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Lista de obras de Tim Vanderhasselt

Abnormal primary gyration in relation to deep brain injury in preterm infants

artículo científico publicado en 2019

Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts

artículo científico publicado en 2017

Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations

scientific article published on 05 June 2018

Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review.

artículo científico publicado en 2013

Encephalitis associated with the SARS-CoV-2 virus: A case report

scientific article published on 10 July 2020

Expanding the clinical spectrum of biallelic ZNF335 variants.

artículo científico publicado en 2018

Hemangioperiocytoma simulating meningioma in a 41-year-old man

artículo científico publicado en 2014

Interhemispheric Connections between the Primary Visual Cortical Areas via the Anterior Commissure in Human Callosal Agenesis.

scientific article published on 26 December 2016

Multi-modality imaging in an exceptional case of aborted sudden cardiac death.

artículo científico publicado en 2013

Multinodular and vacuolating neuronal tumor of the cerebrum (MVNT): do not touch

scientific article published on 14 June 2019

Polymicrogyria with dysmorphic basal ganglia? Think tubulin!

artículo científico publicado en 2013

Postmastectomy lymphoedema: different patterns of fluid distribution visualised by ultrasound imaging compared with magnetic resonance imaging ⬇️

artículo científico publicado el 4 de diciembre de 2010

Synthetic MRI of Preterm Infants at Term-Equivalent Age: Evaluation of Diagnostic Image Quality and Automated Brain Volume Segmentation

scientific article published on 16 April 2020

The effect of acute cocoa flavanol intake on the BOLD response and cognitive function in type 1 diabetes: a randomized, placebo-controlled, double-blinded cross-over pilot study

scientific article published on 25 June 2019

Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: a case report and review of literature.

artículo científico

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