Search Results - "Joosten, Anneke"

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  1. 1

    Idiopathic Hypereosinophilic Syndrome Presenting With Embolic Stroke by Silva, Magda S, Ramalho, Carina, Ferreira, Francelino, Maia, Inês, Joosten, Anneke

    Published in Curēus (Palo Alto, CA) (06-11-2021)
    “…Hypereosinophilic syndrome is a rare condition characterized by eosinophilia associated with organ damage, most commonly affecting the skin, lung,…”
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    Journal Article
  2. 2

    Fatal case of progressive Mpox in a patient with AIDS: viral enteropathy and malabsorption demanding the use of full parenteral ARV and endovenous Cidofovir by Caria, João, Vara-Luiz, Francisco, Maia, Inês, Joosten, Anneke, Val-Flores, Luís, Pinheiro, Hélder, Póvoas, Diana, Germano, Nuno, Maltez, Fernando

    Published in Infectious disease reports (16-03-2023)
    “…© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative…”
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    Journal Article
  3. 3

    Tension Pneumothorax as Initial Manifestation of Granulomatosis with Polyangiitis (GPA) by Reis, Rúben, Joosten, Anneke, Ferreira, Francelino, Silva, Magda, Parente, Catarina, Maia, Inês

    “…Granulomatosis with polyangiitis (Wegener's granulomatosis) is a systemic vasculitis that primarily affects small and medium vessels. Its manifestations are…”
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    Journal Article
  4. 4

    ATP8B1 is essential for maintaining normal hearing by Stapelbroek, Janneke M, Peters, Theo A, van Beurden, Denis H.A, Curfs, Jo H.A.J, Joosten, Anneke, Beynon, Andy J, van Leeuwen, Bibian M, van der Velden, Lieke M, Bull, Laura, Oude Elferink, Ronald P, van Zanten, Bert A, Klomp, Leo W.J, Houwen, Roderick H.J

    “…ATP8B1 deficiency is caused by autosomal recessive mutations in ATP8B1, which encodes the putative phospatidylserine flippase ATP8B1 (formerly called FIC1)…”
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  5. 5

    A patient with unexplained neurological symptoms by Maris-Boes, Ester S, Ramdhani-Joosten, Anneke A J, Scholte-Stalenhoef, Anne Neeltje

    Published in Nederlands tijdschrift voor geneeskunde (29-08-2019)
    “…In this case of a 54-year-old woman, severe impairment of motor and sensory function - that could not be assigned to any neurological disease - was diagnosed…”
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    Journal Article
  6. 6