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Cherine Charfeddine

Showing results (1-10 of 24) with videos related to

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Indian Pediatrics|February 29, 2024
Bathing Suit IchthyosisAnissa Zaouak, Cherine Charfeddine
Heart & Lung : the Journal of Critical Care|June 22, 2010
Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian familiesSonia Nouira, Fatma Ouarda, Cherine Charfeddine, et al.
International Journal of Women'S Dermatology|August 22, 2024
Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosisAnissa Zaouak, Wafa Jouini, Ghaith Abdessalem, et al.
Journal of Human Genetics|July 26, 2006
Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean regionCherine Charfeddine, Mourad Mokni, Selma Kassar, et al.
Archives of Medical Research|April 1, 2008
Clinical and genetic investigation of atrial septal defect with atrioventricular conduction defect in a large consanguineous Tunisian familySonia Nouira, Ikram Kamoun, Houyem Ouragini, et al.
International Journal of Dermatology|April 18, 2014
The first Mal de Meleda case in Libya: identification of a SLURP1 mutationMbarka Bchetnia, Mariam Bozgia, Nadia Laroussi, et al.
Biomed Research International|October 5, 2013
Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean regionMbarka Bchetnia, Nadia Laroussi, Monia Youssef, et al.
Journal of Cutaneous Pathology|March 4, 2008
Immunohistological study of involucrin expression in Darier's disease skinSelma Kassar, Cherine Charfeddine, Hela Zribi, et al.
Archives of Dermatology|June 17, 2009
Clinical and mutational heterogeneity of Darier disease in Tunisian familiesMbarka Bchetnia, Cherine Charfeddine, Selma Kassar, et al.
Journal of Dermatological Science|January 13, 2009
Clinical, histological and genetic investigation of Buschke-Fischer-Brauer's disease in Tunisian familiesMbarka Bchetnia, Cherine Charfeddine, Selma Kassar, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Indian Pediatrics|February 29, 2024
Bathing Suit IchthyosisAnissa Zaouak, Cherine Charfeddine
Heart & Lung : the Journal of Critical Care|June 22, 2010
Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian familiesSonia Nouira, Fatma Ouarda, Cherine Charfeddine, et al.
International Journal of Women'S Dermatology|August 22, 2024
Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosisAnissa Zaouak, Wafa Jouini, Ghaith Abdessalem, et al.
Journal of Human Genetics|July 26, 2006
Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean regionCherine Charfeddine, Mourad Mokni, Selma Kassar, et al.
Archives of Medical Research|April 1, 2008
Clinical and genetic investigation of atrial septal defect with atrioventricular conduction defect in a large consanguineous Tunisian familySonia Nouira, Ikram Kamoun, Houyem Ouragini, et al.
International Journal of Dermatology|April 18, 2014
The first Mal de Meleda case in Libya: identification of a SLURP1 mutationMbarka Bchetnia, Mariam Bozgia, Nadia Laroussi, et al.
Biomed Research International|October 5, 2013
Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean regionMbarka Bchetnia, Nadia Laroussi, Monia Youssef, et al.
Journal of Cutaneous Pathology|March 4, 2008
Immunohistological study of involucrin expression in Darier's disease skinSelma Kassar, Cherine Charfeddine, Hela Zribi, et al.
Archives of Dermatology|June 17, 2009
Clinical and mutational heterogeneity of Darier disease in Tunisian familiesMbarka Bchetnia, Cherine Charfeddine, Selma Kassar, et al.
Journal of Dermatological Science|January 13, 2009
Clinical, histological and genetic investigation of Buschke-Fischer-Brauer's disease in Tunisian familiesMbarka Bchetnia, Cherine Charfeddine, Selma Kassar, et al.
Pageof 3