Search Results - "Achouri, Afef"

Association between H2 haplotype of microtubule associated protein tau gene (deletion / insertion) with Alzheimer Disease in Tunisian patients by Fray, Saloua, Achouri-Rassas, Afef Achouri, Hadj Fredj, Sondes, Messaoud, Taieb, Belal, Samir

“…It is widely recognized that Alzheimer's disease (AD) is the main cause of dementia in the elderly. AD is typically characterized by the extraneuronal plaque…”
Get full text

A Tunisian patient with CLCN2‐related leukoencephalopathy by Ben Mohamed, Dina, Saied, Zacharia, Ben Sassi, Samia, Ben Said, Mariem, Nabli, Fatma, Achouri, Afef, Jeridi, Cyrine, Masmoudi, Saber, Amouri, Rim

“…CLCN2‐related leukoencephalopathy (CC2L OMIM#: 615651) is a recently identified rare disorder. It is caused by autosomal recessive mutations in the CLCN2 gene…”
Get full text

Parkinsonism and Sjögren's Syndrome: A Fortuitous Association or a Shared Immunopathogenesis? by Belal, Samir, Achouri, Afef, Jalleli, Mohamed, Jamoussi, Hela, Fray, Saloua, Hmida, Intissar, Ben Ali, Nadia, Kchaou, Mariem, Echebbi, Slim

“…Background. The Sjögren Syndrome (SS) can include various manifestations of central nervous system impairment. Extrapyramidal signs are known to be very rare…”
Get full text

Identification of RS2234253 T96K polymorphism of TREM2 gene in Tunisian Alzheimer's disease population by Fray, Saloua, Achouri, Afef, Jamoussi, Hela, Mahmoud, Mariem Ben, Ali, Nadia Ben, Messaoud, Taieb, Fradj, Mohamed

Get full text

Role of vitamin D receptor polymorphism in multiple sclerosis disease course by Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ali, Nadia Ben, Messaoud, Taieb, Hannachi, Amal, Fradj, Mohamed

Get full text

Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations by Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ben Ali, Nadia, Messaoud, Taieb, Hannachi Salhi, Amel, Fredj, Mohamed

“…Background Multiple sclerosis (MS) has a complex pathophysiology which depends on many endogenous and exogenous factors. Vitamin D involvement has been largely…”
Get full text

Gastrointestinal Dysfunction and Neuropathologic Correlations in Parkinson Disease by Mrabet, Saloua, Ben Ali, Nadia, Achouri, Afef, Dabbeche, Radhouene, Najjar, Taoufik, Haouet, Slim, Belal, Samir

“…INTRODUCTION:Recently, an increasing interest to nonmotor symptoms of Parkinson disease (PD) has shown. Gastrointestinal dysfunction is a prominent nonmotor…”
Get full text

Toward a New Biomarker of Parkinson’s Disease by Study of Alpha Synuclein on Upper Enteric System by Endoscopy (I1.014) by Ben Ali, Nadia, Afef, Achouri-Rassas, Saloua, Mrabet, Meriem, Kchaou, Saloua, Fray, Radhouane, Debbeche, Taoufik, Najjar, Hawat, Slim, Samir, Belal

“…Abstract only…”
Get full text

Early psychiatrics symptoms in familial Alzheimer’s disease with presenilin 1 mutation (I83T) by Fray, Saloua, Ali, Nadia Ben, Rassas, Afef Achouri, Kechaou, Meriem, Oudiaa, Nouria, Cherif, Aroua, Echebbi, Slim, Messaoud, Taieb, Belal, Samir

“…Several clinical phenotypes were associated with presenilin 1 (PSEN1) mutation in early-onset familial Alzheimer’s disease (EOFAD). We report the clinical…”
Get full text

No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population by Rassas, Afef Achouri, Fredj, Sondess Hadj, Khiari, Hela Mrabet, Sahnoun, Safa, Bibi, Amina, Siala, Hajer, Mrabet, Amel, Messaoud, Taieb

“…We examined the potential involvement of the polymorphism in intron 8 of the presenilin-1 ( PSEN1 ) gene as a risk factor for Alzheimer disease (AD), both…”
Get full text

Obsessive–compulsive disorder: a new risk factor for Alzheimer disease? by Mrabet Khiari, Hela, Achouri, Afef, Ben Ali, Nadia, Cherif, Aroua, Batti, Hend, Messaoud, Taieb, Mrabet, Amel

“…We describe a case of a 75-year-old woman referred to the Memory Clinic of the neurological Department of Charles Nicolle Hospital, Tunis, for cognitive…”
Get full text

High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population by Rassas, Afef Achouri, Mrabet Khiari, Hela, Hadj Fredj, Sondes, Sahnoun, Safa, Batti, Hend, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Anane, Nadia, Ben Ali, Nadia, Messaoud, Taieb, Mrabet, Amel

“…The goal of the study was to examine the Apolipoprotein E ( APOE ) genotypes in a Tunisian sample of patients with Alzheimer disease (AD) and normal controls,…”
Get full text

Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population by Fray, Saloua, Achouri-Rassas, Afef, Belal, Samir, Messaoud, Taieb

“…In this study, we investigate the impact of apolipoprotein E epsilon 4 (APOE ɛ 4) as a major risk factor of Alzheimer’s disease (AD), based on the clinical…”
Get full text

Missing apolipoprotein E ε4 allele associated with nonamnestic Alzheimer's disease in a Tunisian population by Fray, Saloua, Achouri-Rassas, Afef, Belal, Samir, Messaoud, Taieb

Get full text

Neurobehçet : diagnostic différentiel de méningo-encéphalite aiguë by Jellali, Mohamed, Fray, Saloua, Ali, Nadia Ben, Kchaou, Meriem, Achouri, Afef, Echebbi, Selim, Belal, Samir

“…La présence de symptômes neurologiques au cours de la maladie de Behçet constitue le neurobehçet dont les manifestations sont polymorphes : méningite…”
Get full text

Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients by Jemaa, Riadh, Achouri, Afef, Kallel, Amani, Ben Ali, Samir, Mourali, Sami, Feki, Moncef, Elasmi, Monia, Taieb, Samah Haj, Sanhaji, Haïfa, Omar, Souheil, Mechmeche, Rachid, Kaabachi, Naziha

“…Elevated plasma total homocysteine (tHcy), a risk factor for coronary artery disease (CAD), is due to defects in genes encoding for enzymes involved in tHcy…”
Get more information

Étude du polymorphisme de l’ApoE dans les démences chez une population tunisienne by Achouri-Rassas, Afef, Saloua, Fray, Messaoud, Taieb, Blel, Samir

“…L’allèle e4 du gène APOE est établi principal facteur de risque génétique de la maladie d’Alzheimer, mais son association avec d’autres types de démence et…”
Get full text

Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease by Achouri-Rassas, Afef, Ben Ali, Nadia, Fray, Saloua, Hadj Fredj, Sondes, Kechaou, Meriem, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Chabbi, Slim, Anane, Nadia, Messaoud, Taieb, Gouider, Riadh, Belal, Samir

“…Abstract A minority of Alzheimer disease (AD) patients begin presenting symptoms before the age of 65 years. A familial aggregation is often found in this…”
Get full text

Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease by Achouri-Rassas, Afef, Ali, Nadia Ben, Cherif, Aroua, Fray, Saloua, Siala, Hajer, Zakraoui, Nouria Oudiaa, Hadj-Fredj, Sondes, Kechaou, Mariem, Anane, Nadia, Echebi, Slim, Messaoud, Taieb, Belal, Samir

“…Angiotensin-converting enzyme (ACE) has shown altered activity in patients with neurological diseases. An insertion/deletion (I/D) polymorphism of the ACE gene…”
Get full text

Étude de l’association de la maladie d’Alzheimer au polymorphisme rs118104841(T>C) de l’intron 14 du gène microtubule associated protein Tau (MAPT) au sein d’une population tunisienne by Fray, Saloua, Achouri-Rassas, Afef, Ben Ali, Nadia, Jamoussi, Hela, Aroua, Cherif, Messaoud, Taieb, Mohamed, Fradj

“…En plus de l’accumulation extracellulaire du peptide Aβ amyloïde, les mécanismes physiopathologiques de la maladie d’Alzheimer (MA) impliquent une agrégation…”
Get full text