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Your search keyword '"Vercelletto M"' showing total 7 results
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7 results on '"Vercelletto M"'

1. Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation

Author

Sevin, M., Kutalik, Z., Bergman, S., Vercelletto, M., Renou, P., Lamy, E., Vingerhoets, F.J., Di Virgilio, G., Boisseau, P., Bezieau, S., Pasquier, L., Rival, J.-M., Beckmann, J.S., Damier, P., and Jacquemont, S.

Subjects
Gene mutations -- Research, Cognition disorders -- Diagnosis, Cognition disorders -- Genetic aspects, Cognition disorders -- Demographic aspects, Nervous system -- Degeneration, Nervous system -- Diagnosis, Nervous system -- Genetic aspects, Nervous system -- Demographic aspects, Health
Published
2009

2. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

Author

Le Ber, I, Camuzat, A, Berger, E, Hannequin, D, Laquerrière, A, Golfier, V, Seilhean, D, Viennet, G, Couratier, P, Verpillat, P, Heath, S, Camu, W, Martinaud, O, Lacomblez, L, Vercelletto, M, Salachas, F, Sellal, F, Didic, M, Thomas-Anterion, C, Puel, M, Michel, B-F, Besse, C, Duyckaerts, C, Meininger, V, Campion, D, Dubois, B, and Brice, A

Abstract

Frontotemporal dementia associated with motor neuron disease (FTD-MND) is a rare neurodegenerative disorder that may be inherited by autosomal dominant trait. No major gene has been identified but a locus was mapped on chromosome 9 (9p21.3-p13.3).

Published
2009
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3. Frontal type dementia preceding amyotrophic lateral sclerosis: a neuropsychological and SPECT study of five clinical cases

Author

Vercelletto, M., Ronin, M., Huvet, M., Magne, C., and Feve, J.R.

Abstract

Between 1993 and 1995, we observed five sporadic cases of frontotemporal dementia (FTD) which in all cases preceded the appearance of typical amyotrophic lateral sclerosis (ALS). The FTD rapidly became severe (within 12‐18 months) and the delay between the presumed onset of mental change and ALS was short (12–26 months). The frontal dysfunction was characteristic (disinhibited, jocular, impatient, gluttonous, stereotypical gestures). The language impairment (less talkative, persistent errors, fantastic and semantic paraphasia, neologistic errors, echolalia) was constant. Single photon emission computed tomography (SPECT) with 99 TcmHMPAO (hexamethyl propylamine oxime) was done at the same time as neuropsychological testing in four cases and showed serious diffuse bifrontal defect, sometimes with less serious internal temporal hypofixation. All patients died with bulbar ALS complications. The total course can last from 14–48 months. Most of the reported cases suggested a relationship between dementia‐ALS and frontal dysfunction. The mechanism underlying dementia‐ALS remains to be solved. Our five cases resemble those reported by Mitsuyama (1993), who suggested that dementia‐ALS has the same clinicopathological entity.

Published
1999
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7. Fréquence et phénotypes associés aux mutations du gène c9orf72 dans une cohorte française de patients atteints de DLFT

Author

Le Ber, I., Camuzat, A., Hannequin, D., Lacomblez, L., Couratier, P., Guillot-Noel, L., Habert, M.O., Seilhean, D., Golfier, V., Puel, M., Martinaud, O., Deramecourt, V., Vercelletto, M., Sellal, F., Pasquier, F., Salachas, F., Thomas-Anterion, C., Didic, M., Pariente, J., Wargon, I., Blanc, F., Michel, B.F., Berger, E., Sauvee, M., Mondon, K., Fleury, M., Meininger, V., Duyckaerts, C., Dubois, B., Guedj, E., and Brice, A.

Published
2012
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