Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mustapha El Alloussi"'
Autor:
Agnes Bloch-Zupan, Tristan Rey, Alexandra Jimenez-Armijo, Marzena Kawczynski, Naji Kharouf, O-Rare consortium, Muriel de La Dure-Molla, Emmanuelle Noirrit, Magali Hernandez, Clara Joseph-Beaudin, Serena Lopez, Corinne Tardieu, Béatrice Thivichon-Prince, ERN Cranio Consortium, Tatjana Dostalova, Milan Macek, International Consortium, Mustapha El Alloussi, Leila Qebibo, Supawich Morkmued, Patimaporn Pungchanchaikul, Blanca Urzúa Orellana, Marie-Cécile Manière, Bénédicte Gérard, Isaac Maximiliano Bugueno, Virginie Laugel-Haushalter, Yves Alembik, Victorin Ahossi, Isabelle Bailleul-Forestier, Isabelle Blanchet, Ariane Berdal, Marie José Boileau, Nicolas Chassaing, François Clauss, Caroline Delfosse, Anne De-Saint-Martin, Jean-Christophe Dahlet, Bérénice Doray, Jean-Luc Davideau, Tiphaine Davit-Béal, Hélène Dollfus, Jean-Pierre Duprez, Muriel de La Dure Molla, Klauss Dieterich, Dominique Droz, Salima El Chehadeh, Olivier Etienne, Edouard Euvrard, Laurence Faivre, Benjamin Fournier, Elsa Garot, Bruno Grollemund, Nathalie Guffon-Fouilhoux, Mathilde Huckert, Bertand Isidor, Sophie Jung, Didier Lacombe, Alinoe Lavillaurex, Marine Lebrun, Bruno Leheup, Adeline Loing, Sandrine Marlin, Jean-Jacques Morrier, Michèle Muller-Bolla, Sylvie Odent, Marie Paule Gelle, Juliette Piard, Linda Pons, Béatrice Richard, Massimiliano Rossi, Prune Sadones, Elise Schaefer, Jean-Louis Sixou, Sylvie Soskin, Marion Strub, Annick Toutain, Alain Verloes, Frédéric Vaysse, Delphine Wagner
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel phenotypes can be described as hypoplastic, hypomineralized or hypomature a
Externí odkaz:
https://doaj.org/article/be19745ebc994351a79834498f898534
Publikováno v:
Case Reports in Dentistry, Vol 2022 (2022)
Introduction. Oligodontia is a dental abnormality in which the patient is missing teeth. It is a hereditary disorder characterized by agenesis of more than six primary or permanent teeth, excluding the wisdom teeth. Oligodontia is often related with
Externí odkaz:
https://doaj.org/article/032df8196d3d43899b91b4f798787987
Autor:
Yassamine Doubaj, Mustapha El Alloussi, Abdelali Zrhidri, Imane Cherkaoui Jaouad, Jaber Lyahyai, Abdelkrim Boulanouar, Soukaina Guaoua, Abdelaziz Sefiani
Publikováno v:
European Journal of Medical Genetics. 60:239-244
Jalili syndrome is a rare autosomal recessive genetic disease characterized by the association of amelogenesis imperfecta and cone-rod retinal dystrophy. This syndrome is caused by mutations in the CNNM4 gene. Different types of CNNM4 mutations have
Publikováno v:
Clinical dysmorphology. 26(2)
Publikováno v:
Actualités Odonto-Stomatologiques. :123-132
La succion chez l’enfant est decrite dans la litterature sous deux aspects : la succion nutritive et la succion non nutritive. La succion nutritive est relative a l’allaitement au sein, au biberon ou a une combinaison des deux. La succion non nut
Publikováno v:
Médecine Buccale Chirurgie Buccale. 15:189-194
Ce cas concerne une jeune fille âgee de 3 ans qui presente un syndrome de Papillon-Lefevre et dont le diagnostic est base sur les donnees cliniques. Elle presentait des hyperkeratoses plantaires des la premiere consultation avec une parodontite seve
Publikováno v:
The New York state dental journal. 76(2)
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare, proliferative disorder in which the accumulation of pathologic Langerhans cells leads to local tissue infiltration and destruction. The incidence of LCH is estimated
Autor:
Rachida Amezian, Abdelaziz Sefiani, Siham Chafai El alaoui, Abderrahmane Al Bouzidi, Mustapha El Alloussi, Samir Laouina
Publikováno v:
Journal of Medical Case Reports
Introduction Amelogenesis imperfecta is an inherited disease characterized by generalized structural abnormalities of the enamel on all teeth, including both primary and permanent dentition. To the best of our knowledge, this is the first case report
Autor:
Jaber Lyahyai, Siham Chafai El alaoui, Mustapha El Alloussi, Imane Cherkaoui Jaouad, Fatima Zahra Laarabi, Abdelaziz Sefiani
Publikováno v:
BMC Oral Health
Background Amelogenesis imperfecta represents a group of developmental conditions, clinically and genetically heterogeneous, that affect the structure and clinical appearance of enamel. Amelogenesis imperfecta occurred as an isolated trait or as part
Autor:
Karimi Z; Zakaria Karimi DMD, MDentSci Associate Professor in Conservative Dentistry, Department of Conservative Dentistry, Faculty of Dentistry, Mohammed V University, Mohammed V Military teaching hospital, Rabat, Morocco.; Mustapha El Alloussi DMD, MDentSci Private practice and former Professor of higher education, Faculty of Dentistry, Mohammed V University, Mohammed V Military teaching hospital, Rabat, Morocco., Alloussi ME; Zakaria Karimi DMD, MDentSci Associate Professor in Conservative Dentistry, Department of Conservative Dentistry, Faculty of Dentistry, Mohammed V University, Mohammed V Military teaching hospital, Rabat, Morocco.; Mustapha El Alloussi DMD, MDentSci Private practice and former Professor of higher education, Faculty of Dentistry, Mohammed V University, Mohammed V Military teaching hospital, Rabat, Morocco.
Publikováno v:
Primary dental journal [Prim Dent J] 2024 Jun; Vol. 13 (2), pp. 79-83.