Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hela Mesrati"'
Publikováno v:
Skinmed. 20(5)
A 21-year-old woman presented with a 13-year history of a linear lesion on the lip. She experienced no pain and only had an esthetic complaint. Her personal and family history was otherwise unremarkable. She had no history of photosensitivity, Raynau
Publikováno v:
Our Dermatology Online. 11:36-39
Publikováno v:
Néphrologie & Thérapeutique. 17:473-474
Vitiligo is an acquired depigmenting disorder. Vitiligo universalis is a rare form responsible for significant aesthetic damage. To date, the exact pathogenesis remains unknown. Its treatment, a real challenge, consists rather in removing the still p
Publikováno v:
Journal of paediatrics and child health. 57(9)
Autor:
Mariem, Rekik, Khadija, Sellami, Massara, Baklouti, Emna, Bahloul, Hela, Mesrati, Hamida, Turki
Publikováno v:
Nephrologietherapeutique. 17(6)
Vitiligo is an acquired depigmenting disorder. Vitiligo universalis is a rare form responsible for significant aesthetic damage. To date, the exact pathogenesis remains unknown. Its treatment, a real challenge, consists rather in removing the still p
Publikováno v:
International Journal of Dermatology. 54:1370-1375
Background Aplasia cutis congenita (ACC) is a rare malformation characterized by absent or scarred areas of skin at birth. Although most commonly found on the scalp, ACC can also involve other locations. Its etiology and pathogenesis remain unclear.
Autor:
Meriem, Amouri, Hela, Mesrati, Hend, Chaaben, Abderrahmen, Masmoudi, Madiha, Mseddi, Hamida, Turki
Publikováno v:
Cutis. 99(1)
Congenital hemangiomas (CHs) are fully developed hemangiomas that are present at birth. There are 2 possible types: rapidly involuting CHs (RICHs) and noninvoluting CHs (NICHs). We conducted a retrospective study (2008-2012) of 6 patients (2 females,
Autor:
M. Kharfi, Alain Hovnanian, Lilia Romdhane, Mbarka Bchetnia, M.S. Boubaker, Daniele Castiglia, Salaheddine Marrakchi, A.S. Ben Brick, Hamida Turki, Nadia Laroussi, Rym Kefi, Hela Mesrati, Houyem Ouragini, Sonia Abdelhak
Publikováno v:
Journal of the European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology, Wiley, 2014, epub ahead of print. ⟨10.1111/jdv.12645⟩
Journal of the European Academy of Dermatology and Venereology, Wiley, 2014, epub ahead of print. 〈10.1111/jdv.12645〉
Journal of the European Academy of Dermatology and Venereology, Wiley, 2014, epub ahead of print. ⟨10.1111/jdv.12645⟩
Journal of the European Academy of Dermatology and Venereology, Wiley, 2014, epub ahead of print. 〈10.1111/jdv.12645〉
Dystrophic epidermolysis bullosa (DEB) is a rare genodermatosis characterized by extensive fragility of the skin, which forms blisters and scars following a minimal friction or mechanical trauma.1 It is inherited as either autosomal recessive (RDEB)
Autor:
Meriem Amouri, H. Chaaben, Tahia Boudawara, Hela Mesrati, Hamida Turki, Sameh Ellouze, Taha Jalel Meziou, Najla Abid
Publikováno v:
La Presse Médicale. 41:332-334
Autor:
Nizar Ben Halim, Mbarka Bchetnia, Khaled Lasram, Daniele Castiglia, Nadia Laroussi, Sonia Abdelhak, Lilia Romdhane, Rym Kefi, Mounira Meddeb Cherif, Houyem Ouragini, Mohamed Samir Boubaker, Hamida Turki, Ahlem Sabrine Ben Brick, Alain Hovnanian, Salaheddine Marrakchi, Hela Mesrati
Publikováno v:
Archives of Dermatological Research
Archives of Dermatological Research, Springer Verlag, 2014, 306 (4), pp.405-11. ⟨10.1007/s00403-013-1421-y⟩
Archives of Dermatological Research, Springer Verlag, 2014, 306 (4), pp.405-11. 〈10.1007/s00403-013-1421-y〉
Archives of Dermatological Research, Springer Verlag, 2014, 306 (4), pp.405-11. ⟨10.1007/s00403-013-1421-y⟩
Archives of Dermatological Research, Springer Verlag, 2014, 306 (4), pp.405-11. 〈10.1007/s00403-013-1421-y〉
International audience; Dystrophic epidermolysis bullosa (DEB) is a group of heritable bullous skin disorders caused by mutations in the COL7A1 gene. One of the most severe forms of DEB is the severe generalized [recessive dystrophic epidermolysis bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dadbed3d4ad3a3a003b9a9cda16fb6f
https://hal-riip.archives-ouvertes.fr/pasteur-01061249
https://hal-riip.archives-ouvertes.fr/pasteur-01061249