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Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

Neurology, 2003-09, Vol.61 (5), p.631-636

2003

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Four novel cases of periaxin-related neuropathy and review of the literature

Neurology, 2010-11, Vol.75 (20), p.1830-1838

2010

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Ischemic stroke as clinical onset of POEMS syndrome

Journal of neurology, 2013-12, Vol.260 (12), p.3178-3181

2013

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Melanoma Cells Homing to the Brain: An In Vitro Model

BioMed research international, 2015-01, Vol.2015 (2015), p.1-11

2015

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Adult polyglucosan body disease in a patient originally diagnosed with Fabry’s disease

Neuromuscular disorders : NMD, 2014-03, Vol.24 (3), p.272-276

2014

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A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy

European journal of medical genetics, 2015-10, Vol.58 (10), p.540-544

2015

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A novel mutation of CLN3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy

European journal of medical genetics, 2015-10, Vol.58 (10), p.540-544

2015

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A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene

Neurology, 2004-09, Vol.63 (5), p.910-912

2004

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Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

Neurology, 2000-04, Vol.54 (8), p.1696-1698

2000

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Atypical tauopathy with massive involvement of the white matter

Neuropathology and applied neurobiology, 2008-08, Vol.34 (4), p.468-472

2008

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Blurring in patients with temporal lobe epilepsy: clinical, high-field imaging and ultrastructural study

Brain (London, England : 1878), 2012-08, Vol.135 (Pt 8), p.2337-2349

2012

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CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia

American Journal of Neuroradiology, 2006-05, Vol.27 (5), p.1037-1039

2006

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Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis

Neuropediatrics, 2007-02, Vol.38 (1), p.46-49

2007

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Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (9), p.1009-1011

2014

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147th ENMC International Workshop: Guideline on processing and evaluation of sural nerve biopsies, 15–17 December 2006, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2008-01, Vol.18 (1), p.90-96

2008

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Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?

Neurology, 2003-05, Vol.60 (10), p.1721-1722

2003

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Familial frontotemporal dementia associated with the novel MAPT mutation T427M

Journal of neurology, 2005-12, Vol.252 (12), p.1543-1545

2005

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Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis

Human molecular genetics, 2013-04, Vol.22 (7), p.1417-1423

2013

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APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38

Acta neuropathologica, 2012-12, Vol.124 (6), p.809-821

2012

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Focal lesions area feature of chronic inflammatory demyelinating polyneuropathy (CIDP)

Acta neuropathologica, 1998-12, Vol.96 (6), p.603-609

1998

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IgM deposits on skin nerves in anti-myelin-associated glycoprotein neuropathy

Annals of neurology, 2005-02, Vol.57 (2), p.180-187

2005

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Expression of capsaicin receptor immunoreactivity in human peripheral nervous system and in painful neuropathies

Journal of the peripheral nervous system, 2006-09, Vol.11 (3), p.262-271

2006

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Infantile neuroaxonal dystrophy : neuroradiological studies in 11 patients

Neuroradiology, 1999-05, Vol.41 (5), p.376-380

1999

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Conformational Plasticity of the Gerstmann–Sträussler–Scheinker Disease Peptide as Indicated by Its Multiple Aggregation Pathways

Journal of molecular biology, 2008-09, Vol.381 (5), p.1349-1361

2008

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Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome

Journal of neurology, neurosurgery and psychiatry, 1999-03, Vol.66 (3), p.386-389

1999

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Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

Four novel cases of periaxin-related neuropathy and review of the literature

Ischemic stroke as clinical onset of POEMS syndrome

Melanoma Cells Homing to the Brain: An In Vitro Model

Adult polyglucosan body disease in a patient originally diagnosed with Fabry’s disease

A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy

A novel mutation of CLN3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

Atypical tauopathy with massive involvement of the white matter

Blurring in patients with temporal lobe epilepsy: clinical, high-field imaging and ultrastructural study

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia

Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis

Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis

147th ENMC International Workshop: Guideline on processing and evaluation of sural nerve biopsies, 15–17 December 2006, Naarden, The Netherlands

Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?

Familial frontotemporal dementia associated with the novel MAPT mutation T427M

Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis

APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38

Focal lesions area feature of chronic inflammatory demyelinating polyneuropathy (CIDP)

IgM deposits on skin nerves in anti-myelin-associated glycoprotein neuropathy

Expression of capsaicin receptor immunoreactivity in human peripheral nervous system and in painful neuropathies

Infantile neuroaxonal dystrophy : neuroradiological studies in 11 patients

Conformational Plasticity of the Gerstmann–Sträussler–Scheinker Disease Peptide as Indicated by Its Multiple Aggregation Pathways

Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome

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