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Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Annals of neurology, 1999-08, Vol.46 (2), p.224-233

1999

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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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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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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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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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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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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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Amyloid neuropathy: a retrospective study of 35 peripheral nerve biopsies

Journal of the peripheral nervous system, 2004-12, Vol.9 (4), p.232-241

2004

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Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum

Journal of the peripheral nervous system, 2014-12, Vol.19 (4), p.333-342

2014

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Crow–Fukase (POEMS) syndrome: a study of peripheral nerve biopsy in five new cases

Journal of the peripheral nervous system, 2003-09, Vol.8 (3), p.136-144

2003

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Clinical Neuropathology practice guide 3-2014: combined nerve and muscle biopsy in the diagnostic workup of neuropathy - the Bordeaux experience

Clinical neuropathology, 2014-05, Vol.33 (3), p.172-178

2014

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Charcot-Marie-Tooth disease type 1A: clinicopathological correlations in 24 patients

Journal of the peripheral nervous system, 2005-03, Vol.10 (1), p.85-92

2005

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Significance of uncompacted myelin lamellae in POEMS syndrome

Muscle & nerve, 2003-02, Vol.27 (2), p.253-254

2003

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Protein Aggregation in the Aging Retina

Journal of neuropathology and experimental neurology, 2011-01, Vol.70 (1), p.63-68

2011

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A French family with Charcot–Marie–Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations

Neuromuscular disorders : NMD, 2012-08, Vol.22 (8), p.735-741

2012

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Allelic origin of the abnormal prion protein isoform in familial prion diseases

Nature medicine, 1997-09, Vol.3 (9), p.1009-1015

1997

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Neuronal Apoptosis in Fatal Familial Insomnia

Brain pathology (Zurich, Switzerland), 1998-07, Vol.8 (3), p.531-537

1998

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Dementia pugilistica: a severe tribute to a career

Clinical neuropathology, 2015-07, Vol.34 (4), p.193-198

2015

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An Update on Nerve Biopsy

Journal of neuropathology and experimental neurology, 2009-08, Vol.68 (8), p.833-844

2009

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Severe Charcot‐Marie‐Tooth disease type 1E caused by a novel p.Phe84Leufs24 PMP22 point mutation

Journal of the peripheral nervous system, 2013-06, Vol.18 (2), p.181-184

2013

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Severe Charcot‐Marie‐Tooth disease type 1E caused by a novel p. Phe84Leufs 24 PMP22 point mutation

Journal of the peripheral nervous system, 2013-06, Vol.18 (2), p.181-184

2013

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Guillain‐Barré syndrome occurring in two women after ketoacidosic comatose state disclosing an insulin‐dependent diabetes mellitus

Journal of the peripheral nervous system, 2000-03, Vol.5 (1), p.27-31

2000

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The Nigrostriatal Pathway in Creutzfeldt-Jakob Disease

Journal of neuropathology and experimental neurology, 2009-07, Vol.68 (7), p.809-815

2009

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Familial amyloid polyneuropathy associated with nodular lumbosacral radiculoplexopathy

Journal of the peripheral nervous system, 2012-03, Vol.17 (1), p.138-139

2012

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Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Mitochondria and Peripheral Neuropathies

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

Intra-axonal protein aggregation in the peripheral nervous system

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

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

Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)

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

Amyloid neuropathy: a retrospective study of 35 peripheral nerve biopsies

Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum

Crow–Fukase (POEMS) syndrome: a study of peripheral nerve biopsy in five new cases

Clinical Neuropathology practice guide 3-2014: combined nerve and muscle biopsy in the diagnostic workup of neuropathy - the Bordeaux experience

Charcot-Marie-Tooth disease type 1A: clinicopathological correlations in 24 patients

Significance of uncompacted myelin lamellae in POEMS syndrome

Protein Aggregation in the Aging Retina

A French family with Charcot–Marie–Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations

Allelic origin of the abnormal prion protein isoform in familial prion diseases

Neuronal Apoptosis in Fatal Familial Insomnia

Dementia pugilistica: a severe tribute to a career

An Update on Nerve Biopsy

Severe Charcot‐Marie‐Tooth disease type 1E caused by a novel p.Phe84Leufs24 PMP22 point mutation

Severe Charcot‐Marie‐Tooth disease type 1E caused by a novel p. Phe84Leufs 24 PMP22 point mutation

Guillain‐Barré syndrome occurring in two women after ketoacidosic comatose state disclosing an insulin‐dependent diabetes mellitus

The Nigrostriatal Pathway in Creutzfeldt-Jakob Disease

Familial amyloid polyneuropathy associated with nodular lumbosacral radiculoplexopathy

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