Search Results - Karkar, Adnane

  • Showing 1 - 7 results of 7
Refine Results
  1. 1
    The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco

    The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco by Nassereddine, Sanaa, Hassani Idrissi, Hind, Habbal, Rachida, Abouelfath, Rhizlane, Korch, Farah, Haraka, Majda, Karkar, Adnane, Nadifi, Sellama

    Published in BMC medical genetics
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia

    Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia by Kraoua, Ichraf, Karkar, Adnane, Drissi, Cyrine, Benrhouma, Hanene, Klaa, Hedia, Samaan, Simon, Renaldo, Florence, Elmaleh, Monique, Ben Hamouda, Mohamed, Abdelhak, Sonia, Boespflug‐Tanguy, Odile, Ben Youssef‐Turki, Ilfghem, Dorboz, Imen

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome

    Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome by Rachad, Laila, El Otmani, Hicham, Karkar, Adnane, El Moutawakil, Bouchra, El Kadmiri, Nadia, Nadifi, Sellama

    Published in Neuroscience letters
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    The polymorphism G894 T of endothelial nitric oxide synthase in Morocco

    The polymorphism G894 T of endothelial nitric oxide synthase in Morocco by Nassereddine, Sanaa, Hassani Idrissi, Hind, Habbal, Rachida, Abouelfath, Rhizlane, Korch, Farah, Haraka, Majda, Karkar, Adnane, Nadifi, Sellama

    Published in BMC medical genetics
    Get full text
    Article
    Save to List
    Saved in:
  5. 5
    A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report

    A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report by Karkar, Adnane, Barakat, Abdelhamid, Bakhchane, Amina, Fettah, Houda, Slassi, Ilham, Dorboz, Imen, Boespflug-Tanguy, Odile, Nadifi, Sellama

    Published in BMC neurology
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    A novel SGCE gene mutation in a Moroccan sporadic case with myoclonus-dystonia syndrome

    A novel SGCE gene mutation in a Moroccan sporadic case with myoclonus-dystonia syndrome by Rachad, Laila, El Otmani, Hicham, Karkar, Adnane, El Kadmiri, Nadia, Nadifi, Sellama

    Published in Gene reports
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  7. 7
    Genetic aspect of leukodystrophies in Moroccan population

    Genetic aspect of leukodystrophies in Moroccan population by Karkar, Adnane, Dorboz, Imen, Nadifi, Sellama, Boespflug-Tanguy, Odile

    Published in IBRO reports
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: