Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases

RESEARCH

Reducing complexity: explaining inborn errors of metabolism and their treatment to children and adolescents

Nina A. Zeltner, Mendy M. Welsink-Karssies, Markus A. Landolt, Dominique Bosshard-Bullinger, Fabia Keller, Annet M. Bosch, Marike Groenendijk, Sarah C. Grünert, Daniela Karall, Beatrix Rettenbacher, Sabine Scholl-Bürgi, Matthias R. Baumgartner and Martina Huemer

Orphanet Journal of Rare Diseases 2019, 14:248 | Published on: 8 November 2019

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RESEARCH

The effect of impulsivity and inhibitory control deficits in the saccadic behavior of premanifest Huntington’s disease individuals

Filipa Júlio, Gina Caetano, Cristina Januário and Miguel Castelo-Branco

Orphanet Journal of Rare Diseases 2019, 14:246 | Published on: 8 November 2019

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RESEARCH

C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy

Nóra Garam, Zoltán Prohászka, Ágnes Szilágyi, Christof Aigner, Alice Schmidt, Martina Gaggl, Gere Sunder-Plassmann, Dóra Bajcsi, Jürgen Brunner, Alexandra Dumfarth, Daniel Cejka, Stefan Flaschberger, Hana Flögelova, Ágnes Haris, Ágnes Hartmann, Andreas Heilos…

Orphanet Journal of Rare Diseases 2019, 14:247 | Published on: 8 November 2019

Full Text | PDF

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