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	21.	Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene. [electronic resource] by Azzedine, H Ruberg, M Ente, D Gilardeau, C Périé, S Wechsler, B Brice, A LeGuern, E Dubourg, O Producer: 20030819 In: Neuromuscular disorders : NMD vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	22.	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 Publication details: Annals of the New York Academy of Sciences Oct 1999 In: Annals of the New York Academy of Sciences vol. 883 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP. [electronic resource] by Lopes, J Tardieu, S Silander, K Blair, I Vandenberghe, A Palau, F Ruberg, M Brice, A LeGuern, E Producer: 19991214 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	K-complex-induced seizures in autosomal dominant nocturnal frontal lobe epilepsy. [electronic resource] by El Helou, J Navarro, V Depienne, C Fedirko, E LeGuern, E Baulac, M An-Gourfinkel, I Adam, C Producer: 20090409 In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease. [electronic resource] by Dubourg, O Tardieu, S Birouk, N Gouider, R Léger, J M Maisonobe, T Brice, A Bouche, P LeGuern, E Producer: 20011101 In: Brain : a journal of neurology vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33. [electronic resource] by Baulac, S Gourfinkel-An, I Picard, F Rosenberg-Bourgin, M Prud'homme, J F Baulac, M Brice, A LeGuern, E Producer: 20001002 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	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)
	28.	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 Publication details: Annals of the New York Academy of Sciences Oct 1999 In: Annals of the New York Academy of Sciences vol. 883 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family. [electronic resource] by Magnin, E Vidailhet, M Depienne, C Saint-Martin, C Bouteiller, D LeGuern, E Apartis, E Rumbach, L Labauge, P Producer: 20091116 In: Revue neurologique vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity. [electronic resource] by Dubourg, O Tardieu, S Birouk, N Gouider, R Léger, J M Maisonobe, T Brice, A Bouche, P LeGuern, E Producer: 20010830 In: Neuromuscular disorders : NMD vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Autism, language delay and mental retardation in a patient with 7q11 duplication. [electronic resource] by Depienne, C Heron, D Betancur, C Benyahia, B Trouillard, O Bouteiller, D Verloes, A Leguern, E Leboyer, M Brice, A Producer: 20111110 In: BMJ case reports vol. 2009 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Ultrastructural PMP22 expression in inherited demyelinating neuropathies. [electronic resource] by Vallat, J M Sindou, P Preux, P M Tabaraud, F Milor, A M Couratier, P LeGuern, E Brice, A Producer: 19960724 In: Annals of neurology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities. [electronic resource] by Gouider, R LeGuern, E Emile, J Tardieu, S Cabon, F Samid, M Weissenbach, J Agid, Y Bouche, P Brice, A Producer: 19950111 In: Neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2? [electronic resource] by LeGuern, E Gouider, R Ravisé, N Lopes, J Tardieu, S Gugenheim, M Abbas, N Bouche, P Agid, Y Brice, A Producer: 19961022 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group. [electronic resource] by Lopes, J LeGuern, E Gouider, R Tardieu, S Abbas, N Birouk, N Gugenheim, M Bouche, P Agid, Y Brice, A Producer: 19960725 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	36.	Autism, language delay and mental retardation in a patient with 7q11 duplication. [electronic resource] by Depienne, C Heron, D Betancur, C Benyahia, B Trouillard, O Bouteiller, D Verloes, A LeGuern, E Leboyer, M Brice, A Producer: 20080306 In: Journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family. [electronic resource] by Verny, C Ravisé, N Leutenegger, A-L Pouplard, F Dubourg, O Tardieu, S Dubas, F Brice, A Genin, E LeGuern, E Producer: 20060118 In: Neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Edg-2 in myelin-forming cells: isoforms, genomic mapping, and exclusion in Charcot-Marie-Tooth disease. [electronic resource] by Allard, J Barron, S Trottier, S Cervera, P Daumas-Duport, C Leguern, E Brice, A Schwartz, J C Sokoloff, P Producer: 19990903 In: Glia vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1. [electronic resource] by Benomar, A Krols, L Stevanin, G Cancel, G LeGuern, E David, G Ouhabi, H Martin, J J Dürr, A Zaim, A Producer: 19950925 In: Nature genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat length. [electronic resource] by Dejager, S Bry-Gauillard, H Bruckert, E Eymard, B Salachas, F LeGuern, E Tardieu, S Chadarevian, R Giral, P Turpin, G Producer: 20020830 In: The Journal of clinical endocrinology and metabolism vol. 87 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.