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Journal of Pediatric Neurosciences|October 12, 2020
Clinico-radiological Profile of Children with Pontocerebellar HypoplasiaAnanthanarayanan Kasinathan, Naveen Sankhyan, Tessa Van Dijk, et al.Orphanet Journal of Rare Diseases|June 16, 2018
What's new in pontocerebellar hypoplasia? An update on genes and subtypesTessa van Dijk, Frank Baas, Peter G Barth, et al.Neuropediatrics|October 28, 2020
Postnatal Brain Growth Patterns in Pontocerebellar HypoplasiaTessa van Dijk, Peter Barth, Frank Baas, et al.Journal of Vector Borne Diseases|July 30, 2025
The In2Care® EaveTubes improved protection against malaria vectors in a small-scale field study at Kagera Sugar Ltd, Missenyi, TanzaniaEliningaya J Kweka, Marit Farenhorst, Tessa van Dijk, et al.American Journal of Medical Genetics. Part A|November 19, 2016
A de novo missense mutation in the inositol 1,4,5-triphosphate receptor type 1 gene causing severe pontine and cerebellar hypoplasia: Expanding the phenotype of ITPR1-related spinocerebellar ataxia'sTessa van Dijk, Peter Barth, Liesbeth Reneman, et al.International Journal of Neonatal Screening|March 3, 2021
Informing Parents about Newborn Screening: A European Comparison StudyAmber IJzebrink, Tessa van Dijk, Věra Franková, et al.Health Policy (Amsterdam, Netherlands)|June 5, 2021
Power, legitimacy and urgency: Unravelling the relationship between Dutch healthcare organisations and their financial stakeholdersT S Tessa van Dijk, W K Wilma van der Scheer, R T J M Richard JanssenJournal of Inherited Metabolic Disease|February 22, 2018
A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxiaTessa van Dijk, Jan-Dirk Vermeij, Silvana van Koningsbruggen, et al.Orphanet Journal of Rare Diseases|June 2, 2023
A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their childLieke M van den Heuvel, Adriana Kater-Kuipers, Tessa van Dijk, et al.JIMD Reports|September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.Pageof 2