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	81.	Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy. [electronic resource] by Ben Hamida, C Soussi-Yanicostas, N Butler-Browne, G S Bejaoui, K Hentati, F Ben Hamida, M Producer: 19940602 In: Muscle & nerve vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study. [electronic resource] by Larnaout, A Mongalgi, M A Kaabachi, N Khiari, D Debbabi, A Mebazza, A Ben Hamida, M Hentati, F Producer: 19981207 In: Journal of inherited metabolic disease vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence]. [electronic resource] by Ben Hamida, M Chaabouni, H Madani, S Boussen, S Samoud, S Letaief, F Mrabet, A Hentati, F Miladi, N Producer: 19861118 In: Journal de genetique humaine vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	84.	Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient. [electronic resource] by Larnaout, A Belal, S Zouari, M Fki, M Ben Hamida, C Goebel, H H Ben Hamida, M Hentati, F Producer: 19970805 In: Acta neuropathologica vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	[Epidemiologic aspects of cerebrovascular accidents in Tunisia]. [electronic resource] by Mrabet, A Attia-Romdhane, N Ben Hamida, M Gharbi, N Le Noan, H Hentati, R Ben Mansour, J Srairi, I Producer: 19900802 In: Revue neurologique vol. 146 Availability: No items available. Save to lists Add to cart (remove)
	86.	Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0. [electronic resource] by Ben Jelloun-Dellagi, S Dellagi, K Burger, D Ben Younes-Chennoufi, A Hentati, F F Steck, A Ben Hamida, M Producer: 19921229 In: Annals of neurology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Prevalence study of neurologic disorders in Kelibia (Tunisia). [electronic resource] by Attia Romdhane, N Ben Hamida, M Mrabet, A Larnaout, A Samoud, S Ben Hamda, A Ben Hamda, M Oueslati, S Producer: 19940317 In: Neuroepidemiology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency. [electronic resource] by Zouari, M Feki, M Ben Hamida, C Larnaout, A Turki, I Belal, S Mebazaa, A Ben Hamida, M Hentati, F Producer: 19981106 In: Neuromuscular disorders : NMD vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	[Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)]. [electronic resource] by Ben Hamida, M Madani, S Zmerli, S Chami, I Annabi, A Jamoussi, M Marzouki, M Rachdi, M Samoud, S Talbi, M Producer: 19810623 In: Revue neurologique vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	90.	Familial encephalopathy and L-2-hydroxyglutaric aciduria. [electronic resource] by Kaabachi, N Larnaout, A Rabier, D Jakobs, C Belal, S Hentati, F Parvey, P Bardet, J Ben Hamida, M Mebazaa, A Producer: 19940303 In: Journal of inherited metabolic disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein. [electronic resource] by Ouahchi, K Arita, M Kayden, H Hentati, F Ben Hamida, M Sokol, R Arai, H Inoue, K Mandel, J L Koenig, M Producer: 19950524 In: Nature genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. [electronic resource] by Belal, S Cancel, G Stevanin, G Hentati, F Khati, C Ben Hamida, C Auburger, G Agid, Y Ben Hamida, M Brice, A Producer: 19940912 In: Neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Fine localization of the CMT4A locus using a PAC contig and haplotype analysis. [electronic resource] by Ben Othmane, K Rochelle, J M Ben Hamida, M Slotterbeck, B Rao, N Hentati, F Pericak-Vance, M A Vance, J M Producer: 20000407 In: Neurogenetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency. [electronic resource] by Gabsi, S Gouider-Khouja, N Belal, S Fki, M Kefi, M Turki, I Ben Hamida, M Kayden, H Mebazaa, R Hentati, F Producer: 20011025 In: European journal of neurology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. [electronic resource] by Hentati, A Pericak-Vance, M A Hung, W Y Belal, S Laing, N Boustany, R M Hentati, F Ben Hamida, M Siddique, T Producer: 19950110 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. [electronic resource] by Belal, S Panayides, K Sirugo, G Ben Hamida, C Ioannou, P Hentati, F Beckmann, J Koenig, M Mandel, J L Ben Hamida, M Producer: 19930114 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	97.	Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. [electronic resource] by Ben Hamida, M Belal, S Sirugo, G Ben Hamida, C Panayides, K Ionannou, P Beckmann, J Mandel, J L Hentati, F Koenig, M Producer: 19931220 In: Neurology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A. [electronic resource] by Othmane, K B Loeb, D Hayworth-Hodgte, R Hentati, F Rao, N Roses, A D Ben Hamida, M Pericak-Vance, M A Vance, J M Producer: 19960201 In: Genomics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy. [electronic resource] by Ben Jelloun-Dellagi, S Chaffey, P Hentati, F Ben Hamida, C Tome, F Colin, H Dellagi, K Kaplan, J C Fardeau, M Ben Hamida, M Producer: 19910107 In: Neurology vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. [electronic resource] by Ben Othmane, K Hentati, F Lennon, F Ben Hamida, C Blel, S Roses, A D Pericak-Vance, M A Ben Hamida, M Vance, J M Producer: 19940203 In: Human molecular genetics vol. 2 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 112 results.