC, de Vries IAC, Penris WM, Hanny KH, Lavrijsen SW, van Leerdam EK, et al: Growth and prevalence of feeding difficulties in children with Robin sequence: a retrospective[karger.com]

  • Nemaline Myopathy 2

    Leijenaar JF2, Spliet WG3, Lavrijsen SW3, Jansen NJ3, Braun KP1, Mulder M2, Timmers-Raaijmakers B4, Ratsma K2, Dooijes D2, van Haelst MM2.[ncbi.nlm.nih.gov]

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