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Ahmed Bouhouche

Research Profile

Geographic Areas

Disorders

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Genes & Molecular Sequences

Recessive Genes

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Chromosomes, Human, Pair 5

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Publications

TOP 3
Ahmed Bouhouche; Naima Bouslam; Layachi Chabraoui; elmostafa El fahime; Abdeljalil El Quessar; L Errguig; Mohamed Jiddane; Lamiae Lachhab; Sanaa Sefiani; Jehanne Aasfara; Ali Benomar; Mohamed Yahyaoui
An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.
Bouchra Ouled Amar Ben Cheikh; Stéphanie Baulac; Fatiha Lahjouji; Ahmed Bouhouche; Philippe Couarch; Naima Khalili; Wafae Regragui; Stéphane Lehericy; Merle Ruberg; Ali Benomar; Simon Heath; Taib Chkili; Mohamed Yahyaoui; Mohamed Jiddane; Reda Ouazzani; Eric LeGuern
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.
Ahmed Bouhouche; Nazha Birouk; Ali Benomar; Reda Ouazzani; Taïeb Chkili; Mohamed Yahyaoui
A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.

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All Publications

2012: Ahmed Bouhouche; Naima Bouslam; Layachi Chabraoui; elmostafa El fahime; Abdeljalil El Quessar; L Errguig; Mohamed Jiddane; Lamiae Lachhab; Sanaa Sefiani; Jehanne Aasfara; Ali Benomar; Mohamed Yahyaoui
An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.
BMC medical genetics 2012;13():18.
2009: Bouchra Ouled Amar Ben Cheikh; Stéphanie Baulac; Fatiha Lahjouji; Ahmed Bouhouche; Philippe Couarch; Naima Khalili; Wafae Regragui; Stéphane Lehericy; Merle Ruberg; Ali Benomar; Simon Heath; Taib Chkili; Mohamed Yahyaoui; Mohamed Jiddane; Reda Ouazzani; Eric LeGuern
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.
Neurogenetics 2009;10(1):35-42.
2007: Ahmed Bouhouche; Nazha Birouk; Ali Benomar; Reda Ouazzani; Taïeb Chkili; Mohamed Yahyaoui
A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2007;34(4):421-6.
2007: Stephan Klebe; Alexandra Durr; Naima Bouslam; Djamel Grid; Caroline Paternotte; Christel Depienne; Sylvain Hanein; Ahmed Bouhouche; Nizar Elleuch; Hamid Azzedine; Sandrine Poea-Guyon; Sylvie Forlani; Elodie Denis; Céline Charon; Jamilé Hazan; Alexis Brice; Giovanni Stevanin
Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(7):854-61.
2007: Naima Bouslam; Ahmed Bouhouche; Ali Benomar; Sylvain Hanein; Stephan Klebe; Hamid Azzedine; Silvia Di Giandomenico; Anne Boland-Augé; Filippo M Santorelli; Alexandra Durr; Alexis Brice; Mohamed Yahyaoui; Giovanni Stevanin
A novel locus for autosomal recessive spastic ataxia on chromosome 17p.
Human genetics 2007;121(3-4):413-20.
2007: Ahmed Bouhouche; Nazha Birouk; Hamid Azzedine; Ali Benomar; Garry Durosier; Dorothée Ente; Marie-Paule Muriel; Merle Ruberg; Ilham Slassi; Mohamed Yahyaoui; Odile Dubourg; Reda Ouazzani; Eric LeGuern
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
Brain : a journal of neurology 2007;130(Pt 4):1062-75.
2006: Hamid Azzedine; Nicole Ravisé; Christophe Verny; A Gabrëels-Festen; M Lammens; Djamel Grid; Jean-Michel Vallat; Garry Durosier; Jan Senderek; S Nouioua; Tarik Hamadouche; Ahmed Bouhouche; Angele Guilbot; Claudia Stendel; Merle Ruberg; Alexis Brice; Nazha Birouk; Odile Dubourg; Meriem Tazir; Eric LeGuern
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.
Neurology 2006;67(4):602-6.
2006: Ahmed Bouhouche; Ali Benomar; Naima Bouslam; Taïeb Chkili; Mohamed Yahyaoui
Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.
Journal of medical genetics 2006;43(5):441-3.
2006: Ahmed Bouhouche; Ali Benomar; Naima Bouslam; Reda Ouazzani; Taïeb Chkili; Mohamed Yahyaoui
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.
European journal of human genetics : EJHG 2006;14(2):249-52.
2006: Odile Dubourg; Hamid Azzedine; Christophe Verny; Garry Durosier; Nazha Birouk; Riadh Gouider; Mustafa A Salih; Ahmed Bouhouche; A Thiam; Djamel Grid; M Mayer; Merle Ruberg; Meriem Tazir; Alexis Brice; Eric LeGuern
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.
Neuromolecular medicine 2006;8(1-2):75-86.
2005: Naima Bouslam; Ali Benomar; Hamid Azzedine; Ahmed Bouhouche; Michito Namekawa; Stephan Klebe; Céline Charon; Alexandra Durr; Merle Ruberg; Alexis Brice; Mohamed Yahyaoui; Giovanni Stevanin
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).
Annals of neurology 2005;57(4):567-71.
2003: Ahmed Bouhouche; Ali Benomar; Nazha Birouk; Naima Bouslam; Reda Ouazzani; Mohamed Yahyaoui; Taïeb Chkili
High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.
Journal of neurology 2003;250(10):1209-13.
2003: Hamid Azzedine; Alessandra Bolino; T Taïeb; Nazha Birouk; Marco Di Duca; Ahmed Bouhouche; S Benamou; Amel Mrabet; Tarik Hammadouche; Taïeb Chkili; Riadh Gouider; Roberto Ravazzolo; Alexis Brice; Jocelyn Laporte; Eric LeGuern
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.
American journal of human genetics 2003;72(5):1141-53.
2002: Ali Benomar; Mohamed Yahyaoui; Farid Meggouh; Ahmed Bouhouche; Mohammed Boutchich; Naima Bouslam; Abdelhaq Zaim; Michèle Schmitt; Halima Belaidi; Reda Ouazzani; Taïeb Chkili; Michel Koenig
Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.
Journal of the neurological sciences 2002;198(1-2):25-9.
1999: Angele Guilbot; Nicole Ravisé; Ahmed Bouhouche; Philippe Coullin; Nazha Birouk; Thierry Maisonobe; Thierry Kuntzer; C Vial; Djamel Grid; Alexis Brice; Eric LeGuern
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1.
European journal of human genetics : EJHG 1999;7(8):849-59.
1999: Angele Guilbot; M Kessali; Nicole Ravisé; Tarik Hammadouche; Ahmed Bouhouche; Thierry Maisonobe; Djamel Grid; Alexis Brice; Eric LeGuern
The autosomal recessive form of CMT disease linked to 5q31-q33.
Annals of the New York Academy of Sciences 1999;883():453-6.
1999: Angele Guilbot; M Kessali; Nicole Ravisé; Tarik Hammadouche; Ahmed Bouhouche; Thierry Maisonobe; Djamel Grid; Alexis Brice; Eric LeGuern
The autosomal recessive form of CMT disease linked to 5q31-q33.
Annals of the New York Academy of Sciences 1999;883():56-9.
1999: Ahmed Bouhouche; Ali Benomar; Nazha Birouk; A Mularoni; Farid Meggouh; JP Tassin; Djamel Grid; Antoon Vandenberghe; Mohamed Yahyaoui; Taïeb Chkili; Alexis Brice; Eric LeGuern
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.
American journal of human genetics 1999;65(3):722-7.