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1
A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson’s Disease Associated with Epilepsy
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A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson’s Disease Associated with Epilepsy

Ben Romdhan, Sawssan ; Sakka, Salma ; Farhat, Nouha ; Triki, Siwar ; Dammak, Mariem ; Mhiri, Chokri

Journal of molecular neuroscience, 2018-10, Vol.66 (2), p.273-278 [Periódico revisado por pares]

New York: Springer US

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2
Predictors of maternal and neonatal complications in women with severe valvular heart disease during pregnancy in Tunisia: a retrospective cohort study
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Artigo
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Predictors of maternal and neonatal complications in women with severe valvular heart disease during pregnancy in Tunisia: a retrospective cohort study

Hammami, Rania ; Ibn Hadj, Mohamed Ali ; Mejdoub, Yosra ; Bahloul, Amine ; Charfeddine, Selma ; Abid, Leila ; Kammoun, Samir ; Dammak, Abdallah ; Chaabene, Kais

BMC pregnancy and childbirth, 2021-12, Vol.21 (1), p.813-813, Article 813 [Periódico revisado por pares]

England: BioMed Central

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3
Primary membranoproliferative glomerulonephritis in Sfax, Tunisia: epidemiologic profile and prognostic factors
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Primary membranoproliferative glomerulonephritis in Sfax, Tunisia: epidemiologic profile and prognostic factors

Agrebi, Ikram ; Kammoun, Khawla ; Dammak, Najla ; Hachicha, Jamil ; Boudawara, Tahya ; Jarraya, Faiçal ; Hmida, Mohamed Ben

The Pan African medical journal, 2021, Vol.38 (218), p.218-218 [Periódico revisado por pares]

Uganda: African Field Epidemiology Network

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4
Management of COVID-19-Associated Guillain-Barré Syndrome in a Full-Term Pregnant Woman: A Case Report
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Artigo
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Management of COVID-19-Associated Guillain-Barré Syndrome in a Full-Term Pregnant Woman: A Case Report

Jarraya, Anouar ; Kammoun, Manel ; Dammak, Sonda ; Kolsi, Kamel

Journal of Mother and Child, 2023-06, Vol.27 (1), p.52-54 [Periódico revisado por pares]

Poland: Sciendo

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5
Neuromyelitis optica spectrum disorders in South of Tunisia: A rare entity with low seroprevalence of anti-aquaporin 4 autoantibodies
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Artigo
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Neuromyelitis optica spectrum disorders in South of Tunisia: A rare entity with low seroprevalence of anti-aquaporin 4 autoantibodies

Mejdoub, S. ; Feki, S. ; Dammak, M. ; Farhat, N. ; Hdiji, O. ; Boukthir, S. ; Hachicha, H. ; Mhiri, C. ; Masmoudi, H.

Revue neurologique, 2020-05, Vol.176 (4), p.261-267 [Periódico revisado por pares]

France: Elsevier Masson SAS

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6
Safety and efficacy of colistin compared with imipenem in the treatment of ventilator-associated pneumonia : a matched case-control study
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Artigo
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Safety and efficacy of colistin compared with imipenem in the treatment of ventilator-associated pneumonia : a matched case-control study

KALLEL, H ; HERGAFI, L ; BAHLOUL, M ; HAKIM, A ; DAMMAK, H ; CHELLY, H ; BEN HAMIDA, C ; CHAARI, A ; REKIK, N ; BOUAZIZ, M

Intensive care medicine, 2007-07, Vol.33 (7), p.1162-1167 [Periódico revisado por pares]

Heidelberg: Springer

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7
Factors associated with Internet addiction among Tunisian adolescents
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Artigo
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Factors associated with Internet addiction among Tunisian adolescents

Ben Thabet, J ; Ellouze, A S ; Ghorbel, N ; Maalej, M ; Yaich, S ; Omri, S ; Feki, R ; Zouari, N ; Zouari, L ; Dammak, J ; Charfi, N

Encéphale, 2019-12, Vol.45 (6), p.474 [Periódico revisado por pares]

France

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8
Adrenal Diseases During Pregnancy: Pathophysiology, Diagnosis and Management Strategies
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Artigo
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Adrenal Diseases During Pregnancy: Pathophysiology, Diagnosis and Management Strategies

Kamoun, Mahdi, MD ; Mnif, Mouna F., PhD ; Charfi, Nadia, PhD ; Kacem, Faten H., MD ; Naceur, Basma B., MD ; Mnif, Fatma, PhD ; Dammak, Mohamed, MD ; Rekik, Nabila, PhD ; Abid, Mohamed, PhD

The American journal of the medical sciences, 2014-01, Vol.347 (1), p.64-73 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Novel splicing dysferlin mutation causing myopathy with intra-familial heterogeneity
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Artigo
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Novel splicing dysferlin mutation causing myopathy with intra-familial heterogeneity

Rekik, Sabrine ; Sakka, Salma ; Romdhane, Sawsan Ben ; Amer, Yasmine Baba ; Lehkim, Leila ; Farhat, Nouha ; Mahfoudh, Khaireddine Ben ; Authier, François Jérôme ; Dammak, Mariem ; Mhiri, Chokri

Molecular biology reports, 2020-08, Vol.47 (8), p.5755-5761 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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10
Predominance of the Rare EGFR Mutation p.L861Q in Tunisian Patients with Non-Small Cell Lung Carcinoma
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Artigo
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Predominance of the Rare EGFR Mutation p.L861Q in Tunisian Patients with Non-Small Cell Lung Carcinoma

Abdelmaksoud-Dammak, Rania ; Ammous-Boukhris, Nihel ; Saadallah-Kallel, Amèna ; Charfi, Slim ; Khemiri, Souhir ; Khemakhem, Rim ; Kallel, Nesrin ; Ben Kridis-Rejeb, Wala ; Sallemi-Boudawara, Tahya ; Khanfir, Afef ; Yangui, Ilhem ; Daoud, Jamel ; Mokdad-Gargouri, Raja

Genes, 2022-08, Vol.13 (8), p.1499 [Periódico revisado por pares]

Switzerland: MDPI AG

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