Andoni Laguna-Echaniz

Paris, France

Last Updated: 09/26/2026

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Found 148 publications

Asymptomatic Carrier Neurologic Assessment: A Tool for Early Detection of Symptomatic Transition in Pathogenic TTR Gene Variant Carriers.

Asymptomatic Carrier Neurologic Assessment: A Tool for Early Detection of Symptomatic Transition in Pathogenic TTR Gene Variant Carriers.

Journal: European journal of neurology

Published: April 10, 2026

Long-term treatment outcomes of immune checkpoint inhibitor-related neuropathies: a French multicenter cohort study.

Long-term treatment outcomes of immune checkpoint inhibitor-related neuropathies: a French multicenter cohort study.

Journal: Scientific reports

Published: February 25, 2026

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Journal: Neurology

Published: January 15, 2026

Nexiguran Ziclumeran Gene Editing in Hereditary ATTR with Polyneuropathy.

Nexiguran Ziclumeran Gene Editing in Hereditary ATTR with Polyneuropathy.

Journal: The New England journal of medicine

Published: September 26, 2025

Characteristics of Patients with Myasthenia Gravis in the French Rare Disease Registry.

Characteristics of Patients with Myasthenia Gravis in the French Rare Disease Registry.

Journal: European journal of neurology

Published: July 08, 2025

Myasthenia Gravis Outcomes After Use of Statins and Other Contraindicated Treatments: Results From the French National Insurance Database.

Myasthenia Gravis Outcomes After Use of Statins and Other Contraindicated Treatments: Results From the French National Insurance Database.

Journal: European journal of neurology

Published: June 17, 2025

Laminopathies: natural history and risk prediction of heart failure.

Laminopathies: natural history and risk prediction of heart failure.

Journal: European heart journal

Published: June 06, 2025

Diagnostic & therapeutic challenges of presymptomatic hereditary transthyretin amyloidosis.

Diagnostic & therapeutic challenges of presymptomatic hereditary transthyretin amyloidosis.

Journal: Revue neurologique

Published: April 09, 2025

Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy.

Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy.

Journal: European journal of neurology

Published: April 08, 2025

Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR).

Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR).

Journal: European journal of neurology

Published: April 03, 2025

Intracutaneous Amyloid Deposition is Associated With Nerve Conduction Studies Deterioration in Presumed Asymptomatic Pathogenic Variant TTR Carriers.

Intracutaneous Amyloid Deposition is Associated With Nerve Conduction Studies Deterioration in Presumed Asymptomatic Pathogenic Variant TTR Carriers.

Journal: European journal of neurology

Published: February 13, 2025

Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.

Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.

Journal: medRxiv : the preprint server for health sciences

Published: January 13, 2025

Showing 1-12 of 148

Last Updated: 09/26/2026