Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Bourane, Kammoun"'
Autor:
N. Hmida, Mongia Hchicha, Imen Chabchoub, Bourane Kammoun, H. Kammoun, Neila Belguith, Olfa Siala, Faiza Fakhfakh
Publikováno v:
Gene. 507(1)
Peters plus syndrome is an autosomal recessive rare disorder comprising ocular anterior segment dysgenesis, short stature, hand abnormalities, distinctive facial features, and often other major/minor additional defects. Peters plus syndrome is relate
Autor:
Madiha, Mseddi, Dorra, Sellami, Y, Elloumi, Yacine, Aloulou, Bourane, Kammoun, Hamida, Turki, Jamel, Feki, Abdelmajid, Zahaf
Publikováno v:
La Tunisie medicale. 84(9)
Xéroderma pigmentosum (XP) is a rare genetic disease characterised by defective repair of DNA damage. We report a retrospective study of the ophtalmologic manifestations of 16 patients with xéroderma pigmentosum, the ophtalmologic manifestations we
Autor:
Dorra, Sellami, Abderrahmen, Masmoudi, Hamida, Turki, Madiha, Mseddi, Bourane, Kammoun, Naila, Elleuch, Fatma, Chaabouni, Zeineb, Ben Zina, Jamel, Feki, Abdelmajid, Zahaf
Publikováno v:
Presse medicale (Paris, France : 1983). 35(5 Pt 1)
Lipoid proteinosis (LP), also known as hyalinosis (or lipoidosis) cutis et mucosae or Urbach-Wiethe disease, is a rare autosomal recessive disorder. It is associated with deposits of protein-lipid complexes in various tissues including the skin and m
Autor:
Zineb, Benzina, Héla, Khlif, Dorra, Sellami, Imen, Sayadi, Sameh, Abdelmoula, Amira, Trigui, Bourane, Kammoun, Jamel, Daoud, Jamel, Féki
Publikováno v:
La Tunisie medicale. 82(9)
The non-Hodgkin's lymphomas are a group of neoplasms characterized by proliferation of malignant lymphocytes. There is a wide variety of presenting signs and symptoms depending on the site of involvement and aggressiveness of the disease. Many organs