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Publications by Kåre Lehmann Nielsen

The Hsp60-(p.V98I) Mutation Associated With Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Bothin Vitroandin Vivo

Journal of Biological Chemistry

Molecular Biology

English

Related publications

Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

American Journal of Human Genetics

English

Hereditary Spastic Paraplegia

Schweizer Archiv für Neurologie und Psychiatrie

English

Protrudin Regulates Endoplasmic Reticulum Morphology and Function Associated With the Pathogenesis of Hereditary Spastic Paraplegia

Journal of Biological Chemistry

Molecular Biology

English

A Hereditary Spastic Paraplegia Mutation in Kinesin-1a/Kif5a Disrupts Neurofilament Transport

Molecular Neurodegeneration

Molecular Neuroscience

Molecular Biology

English

Hereditary Spastic Paraplegia and Amyotrophy Associated With a Novel Locus on Chromosome 19

Molecular Neuroscience

English

Hereditary Spastic Paraplegia Type 8 - Neuropathological Findings

Brain Pathology

Forensic Medicine

English

Hereditary Ataxia and Spastic Paraplegia in Portugal

English

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

American Journal of Human Genetics

English

AP4B1-associated Hereditary Spastic Paraplegia: Expansion of Phenotypic Spectrum Related to Homozygous p.Thr387fs Variant

Journal of Applied Genetics

English