Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals

Por Hamzi, Khalil, Tazzite, Amal, Nadifi, Sellama
Publicado em 2011

MTHFR C677T polymorphism and risk of nonsyndromic cleft lip with or without cleft palate in the Moroccan population

Por Rafik A, Rachad L, Kone A, Nadifi S
Publicado em 2019-03-01

Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals

Por Hamzi, Khalil, Diakité, Bréhima, Tazzite, Amal, Nadifi, Sellama
Publicado em 2013

Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?

Por Hamzi, Khalil, Itto, Afaf Ben, Nassereddine, Sanaa, Nadifi, Sellama
Publicado em 2010

Methylenetetrahydrofolate Reductase C677T polymorphism and breast cancer risk in Moroccan women

Por Diakite, B, Tazzite, A, Hamzi, K, Jouhadi, H, Nadifi, S
Publicado em 2012

FLT3-ITD Incidence and FLT-D835 Mutations in Acute Myeloid Leukemia Patients with Normal Karyotype in Morocco: A Preliminary Study

Por Hind Dehbi, Yaya Kassogue, Sanaa Nasserddine, Asma Quessar, Sellama Nadifi
Publicado em 2013-01-01

Duchenne muscular dystrophy: Advances in molecular appraoch

Por Benitto, Afaf, Hamzi, Khalil, Itri, Mohammed, Slassi, Ilham, Nadifi, Sellama
Publicado em 2013

Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations

Por Tazzite, Amal, Jouhadi, Hassan, Hamzi, Khalil, Benider, Abdellatif, Nadifi, Sellama
Publicado em 2013

Relationship Between Family History of Breast Cancer and Clinicopathological Features in Moroccan Patients

Por Tazzite, Amal, Jouhadi, Hassan, Saiss, Kamal, Benider, Abdellatif, Nadifi, Sellama
Publicado em 2013

IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease

Por Serbati, Nadia, Senhaji, Nezha, Diakite, Brehima, Badre, Wafaa, Nadifi, Sellama
Publicado em 2014

Association of methylenetetrahydrofolate reductase gene (C677T) with the risk of hypertension in Morocco

Por Nassereddine, Sanaa, Kassogue, Yaya, Korchi, Farah, Habbal, Rachida, Nadifi, Sellama
Publicado no BMC Res Notes (2015)

Genetics of Glioblastoma in Moroccan population: Review of literature

Por Hossam Hilal El Idrissi, Oum Kaltoum Ait Boujmia, Sellama Nadifi, Hind Dehbi
Publicado em 2018-12-01

Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: New data and a meta-analysis

Por Senhaji, Nezha, Diakité, Brehima, Serbati, Nadia, Zaid, Younes, Badre, Wafaa, Nadifi, Sellama
Publicado no BMC Gastroenterol (2014)

Association of glutathione S-transferase (GSTM1 and GSTT1) genes with chronic myeloid leukemia

Por Kassogue, Yaya, Dehbi, Hind, Quachouh, Meryem, Quessar, Asma, Benchekroun, Said, Nadifi, Sellama
Publicado no Springerplus (2015)

Genetic Polymorphisms of Multidrug Resistance Gene-1 (MDR1/ABCB1) and Glutathione S-Transferase Gene and the Risk of Inflammatory Bowel Disease among Moroccan Patients

Por Senhaji, Nezha, Kassogue, Yaya, Fahimi, Mina, Serbati, Nadia, Badre, Wafaa, Nadifi, Sellama
Publicado no Mediators Inflamm (2015)

Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients

Por Jouhadi, Hassan, Tazzite, Amal, Azeddoug, Houssine, Naim, Asmâa, Nadifi, Sellama, Benider, Abdellatif
Publicado no BMC Res Notes (2016)

Association of Glutathione S-transferase Genes (M1 and T1) with the Risk of Acute Myeloid Leukemia in a Moroccan Population

Por Ait Boujmia Oum Kaltoum, Nadifi Sellama, Dehbi Hind, Kassogue Yaya, Lamchahab Mouna, Quessar Asma
Publicado em 2017-01-01

A synergic effect between CYP2C19*2, CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function alleles is associated with Clopidogrel resistance among Moroccan Acute Coronary Synd...

Por Hind Hassani Idrissi, Wiam Hmimech, Nada El Khorb, Hafid Akoudad, Rachida Habbal, Sellama Nadifi
Publicado em 2018-01-01

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population

Por Marouf, Chaymaa, Hajji, Omar, Diakité, Brehima, Tazzite, Amal, Jouhadi, Hassan, Benider, Abdellatif, Nadifi, Sellama
Publicado no Springerplus (2015)

Atteinte cardiaque au cours de la dystrophie myotonique de Steinert: expérience marocaine, à propos de 18 cas

Por Saghi, Ghita, Bouhouch, Rachida, Salaheddine, Loubna, Birouk, Nezha, Nadifi, Salama, Fellat, Ibtissam, Cherti, Mohamed
Publicado no Pan Afr Med J (2015)