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Your search keyword '"Ricard, D."' showing total 26 results
Start Over Author "Ricard, D." Journal revue neurologique
26 results on '"Ricard, D."'

4. Subacute monomelic radiculoplexus neuropathy following Comirnaty© (Pfizer-BioNTech COVID-19) vaccination: A case report

Author

Coly, M., primary, Balcerac, A., additional, Brasseur, N., additional, Sallansonnet-Froment, M., additional, Tafani, C., additional, Taifas, I., additional, Bréchemier, M.L., additional, Drouard, E., additional, Foissaud, V., additional, Vest, P., additional, Vandendries, C., additional, Bompaire, F., additional, Bihan, K., additional, and Ricard, D., additional

Published
2023
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5. Pseudo-tumour lesion of the brainstem: A case and discussion

Author

Maillot, J., primary, Brunet de Courssou, J.-B., additional, Brechemier, M.-L., additional, Tafani, C., additional, Sallansonnet-Froment, M., additional, Taifas, I., additional, Cournac, J.-M., additional, Drouard, E., additional, Bompaire, F., additional, Faivre, A., additional, and Ricard, D., additional

Published
2022
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12. La mémoire brûlée

Author

Ouologuem, M., primary, Bompaire, F., additional, Ricard, D., additional, de Greslan, T., additional, Sallansonnet-Froment, M., additional, Taillia, H., additional, and Renard, J.-L., additional

Published
2013
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21. Fatigue physique dans la sclérose en plaques

Author

Renard, J.L., primary, Gomez-Merino, D., additional, Dussault, C., additional, de Greslan, T., additional, Ricard, D., additional, Bounolleau, P., additional, Sallansonnet, M., additional, Taillia, H., additional, and Jouanin, J.C., additional

Published
2007
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24. [A fragile writer. FTXA (fragile X associated tremor ataxia syndrome)].

Author

Ricard D, Sallansonnet-Froment M, and De Greslan T

Subjects
Atrophy, Cerebellar Ataxia genetics, Cerebellum pathology, Cerebral Cortex pathology, Cerebral Ventricles pathology, Chromosomes, Human, X, DNA Mutational Analysis, Fragile X Mental Retardation Protein genetics, Fragile X Syndrome genetics, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Sex Chromosome Aberrations, Tremor genetics, Cerebellar Ataxia diagnosis, Fragile X Syndrome diagnosis, Handwriting, Image Enhancement, Tremor diagnosis
Published
2009

26. [Eulenburg's paramyotonia congenita].

Author

Sallansonnet-Froment M, Bounolleau P, De Greslan T, Ricard D, Taillia H, and Renard JL

Subjects
Adult, Chromosomes, Human, Pair 17 genetics, Cold Temperature adverse effects, Electromyography, Exercise Tolerance, Exons genetics, Eyelids physiopathology, Hand Strength physiology, Humans, Male, Muscle Weakness etiology, Muscle Weakness physiopathology, Muscle, Skeletal physiopathology, Mutation genetics, Mutation physiology, Myotonic Disorders diagnosis, Myotonic Disorders physiopathology, NAV1.4 Voltage-Gated Sodium Channel, Pedigree, Percussion, Sodium Channels genetics, Syndrome, Myotonic Disorders pathology
Abstract

Introduction: Paramyotonia congenita is an autosomal dominant sodium channelopathy, caused by mutations in gene coding for muscle voltage-gated sodium channel alpha subunit., Case Report: We report the case of a 38-year-old man who described since childhood muscle stiffness with attacks ok weakness induced by two provocative stimuli: cold exposure and exercise. It primarily concerned eyelids and hands, occasionally limbs. Family history suggested an autosomal dominant mode of transmission. Clinical examination revealed myotonia at the thenar eminence percussion. Generalized myotonic discharges were observed on electromyography. Molecular diagnosis reported an Arg1448Cys mutation in exon 24 in gene coding for muscle voltage-gated sodium channel alpha subunit (SCN4A) in chromosome 17., Conclusion: Paramyotonia congenita is not evolutive. Treatment is essentially preventive. Some medications could be proposed: membrane stabilizing agents like antiarrhythmic drugs (mexiletine, tocainide), or the carbonic anhydrase inhibitor (acetazolamide). Precautions may be taken during general anaesthesia because of diaphragm myotonia risk.

Published
2007
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