Nadifi S - Search Results

1

Dilated cardiomyopathy: A rare and late complication of the hemolytic-uremic syndrome.

Naour O, Drighil A, Idouz K, Nadifi S, Rochdi FE, Bouayed K, Mikou N. Naour O, et al. Among authors: nadifi s. J Cardiol Cases. 2019 Aug 2;20(4):125-128. doi: 10.1016/j.jccase.2019.07.002. eCollection 2019 Oct. J Cardiol Cases. 2019. PMID: 31969940 Free PMC article.

2

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

Hamzi K, Itto AB, Nassereddine S, Nadifi S. Hamzi K, et al. Among authors: nadifi s. Indian J Hum Genet. 2010 Sep;16(3):172-4. doi: 10.4103/0971-6866.73417. Indian J Hum Genet. 2010. PMID: 21206709 Free PMC article.

3

Sickle cell disease with double stroke in a Moroccan family.

Hamzi K, Itto AB, Jouhadi Z, Slassi I, Nadifi S. Hamzi K, et al. Among authors: nadifi s. J Mol Neurosci. 2013 Jun;50(2):311-3. doi: 10.1007/s12031-013-9967-x. Epub 2013 Jan 23. J Mol Neurosci. 2013. PMID: 23340961

4

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 Syndromes patients.

Hassani Idrissi H, Hmimech W, Khorb NE, Akoudad H, Habbal R, Nadifi S. Hassani Idrissi H, et al. Among authors: nadifi s. BMC Res Notes. 2018 Jan 18;11(1):46. doi: 10.1186/s13104-018-3132-0. BMC Res Notes. 2018. PMID: 29347970 Free PMC article.

5

Prenatal diagnosis of BMD in Morocco: evolution and limits.

Hamzi K, Itto AB, Itri M, Nadifi S. Hamzi K, et al. Among authors: nadifi s. J Mol Neurosci. 2014 Apr;52(4):459-60. doi: 10.1007/s12031-013-0106-5. Epub 2013 Sep 8. J Mol Neurosci. 2014. PMID: 24014122

6

Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).

Rachad L, El Kadmiri N, Slassi I, El Otmani H, Nadifi S. Rachad L, et al. Among authors: nadifi s. Mol Neurobiol. 2017 Mar;54(2):939-942. doi: 10.1007/s12035-016-9712-x. Epub 2016 Jan 20. Mol Neurobiol. 2017. PMID: 26790671 Review.

7

Genetics of Glioblastoma in Moroccan population: Review of literature.

Idrissi HHE, Boujmia OKA, Nadifi S, Dehbi H. Idrissi HHE, et al. Among authors: nadifi s. IBRO Rep. 2018 Nov 17;5:133-136. doi: 10.1016/j.ibror.2018.11.005. eCollection 2018 Dec. IBRO Rep. 2018. PMID: 30569026 Free PMC article. Review.

8

Association of Multidrug Resistance Gene-1 (MDR1 C1236T) Polymorphism with the Risk of Acute Myeloid Leukemia in a Moroccan Population.

Ait Boujmia OK, Nadifi S, Dehbi H, Lamchahab M, Quessar A. Ait Boujmia OK, et al. Among authors: nadifi s. Asian Pac J Cancer Prev. 2020 Jul 1;21(7):1899-1904. doi: 10.31557/APJCP.2020.21.7.1899. Asian Pac J Cancer Prev. 2020. PMID: 32711413 Free PMC article.

9

The influence of DNMT3A and DNMT3B gene polymorphisms on acute myeloid leukemia risk in a Moroccan population.

Ait Boujmia OK, Nadifi S, Dehbi H, Lamchahab M, Quessar A. Ait Boujmia OK, et al. Among authors: nadifi s. Curr Res Transl Med. 2020 Nov;68(4):191-195. doi: 10.1016/j.retram.2020.08.001. Epub 2020 Sep 8. Curr Res Transl Med. 2020. PMID: 32912818

10

BRCA Mutational Status is a Promising Predictive Biomarker for Platinum- based Chemotherapy in Triple-Negative Breast Cancer.

Tazzite A, Jouhadi H, Benider A, Nadifi S. Tazzite A, et al. Among authors: nadifi s. Curr Drug Targets. 2020;21(10):962-973. doi: 10.2174/1389450121666200203162541. Curr Drug Targets. 2020. PMID: 32013831 Review.

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