Inger Nennesmo

Solna, AB 17176, Sweden

Last Updated: 09/26/2026

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Found 58 publications

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Journal: Human molecular genetics

Published: April 28, 2026

The Importance of Neuropathology in a Complex Movement Disorder with Primary Familial Brain Calcification.

The Importance of Neuropathology in a Complex Movement Disorder with Primary Familial Brain Calcification.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: November 09, 2025

Acquired Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline in Sweden-A Nationwide Population-Based Study.

Acquired Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline in Sweden-A Nationwide Population-Based Study.

Journal: European journal of neurology

Published: October 28, 2025

N-formyl methionine peptide-driven neutrophil activation in idiopathic inflammatory myopathies.

N-formyl methionine peptide-driven neutrophil activation in idiopathic inflammatory myopathies.

Journal: Rheumatology (Oxford, England)

Published: March 27, 2025

Phenotypic variability in early-onset dementia segregating with a novel APP (p.I718M) variant.

Phenotypic variability in early-onset dementia segregating with a novel APP (p.I718M) variant.

Journal: Alzheimer's research & therapy

Published: March 27, 2025

Author Correction: A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease.

Author Correction: A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease.

Journal: Scientific reports

Published: March 25, 2025

Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies.

Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies.

Journal: Muscle & nerve

Published: October 01, 2024

A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease.

A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease.

Journal: Scientific reports

Published: September 06, 2024

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder.

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: August 07, 2024

Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs.

Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs.

Journal: Journal of internal medicine

Published: July 08, 2024

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues.

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues.

Journal: NPJ Parkinson's disease

Published: September 12, 2023

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.

Journal: Neurology. Genetics

Published: June 07, 2023

Showing 1-12 of 58

Last Updated: 09/26/2026