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Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene. [electronic resource] by
- Birouk, Nazha
- Azzedine, Hamid
- Dubourg, Odile
- Muriel, Marie-Paule
- Benomar, Ali
- Hamadouche, Tarik
- Maisonobe, Thierry
- Ouazzani, Reda
- Brice, Alexis
- Yahyaoui, Mohamed
- Chkili, Taïb
- Le Guern, Eric
Producer: 20030507
In:
Archives of neurology vol. 60
Availability: No items available.
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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families. [electronic resource] by
- Bouhouche, Ahmed
- Birouk, Nazha
- Azzedine, Hamid
- Benomar, Ali
- Durosier, Garry
- Ente, Dorothée
- Muriel, Marie-Paule
- Ruberg, Merle
- Slassi, Ilham
- Yahyaoui, Mohamed
- Dubourg, Odile
- Ouazzani, Reda
- LeGuern, Eric
Producer: 20070530
In:
Brain : a journal of neurology vol. 130
Availability: No items available.
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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
Availability: No items available.
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia. [electronic resource] by
- Gan-Or, Ziv
- Bouslam, Naima
- Birouk, Nazha
- Lissouba, Alexandra
- Chambers, Daniel B
- Vérièpe, Julie
- Androschuk, Alaura
- Laurent, Sandra B
- Rochefort, Daniel
- Spiegelman, Dan
- Dionne-Laporte, Alexandre
- Szuto, Anna
- Liao, Meijiang
- Figlewicz, Denise A
- Bouhouche, Ahmed
- Benomar, Ali
- Yahyaoui, Mohamed
- Ouazzani, Reda
- Yoon, Grace
- Dupré, Nicolas
- Suchowersky, Oksana
- Bolduc, Francois V
- Parker, J Alex
- Dion, Patrick A
- Drapeau, Pierre
- Rouleau, Guy A
- Ouled Amar Bencheikh, Bouchra
Producer: 20171229
In:
American journal of human genetics vol. 98
Availability: No items available.
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia. [electronic resource] by
- Gan-Or, Ziv
- Bouslam, Naima
- Birouk, Nazha
- Lissouba, Alexandra
- Chambers, Daniel B
- Vérièpe, Julie
- Androschuk, Alaura
- Laurent, Sandra B
- Rochefort, Daniel
- Spiegelman, Dan
- Dionne-Laporte, Alexandre
- Szuto, Anna
- Liao, Meijiang
- Figlewicz, Denise A
- Bouhouche, Ahmed
- Benomar, Ali
- Yahyaoui, Mohamed
- Ouazzani, Reda
- Yoon, Grace
- Dupré, Nicolas
- Suchowersky, Oksana
- Bolduc, Francois V
- Parker, J Alex
- Dion, Patrick A
- Drapeau, Pierre
- Rouleau, Guy A
- Ouled Amar Bencheikh, Bouchra
Publication details: American journal of human genetics 06 2016
In:
American journal of human genetics vol. 98
Availability: No items available.
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