J. Praline

发表

Malnutrition at the time of diagnosis is associated with a shorter disease duration in ALS

C. Andres, P. Corcia, P. Gordon, 2010, Journal of the Neurological Sciences.

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

V. Meininger, P. Vourc'h, C. Andres, 2008, Archives of neurology.

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.

Somatosensory Evoked Potentials in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

P. Corcia, J. Praline, H. Salhi, 2014, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Epilepsy and Language Development: The Continuous Spike‐Waves during Slow Sleep Syndrome

C. Barthélémy, C. Hommet, Laurie Tuller, 2007, Epilepsia.

Long‐term benefit of enzyme replacement therapy with alglucosidase alfa in adults with Pompe disease: Prospective analysis from the French Pompe Registry

F. Chapon, T. Perez, G. Bassez, 2020, Journal of inherited metabolic disease.

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis

V. Meininger, P. Vourc'h, C. Andres, 2011, Journal of the Neurological Sciences.

Long-term exposure to Myozyme results in a decrease of anti-drug antibodies in late-onset Pompe disease patients

F. Chapon, G. Bassez, D. Orlikowski, 2016, Scientific Reports.

ALS and mercury intoxication: A relationship?

P. Corcia, N. Limousin, B. Toffol, 2007, Clinical Neurology and Neurosurgery.

Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2013, The International journal of neuroscience.

The importance of the SMN genes in the genetics of sporadic ALS

C. Andres, P. Corcia, P. Gordon, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Homozygous SMN2 deletion is a protective factor in the Swedish ALS population

P. Andersen, P. Vourc'h, C. Andres, 2012, European Journal of Human Genetics.

Association of a paraneoplastic motor neuron disease with anti-Ri antibodies and a novel SOD1 I18del mutation

C. Diard-Detoeuf, P. Vourc'h, C. Andres, 2014, Journal of the Neurological Sciences.

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

CADASIL and ALS: A link?

P. Vourc'h, C. Andres, P. Corcia, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma

P. Vourc'h, P. Corcia, P. Gordon, 2011, Journal of the Neurological Sciences.

Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease.

D. Orlikowski, J. Hogrel, D. Hamroun, 2016, Molecular genetics and metabolism.

Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family

P. Vourc'h, P. Corcia, C. Veyrat-Durebex, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Adjunctive perampanel in refractory epilepsy: Experience at tertiary epilepsy care center in Tours

P. Corcia, N. Limousin, B. Toffol, 2016, Epilepsy & Behavior.

Brain biopsy is required in steroid-resistant patients with chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS)

J. Cottier, K. Mokhtari, N. Limousin, 2012, Journal of Neuro-Oncology.

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees

P. Vourc'h, P. Corcia, J. Praline, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Preliminary results of PET with 18F-DPA 714 in humans for detection of microglial activation in amyotrophic lateral sclerosis (ALS)

D. Visvikis, S. Meikle, M. Kassiou, 2008 .

1H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis

Patrick Emond, Caroline Moreau, David Devos, 2010, PloS one.

[Genetics of motor neuron disorders].

P. Vourc'h, P. Corcia, J. Praline, 2008, Revue neurologique.

Outcome at Adulthood of the Continuous Spike–waves During Slow Sleep and Landau–Kleffner Syndromes

C. Hommet, C. Billard, B. Toffol, 2003, Epilepsia.

Nutritional assessment of amyotrophic lateral sclerosis in routine practice: Value of weighing and bioelectrical impedance analysis

P. Corcia, H. Blasco, J. Praline, 2015, Muscle & nerve.

Emergent EEG in clinical practice

C. Hommet, P. Corcia, B. Toffol, 2007, Clinical Neurophysiology.

Correction: 1H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis

Patrick Emond, Caroline Moreau, David Devos, 2010, PLoS ONE.

High incidence of obstructive sleep apnea syndrome in patients with late-onset epilepsy

N. Limousin, B. Toffol, J. Praline, 2017, Neurophysiologie Clinique/Clinical Neurophysiology.

Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.

R. Porcher, É. Marijon, A. Lazarus, 2019, Circulation.

The high frequency of restless legs syndrome in patients with amyotrophic lateral sclerosis

I. Arnulf, P. Corcia, N. Limousin, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Molecular Imaging of Microglial Activation in Amyotrophic Lateral Sclerosis

Caroline Prunier, Denis Guilloteau, Clovis Tauber, 2012, PloS one.

APOE ε4 allele is associated with an increased risk of bulbar‐onset amyotrophic lateral sclerosis in men

P. Vourc'h, C. Andres, P. Corcia, 2011, European journal of neurology.

Predictive value of motor evoked potentials in clinically isolated syndrome

P. Corcia, H. Blasco, J. Praline, 2011, Acta neurologica Scandinavica.

Pure bulbar motor neuron involvement linked to an abnormal CAG repeat expansion in the androgen receptor gene

P. Corcia, J. Praline, B. de Toffol, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS

P. Vourc'h, C. Andres, P. Corcia, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, W. Camu, 2012, Journal of the Neurological Sciences.

Myasthenia gravis in the elderly: a rare cause of undernutrition

C. Hommet, K. Mondon, J. Praline, 2012, Aging Clinical and Experimental Research.

[Narcolepsy associated with systemic lupus erythematosus].

D. Jacobi, F. Maillot, C. Couet, 2011, La Revue de medecine interne.

[Ataxia phenotype of type 1 Charcot-Marie-Tooth disease: an atypical presentation].

P. Corcia, J. Praline, A. Guennoc, 2013, Revue neurologique.

Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2013, The International journal of neuroscience.

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees

P. Vourc'h, P. Corcia, J. Praline, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.