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Focus on 1,25-Dihydroxyvitamin D3 in the Peripheral Nervous System

Frontiers in neuroscience, 2019-04, Vol.13, p.348

2019

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Deciphering the links between psychological stress, depression, and neurocognitive decline in patients with Down syndrome

Neurobiology of stress, 2021-05, Vol.14, p.100305-100305, Article 100305

2021

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Neuroprotective effect of angiotensin II type 2 receptor stimulation in vincristine-induced mechanical allodynia

Pain (Amsterdam), 2018-12, Vol.159 (12), p.2538-2546

2018

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Candesartan prevents resiniferatoxin-induced sensory small-fiber neuropathy in mice by promoting angiotensin II-mediated AT2 receptor stimulation

Neuropharmacology, 2017-11, Vol.126, p.142-150

2017

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The Efficacy of a Social Skills Group Intervention for Improving Social Behaviors in Children with High Functioning Autism Spectrum Disorders

Journal of autism and developmental disorders, 2011-08, Vol.41 (8), p.1033-1043

2011

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Local low dose curcumin treatment improves functional recovery and remyelination in a rat model of sciatic nerve crush through inhibition of oxidative stress

Neuropharmacology, 2018-09, Vol.139, p.98-116

2018

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Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants

Journal of the neurological sciences, 2019-11, Vol.406, p.116376-116376, Article 116376

2019

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Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model

Neuroscience letters, 2009-09, Vol.461 (2), p.126-130

2009

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Acute Regression in Young People with Down Syndrome

Brain sciences, 2017-05, Vol.7 (6), p.57

2017

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Optimized Protocol to Generate Spinal Motor Neuron Cells from Induced Pluripotent Stem Cells from Charcot Marie Tooth Patients

Brain sciences, 2020-07, Vol.10 (7), p.407

2020

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A reversible functional sensory neuropathy model

Neuroscience letters, 2014-06, Vol.571, p.39-44

2014

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One Multilocus Genomic Variation Is Responsible for a Severe Charcot-Marie-Tooth Axonal Form

Brain sciences, 2020-12, Vol.10 (12), p.986

2020

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Clinical features of homozygous FIG4‐p.Ile41Thr Charcot‐Marie‐Tooth 4J patients

Annals of clinical and translational neurology, 2021-02, Vol.8 (2), p.471-476

2021

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A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature

Journal of the peripheral nervous system, 2017-06, Vol.22 (2), p.77-84

2017

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A novel pathogenic variant of NEFL responsible for deafness associated with peripheral neuropathy discovered through next‐generation sequencing and review of the literature

Journal of the peripheral nervous system, 2019-03, Vol.24 (1), p.139-144

2019

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Pharmacoresistant Epilepsy in Childhood: Think of the Cerebral Folate Deficiency, a Treatable Disease

Brain sciences, 2020-11, Vol.10 (11), p.1

2020

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Homozygous deletion of an EGR2 enhancer in congenital amyelinating neuropathy

Annals of neurology, 2012-05, Vol.71 (5), p.719-723

2012

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Autosomal-recessive charcot-marie-tooth diseases

Journal of neuropathology and experimental neurology, 2005-05, Vol.64 (5), p.363-370

2005

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Congenital hypomyelinating neuropathy due to the association of a truncating mutation in PMP22 with the classical HNPP deletion

Neuromuscular disorders : NMD, 2016-04, Vol.26 (4-5), p.316-321

2016

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Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance

Acta neuropathologica, 2007-04, Vol.113 (4), p.443-449

2007

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Clinical and electrophysiological phenotype of a homozygously duplicated Charcot-Marie-Tooth (type 1A) disease

European neurology, 1997-01, Vol.38 (1), p.26-30

1997

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Detection of 2,4-dichlorophenoxyacetic acid (2,4-D) residues in neonates breast-fed by 2,4-D exposed dams

Neurotoxicology (Park Forest South), 2000-02, Vol.21 (1-2), p.147-154

2000

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Modelization of Motor Nerve Conduction Velocities for Charcot-Marie-Tooth (Type-1) Patients

European neurology, 1996-01, Vol.36 (4), p.224-228

1996

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Iron, zinc and copper levels in brain, serum and liver of neonates exposed to 2,4-dichlorophenoxyacetic acid

Neurotoxicology and teratology, 2003-09, Vol.25 (5), p.607-613

2003

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Regionally specific changes in central brain monoamine levels by 2,4-dichlorophenoxyacetic acid in acute treated rats

Neurotoxicology (Park Forest South), 1998-12, Vol.19 (6), p.839-851

1998

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Focus on 1,25-Dihydroxyvitamin D3 in the Peripheral Nervous System

Deciphering the links between psychological stress, depression, and neurocognitive decline in patients with Down syndrome

Neuroprotective effect of angiotensin II type 2 receptor stimulation in vincristine-induced mechanical allodynia

Candesartan prevents resiniferatoxin-induced sensory small-fiber neuropathy in mice by promoting angiotensin II-mediated AT2 receptor stimulation

The Efficacy of a Social Skills Group Intervention for Improving Social Behaviors in Children with High Functioning Autism Spectrum Disorders

Local low dose curcumin treatment improves functional recovery and remyelination in a rat model of sciatic nerve crush through inhibition of oxidative stress

Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants

Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model

Acute Regression in Young People with Down Syndrome

Optimized Protocol to Generate Spinal Motor Neuron Cells from Induced Pluripotent Stem Cells from Charcot Marie Tooth Patients

A reversible functional sensory neuropathy model

One Multilocus Genomic Variation Is Responsible for a Severe Charcot-Marie-Tooth Axonal Form

Clinical features of homozygous FIG4‐p.Ile41Thr Charcot‐Marie‐Tooth 4J patients

A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature

A novel pathogenic variant of NEFL responsible for deafness associated with peripheral neuropathy discovered through next‐generation sequencing and review of the literature

Pharmacoresistant Epilepsy in Childhood: Think of the Cerebral Folate Deficiency, a Treatable Disease

Homozygous deletion of an EGR2 enhancer in congenital amyelinating neuropathy

Autosomal-recessive charcot-marie-tooth diseases

Congenital hypomyelinating neuropathy due to the association of a truncating mutation in PMP22 with the classical HNPP deletion

Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance

Clinical and electrophysiological phenotype of a homozygously duplicated Charcot-Marie-Tooth (type 1A) disease

Detection of 2,4-dichlorophenoxyacetic acid (2,4-D) residues in neonates breast-fed by 2,4-D exposed dams

Modelization of Motor Nerve Conduction Velocities for Charcot-Marie-Tooth (Type-1) Patients

Iron, zinc and copper levels in brain, serum and liver of neonates exposed to 2,4-dichlorophenoxyacetic acid

Regionally specific changes in central brain monoamine levels by 2,4-dichlorophenoxyacetic acid in acute treated rats

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