Vincent Huin

Associate professor

Université de Lille

France

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Dr. Vincent Huin is an Associate Professor at the University of Lille Nord de France, France. His research focuses on areas including iron chelation, neurodegenerative diseases, and genetic mutations associated with varying phenotypes of parkinsonism and Alzheimer's disease. He has contributed to the field through several recent publications, exploring critical links between tau pathology, insulin resistance, and clinical presentations in neurological disorders.

Articles (22)

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2025

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2021

Collaborators (10)

Cécile Delarasse

Sorbonne Université

FRANCE

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Franco Taroni

Head

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Benoît Delatour

CNRS Délégation Paris B

FRANCE

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danielle seilhean

Professor

Assistance Publique - Hôpitaux de Paris

FRANCE

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Cyril Goizet

Professeur PU-PH

University of Bordeaux

FRANCE

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Daniela Di Bella

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Elena Rossini

Sapienza University of Rome

ITALY

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Jean-Marc Taymans

Associate Professor

Université de Lille

FRANCE

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Giovanni Stevanin

Directeur d'Etudes Cumulant (Professor)

École Pratique des Hautes Études

FRANCE

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Alexandra Durr

Professor, MD, PhD,

Sorbonne Université

FRANCE

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Vincent Huin

Research Interests

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Articles (22)

Conservative iron chelation for VAC14: Two-year clinical-radiological follow-up

Two case reports of RAB39B deletion displaying highly variable parkinsonism

Two case reports of<i> RAB39B</i> deletion displaying highly variable parkinsonism

Comparing high and low amyloid producers in Alzheimer's disease: An in-depth analysis

Comparing high and low amyloid producers in Alzheimer's disease: An in-depth analysis

HMGA1 deficiency: a pathogenic link between tau pathology and insulin resistance

HMGA1 deficiency: a pathogenic link between tau pathology and insulin resistance

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease

Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case report

Reply to: “Further Evidence of Cerebellar Cognitive Affective/Schmahmann Syndrome in RFC1‐Related Syndrome”

Pseudohypoaldosteronism type II and sensory neuropathy associated with a heterozygous pathogenic variant in KLHL3 gene, a case report

Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case report

Two RFC1 splicing variants in CANVAS

Indication for molecular testing by multiplex ligation-dependent probe amplification in parkinsonism.

Motor neuron pathology in CANVAS due to RFC1 expansions.

Conservative Iron Chelation for Neuroferritinopathy.

Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.

Cramp-fasciculation syndrome phenotype of cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) due to RFC1 repeat expansion

Neuronal ApoE4 stimulates C/EBPβ activation, promoting Alzheimer’s disease pathology in a mouse model

Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson's Disease.

P2X7-deficiency improves plasticity and cognitive abilities in a mouse model of Tauopathy

Equilibrative nucleoside transporter 1 inhibition rescues energy dysfunction and pathology in a model of tauopathy

Collaborators (10)

Cécile Delarasse

Franco Taroni

Benoît Delatour

danielle seilhean

Cyril Goizet

Daniela Di Bella

Elena Rossini

Jean-Marc Taymans

Giovanni Stevanin

Alexandra Durr

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