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List of works by Nadine G Andersson

Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.

scientific article published on 27 July 2017

Common themes and challenges in hemophilia care: a multinational perspective

scientific article published on 03 August 2018

Genetic screening of children with suspected inherited bleeding disorders

scientific article published on 26 February 2020

Intracranial haemorrhage in children and adolescents with severe haemophilia A or B - the impact of prophylactic treatment.

scientific article published on 12 July 2017

Long-term follow-up of neonatal intracranial haemorrhage in children with severe haemophilia

scientific article published on 09 June 2020

Novel F8 and F9 gene variants from the PedNet Hemophilia Registry classified according to ACMG/AMP guidelines

scientific article published on 15 September 2020

Safety and efficacy of nonacog alfa for the treatment of haemophilia B in children younger than 6 years of age in a routine clinical care setting: the EUREKIX registry study

scientific article published on 05 December 2020

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