Results 91 to 100 of about 5,937 (217)

Restauración estética y funcional de un paciente con amelogénesis imperfecta Esthetic and functional restoration in a patient with amelogenesis imperfecta

Revista de la Asociación Odontológica Argentina, 2012
sumen Objetivo. Describir el manejo clínico para la restauración estética y funcional de un caso con amelogénesis imperfecta. Caso clínico. Paciente femenina de 15 años que presentaba alteración en la apariencia estética de sus dientes y episodios ...
Weider de Oliveira, Juan Carlos Pontons Melo, Valkyria Ceruti, Gil Montenegro, Tarcísio Pinto, Janyne Andrade   +5 more
doaj  

Amelogenesis imperfecta: Four case reports

Journal of Natural Science, Biology and Medicine, 2013
Amelogenesis Imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner. AI is a serious problem that reduces oral health-related quality of life and causes some physiological problems.
Mehta, Dhaval N., Shah, Jigna, Thakkar, Bhavik   +2 more
openaire   +3 more sources

Aesthetic full-mouth oral rehabilitation of a young adult with amelogenesis imperfecta: a clinical report

Cumhuriyet Dental Journal, 2014
Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause developmental alterations in the structure of the enamel in the absence of a systemic disorder.
Derya Özdemir Doğan, Fatih Sarı, Onur Şahin   +2 more
doaj   +1 more source

Asthma, a chronic disease whose manifestations go beyond respiratory distress, physical limitation and impaired quality of life [PDF]

, 2009
Universidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaUNIFESP ...
Fernandes, Ana Luisa Godoy
core   +3 more sources

Experiences of Being a Parent to a Child with Amelogenesis Imperfecta

Dentistry Journal, 2019
Amelogenesis imperfecta (AI) is a hereditary developmental disorder affecting the enamel of teeth. Affected patients present with tooth hypersensitivity, rapid tooth wear, or fractures of enamel as well as alterations in color and shape, all of which ...
Gunilla Pousette Lundgren, Tove Hasselblad, Anna Stigsdotter Johansson, Anna Johansson, Göran Dahllöf   +4 more
doaj   +1 more source

How do children with amelogenesis imperfecta feel about their teeth? [PDF]

, 2014
Amelogenesis imperfecta (AI) is an inherited dental condition affecting enamel, which can result in significant tooth discolouration and enamel breakdown, requiring lifelong dental care.
Almehateb, M, Cunningham, SJ, Parekh, S
core  

Tricho-dento-osseous syndrome and precocious eruption [PDF]

, 2017
Tricho-dento-osseous syndrome (TDO), an uncommon form of ectodermal dysplasia is an autosomal dominant genetic disorder which is characterized by inherited defects in tissues arising from epithelial-mesenchymal interaction.
Jain, Parul, Kaul, Rahul, Saha, Subrata, Sarkar, Subir   +3 more
core   +2 more sources

Scanning Еlectron Мicroscopy of Еnamel and Dentin of Тeeth with Hypocalcified Аmelogenesis Imperfecta

Folia Medica, 2016
The histological features of teeth with hypocalcified amelogenesis imperfecta (AI) have been poorly studied, which calls into question the effectiveness of modern adhesive techniques used in the treatment of these noncarious defects.
Belcheva Ani B., Philipov Ivan At., Tomov Georgi T.   +2 more
doaj   +1 more source

Enamel proteins and proteases in Mmp20 and Klk4 null and double‐null mice [PDF]

, 2011
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90347/1/j.1600-0722.2011.00866.x ...
Bartlett, Bartlett, Bartlett, Bartlett, Begue-Kirn, Bourd-Boittin, Boyde, Bronckers, Caterina, Chun, Chun, Fincham, Fincham, Fincham, Fukae, Fukae, Fukae, Fukae, Hart, Hu, Hu, Hu, Hu, Hu, Iwata, Kim, Kobayashi, Krebsbach, Lau, Li, Lu, Nagano, Nanci, Nanci, Ronnholm, Ryu, Ryu, Ryu, Simmer, Simmer, Simmer, Simmer, Simmer, Simmer, Simmer, Simmer, Smith, Smith, Smith, Smith, Suga, Sun, Tye, Uchida, Yamada, Yamakoshi   +55 more
core   +1 more source

The crystal structure of human Rogdi provides insight into the causes of Kohlschutter-Tonz Syndrome [PDF]

, 2017
Kohlschutter-Tönz syndrome (KTS) is a rare autosomal-recessive disorder of childhood onset characterized by global developmental delay, spasticity, epilepsy, and amelogenesis imperfecta.
A Kohlschütter, A Mory, A Mory, A Schossig, A Schossig, A Schossig, A Tucci, AJ McCoy, CM Souza De, DC Soares, E Haberlandt, EG Hutchinson, H Suzuki, J Christodoulou, J Ma, J Zlotogora, L Holm, L Pauling, L-M Dong, LM Dong, M Huckert, MC Abba, MD Hoban, NJ Greenfield, P Emsley, PD Adams, R Rupaimoole, S Kamtekar, S Nakagawa, SJ Busch, T Alber, T Shinoda, TC Terwilliger, TV Lipina, V Narayanaswami, VM Ingram, Y Saitoh, Y-F Chen   +37 more
core   +1 more source