1 – 10 of 23
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2024
-
Mark
Inventory of current practices regarding hematopoietic stem cell transplantation in metachromatic leukodystrophy in Europe and neighboring countries
(
- Contribution to journal › Article
-
Mark
Needs of amyloidosis patients and their care providers : design & first results of the AMY-NEEDS research and care program
(
- Contribution to journal › Article
-
Mark
Comment on Ombashi, van der Goes, Versnel, Khonsari, van der Molen: guidance to develop a multidisciplinary, international, pediatric registry: a systematic review, Orphanet Journal of Rare diseases, 2023
(
- Contribution to journal › Debate/Note/Editorial
- 2023
-
Mark
Overcoming challenges in rare disease registry integration using the semantic web - a clinical research perspective
(
- Contribution to journal › Letter
-
Mark
Schooling experiences in children with long-gap esophageal atresia compared with children with esophageal atresia and primary anastomosis : a Swedish study
(
- Contribution to journal › Article
- 2022
-
Mark
Postoperative morbidity and health-related quality of life in children with delayed reconstruction of esophageal atresia : a nationwide Swedish study
(
- Contribution to journal › Article
- 2020
-
Mark
Cross-cutting view of current challenges in paediatric solid organ and haematopoietic stem cell transplantation in Europe : The European Reference Network TransplantChild
(
- Contribution to journal › Article
- 2019
-
Mark
Arabidopsis thaliana alternative dehydrogenases : A potential therapy for mitochondrial complex i deficiency? Perspectives and pitfalls
(
- Contribution to journal › Article
-
Mark
Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; A consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability
(
- Contribution to journal › Article
-
Mark
Recommendations for patient screening in ultra-rare inherited metabolic diseases : What have we learned from Niemann-Pick disease type C?
(
- Contribution to journal › Scientific review