Determinants of cognitive impairment in multiple system atrophy: Clinical and genetic study von Nasri, Amina, Gharbi, Alya, Sghaier, Ikram, Mrabet, Saloua, Souissi, Amira, Gargouri, Amina, Djebara, Mouna Ben, Kacem, Imen, Gouider, Riadh

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Western influenced lifestyle and Kv2.1 association as predicted biomarkers for Tunisian colorectal cancer von Barbirou, Mouadh, Woldu, Henok G, Sghaier, Ikram, Bedoui, Sinda A, Mokrani, Amina, Aami, Radhia, Mezlini, Amel, Yacoubi-Loueslati, Besma, Tonellato, Peter J, Bouhaouala-Zahar, Balkiss

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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 von Sghaier, Ikram, Zidi, Sabrina, Mouelhi, Leila, Dabbech, Radhouane, Ghazouani, Ezzedine, Brochot, Etienne, Stayoussef, Mouna, Yacoubi-Loueslati, Besma

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KCNB1 gene polymorphisms and related indel as predictor biomarkers of treatment response for colorectal cancer – toward a personalized medicine von Barbirou, Mouadh, Sghaier, Ikram, Bedoui, Sinda, Ben Abderrazek, Rahma, Kraiem, Hazar, Farah, Azer, Hassiki, Rym, Mokrani, Amina, Mezlini, Amel, Almawi, Wassim Y, Loueslati-Yacoubi, Besma, Bouhaouala-Zahar, Balkiss

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Atypical parkinsonian syndromes in a North African tertiary referral center von Nasri, Amina, Ben Djebara, Mouna, Sghaier, Ikram, Mrabet, Saloua, Zidi, Sabrina, Gargouri, Amina, Kacem, Imen, Gouider, Riadh

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Common variants in IL-1RN, IL-1β and TNF-α and the risk of ovarian cancer: a case control study von Ahmed, Amira Ben, Zidi, Sabrina, Sghaier, Ikram, Ghazouani, Ezzeddine, Mezlini, Amel, Almawi, Wassim, Loueslati, Besma Yacoubi

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Rare genetic mutation of TARDBP leading to intrafamilial clinical phenotype variability; from pathogenic variant to genetic features modifier (P1-1.Virtual) von Kacem, Imen, Sghaier, Ikram, Ticozzi, Nicolas, Nasri, Amina, Ratti, Antonis, Gargouri, Amina, Silani, Vincenzo, Gouider, Riadh

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Predictors of Survival in Atypical Parkinsonian Syndromes in a Tunisian Cohort (P8-11.006) von Nasri, amina, Sghaier, Ikram, Mrabet, Saloua, Abida, Youssef, Gharbi, Alya, Souissi, Amira, BenDjebara, Mouna, Gargouri, Amina, Kacem, Imen, Gouider, Riadh

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Association of Amyotrophic Lateral Sclerosis and Dopa-responsive dystonia in a Tunisian patient von Kacem, Imen, Sghaier, Ikram, Ben Rhouma, Hanene, Ratti, Antonia, Ticozzi, Nicola, Silani, Vincenzo, Gouider-Khouja, Neziha, Gouider, Riadh

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Impact of MAPT haplotype on the phenotypic spectrum of progressive supranuclear palsy von Sghaier, Ikram, Nasri, Amina, Frikha, Sana, Gharbi, Alya, Mrabet, Saloua, Souissi, Amira, Atrous, Amal, Berrechid, Amina Gargouri, Gouider, Riadh

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Role of Apolipoprotein E genotype in the occurrence of atypical parkinsonian syndromes (4661) von Nasri, Amina, Sghaier, Ikram, Mrabet, Saloua, Gharbi, Alya, Ben Djebara, Mouna, Kacem, Imen, Gouider, Riadh

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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 von Sghaier, Ikram, Zidi, Sabrina, El-Ghali, Rabeb M., Daldoul, Amira, Aimagambetova, Gulzhanat, Almawi, Wassim Y.

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Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis von Kacem, Imen, Sghaier, Ikram, Peverelli, Silvia, Souissi, Emira, Ticozzi, Nicola, Gharbi, Alya, Ratti, Antonia, Berrechid, Amina Gargouri, Silani, Vincenzo, Gouider, Riadh

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Clinical and molecular predictors of survival among atypical parkinsonian syndromes in a North African tertiary referral center von Sghaier, Ikram, Nasri, Amina, Atrous, Amal, Abida, Youssef, Gharbi, Alya, Souissi, Amira, Mrabet, Saloua, Ben Djebara, Mouna, Kacem, Imen, Gargouri-Berrechid, Amina, Gouider, Riadh

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Role of Apolipoprotein E in the clinical profile of atypical Parkinsonian syndromes von Nasri, Amina, Sghaier, Ikram, Mrabet, Saloua, Djebara, Mouna Ben, Kacem, Imen, Gouider, Riadh

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Glutathione S-transferase polymorphisms (GSTM1/GSTT1) outcomes in clinical profile and treatment responsiveness among Tunisian cohort of Parkinson’s disease von Guedi, Ali Barreh, Ikram, Sghaier, Youssef, Abida, Alya, Gharbi, Amira, Souissi, Saloua, Mrabet, Amina, Nasri, Mouna, Ben Djebara, Imen, Kacem, Amina, Gargouri-Berrechid, Riadh, Gouider

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The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families von Sghaier, Ikram, Kacem, Imen, Ticozzi, Nicola, Mrabet, Saloua, Paverelli, Silvia, Abida, Youssef, Ratti, Antonia, Silani, Vincenzo, Gouider, Riadh

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Clinical and genetic features in young-adult amyotrophic lateral sclerosis – a Tunisian cohort study von Kacem, Imen, Abbes, Amal, Sghaier, Ikram, Abida, Youssef, Souissi, Amira, Berrechid, Amina Gargouri, Mrabet, Saloua, Nasri, Amina, Silani, Vincenzo, Gouider, Riadh

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Interactions between environmental factors and LRRK2-G2019S mutation in Parkinson's disease von Mrad, Yasmine, Nasri, Amina, Sghaier, Ikram, Gharbi, Alya, Mrabet, Saloua, Atrous, Amal, Souissi, Amira, Berrechid, Amina Gargouri, Kacem, Imen, Gouider, Riadh

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28. Relationship between Neurofilament Light Chain levels and Disability Progression in Patients with Multiple Sclerosis von Mrabet, Saloua, Sghaier, Ikram, Souissi, Amira, Gharbi, Alya, Abida, Youssef, Kacem, Imen, Gargouri, Amina, Gouider, Riadh

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