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Determinants of cognitive impairment in multiple system atrophy: Clinical and genetic study

PloS one, 2022-12, Vol.17 (12), p.e0277798-e0277798

2022

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Western influenced lifestyle and Kv2.1 association as predicted biomarkers for Tunisian colorectal cancer

BMC cancer, 2020-11, Vol.20 (1), p.1086-12, Article 1086

2020

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The relationship between TNF alpha gene polymorphisms (−238/−308), TNF RII VNTR (p75) and outcomes of hepatitis B virus infection in Tunisian population

Gene, 2015-09, Vol.568 (2), p.140-145

2015

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KCNB1 gene polymorphisms and related indel as predictor biomarkers of treatment response for colorectal cancer – toward a personalized medicine

Tumor biology, 2020-06, Vol.42 (6), p.101042832092523-1010428320925237

2020

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Atypical parkinsonian syndromes in a North African tertiary referral center

Brain and behavior, 2021-01, Vol.11 (1), p.e01924-n/a

2021

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Common variants in IL-1RN, IL-1β and TNF-α and the risk of ovarian cancer: a case control study

Central-European journal of immunology, 2017-01, Vol.42 (2), p.150-155

2017

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Impact of MAPT haplotype on the phenotypic spectrum of progressive supranuclear palsy

Journal of the neurological sciences, 2023-12, Vol.455, p.121758, Article 121758

2023

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Clinical and molecular predictors of survival among atypical parkinsonian syndromes in a North African tertiary referral center

Journal of the neurological sciences, 2024-09, Vol.464, p.123155, Article 123155

2024

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Role of Apolipoprotein E in the clinical profile of atypical Parkinsonian syndromes

Journal of the neurological sciences, 2021-10, Vol.429, p.119554, Article 119554

2021

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Unique ESR1 and ESR2 estrogen receptor gene variants associated with altered risk of triple-negative breast cancer: A case-control study

Gene, 2023-01, Vol.851, p.146969-146969, Article 146969

2023

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Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis

Neurobiology of aging, 2022-12, Vol.120, p.27-33

2022

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Glutathione S-transferase polymorphisms (GSTM1/GSTT1) outcomes in clinical profile and treatment responsiveness among Tunisian cohort of Parkinson’s disease

Journal of Neural Transmission, 2024-08

2024

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The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families

Clinical genetics, 2022-12, Vol.102 (6), p.555-556

2022

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Interactions between environmental factors and LRRK2-G2019S mutation in Parkinson's disease

Journal of the neurological sciences, 2023-12, Vol.455, p.121935, Article 121935

2023

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Clinical and genetic features in young-adult amyotrophic lateral sclerosis – a Tunisian cohort study

Journal of the neurological sciences, 2023-12, Vol.455, p.121713, Article 121713

2023

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Epidemiological and clinical features of amyotrophic lateral sclerosis in a Tunisian cohort

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-01, Vol.21 (1-2), p.131-139

2020

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Role of Apolipoprotein E in the Clinical Profile of Atypical Parkinsonian Syndromes

Alzheimer disease and associated disorders, 2022-01, Vol.36 (1), p.36

2022

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Clinical and genetic spectrum of amyotrophic lateral sclerosis in a Tunisian series

Journal of the neurological sciences, 2021-10, Vol.429, p.119402, Article 119402

2021

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Progression de la maladie de Parkinson en fonction du profil génétique LRRK2-G2019S

Revue neurologique, 2023-04, Vol.179, p.S33-S33

2023

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Novel Association of IGF2BP2 Gene Variants With Altered Risk of Breast Cancer and as Potential Molecular Biomarker of Triple Negative Breast Cancer

Clinical breast cancer, 2023-04, Vol.23 (3), p.272-280

2023

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Association of IL-1β gene polymorphisms rs1143627, rs1799916, and rs16944 with altered risk of triple-negative breast cancer

Cytokine (Philadelphia, Pa.), 2024-08, Vol.180, p.156659, Article 156659

2024

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IL-10 and IL-28B gene variants as predictors of sustained response to peginterferon and ribavirin therapy in chronic HCV infection

Cytokine (Philadelphia, Pa.), 2022-03, Vol.151, p.154008-154008, Article 154008

2022

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Hepatitis C virus protein interaction network for HCV clearance and association of DAA to HCC occurrence via data mining approach: A systematic review and critical analysis

Reviews in medical virology, 2019-03, Vol.29 (2), p.e2033-n/a

2019

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Circulating leptin concentration, LEP gene variants and haplotypes, and polycystic ovary syndrome in Bahraini and Tunisian Arab women

Gene, 2019-04, Vol.694, p.19-25

2019

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Genetic variants in IL-6 and IL-10 genes and susceptibility to hepatocellular carcinoma in HCV infected patients

Cytokine (Philadelphia, Pa.), 2017-01, Vol.89, p.62-67

2017

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Determinants of cognitive impairment in multiple system atrophy: Clinical and genetic study

Western influenced lifestyle and Kv2.1 association as predicted biomarkers for Tunisian colorectal cancer

The relationship between TNF alpha gene polymorphisms (−238/−308), TNF RII VNTR (p75) and outcomes of hepatitis B virus infection in Tunisian population

KCNB1 gene polymorphisms and related indel as predictor biomarkers of treatment response for colorectal cancer – toward a personalized medicine

Atypical parkinsonian syndromes in a North African tertiary referral center

Common variants in IL-1RN, IL-1β and TNF-α and the risk of ovarian cancer: a case control study

Impact of MAPT haplotype on the phenotypic spectrum of progressive supranuclear palsy

Clinical and molecular predictors of survival among atypical parkinsonian syndromes in a North African tertiary referral center

Role of Apolipoprotein E in the clinical profile of atypical Parkinsonian syndromes

Unique ESR1 and ESR2 estrogen receptor gene variants associated with altered risk of triple-negative breast cancer: A case-control study

Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis

Glutathione S-transferase polymorphisms (GSTM1/GSTT1) outcomes in clinical profile and treatment responsiveness among Tunisian cohort of Parkinson’s disease

The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families

Interactions between environmental factors and LRRK2-G2019S mutation in Parkinson's disease

Clinical and genetic features in young-adult amyotrophic lateral sclerosis – a Tunisian cohort study

Epidemiological and clinical features of amyotrophic lateral sclerosis in a Tunisian cohort

Role of Apolipoprotein E in the Clinical Profile of Atypical Parkinsonian Syndromes

Clinical and genetic spectrum of amyotrophic lateral sclerosis in a Tunisian series

Progression de la maladie de Parkinson en fonction du profil génétique LRRK2-G2019S

Novel Association of IGF2BP2 Gene Variants With Altered Risk of Breast Cancer and as Potential Molecular Biomarker of Triple Negative Breast Cancer

Association of IL-1β gene polymorphisms rs1143627, rs1799916, and rs16944 with altered risk of triple-negative breast cancer

IL-10 and IL-28B gene variants as predictors of sustained response to peginterferon and ribavirin therapy in chronic HCV infection

Hepatitis C virus protein interaction network for HCV clearance and association of DAA to HCC occurrence via data mining approach: A systematic review and critical analysis

Circulating leptin concentration, LEP gene variants and haplotypes, and polycystic ovary syndrome in Bahraini and Tunisian Arab women

Genetic variants in IL-6 and IL-10 genes and susceptibility to hepatocellular carcinoma in HCV infected patients

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