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5-Oxoprolinuria in hyperammonemic encephalopathy: Coincidence or worsening factor?

Clinical biochemistry, 2017-12, Vol.50 (18), p.1115-1117

2017

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The accumulation of assembly intermediates of the mitochondrial complex I matrix arm is reduced by limiting glucose uptake in a neuronal-like model of MELAS syndrome

Biochimica et biophysica acta. Molecular basis of disease, 2018-05, Vol.1864 (5), p.1596-1608

2018

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An autopsy case of acute multiple sclerosis (Marburg's type) during pregnancy

Clinical neurology and neurosurgery, 2008-05, Vol.110 (5), p.514-517

2008

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Axonal regeneration is compromised in NFH-LacZ transgenic mice but not in NFH-GFP mice

Neuroscience, 2013-01, Vol.228, p.101-108

2013

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Characterization of Cells Interactions with Patterned Azopolymer-Based Materials using SEM, AFM and Video Microscopy

The open biomedical engineering journal, 2018-11, Vol.12 (1), p.92-100

2018

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A chasing dead-end case report: a fatal lead intoxication following an attempted homicide

Forensic toxicology, 2020-07, Vol.38 (2), p.505-510

2020

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Chronic inflammatory demyelinating polyneuropathy in Waldenström's macroglobulinemia

Revue neurologique, 2011-04, Vol.167 (4), p.343-347

2011

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Correction: Mycolactone Gene Expression Is Controlled by Strong SigA-Like Promoters with Utility in Studies of and Buruli Ulcer

PLoS neglected tropical diseases, 2010-02, Vol.4 (2)

2010

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Correction: Mycolactone Gene Expression Is Controlled by Strong SigA-Like Promoters with Utility in Studies of Mycobacterium ulcerans and Buruli Ulcer

PLoS neglected tropical diseases, 2010-02, Vol.4 (2)

2010

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Correction to: A chasing dead-end case report: a fatal lead intoxication following an attempted homicide

Forensic toxicology, 2023, Vol.41 (1), p.184-184

2023

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Création et application d’une base de données relationnelle pour analyser les corrélations clinico-pathologiques dans les maladies neurodégénératives

Revue neurologique, 2023-04, Vol.179, p.S72-S74

2023

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Cytoskeleton abnormalities in axonopathies of unknown aetiology: correlations with morphometry

Journal of the neurological sciences, 2002-04, Vol.196 (1), p.53-61

2002

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Dedifferentiated cells obtained from glioblastoma cell lines are an easy and robust model for mesenchymal glioblastoma stem cells studies

American journal of cancer research, 2023-01, Vol.13 (4), p.1425-1442

2023

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Démences : où sont les corps de Lewy ?

Revue neurologique, 2013-11, Vol.169 (11), p.844-857

2013

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Design and application of a customizable relational DataBase to assess clinicopathological correlations and concomitant pathology in neurodegenerative diseases

Brain pathology (Zurich, Switzerland), 2023-05, Vol.33 (3), p.e13138-n/a

2023

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Diagnostic value of minor salivary glands biopsy for the detection of Lewy pathology

Neuroscience letters, 2013-09, Vol.551, p.62-64

2013

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Differences in clinical features between small fiber and sensitive large fiber neuropathies in Sjögren's syndrome

European journal of internal medicine, 2020-09, Vol.79, p.58-62

2020

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Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity

Mitochondrion, 2010-03, Vol.10 (2), p.115-124

2010

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Étude du cerveau humain à l’échelle nanoscopique par microscopie Super-Résolutive STORM

Revue neurologique, 2020-09, Vol.176, p.S105-S105

2020

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Evaluation of alpha-synuclein immunohistochemical methods for the detection of Lewy-type synucleinopathy in gastrointestinal biopsies

Acta neuropathologica communications, 2016-04, Vol.4 (35), p.35-35, Article 35

2016

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Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A

Neurology, 2017-01, Vol.88 (4), p.414-416

2017

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G51D [alpha]-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome

Annals of neurology, 2013-04, Vol.73 (4), p.459-471

2013

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G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome

Annals of neurology, 2013-04, Vol.73 (4), p.459-471

2013

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Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin

Journal of the peripheral nervous system : JPNS, 2008, Vol.13 (3), p.251-254

2008

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5-Oxoprolinuria in hyperammonemic encephalopathy: Coincidence or worsening factor?

The accumulation of assembly intermediates of the mitochondrial complex I matrix arm is reduced by limiting glucose uptake in a neuronal-like model of MELAS syndrome

An autopsy case of acute multiple sclerosis (Marburg's type) during pregnancy

Axonal regeneration is compromised in NFH-LacZ transgenic mice but not in NFH-GFP mice

Characterization of Cells Interactions with Patterned Azopolymer-Based Materials using SEM, AFM and Video Microscopy

A chasing dead-end case report: a fatal lead intoxication following an attempted homicide

Chronic inflammatory demyelinating polyneuropathy in Waldenström's macroglobulinemia

Correction: Mycolactone Gene Expression Is Controlled by Strong SigA-Like Promoters with Utility in Studies of and Buruli Ulcer

Correction: Mycolactone Gene Expression Is Controlled by Strong SigA-Like Promoters with Utility in Studies of Mycobacterium ulcerans and Buruli Ulcer

Correction to: A chasing dead-end case report: a fatal lead intoxication following an attempted homicide

Création et application d’une base de données relationnelle pour analyser les corrélations clinico-pathologiques dans les maladies neurodégénératives

Cytoskeleton abnormalities in axonopathies of unknown aetiology: correlations with morphometry

Dedifferentiated cells obtained from glioblastoma cell lines are an easy and robust model for mesenchymal glioblastoma stem cells studies

Démences : où sont les corps de Lewy ?

Design and application of a customizable relational DataBase to assess clinicopathological correlations and concomitant pathology in neurodegenerative diseases

Diagnostic value of minor salivary glands biopsy for the detection of Lewy pathology

Differences in clinical features between small fiber and sensitive large fiber neuropathies in Sjögren's syndrome

Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity

Étude du cerveau humain à l’échelle nanoscopique par microscopie Super-Résolutive STORM

Evaluation of alpha-synuclein immunohistochemical methods for the detection of Lewy-type synucleinopathy in gastrointestinal biopsies

Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A

G51D [alpha]-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome

G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome

Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure

Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin

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