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Topical paromomycin with or without gentamicin for cutaneous leishmaniasis.
Afif Ben Salah
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Nathalie Ben Messaoud
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Evelyn Guedri
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Amor Zaatour
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Nissaf Ben Alaya
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et al.
Journal articles
pasteur-00793585v1
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Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family
Cherine Charfeddine
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Hamza Dallali
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Ghaith Abdessalem
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Kais Ghedira
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Yosr Hamdi
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et al.
Journal articles
pasteur-03261809v1
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Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations.
C Charfeddine
,
K Monastiri
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M Mokni
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A Laadjimi
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N Kaabachi
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et al.
Journal articles
istex
hal-01974010v1
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Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity
Nizar Ben Halim
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Majdi Nagara
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Béatrice Regnault
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Sana Hsouna
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Khaled Lasram
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et al.
Journal articles
pasteur-01375019v1
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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.
Zied Riahi
,
Crystel Bonnet
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Rim Zainine
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Saida Lahbib
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Yosra Bouyacoub
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et al.
Journal articles
pasteur-01221041v1
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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
Zied Riahi
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Crystel Bonnet
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Rim Zainine
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Malek Louha
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Yosra Bouyacoub
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et al.
Journal articles
pasteur-01060192v1
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Hepatitis viruses take advantage of traditional practices to increase the burden of hepatocellular carcinoma in Tunisia
Ines Dhifallah
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Marwa Khedhiri
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Anissa Chouikha
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Ghassen Kharroubi
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Walid Hammami
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et al.
Journal articles
pasteur-02641737v1
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Identification of a novel mutation of LAMB3 gene in a lybian patient with hereditary epidermolysis bullosa by whole exome sequencing
N. Laroussi
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O. Messaoud
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M. Chargui
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C.B. Fayala
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A. Elahlafi
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et al.
Journal articles
hal-01534741v1
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High Frequency of Enterocytozoon bieneusi Genotype WL12 Occurrence among Immunocompromised Patients with Intestinal Microsporidiosis
Mariem Messaoud
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Salma Abbes
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Mayssa Gnaien
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Yasmine Rebai
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Aicha Kallel
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et al.
Journal articles
pasteur-03542424v1
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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Rahma Mkaouar
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Zied Riahi
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Cherine Charfeddine
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Imen Chelly
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Hela Boudabbous
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et al.
Journal articles
pasteur-04072687v1
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A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene
Marwa Sayeb
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Zied Riahi
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Nadia Laroussi
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Crystel Bonnet
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Lilia Romdhane
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et al.
Journal articles
pasteur-03219630v1
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Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region
Cherine Charfeddine
,
Mourad Mokni
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Selma Kassar
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Hela Zribi
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Chiraz Bouchlaka
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et al.
Journal articles
pasteur-01375261v1
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In Vivo Efficacy of Voriconazole in a Galleria mellonella Model of Invasive Infection Due to Azole-Susceptible or Resistant Aspergillus fumigatus Isolates
Sana Jemel
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Jacques Guillot
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Kalthoum Kallel
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Grégory Jouvion
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Elise Brisebard
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et al.
Journal articles
hal-03944250v1
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HIBISCUS: Hydroxychloroquine for the secondary prevention of thrombotic and obstetrical events in primary antiphospholipid syndrome
Cristina Belizna
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Francesca Pregnolato
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Sébastien Abad
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Jaume Alijotas-Reig
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Howard Amital
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et al.
Journal articles
hal-01936357v1
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