An Unusual Case of Gullo's Syndrome Concomitant with Serious Endometriosis Disease in a Postmenopausal Woman

por Ainahi, Abdelhakim, Ziane, Abdellaziz, Wakrim, Lahcen, Elmdaghri, Naima, Barakat, Abdelhamid
Publicado 2018

Molecular docking analysis of PPARγ with phytochemicals from Moroccan medicinal plants

por Elkhattabi, Lamiae, Zouhdi, Salwa, Moussetad, Fairouz, Kettani, Anass, Barakat, Abdelhamid, Saile, Rachid
Publicado 2023

Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility

por Harmak, Houda, Charoute, Hicham, Redouane, Salaheddine, Filali, Ouafaa Aniq, Barakat, Abdelhamid, Rouba, Hassan
Publicado 2022

Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes

por Bouzidi, Aymane, Charif, Majida, Bouzidi, Adil, Amalou, Ghita, Kandil, Mostafa, Barakat, Abdelhamid, Lenaers, Guy
Publicado 2021

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies

por Bouzidi, Aymane, Charoute, Hicham, Charif, Majida, Amalou, Ghita, Kandil, Mostafa, Barakat, Abdelhamid, Lenaers, Guy
Publicado 2022

Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile

por Kindil, Zineb, Senhaji, Mohamed Amine, Bakhchane, Amina, Charoute, Hicham, Chihab, Soumia, Nadifi, Sellama, Barakat, Abdelhamid
Publicado 2017

Computational screening of potential drugs against COVID-19 disease: the Neuropilin-1 receptor as molecular target

por Charoute, Hicham, Elkarhat, Zouhair, Elkhattabi, Lamiae, El Fahime, Elmostafa, Oukkache, Naoual, Rouba, Hassan, Barakat, Abdelhamid
Publicado 2022

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome

por Ajjemami, Maria, Ouatou, Sanaa, Charoute, Hicham, Fakiri, Malika, Rhaissi, Houria, Benrahma, Houda, Rouba, Hassan, Barakat, Abdelhamid
Publicado 2015

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

por Bakhchane, Amina, Charif, Majida, Salime, Sara, Boulouiz, Redouane, Nahili, Halima, Roky, Rachida, Lenaers, Guy, Barakat, Abdelhamid
Publicado 2015

Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis

por Morjane, Imane, Charoute, Hicham, Ouatou, Sanaa, Elkhattabi, Lamiae, Benrahma, Houda, Saile, Rachid, Rouba, Hassan, Barakat, Abdelhamid
Publicado 2020

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco

por Naasse, Yassine, Charoute, Hicham, El Houate, Brahim, Elbekkay, Chadli, Razoki, Lunda, Malki, Abderrahim, Barakat, Abdelhamid, Rouba, Hassan
Publicado 2015

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report

por Karkar, Adnane, Barakat, Abdelhamid, Bakhchane, Amina, Fettah, Houda, Slassi, Ilham, Dorboz, Imen, Boespflug-Tanguy, Odile, Nadifi, Sellama
Publicado 2015

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation

por Essadssi, Soukaina, Krami, Al Mehdi, Elkhattabi, Lamiae, Elkarhat, Zouhair, Amalou, Ghita, Abdelghaffar, Houria, Rouba, Hassan, Barakat, Abdelhamid
Publicado 2019

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients

por Ouatou, Sanaa, Ajjemami, Maria, Charoute, Hicham, Sefri, Hajar, Ghalim, Noreddine, Rhaissi, Houria, Benrahma, Houda, Barakat, Abdelhamid, Rouba, Hassan
Publicado 2014

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

por Bousfiha, Amale, Bakhchane, Amina, Charoute, Hicham, Riahi, Zied, Snoussi, Khalid, Rouba, Hassan, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid
Publicado 2017

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss

por Bakhchane, Amina, Charif, Majida, Bousfiha, Amale, Boulouiz, Redouane, Nahili, Halima, Rouba, Hassan, Charoute, Hicham, Lenaers, Guy, Barakat, Abdelhamid
Publicado 2017

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure

por Elkhattabi, Lamiae, Morjane, Imane, Charoute, Hicham, Amghar, Soumaya, Bouafi, Hind, Elkarhat, Zouhair, Saile, Rachid, Rouba, Hassan, Barakat, Abdelhamid
Publicado 2019

Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity

por Bouafi, Hind, Bencheikh, Sara, Mehdi Krami, AL, Morjane, Imane, Charoute, Hicham, Rouba, Hassan, Saile, Rachid, Benhnini, Fouad, Barakat, Abdelhamid
Publicado 2019

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study

por Ait El Cadi, Chaimaa, Krami, Al Mehdi, Charoute, Hicham, Elkarhat, Zouhair, Sifeddine, Najat, Lakhiari, Hamid, Rouba, Hassan, Barakat, Abdelhamid, Nahili, Halima
Publicado 2020

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss

por Charif, Majida, Boulouiz, Redouane, Bakhechane, Amina, Benrahma, Houda, Nahili, Halima, Eloualid, Abdelmajid, Rouba, Hassan, Kandil, Mostafa, Abidi, Omar, Lenaers, Guy, Barakat, Abdelhamid
Publicado 2013