Search research articles
Contact Us
Filters
Showing results (11-20 of 51) with videos related to
Page
of 6
Sort By:
Medecine Sciences : M/S
|
January 17, 2023
[The high phenotypic variability of RYR1 gene mutations]
Mohamed Islam Kediha, Sonia Nouioua, Meriem Tazir, et al.
Journal of Medical Genetics
|
August 7, 2015
Charcot-Marie-Tooth diseases: an update and some new proposals for the classification
Stéphane Mathis, Cyril Goizet, Meriem Tazir, et al.
Neuroimmunomodulation
|
August 18, 2015
All-trans-retinoic acid modulates nitric oxide and interleukin-17A production by peripheral blood mononuclear cells from patients with Alzheimer's disease
Nassima Behairi, Mourad Belkhelfa, Hamida Mesbah-Amroun, et al.
Journal of Neuropathology and Experimental Neurology
|
January 5, 2018
Nerve Biopsy Is Still Useful in Some Inherited Neuropathies
Mathilde Duchesne, Stéphane Mathis, Laurence Richard, et al.
Archives of Medical Research
|
March 25, 2014
Hyperhomocysteinemia is a risk factor for Alzheimer's disease in an Algerian population
Khaled Nazef, Malika Khelil, Hiba Chelouti, et al.
Neuromuscular Disorders : NMD
|
February 24, 2009
Phenotypic variability in giant axonal neuropathy
Meriem Tazir, Sonia Nouioua, Laurent Magy, et al.
BMC Medical Genetics
|
June 13, 2015
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia
Wahiba Hamza, Lamia Ali Pacha, Tarik Hamadouche, et al.
Neuromuscular Disorders : NMD
|
July 12, 2011
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes
Sonia Nouioua, Tarik Hamadouche, Benoit Funalot, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research
|
May 17, 2014
IFN-γ and TNF-α are involved during Alzheimer disease progression and correlate with nitric oxide production: a study in Algerian patients
Mourad Belkhelfa, Hayet Rafa, Oussama Medjeber, et al.
Neuromuscular Disorders : NMD
|
May 6, 2014
Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
Stéphane Mathis, Philippe Corcia, Meriem Tazir, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
Medecine Sciences : M/S
|
January 17, 2023
[The high phenotypic variability of RYR1 gene mutations]
Mohamed Islam Kediha, Sonia Nouioua, Meriem Tazir, et al.
Journal of Medical Genetics
|
August 7, 2015
Charcot-Marie-Tooth diseases: an update and some new proposals for the classification
Stéphane Mathis, Cyril Goizet, Meriem Tazir, et al.
Neuroimmunomodulation
|
August 18, 2015
All-trans-retinoic acid modulates nitric oxide and interleukin-17A production by peripheral blood mononuclear cells from patients with Alzheimer's disease
Nassima Behairi, Mourad Belkhelfa, Hamida Mesbah-Amroun, et al.
Journal of Neuropathology and Experimental Neurology
|
January 5, 2018
Nerve Biopsy Is Still Useful in Some Inherited Neuropathies
Mathilde Duchesne, Stéphane Mathis, Laurence Richard, et al.
Archives of Medical Research
|
March 25, 2014
Hyperhomocysteinemia is a risk factor for Alzheimer's disease in an Algerian population
Khaled Nazef, Malika Khelil, Hiba Chelouti, et al.
Neuromuscular Disorders : NMD
|
February 24, 2009
Phenotypic variability in giant axonal neuropathy
Meriem Tazir, Sonia Nouioua, Laurent Magy, et al.
BMC Medical Genetics
|
June 13, 2015
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia
Wahiba Hamza, Lamia Ali Pacha, Tarik Hamadouche, et al.
Neuromuscular Disorders : NMD
|
July 12, 2011
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes
Sonia Nouioua, Tarik Hamadouche, Benoit Funalot, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research
|
May 17, 2014
IFN-γ and TNF-α are involved during Alzheimer disease progression and correlate with nitric oxide production: a study in Algerian patients
Mourad Belkhelfa, Hayet Rafa, Oussama Medjeber, et al.
Neuromuscular Disorders : NMD
|
May 6, 2014
Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
Stéphane Mathis, Philippe Corcia, Meriem Tazir, et al.
Page
of 6