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STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brain

Neuropathology and applied neurobiology, 2021-02, Vol.47 (1), p.127-142

2021

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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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Mitochondrial complex I defect resulting from exercise-induced lower-limb ischemia in patients with peripheral arterial disease

Journal of applied physiology (1985), 2018-09, Vol.125 (3), p.938-946

2018

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Abundant electrical myotonia and left ventricular noncompaction: Unusual features of Danon disease due to a novel mutation in LAMP2 gene

Revue neurologique, 2019-03, Vol.175 (3), p.201-203

2019

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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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Neuropathologie de la sclérose latérale amyotrophique sporadique

Pratique neurologique - FMC, 2021-12, Vol.12 (4), p.267-276

2021

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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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Wernicke encephalopathy and Creutzfeldt-Jakob disease

Journal of neurology, 2009-06, Vol.256 (6), p.904-909

2009

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Neurofilament high molecular weight–green fluorescent protein fusion is normally expressed in neurons and transported in axons: A neuronal marker to investigate the biology of neurofilaments

Neuroscience, 2006, Vol.137 (1), p.103-111

2006

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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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Dementia: Where are the Lewy bodies?

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

2013

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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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Chronic inflammatory demyelinating polyneuropathy in Waldenström's macroglobulinemia

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

2011

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Demyelinating neuropathy during anti-TNF alpha treatment with a review of the literature

Revue neurologique, 2007-12, Vol.163 (12), p.1232

2007

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Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis

Diabetes & metabolism, 2008-12, Vol.34 (6), p.620-626

2008

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Nemaline bodies as unique pathological feature in the course of treated dermatomyositis

Clinical neuropathology, 2010-11, Vol.29 (6), p.357

2010

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Étude du phénotype de la réponse musculaire au cours des syndrome des anti-synthétases par transcriptomique spatiale : implication de l’IFN-II et des macrophages dans la survie des lymphocytes B

La revue de medecine interne, 2023-12, Vol.44, p.A373-A374

2023

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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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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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Stable Tubule Only Polypeptides (STOP) Proteins Co-Aggregate with Spheroid Neurofilaments in Amyotrophic Lateral Sclerosis

Journal of neuropathology and experimental neurology, 2003-12, Vol.62 (12), p.1211-1219

2003

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DISTAL MYOPATHIES

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S72

2021

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DISTAL MYOPATHIES: EP.76 Mutations in the prion-like domain of heterogenous nuclear ribonuclearprotein A1 (HNRNPA1) cause proximal and distal myopathies

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S72-S72

2021

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

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

2017

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Two clinicopathological cases of a dominantly inherited, adult onset orthochromatic leucodystrophy

Journal of neurology, neurosurgery and psychiatry, 2003-05, Vol.74 (5), p.671-673

2003

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STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brain

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

Mitochondrial complex I defect resulting from exercise-induced lower-limb ischemia in patients with peripheral arterial disease

Abundant electrical myotonia and left ventricular noncompaction: Unusual features of Danon disease due to a novel mutation in LAMP2 gene

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

Neuropathologie de la sclérose latérale amyotrophique sporadique

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

Wernicke encephalopathy and Creutzfeldt-Jakob disease

Neurofilament high molecular weight–green fluorescent protein fusion is normally expressed in neurons and transported in axons: A neuronal marker to investigate the biology of neurofilaments

Démences : où sont les corps de Lewy ?

Dementia: Where are the Lewy bodies?

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

Chronic inflammatory demyelinating polyneuropathy in Waldenström's macroglobulinemia

Demyelinating neuropathy during anti-TNF alpha treatment with a review of the literature

Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis

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

Nemaline bodies as unique pathological feature in the course of treated dermatomyositis

Étude du phénotype de la réponse musculaire au cours des syndrome des anti-synthétases par transcriptomique spatiale : implication de l’IFN-II et des macrophages dans la survie des lymphocytes B

Increased prevalence of granulovacuolar degeneration in C9orf72 mutation

Phenotype associated with APP duplication in five families

Stable Tubule Only Polypeptides (STOP) Proteins Co-Aggregate with Spheroid Neurofilaments in Amyotrophic Lateral Sclerosis

DISTAL MYOPATHIES

DISTAL MYOPATHIES: EP.76 Mutations in the prion-like domain of heterogenous nuclear ribonuclearprotein A1 (HNRNPA1) cause proximal and distal myopathies

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

Two clinicopathological cases of a dominantly inherited, adult onset orthochromatic leucodystrophy

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