Your search returned 29 results.

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	1.	Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1. [electronic resource] by Bouhouche, Ahmed Benomar, Ali Bouslam, Naima Ouazzani, Reda Chkili, Taïeb Yahyaoui, Mohamed Producer: 20060915 In: European journal of human genetics : EJHG vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan family. [electronic resource] by Bouhouche, Ahmed Regragui, Wafae El Fahime, Elmostafa Bouslam, Naima Tazi-Ahnini, Rachid Melloul, Marouane Benomar, Ali Yahyaoui, Mohamed Producer: 20140318 In: Indian journal of pediatrics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing. [electronic resource] by Bouhouche, Ahmed Tibar, Houyam Kriouale, Yamna Jiddane, Mohammed Smaili, Imane Bouslam, Naima Benomar, Ali Yahyaoui, Mohamed El Fahime, Elmostafa Publication details: Case reports in genetics 2018 In: Case reports in genetics vol. 2018 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. [electronic resource] by Stevanin, Giovanni Bouslam, Naima Thobois, Stéphane Azzedine, Hamid Ravaux, Lucas Boland, Anne Schalling, Martin Broussolle, Emmanuel Dürr, Alexandra Brice, Alexis Producer: 20040312 In: Annals of neurology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism. [electronic resource] by Ben El Haj, Rafiqua Regragui, Wafaa Tazi-Ahnini, Rachid Skalli, Asmae Bouslam, Naima Benomar, Ali Yahyaoui, Mohamed Bouhouche, Ahmed Producer: 20170315 In: BioMed research international vol. 2016 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A new phenotype linked to SPG27 and refinement of the critical region on chromosome. [electronic resource] by Ribai, Pascale Stevanin, Giovanni Bouslam, Naima Pontier, Bénédicte Nelson, Isabelle Fontaine, Bertrand Dussert, Christel Charon, Céline Durr, Alexandra Brice, Alexis Producer: 20061212 In: Journal of neurology vol. 253 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Evidence for prehistoric origins of the G2019S mutation in the North African Berber population. [electronic resource] by Ben El Haj, Rafiqua Salmi, Ayyoub Regragui, Wafa Moussa, Ahmed Bouslam, Naima Tibar, Houyam Benomar, Ali Yahyaoui, Mohamed Bouhouche, Ahmed Producer: 20170926 In: PloS one vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families. [electronic resource] by Benomar, Ali Yahyaoui, Mohammed Meggouh, Farid Bouhouche, Ahmed Boutchich, Mohammed Bouslam, Naima Zaim, Abdelhaq Schmitt, Michèle Belaidi, Halima Ouazzani, Reda Chkili, Taïb Koenig, Michel Producer: 20020731 In: Journal of the neurological sciences vol. 198 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3. [electronic resource] by Klebe, Stephan Azzedine, Hamid Durr, Alexandra Bastien, Patrick Bouslam, Naima Elleuch, Nizar Forlani, Sylvie Charon, Celine Koenig, Michel Melki, Judith Brice, Alexis Stevanin, Giovanni Producer: 20060619 In: Brain : a journal of neurology vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28). [electronic resource] by Bouslam, Naima Benomar, Ali Azzedine, Hamid Bouhouche, Ahmed Namekawa, Michito Klebe, Stephan Charon, Céline Durr, Alexandra Ruberg, Merle Brice, Alexis Yahyaoui, Mohamed Stevanin, Giovanni Producer: 20050520 In: Annals of neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. [electronic resource] by Stevanin, Giovanni Hahn, Valérie Lohmann, Ebba Bouslam, Naima Gouttard, Michel Soumphonphakdy, Caroline Welter, Marie-Laure Ollagnon-Roman, Elisabeth Lemainque, Arnaud Ruberg, Merle Brice, Alexis Durr, Alexandra Producer: 20040907 In: Archives of neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3. [electronic resource] by Bouhouche, Ahmed Benomar, Ali Errguig, Leila Lachhab, Lamiae Bouslam, Naima Aasfara, Jehanne Sefiani, Sanaa Chabraoui, Layachi El Fahime, Elmostafa El Quessar, Abdeljalil Jiddane, Mohamed Yahyaoui, Mohamed Producer: 20120627 In: BMC medical genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	None [electronic resource] by Bouhouche, Ahmed Tibar, Houyam Ben El Haj, Rafiqua El Bayad, Khalil Razine, Rachid Tazrout, Sanaa Skalli, Asmae Bouslam, Naima Elouardi, Loubna Benomar, Ali Yahyaoui, Mohammed Regragui, Wafa Publication details: Parkinson's disease 2017 In: Parkinson's disease vol. 2017 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction. [electronic resource] by Dor, Talya Cinnamon, Yuval Raymond, Laure Shaag, Avraham Bouslam, Naima Bouhouche, Ahmed Gaussen, Marion Meyer, Vincent Durr, Alexandra Brice, Alexis Benomar, Ali Stevanin, Giovanni Schuelke, Markus Edvardson, Simon Producer: 20140908 In: Journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel. [electronic resource] by Bouhouche, Ahmed Tesson, Christelle Regragui, Wafaa Rahmani, Mounia Drouet, Valérie Tibar, Houyam Souirti, Zouhayr Ben El Haj, Rafiqua Bouslam, Naima Yahyaoui, Mohamed Brice, Alexis Benomar, Ali Lesage, Suzanne Publication details: Frontiers in neurology 2017 In: Frontiers in neurology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A novel locus for autosomal recessive spastic ataxia on chromosome 17p. [electronic resource] by Bouslam, Naima Bouhouche, Ahmed Benomar, Ali Hanein, Sylvain Klebe, Stephan Azzedine, Hamid Di Giandomenico, Silvia Boland-Augé, Anne Santorelli, Filippo M Durr, Alexandra Brice, Alexis Yahyaoui, Mohamed Stevanin, Giovanni Producer: 20070710 In: Human genetics vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Clinical and genetic data of Huntington disease in Moroccan patients. [electronic resource] by Bouhouche, Ahmed Regragui, Wafaa Lamghari, Hind Khaldi, Khadija Birouk, Nazha Lytim, Safaa Bellamine, Soufiane Kriouile, Yamna Bouslam, Naima Haddou, El Hachmia Ait Ben Faris, Mustapha Alaoui Benomar, Ali Yahyaoui, Mohamed Producer: 20170310 In: African health sciences vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. [electronic resource] by Klebe, Stephan Durr, Alexandra Bouslam, Naima Grid, Djamel Paternotte, Caroline Depienne, Christel Hanein, Sylvain Bouhouche, Ahmed Elleuch, Nizar Azzedine, Hamid Poea-Guyon, Sandrine Forlani, Sylvie Denis, Elodie Charon, Céline Hazan, Jamile Brice, Alexis Stevanin, Giovanni Producer: 20071206 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 144B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity. [electronic resource] by Lossos, Alexander Stevanin, Giovanni Meiner, Vardiella Argov, Zohar Bouslam, Naima Newman, J P Gomori, John M Klebe, Stephan Lerer, Israela Elleuch, Nizar Silverstein, Shira Durr, Alexandra Abramsky, Oded Ben-Nariah, Ziva Brice, Alexis Producer: 20060628 In: Archives of neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients. [electronic resource] by Le Ber, Isabelle Bouslam, Naïma Rivaud-Péchoux, Sophie Guimarães, João Benomar, Ali Chamayou, Céline Goizet, Cyril Moreira, Maria-Ceù Klur, Sandra Yahyaoui, Mohamed Agid, Yves Koenig, Michel Stevanin, Giovanni Brice, Alexis Dürr, Alexandra Producer: 20040520 In: Brain : a journal of neurology vol. 127 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 29 results.