Publications by authors named "Eline Hamilton"

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The natural history of variable subtypes in pediatric-onset TUBB4A-related leukodystrophy.
Francesco Gavazzi, Brittany Charsar, Eline Hamilton, Jacqueline A Erler, Virali Patel

Mol Genet Metab· March 2025

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Letter to the Editor: The Application of Interleukin-1 Antagonists in Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: Caution Warranted.
Eline M C Hamilton, Pinar Topaloglu, Jigyasha Sinha, Francesco Nicita, Geneviève Bernard

Pediatr Neurol· January 2024

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Aquaporin-4 and GPRC5B: old and new players in controlling brain oedema.
Emma M J Passchier, Sven Kerst, Eelke Brouwers, Eline M C Hamilton, Quinty Bisseling

Brain· August 2023

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Vanishing white matter: Eukaryotic initiation factor 2B model and the impact of missense mutations.
Inna Slynko, Stephanie Nguyen, Eline M C Hamilton, Lisanne E Wisse, Iwan J P de Esch

Mol Genet Genomic Med· March 2021

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Natural History of Vanishing White Matter.
Eline M C Hamilton, Hannemieke D W van der Lei, Gerre Vermeulen, Jan A M Gerver, Charles M Lourenço

Ann Neurol· August 2018

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Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.
Eline M C Hamilton, Pinar Tekturk, Fia Cialdella, Diane F van Rappard, Nicole I Wolf

Neurology· April 2018

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Seizures and disturbed brain potassium dynamics in the leukodystrophy megalencephalic leukoencephalopathy with subcortical cysts.
Mohit Dubey, Eelke Brouwers, Eline M C Hamilton, Oliver Stiedl, Marianna Bugiani

Ann Neurol· March 2018

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founder mutation in the Roma population causes recessive variant of H-ABC.
Eline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, Bharti Morar, Dana Dojčáková

Neurology· October 2017

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Reply: A novel TUBB4A mutation suggests that genotype-phenotype correlation of H-ABC syndrome needs to be revisited.
Eline M Hamilton, Nicole I Wolf, Marjo S van der Knaap

Brain· August 2015

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Reply: TUBB4A novel mutation reinforces the genotype-phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum.
Eline M Hamilton, Nicole I Wolf, Marjo S van der Knaap

Brain· February 2015

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Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation.
Eline M Hamilton, Emiel Polder, Adeline Vanderver, Sakkubai Naidu, Raphael Schiffmann

Brain· July 2014

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Reply: DARS2 gene clinical spectrum: new ideas regarding an underdiagnosed leukoencephalopathy.
Marjo S van der Knaap, Eline M Hamilton, Laura van Berge

Brain· July 2014

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Novel (ovario) leukodystrophy related to AARS2 mutations.
Cristina Dallabona, Daria Diodato, Sietske H Kevelam, Tobias B Haack, Lee-Jun Wong, Eline M Hamilton

Neurology· June 2014

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Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy.
Laura van Berge, Eline M Hamilton, Tarja Linnankivi, Graziella Uziel, Marjan E Steenweg

Brain· April 2014

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Novel cases of D-2-hydroxyglutaric aciduria with IDH1 or IDH2 mosaic mutations identified by amplicon deep sequencing.
Benjamin Nota, Eline M Hamilton, Daoud Sie, Senay Ozturk, Silvy J M van Dooren

J Med Genet· November 2013

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