Showing results (21-30 of 128) with videos related to

Sort By:
Pageof 13
Journal of Inherited Metabolic Disease|February 3, 2018
Timing of cognitive decline in CLN3 diseaseWillemijn F E Kuper, Claudia van Alfen, Roeliene H Rigterink, et al.
JIMD Reports|March 17, 2021
Automatic quantification of lymphocyte vacuolization in peripheral blood smears of patients with Batten's disease (CLN3 disease)Lourens J P Nonkes, Willemijn F E Kuper, Karin Berrens-Hogenbirk, et al.
The Journal of Bone and Joint Surgery. American Volume|January 14, 2021
Quantifying the Effects of Hip Surgery on the Sphericity of the Femoral Head in Patients with Mucopolysaccharidosis Type IEline L van der Veer, Willem Paul Gielis, Harry Weinans, et al.
The Journal of Hand Surgery|April 3, 2026
Trigger Digits in Mucopolysaccharidosis Type I: Clinical Characteristics, Surgical Outcomes, and Histopathological FindingsBoudewijn A W van Binsbergen, Joris A van Dongen, Linda Vriend, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|June 16, 2018
Salivary α-Iduronidase Activity as a Potential New Biomarker for the Diagnosis and Monitoring the Effect of Therapy in Mucopolysaccharidosis Type IJaap van Doorn, Brigitte T A van den Broek, Ans J Geboers, et al.
JIMD Reports|February 23, 2013
High incidence of symptomatic hyperammonemia in children with acute lymphoblastic leukemia receiving pegylated asparaginaseKatja M J Heitink-Pollé, Berthil H C M T Prinsen, Tom J de Koning, et al.
International Journal of Pediatrics|August 14, 2010
Exercise stress testing in children with metabolic or neuromuscular disordersTim Takken, Wim G Groen, Erik H Hulzebos, et al.
The Journal of Hand Surgery, European Volume|February 9, 2026
Carpal tunnel syndrome in mucopolysaccharidosis type I: clinical, surgical and histopathological findingsBoudewijn Aw van Binsbergen, Joris A van Dongen, Linda Vriend, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 16, 2011
[New Dutch practice guideline for administration of vitamin K to full-term newborns]J Peter de Winter, Koen F M Joosten, Marloes M Ijland, et al.
Human Molecular Genetics|July 8, 2010
Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylationJürgen Lübbehusen, Christian Thiel, Nina Rind, et al.
Pageof 13