Federación Chilena de Enfermedades Raras,
sindrome hemolitico uremico atipico
sindrome hemolitico uremico atipico
aHUS international patient registry, families making a difference in moving forward atypical HUS research. Thanks to all the…
It's Rare DiseaseDay 2018: Celebrate the value of patient engagement in research. Published research with aHUS Alliance…
Patients as Partners - Patient Experiences add Insight Len Woodward and Emma Woodward of aHUSUK recently shared information…