List of works - Leila Ammar-Keskes

A novel C-terminal truncated mutation in hCDKL5 protein causing a severe West syndrome: Comparison with previous truncated mutations and genotype/phenotype correlation

scientific article published on 17 September 2018

A novel m.6307A>G mutation in the mitochondrialCOXIgene in asthenozoospermic infertile men ⬇️

scientific article published on June 17, 2013

Antioxidant supplementations in vitro improve rat sperm parameters and enhance antioxidant enzyme activities against dimethoate-induced sperm damages ⬇️

scientific article published on August 2, 2011

Antioxidative potential of Quercetin against hydrogen peroxide induced oxidative stress in spermatozoa in vitro ⬇️

scientific article published on February 25, 2011

Caffeic acid and quercetin protect erythrocytes against the oxidative stress and the genotoxic effects of lambda-cyhalothrin in vitro ⬇️

scientific article published on October 25, 2011

Deletion of CDY1b copy of Y chromosome CDY1 gene is a risk factor of male infertility in Tunisian men.

scientific article published on 15 July 2014

Effect of freezing–thawing process and quercetin on human sperm survival and DNA integrity ⬇️

scientific article published on September 23, 2012

First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation

scientific article published on 5 February 2018

Genetic Determinants of Methotrexate Toxicity in Tunisian Patients with Rheumatoid Arthritis: A Study of Polymorphisms Involved in the MTX Metabolic Pathway

scientific article

Inter-and intra-operator variability in the analysis of semen parameters: results from a quality control program

scientific article published on 26 October 2016

Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency ⬇️

scientific article published on November 1, 2012

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men ⬇️

scientific article published on May 6, 2013

Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion

scientific article published on 03 November 2018

Novel mutations in the CDKL5 gene in complex genotypes associated with West syndrome with variable phenotype: First description of somatic mosaic state

scientific article published on 2 August 2017

Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian man ⬇️

scientific article published on February 8, 2013

Possible Association of a Novel Missense Mutation A6375G in the MitochondrialCytochrome C Oxidase IGene with Asthenospermia in the Tunisian Population ⬇️

scientific article published on October 2, 2012

Protective role of caffeic acid on lambda cyhalothrin-induced changes in sperm characteristics and testicular oxidative damage in rats ⬇️

scientific article published on October 24, 2011

Quercetin attenuates lambda cyhalothrin‐induced reproductive toxicity in male rats ⬇️

scientific article published on September 2, 2011

The CAG repeat polymorphism of mitochondrial polymerase gamma (POLG) is associated with male infertility in Tunisia ⬇️