Paul J. Van Vught
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 15 publications
SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis.
Journal: Neurology. Genetics
Published: January 21, 2021
Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common Aneuploidies.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: December 04, 2018
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.
Journal: PloS one
Published: February 12, 2018
Same-day subtyping of Campylobacter jejuni and C. coli isolates by use of multiplex ligation-dependent probe amplification-binary typing.
Journal: Journal of clinical microbiology
Published: July 04, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study.
Journal: Neurobiology of aging
Published: March 08, 2014
Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: January 10, 2013
Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.
Journal: Neurobiology of aging
Published: June 28, 2012
Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophy.
Journal: Archives of neurology
Published: June 13, 2012
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.
Journal: Neurobiology of aging
Published: May 31, 2012
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.
Journal: Human molecular genetics
Published: March 02, 2012
SMN1 gene duplications are associated with sporadic ALS.
Journal: Neurology
Published: February 11, 2012
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.
Journal: Annals of neurology
Published: December 23, 2011
Last Updated: 09/26/2026