Rudy Van Coster - Ghent University Hospital

基本信息

Career Trajectory

Bio

Additional expertise
Doctorate in Medical Sciences
Brain Metabolic Disorders
Genetic Brain Disorders in Children
Genetic Muscular Disorders in Children
Professor Emeritus Paediatric Neurology, Ghent University

Research Interests

Papers共 233 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选

Mtor Inhibition Enhances Delivery and Activity of Antisense Oligonucleotides in Uveal Melanoma Cells

Shanna Dewaele,Louis Delhaye,Boel De Paepe,Bram Bogaert, Ramiro Martinez,Jasper Anckaert,Nurten Yigit,Justine Nuytens,Rudy Van Coster,Sven Eyckerman,Koen Raemdonck,Pieter Mestdagh

NUCLEIC ACID THERAPEUTICS（2023）

Cited2Views0WOSBibtex

Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression

Sofie Boterberg,Elise Vantroys,Boel De Paepe,Rudy Van Coster,Herbert Roeyers

PLoS One（2022）

Cited2Views0WOSBibtex

RFC1 Repeat Expansions: A Recurrent Cause of Sensory and Autonomic Neuropathy with Cough and Ataxia

Danique Beijer,Maike F. Dohrn,Jonathan De Winter,Sarah Fazal,Andrea Cortese,Tanya Stojkovic,Gorka Fernandez-Eulate,Gauthier Remiche,Mattia Gentile,Rudy Van Coster,Claudia Dufke,Matthis Synofzik,Peter De Jonghe,Stephan Zuchner,Jonathan Baets

European Journal of Neurology（2022）

Cited19Views0WOSBibtex

Neonatal Lactic Acidosis Explained by LARS2 Defect

Boel De Paepe,Joél Smet,Robert Kopajtich,Holger Prokisch,Rudy Van Coster,Arnaud Vanlander

Pediatric research（2022）

Cited0Views0WOSNATUREBibtex

Nonketotic Hyperglycinaemia and Lipoate Deficiency Disorders

Johan L. K. Van Hove,Rudy Van Coster

Inborn Metabolic Diseasespp.459-469, (2022)

Cited1Views0Bibtex

Clinical Implementation of RNA Sequencing for Mendelian Disease Diagnostics

Yépez Vicente A.,Gusic Mirjana,Kopajtich Robert,Mertes Christian,Smith Nicholas H.,Alston Charlotte L.,Ban Rui,Beblo Skadi,Berutti Riccardo,Blessing Holger,Ciara Elżbieta,Distelmaier Felix,Freisinger Peter,Häberle Johannes,Hayflick Susan J.,Hempel Maja,Itkis Yulia S.,Kishita Yoshihito,Klopstock Thomas,Krylova Tatiana D.,Lamperti Costanza,Lenz Dominic,Makowski Christine,Mosegaard Signe,Müller Michaela F.,Muñoz-Pujol Gerard,Nadel Agnieszka,Ohtake Akira,Okazaki Yasushi,Procopio Elena,Schwarzmayr Thomas,Smet Joél,Staufner Christian,Stenton Sarah L.,Strom Tim M.,Terrile Caterina,Tort Frederic,Van Coster Rudy,Vanlander Arnaud,Wagner Matias,Xu Manting, Fang,Ghezzi Daniele,Mayr Johannes A.,Piekutowska-Abramczuk Dorota,Ribes Antonia,Rötig Agnès,Taylor Robert W.,Wortmann Saskia B.,Murayama Kei,Meitinger Thomas,Gagneur Julien,Prokisch Holger

Genome Medicineno. 1 (2022)

Cited82Views0WOSBibtex

Author Statistics

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