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	1.	Levetiracetam in progressive myoclonic epilepsy: an exploratory study in 9 patients. [electronic resource] by Crest, C Dupont, S Leguern, E Adam, C Baulac, M Producer: 20050121 In: Neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies. [electronic resource] by Dubourg, O Mouton, P Brice, A LeGuern, E Bouche, P Producer: 20000519 In: Neuromuscular disorders : NMD vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Genetics of inherited human epilepsies. [electronic resource] by Gourfinkel-An, I Baulac, S Brice, A Leguern, E Baulac, M Producer: 20120910 In: Dialogues in clinical neuroscience vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	4.	The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q. [electronic resource] by Ring, H Z Chang, H Guilbot, A Brice, A LeGuern, E Francke, U Producer: 19990625 In: Human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions]. [electronic resource] by Gourfinkel-An, I Baulac, S Nabbout, R Brice, A Baulac, M Leguern, E Producer: 20040831 In: Revue neurologique vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness. [electronic resource] by Dubourg, O Barhoumi, C Azzedine, H Birouk, N Brice, A Bouche, P Leguern, E Producer: 20020719 In: Muscle & nerve vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa. [electronic resource] by Coullin, P Diatta, A L Boufettal, H Feingold, J Leguern, E Candelier, J J Producer: 20150821 In: Placenta vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease. [electronic resource] by Kessali, M Zemmouri, R Guilbot, A Maisonobe, T Brice, A LeGuern, E Grid, D Producer: 19970515 In: Neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variant. [electronic resource] by Querin, G Corcia, P Lenglet, T Stojkovic, T Leguern, E Cazeneuve, C Pradat, P-F Producer: 20180730 In: Revue neurologique vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	[A genetically confirmed CMT1A mimicking relapsing CIDP]. [electronic resource] by Ben Youssef-Turki, I Kraoua, I Gargouri, A Bouche, P Leguern, E Gouider-Khouja, N Producer: 20120508 In: Revue neurologique vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. [electronic resource] by LeGuern, E Guilbot, A Kessali, M Ravisé, N Tassin, J Maisonobe, T Grid, D Brice, A Producer: 19970204 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease. [electronic resource] by LeGuern, E Gouider, R Mabin, D Tardieu, S Birouk, N Parent, P Bouche, P Brice, A Producer: 19970225 In: Annals of neurology vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosis. [electronic resource] by LeGuern, E Ravise, N Gouider, R Gugenheim, M Lopes, J Bouche, P Agid, Y Brice, A Producer: 19960304 In: Cytogenetics and cell genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33. [electronic resource] by Gabreëls-Festen, A van Beersum, S Eshuis, L LeGuern, E Gabreëls, F van Engelen, B Mariman, E Producer: 19990525 In: Journal of neurology, neurosurgery, and psychiatry vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p. [electronic resource] by Nabbout, R Baulac, S Desguerre, I Bahi-Buisson, N Chiron, C Ruberg, M Dulac, O LeGuern, E Producer: 20070510 In: Neurology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	The autosomal recessive form of CMT disease linked to 5q31-q33. [electronic resource] by Guilbot, A Kessali, M Ravisé, N Hammadouche, T Bouhouche, A Maisonobe, T Grid, D Brice, A Leguern, E Producer: 19991221 In: Annals of the New York Academy of Sciences vol. 883 Availability: No items available. Save to lists Add to cart (remove)
	17.	Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion. [electronic resource] by Mouton, P Tardieu, S Gouider, R Birouk, N Maisonobe, T Dubourg, O Brice, A LeGuern, E Bouche, P Producer: 19990517 In: Neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Recurrent polyradiculoneuropathy with the 17p11.2 deletion. [electronic resource] by Le Forestier, N LeGuern, E Coullin, P Birouk, N Maisonobe, T Brice, A Léger, J M Bouche, P Producer: 19970917 In: Muscle & nerve vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patients. [electronic resource] by Rouger, H LeGuern, E Gouider, R Tardieu, S Birouk, N Gugenheim, M Bouche, P Agid, Y Brice, A Producer: 19960716 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	20.	SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease. [electronic resource] by Hanash, A Leguern, E Birouk, N Clermont, O Pouget, J Bouche, P Munnich, A Brice, A Melki, J Producer: 19970822 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 77 results.