M. Martin-Négrier

发表

Mutation of TP53 gene is involved in carcinogenesis of hepatic undifferentiated (embryonal) sarcoma of the adult, in contrast with Wnt or telomerase pathways: an immunohistochemical study of three cases with genomic relation in two cases.

B. Bloch, J. Zucman‐Rossi, S. Lepreux, 2005, Journal of hepatology.

Concurrent herpes simplex type 1 necrotizing encephalitis, cytomegalovirus ventriculoencephalitis and cerebral lymphoma in an AIDS patient

M. Martin-Négrier, M. Bras, A. Vital, 2004, Acta Neuropathologica.

Fatal brain stem encephalitis due to herpes simplex virus type 1 in AIDS

M. Martin-Négrier, A. Moulignier, M. Baudrimont, 1996, Journal of Neurology.

Intra‐axonal protein aggregation in the peripheral nervous system

E. Bézard, M. Martin-Négrier, F. Tison, 2014, Journal of the peripheral nervous system : JPNS.

Neurologic manifestations of giant cell arteritis

M. Martin-Négrier, J. Vallat, I. Sibon, 2022, Journal of Neurology.

Leber’s optic neuropathy associated with disseminated white matter disease: A case report and review

B. Brochet, M. Martin-Négrier, C. Goizet, 2009, Clinical Neurology and Neurosurgery.

Peripheral neuropathy associated with mitochondrial disorders: 8 cases and review of the literature

J. Orgogozo, M. Martin-Négrier, X. Ferrer, 2002, Journal of the peripheral nervous system : JPNS.

Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)

M. Martin-Négrier, P. Latour, X. Ferrer, 2009, Journal of the peripheral nervous system : JPNS.

Biochemical consequences of two clinically relevant ND-gene mutations in Escherichia coli respiratory complex I

M. Martin-Négrier, V. Procaccio, J. di Rago, 2021, Scientific Reports.

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

C. Duyckaerts, V. Deramecourt, F. Chapon, 2019, Acta Neuropathologica.

Ontogeny of the striatal neurons expressing neuropeptide genes in the human fetus and neonate

B. Bloch, I. Aubert, M. Martin-Négrier, 1995, The Journal of comparative neurology.

REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho‐functional dysfunction

A. Durr, D. Hannequin, S. Forlani, 2011, Human mutation.

Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders

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

Proteomic remodeling of proteasome in right heart failure.

M. Martin-Négrier, Marie-Laure Thiolat, S. Claverol, 2014, Journal of molecular and cellular cardiology.

TWINKLE gene mutation: report of a French family with an autosomal dominant progressive external ophthalmoplegia and literature review

M. Martin-Négrier, X. Ferrer, C. Jardel, 2011, European journal of neurology.

[Diagnostic procedure of limb girdle muscular dystrophies 2A or calpainopathies: French cohort from a neuromuscular center (Bordeaux)].

M. Martin-Négrier, X. Ferrer, A. Vital, 2010, Revue neurologique.

Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination

A. Laquérriere, C. Rooryck, M. Martin-Négrier, 2020, Acta Neuropathologica Communications.

Cytoplasmic Expression of Human Telomerase Catalytic Protein (hTERT) in Neutrophils: An Immunoelectron Microscopy Study

B. Bloch, I. Aubert, S. Lepreux, 2008, Ultrastructural pathology.

The lipid phosphatase Synaptojanin 1 undergoes a significant alteration in expression and solubility and is associated with brain lesions in Alzheimer’s disease

C. Duyckaerts, V. Deramecourt, F. Chapon, 2020, Acta Neuropathologica Communications.

An Update on Nerve Biopsy

M. Martin-Négrier, J. Vallat, A. Vital, 2009, Journal of neuropathology and experimental neurology.

The Nigrostriatal Pathway in Creutzfeldt-Jakob Disease

E. Bézard, M. Martin-Négrier, F. Tison, 2009, Journal of neuropathology and experimental neurology.

RGS4 is involved in the generation of abnormal involuntary movements in the unilateral 6-OHDA-lesioned rat model of Parkinson's disease

W. Ko, E. Bézard, P. Ravenscroft, 2014, Neurobiology of Disease.

Lhermitte-Duclos type cerebellum hamartoma and Cowden disease.

A. Rougier, M. Martin-Négrier, A. Vital, 1994, Clinical neuropathology.

New evidence of a mitochondrial genetic background paradox: Impact of the J haplogroup on the A3243G mutation

M. Crouzet, M. Martin-Négrier, P. Reynier, 2008, BMC Medical Genetics.

Receptor recycling mediates plasma membrane recovery of dopamine D1 receptors in dendrites and axons after agonist‐induced endocytosis in primary cultures of striatal neurons

B. Bloch, M. Martin-Négrier, G. Charron, 2006, Synapse.

Increased prevalence of granulovacuolar degeneration in C9orf72 mutation

C. Duyckaerts, F. Salachas, G. Sobue, 2019, Acta Neuropathologica.

Adult onset tubulo‐interstitial nephropathy in MT‐ND5‐related phenotypes

M. Martin-Négrier, D. Lacombe, C. Combe, 2019, Clinical genetics.

[Mutism and acute behavioral disorders revealing MELAS syndrome].

M. Martin-Négrier, B. Barroso, S. Demasles, 2011, Revue neurologique.

Pathological changes induced by Alzheimer’s brain inoculation in amyloid-beta plaque-bearing mice

F. Petit, C. Duyckaerts, M. Dhenain, 2022, Acta Neuropathologica Communications.

Differential transcript usage unravels gene expression alterations in Alzheimer’s disease human brains

C. Duyckaerts, J. Lambert, V. Deramecourt, 2021, npj Aging and Mechanisms of Disease.

Parkinsonism in a patient with Leber hereditary optic neuropathy (LHON).

M. Martin-Négrier, X. Ferrer, A. Vital, 2015, Revue neurologique.

Primitive malignant fibrous histiocytoma of the neck with carotid occlusion and multiple cerebral ischemic lesions.

J. Orgogozo, M. Martin-Négrier, C. Vital, 1996, Stroke.

Peripheral neuropathy and livedoid vasculopathy

M. Martin-Négrier, T. Maisonobe, J. Vallat, 2022, Journal of Neurology.

PSD-95 expression controls L-DOPA dyskinesia through dopamine D1 receptor trafficking.

Qin Li, E. Bézard, B. Bloch, 2012, The Journal of clinical investigation.

Renal involvement is frequent in adults with primary mitochondrial disorders: an observational study

M. Martin-Négrier, C. Combe, C. Goizet, 2022, Clinical kidney journal.

l-DOPA Impairs Proteasome Activity in Parkinsonism through D1 Dopamine Receptor

Qin Li, E. Bézard, B. Bloch, 2012, The Journal of Neuroscience.

Regulation of G-Protein-Coupled Receptor (GPCR) Trafficking in the Striatum in Parkinson’s Disease

E. Bézard, B. Bloch, M. Martin-Négrier, 2009 .

D1 dopamine receptor stimulation impairs striatal proteasome activity in Parkinsonism through 26S proteasome disassembly

E. Bézard, B. Bloch, J. Baufreton, 2015, Neurobiology of Disease.