J. Cassereau

发表

Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function.

V. Desquiret-Dumas, D. Bonneau, P. Amati‐Bonneau, 2012, The international journal of biochemistry & cell biology.

Improved Locus‐Specific Database for OPA1 Mutations Allows Inclusion of Advanced Clinical Data

D. Milea, D. Bonneau, P. Amati‐Bonneau, 2015, Human mutation.

Metabo-lipidomics of Fibroblasts and Mitochondrial-Endoplasmic Reticulum Extracts from ALS Patients Shows Alterations in Purine, Pyrimidine, Energetic, and Phospholipid Metabolisms

C. Bris, G. Lenaers, P. Reynier, 2019, Molecular Neurobiology.

Guillain‐BarrÉ syndrome subtype diagnosis: A prospective multicentric European study

J. Raymackers, J. Woodard, J. Cassereau, 2018, Muscle & nerve.

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

L. Brunereau, E. Malfatti, I. Richard, 2021, Neuromuscular Disorders.

Somatosensory evoked potentials in the assessment of peripheral neuropathies: Commented results of a survey among French-speaking practitioners and recommendations for practice

D. Guehl, O. Etard, P. Convers, 2015, Neurophysiologie Clinique/Clinical Neurophysiology.

Inherited peripheral neuropathies due to mitochondrial disorders.

B. Funalot, J. Cassereau, P. Codron, 2014, Revue neurologique.

Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions

G. Lenaers, P. Reynier, V. Procaccio, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Mitochondrial dysfunction and pathophysiology of Charcot–Marie–Tooth disease involving GDAP1 mutations

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2011, Experimental Neurology.

Towards personalized medicine for amyotrophic lateral sclerosis

P. Reynier, P. Corcia, J. Cassereau, 2021, Trends in Endocrinology & Metabolism.

Chronic inflammatory demyelinating polyneuropathy in Waldenström's macroglobulinemia.

F. Dubas, J. Cassereau, S. François, 2011, Revue neurologique.

Therapeutic plasma exchange in chronic dysimmune peripheral neuropathies: A 10‐year retrospective study

C. Verny, J. Subra, J. Cassereau, 2017, Journal of clinical apheresis.

InFUSing antisense oligonucleotides for treating ALS.

P. Vourc'h, J. Cassereau, P. Codron, 2022, Trends in molecular medicine.

Phenotypic spectrum of MFN2 mutations in the Spanish population

D. Bonneau, V. Volpini, A. Chevrollier, 2009, Journal of Medical Genetics.

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

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2009, neurogenetics.

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

C. Duyckaerts, J. Julien, G. Lenaers, 2020, Neuropathology and applied neurobiology.

Strength of the Association of Elevated Vitamin B12 and Solid Cancers: An Adjusted Case-Control Study

C. Annweiler, J. Hamel, J. Cassereau, 2020, Journal of clinical medicine.

Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathy.

C. Sommer, F. Zimprich, W. Löscher, 2021, Brain : a journal of neurology.

Genotype–phenotype correlation in French patients with myelin protein zero gene‐related inherited neuropathy

N. Lévy, A. Echaniz-Laguna, Y. Péréon, 2021, European journal of neurology.

Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2011, Neurology.

Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutations

D. Bonneau, G. Lenaers, P. Reynier, 2016, Journal of the peripheral nervous system : JPNS.

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

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2010, Mitochondrion.

Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration

D. Milea, V. Desquiret-Dumas, D. Bonneau, 2011, BMC Research Notes.

Current mechanistic insights into the CCCP‐induced cell survival response

Guy Lenaers, Vincent Procaccio, Pascal Reynier, 2018, Biochemical pharmacology.

Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders

M. Martin-Négrier, C. Bris, D. Goudenège, 2021, Genetics in Medicine.

Pathogens infecting the central nervous system

Y. Bahn, N. Papon, J. Cassereau, 2022, PLoS pathogens.

Neuronal Intermediate Filaments in Amyotrophic Lateral Sclerosis

J. Cassereau, J. Eyer, F. Letournel, 2016 .

Metabo-lipidomics of Fibroblasts and Mitochondrial-Endoplasmic Reticulum Extracts from ALS Patients Shows Alterations in Purine, Pyrimidine, Energetic, and Phospholipid Metabolisms

C. Bris, G. Lenaers, P. Reynier, 2019, Molecular Neurobiology.

Posterior Spinal Cord Syndrome after Flexible Ureteroscopy for Kidney Stones

P. Bigot, J. Cassereau, C. Nedelcu, 2015, Urologia Internationalis.

Anti‐disialosyl‐immunoglobulin M chronic autoimmune neuropathies: a nationwide multicenter retrospective study

A. Echaniz-Laguna, Y. Péréon, P. Cintas, 2022, European journal of neurology.

Determinants of health‐related quality of life in anti‐MAG neuropathy: a cross‐sectional multicentre European study

J. Cassereau, A. Grapperon, S. Attarian, 2017, Journal of the peripheral nervous system : JPNS.

An intraventricular clear cell meningioma revealed by an inflammatory syndrome in a male adult: A case report

H. Fournier, F. Dubas, J. Cassereau, 2008, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).

Prevalence, correlates and impact of pain and cramps in anti‐MAG neuropathy: a multicentre European study

J. Cassereau, S. Attarian, E. Delmont, 2018, European journal of neurology.

Retinal vessels as a window on amyotrophic lateral sclerosis pathophysiology: A systematic review.

P. Gohier, J. Cassereau, P. Codron, 2023, Revue neurologique.

Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2K

D. Bonneau, G. Lenaers, P. Reynier, 2020, Experimental Neurology.

Current clinical management of CIDP with immunoglobulins in France: An expert opinion.

Y. Péréon, P. Cintas, M. Michaud, 2023, Revue neurologique.

Disease status in chronic inflammatory demyelinating polyneuropathy: inter‐centre comparative analysis and correlates

J. Cassereau, G. Nicolas, Y. Rajabally, 2015, European journal of neurology.

A European multicentre reappraisal of distal compound muscle action potential duration in chronic inflammatory demyelinating polyneuropathy

E. Fournier, J. Cassereau, J. Lagarde, 2012, European journal of neurology.

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation.

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2011, Mitochondrion.

Neurotoxicity of Insecticides.

G. Lenaers, P. Reynier, V. Procaccio, 2017, Current medicinal chemistry.

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

A. Mercat, F. Dubas, J. Cassereau, 2008, Clinical Neurology and Neurosurgery.

Effect of familial clustering in the genetic screening of 235 French ALS families

V. Meininger, F. Salachas, F. Viader, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

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

F. Etcharry-Bouyx, V. Chauviré, C. Verny, 2022, Brain pathology.

Efficacy and safety of rituximab in myasthenia gravis: a French multicentre real‐life study

Y. Péréon, A. Magot, A. Nadaj-Pakleza, 2020, European journal of neurology.

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

F. Dubas, C. Verny, J. Cassereau, 2008, Journal of the peripheral nervous system : JPNS.

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

J. Cassereau, P. Lonchampt, G. Nicolas, 2013, Neuroscience.

Comparison of spinal magnetic resonance imaging and classical clinical factors in predicting motor capacity in amyotrophic lateral sclerosis

Jeanne M. Miller, K. Dujardin, V. Marchand-Pauvert, 2023, Journal of Neurology.

Clinical and electrophysiological characteristics of women with X-linked Charcot-Marie-Tooth disease.

A. Echaniz-Laguna, Y. Péréon, P. Latour, 2023, European journal of neurology.

Post-herpetic anti-N-methyl-d-aspartate receptor encephalitis in a pregnant woman.

J. Honnorat, J. Cassereau, M. Tailland, 2019, Revue neurologique.

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

F. Dubas, J. Cassereau, C. Lavigne, 2012, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).

A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K

D. Bonneau, P. Reynier, V. Procaccio, 2011, Orphanet journal of rare diseases.

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

J. Cassereau, C. Lavigne, F. Letournel, 2020, European journal of internal medicine.

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

J. Julien, D. Bohl, S. Pozzi, 2023, Brain : a journal of neurology.

A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K

D. Bonneau, P. Reynier, V. Procaccio, 2011, Orphanet journal of rare diseases.

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

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2010, Mitochondrion.