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Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration

Proceedings of the National Academy of Sciences - PNAS, 2012-06, Vol.109 (24), p.9611-9616

2012

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Insulin resistance and exendin-4 treatment for multiple system atrophy

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.1420-1436

2017

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Recurrent Mutations of MYD88 and TBL1XR1 in Primary Central Nervous System Lymphomas

Clinical cancer research, 2012-10, Vol.18 (19), p.5203-5211

2012

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Increasing incidence of central nervous system (CNS) tumors (2000-2012): findings from a population based registry in Gironde (France)

BMC cancer, 2018-06, Vol.18 (1), p.653-653, Article 653

2018

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Spinal miRNA-124 regulates synaptopodin and nociception in an animal model of bone cancer pain

Scientific reports, 2017-09, Vol.7 (1), p.10949-13, Article 10949

2017

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Genetic Alterations in Gliosarcoma and Giant Cell Glioblastoma

Brain pathology (Zurich, Switzerland), 2016-07, Vol.26 (4), p.517-522

2016

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Phenotype and imaging features associated with APP duplications

Alzheimer's research & therapy, 2023-05, Vol.15 (1), p.93-93, Article 93

2023

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Deep brain stimulation does not enhance neuroinflammation in multiple system atrophy

Neurobiology of disease, 2018-10, Vol.118, p.155-160

2018

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New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers

Frontiers in neuroscience, 2018-08, Vol.12, p.589-589

2018

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Autophagy inhibition cooperates with erlotinib to induce glioblastoma cell death

Cancer biology & therapy, 2011-06, Vol.11 (12), p.1017-1027

2011

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Combined nerve and muscle biopsy in the diagnosis of vasculitic neuropathy. A 16-year retrospective study of 202 cases

Journal of the peripheral nervous system, 2006-03, Vol.11 (1), p.20-29

2006

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Region-Specific Alterations of Matrix Metalloproteinase Activity in Multiple System Atrophy

Movement disorders, 2015-11, Vol.30 (13), p.1802-1812

2015

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Mitochondria and Peripheral Neuropathies

Journal of neuropathology and experimental neurology, 2012-12, Vol.71 (12), p.1036-1046

2012

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Astrocytosis in parkinsonism: considering tripartite striatal synapses in physiopathology?

Frontiers in aging neuroscience, 2014-09, Vol.6, p.258-258

2014

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Alterations in the RB1 Pathway in Low-grade Diffuse Gliomas Lacking Common Genetic Alterations

Brain pathology (Zurich, Switzerland), 2011-11, Vol.21 (6), p.645-651

2011

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Axonal sensory motor neuropathy in copper-deficient Wilson's disease

Muscle & nerve, 2009-08, Vol.40 (2), p.294-296

2009

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Intra-axonal protein aggregation in the peripheral nervous system

Journal of the peripheral nervous system, 2014-03, Vol.19 (1), p.44-49

2014

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Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old man

BMC neurology, 2016-07, Vol.16 (1), p.122-122, Article 122

2016

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11th European Congress 194 of Neuropathology Bordeaux, France, July 6 − 9, 2016

Clinical neuropathology, 2016-07, Vol.35 (7), p.194-261

Vital, Anne

2016

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Presence of crystalline inclusions in the peripheral nerve of a patient with IgA lambda monoclonal gammopathy of undetermined significance

Neuropathology, 2008-10, Vol.28 (5), p.526-531

2008

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Ambiguous mechanisms of dysphagia in multiple system atrophy

Brain (London, England : 1878), 2012-02, Vol.135 (2), p.e205-e205

2012

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Are substantia nigra neurons subject to mitochondrial dysfunction in early life more able to adapt?

Movement disorders, 2013-10, Vol.28 (12), p.1638-1638

2013

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Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)

Journal of the peripheral nervous system, 2009-09, Vol.14 (3), p.206-207

2009

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Genes regulated in MPTP-treated macaques and human Parkinson's disease suggest a common signature in prefrontal cortex

Neurobiology of disease, 2010-06, Vol.38 (3), p.386-394

2010

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A sporadic case of Creutzfeldt–Jakob disease with beta‐amyloid deposits and alpha‐synuclein inclusions

Neuropathology, 2007-06, Vol.27 (3), p.273-277

2007

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Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration

Insulin resistance and exendin-4 treatment for multiple system atrophy

Recurrent Mutations of MYD88 and TBL1XR1 in Primary Central Nervous System Lymphomas

Increasing incidence of central nervous system (CNS) tumors (2000-2012): findings from a population based registry in Gironde (France)

Spinal miRNA-124 regulates synaptopodin and nociception in an animal model of bone cancer pain

Genetic Alterations in Gliosarcoma and Giant Cell Glioblastoma

Phenotype and imaging features associated with APP duplications

Deep brain stimulation does not enhance neuroinflammation in multiple system atrophy

New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers

Autophagy inhibition cooperates with erlotinib to induce glioblastoma cell death

Combined nerve and muscle biopsy in the diagnosis of vasculitic neuropathy. A 16-year retrospective study of 202 cases

Region-Specific Alterations of Matrix Metalloproteinase Activity in Multiple System Atrophy

Mitochondria and Peripheral Neuropathies

Astrocytosis in parkinsonism: considering tripartite striatal synapses in physiopathology?

Alterations in the RB1 Pathway in Low-grade Diffuse Gliomas Lacking Common Genetic Alterations

Axonal sensory motor neuropathy in copper-deficient Wilson's disease

Intra-axonal protein aggregation in the peripheral nervous system

Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old man

11th European Congress 194 of Neuropathology Bordeaux, France, July 6 − 9, 2016

Presence of crystalline inclusions in the peripheral nerve of a patient with IgA lambda monoclonal gammopathy of undetermined significance

Ambiguous mechanisms of dysphagia in multiple system atrophy

Are substantia nigra neurons subject to mitochondrial dysfunction in early life more able to adapt?

Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)

Genes regulated in MPTP-treated macaques and human Parkinson's disease suggest a common signature in prefrontal cortex

A sporadic case of Creutzfeldt–Jakob disease with beta‐amyloid deposits and alpha‐synuclein inclusions

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