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RISK and SAFE signaling pathway involvement in apolipoprotein A-I-induced cardioprotection

PloS one, 2014-09, Vol.9 (9), p.e107950-e107950

2014

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Human subiculo-fornico-mamillary system in Alzheimer’s disease: Tau seeding by the pillar of the fornix

Acta neuropathologica, 2020-03, Vol.139 (3), p.443-461

2020

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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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Mycolactone gene expression is controlled by strong SigA-like promoters with utility in studies of Mycobacterium ulcerans and buruli ulcer

PLoS neglected tropical diseases, 2009-11, Vol.3 (11), p.e553-e553

2009

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Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletion

Neuromuscular disorders : NMD, 2021-05, Vol.31 (5), p.450-455

2021

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Increased prevalence of granulovacuolar degeneration in C9orf72 mutation

Acta neuropathologica, 2019-11, Vol.138 (5), p.783-793

2019

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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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Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells

Brain (London, England : 1878), 2023-09, Vol.146 (9), p.3624-3633

2023

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Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in mice

Progress in neurobiology, 2020-01, Vol.184, p.101698-101698, Article 101698

2020

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Melanoma tumour vasculature heterogeneity: from mice models to human

Journal of cancer research and clinical oncology, 2019-03, Vol.145 (3), p.589-597

2019

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Normal meninges harbor oncogenic somatic mutations in meningioma-driver genes

Acta neuropathologica, 2023-12, Vol.146 (6), p.833-835

2023

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Photo-responsive polymer with erasable and reconfigurable micro- and nano-patterns: An in vitro study for neuron guidance

Colloids and surfaces, B, Biointerfaces, 2011-11, Vol.88 (1), p.63-71

2011

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Phenotype associated with APP duplication in five families

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.2966-2976

2006

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Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4)

Journal of neuropathology and experimental neurology, 2018-09, Vol.77 (9), p.793-802

2018

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

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

2017

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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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Myoadenylate deaminase deficiency: a frequent cause of muscle pain A case detected by exercise testing

Annales de biologie clinique (Paris), 2017-07, Vol.75 (4), p.445-449

2017

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Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Neurogenetics, 2009-04, Vol.10 (2), p.145-150

2009

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Myoadenylate deaminase deficiency: a frequent cause of muscle pain A case detected by exercise testing

Annales de biologie clinique (Paris), 2017-08, Vol.75 (4), p.445-449

2017

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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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Necrotizing vasculitis revealed in a case of multiple mononeuropathy after a 14-year course of spontaneous remissions and relapses

Clinical neurology and neurosurgery, 2012-04, Vol.114 (3), p.290-293

2012

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RISK and SAFE signaling pathway involvement in apolipoprotein A-I-induced cardioprotection

Human subiculo-fornico-mamillary system in Alzheimer’s disease: Tau seeding by the pillar of the fornix

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

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

Mycolactone gene expression is controlled by strong SigA-like promoters with utility in studies of Mycobacterium ulcerans and buruli ulcer

Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletion

Increased prevalence of granulovacuolar degeneration in C9orf72 mutation

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

Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells

OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in mice

Melanoma tumour vasculature heterogeneity: from mice models to human

Normal meninges harbor oncogenic somatic mutations in meningioma-driver genes

Photo-responsive polymer with erasable and reconfigurable micro- and nano-patterns: An in vitro study for neuron guidance

Phenotype associated with APP duplication in five families

Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4)

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

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

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

MELAS syndrome causes glutamate and tricarboxylic acid cycle dysfunctions alleviated by ketone body treatment

Myoadenylate deaminase deficiency: a frequent cause of muscle pain A case detected by exercise testing

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Myoadenylate deaminase deficiency: a frequent cause of muscle pain A case detected by exercise testing

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

Necrotizing vasculitis revealed in a case of multiple mononeuropathy after a 14-year course of spontaneous remissions and relapses

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