Reducing complexity: explaining inborn errors of metabolism and their treatment to children and adolescentsZeltner, Nina A.; Welsink-Karssies, Mendy M.; Landolt, Markus A.; Bosshard-Bullinger, Dominique; Keller, Fabia; Bosch, Annet M.; Groenendijk, Marike; Grünert, Sarah C.; Karall, Daniela; Rettenbacher, Beatrix; Scholl-Bürgi, Sabine; Baumgartner, Matthias R.; Huemer, Martina · Orphanet Journal of Rare Diseases · 2019

Reviewer acknowledgement 2014Aymé, Ségolène · Orphanet Journal of Rare Diseases · 2014

National plans: case study BelgiumRi De Ridder · Orphanet Journal of Rare Diseases · 2012

Spina Bifida and primary preventionPierre Mertens · Orphanet Journal of Rare Diseases · 2012

Exon skipping for DMDAnnemieke Aartsma-Rus,Jan JGM Verschuuren… · Orphanet Journal of Rare Diseases · 2012

Gestational pemphigoidLaura Huilaja,Kaarin Mäkikallio,Kaisa Tasanen · Orphanet Journal of Rare Diseases · 2014

Ventricular septal defectSpicer, Diane E; Hsu, Hao H; Co-Vu, Jennifer; Anderson, Robert H; Fricker, F · Orphanet Journal of Rare Diseases · 2014

Managed entry agreementsMuscolo, Luisa AA; Bernardini, Claudia; Siviero, Paolo D; Montilla, Simona; Pani, Luca · Orphanet Journal of Rare Diseases · 2014

Empowerment Weekends for young adultsLemli, Annette; Schwarzer, Nicole · Orphanet Journal of Rare Diseases · 2014