Found: 5

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  • Infliximab for Paradoxical Reactions in Pediatric Central Nervous System Tuberculosis.

    Published in:
    Journal of the Pediatric Infectious Diseases Society, 2021, v. 10, n. 12, p. 1087, doi. 10.1093/jpids/piab094
    By:
    • Abo, Yara-Natalie;
    • Curtis, Nigel;
    • Osowicki, Joshua;
    • Haeusler, Gabrielle;
    • Purcell, Rachael;
    • Kadambari, Seilesh;
    • Wachter, Matthias De;
    • Driessche, Koen Vanden;
    • Dekeyzer, Sven;
    • Coleman, Lee;
    • Crawford, Nigel;
    • Graham, Steve;
    • Marais, Ben;
    • Gwee, Amanda
    Publication type:
    Article

  • The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders.

    Published in:
    Brain: A Journal of Neurology, 2024, v. 147, n. 8, p. 2775, doi. 10.1093/brain/awae056
    By:
    • Sidpra, Jai;
    • Sudhakar, Sniya;
    • Biswas, Asthik;
    • Massey, Flavia;
    • Turchetti, Valentina;
    • Lau, Tracy;
    • Cook, Edward;
    • Alvi, Javeria Raza;
    • Elbendary, Hasnaa M;
    • Jewell, Jerry L;
    • Riva, Antonella;
    • Orsini, Alessandro;
    • Vignoli, Aglaia;
    • Federico, Zara;
    • Rosenblum, Jessica;
    • Schoonjans, An-Sofie;
    • Wachter, Matthias de;
    • Alvarez, Ignacio Delgado;
    • Felipe-Rucián, Ana;
    • Haridy, Nourelhoda A
    Publication type:
    Article

  • Developmental epileptic encephalopathy in DLG4‐related synaptopathy.

    Published in:
    Epilepsia (Series 4), 2024, v. 65, n. 4, p. 1029, doi. 10.1111/epi.17876
    By:
    • Kassabian, Benedetta;
    • Levy, Amanda M.;
    • Gardella, Elena;
    • Aledo‐Serrano, Angel;
    • Ananth, Amitha L.;
    • Brea‐Fernández, Alejandro J.;
    • Caumes, Roseline;
    • Chatron, Nicolas;
    • Dainelli, Alice;
    • De Wachter, Matthias;
    • Denommé‐Pichon, Anne‐Sophie;
    • Dye, Thomas J.;
    • Fazzi, Elisa;
    • Felt, Roxanne;
    • Fernández‐Jaén, Alberto;
    • Fernández‐Prieto, Montse;
    • Gantz, Emily;
    • Gasperowicz, Piotr;
    • Gil‐Nagel, Antonio;
    • Gómez‐Andrés, David
    Publication type:
    Article

  • Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.

    Published in:
    Clinical Genetics, 2022, v. 102, n. 2, p. 98, doi. 10.1111/cge.14165
    By:
    • Christensen, Maria B.;
    • Levy, Amanda M.;
    • Mohammadi, Nazanin A.;
    • Niceta, Marcello;
    • Kaiyrzhanov, Rauan;
    • Dentici, Maria Lisa;
    • Al Alam, Chadi;
    • Alesi, Viola;
    • Benoit, Valérie;
    • Bhatia, Kailash P.;
    • Bierhals, Tatjana;
    • Boßelmann, Christian M.;
    • Buratti, Julien;
    • Callewaert, Bert;
    • Ceulemans, Berten;
    • Charles, Perrine;
    • De Wachter, Matthias;
    • Dehghani, Mohammadreza;
    • D'haenens, Erika;
    • Doco‐Fenzy, Martine
    Publication type:
    Article

  • ADA2 Deficiency Mimicking Acute Disseminated Encephalomyelitis.

    Published in:
    Journal of Clinical Immunology, 2023, v. 43, n. 3, p. 536, doi. 10.1007/s10875-022-01413-3
    By:
    • Ehlers, Lisa;
    • Bucciol, Giorgia;
    • KU Leuven - UZA DADA2 team;
    • Moens, Leen;
    • Hombrouck, Anneleen;
    • Delafontaine, Selket;
    • Ogunjimi, Benson;
    • De Wachter, Matthias;
    • Beysen, Diane;
    • Meyts, Isabelle
    Publication type:
    Article