Laura V. Vandervore

Brussels, BRU, Belgium

Last Updated: 09/26/2026

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Found 10 publications

Aztreonam-avibactam synergy, a validation and comparison of diagnostic tools.

Aztreonam-avibactam synergy, a validation and comparison of diagnostic tools.

Journal: Frontiers in microbiology

Published: October 15, 2023

False positive Herpes Simplex IgM serology in COVID-19 patients correlates with SARS-CoV-2 IgM/IgG seropositivity.

False positive Herpes Simplex IgM serology in COVID-19 patients correlates with SARS-CoV-2 IgM/IgG seropositivity.

Journal: Diagnostic microbiology and infectious disease

Published: October 01, 2021

TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.

TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.

Journal: American journal of human genetics

Published: June 04, 2019

Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.

Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.

Journal: American journal of human genetics

Published: May 07, 2019

Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.

Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.

Journal: Brain : a journal of neurology

Published: September 07, 2018

MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance.

MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance.

Journal: American journal of human genetics

Published: June 30, 2018

Expanding the clinical spectrum of biallelic ZNF335 variants.

Expanding the clinical spectrum of biallelic ZNF335 variants.

Journal: Clinical genetics

Published: December 25, 2017

Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis.

Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis.

Journal: European journal of medical genetics

Published: September 28, 2017

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

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

Journal: European journal of medical genetics

Published: September 22, 2017

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

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

Journal: Journal of medical genetics

Published: November 01, 2016

Showing 1-10 of 10

Last Updated: 09/26/2026