Results 181 to 190 of about 12,368 (291)

Retraction Note: Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis. [PDF]

Cell Death Dis
Chang H, Wang Y, Liu H, Nan X, Wong S, Peng S, Gu Y, Zhao H, Feng H.   +8 more
europepmc   +1 more source

Amelogenesis Imperfecta: A Conservative and Progressive Adhesive Treatment Concept [PDF]

, 2012
Stefano Ardu, Olivier Duc, Ivo Krejci, R Perroud   +3 more
openalex   +1 more source

Heimler Syndrome With Tooth Agenesis, Abnormal Enamel and Dentin Mineralization, Root Maldevelopment, and PEX1 Mutation. [PDF]

Int Dent J
Kantaputra PN, Apivatthakakul A, Kaewgahya M, Tongsima S, Ngamphiw C, Sastraruji T, Sukantamala P, Carlson BM, Kawasaki K, Ketudat Cairns JR, Sonsuwan N, Ohazama A.   +11 more
europepmc   +1 more source

Comparative aspects of amelogenesis imperfecta.

, 1969
H.W. Noble
openalex  

Oral health-related quality of life before and after crown therapy in young patients with amelogenesis imperfecta [PDF]

, 2015
G. Lundgren, Agneta Karsten, Göran Dahllöf   +2 more
openalex   +1 more source

The Evolutionary Young Actin Nucleator Cobl Is Important for Proper Amelogenesis. [PDF]

Cells
Janitzek H, González Delgado J, Haag N, Seemann E, Nietzsche S, Sigusch B, Qualmann B, Kessels MM.   +7 more
europepmc   +1 more source

Partial Amelogenesis Imperfecta: A Report of a Rare Case. [PDF]

Cureus
AlBagieh HN, Alomran LM, AlBishry FY, Aloraini TK, Almofarej NM, Alhamzah NH, Alqahtani MM.   +6 more
europepmc   +1 more source

Corrections of Dental Anomalies in the Maxillary Incisors and Their Influence on Perceived Smile Esthetics: A Systematic Review. [PDF]

Bioengineering (Basel)
McGarty NR, Delre C, Gaeta C, Doldo T.
europepmc   +1 more source

Aesthetic and Functional Rehabilitation of the Primary Dentition Affected by Amelogenesis Imperfecta [PDF]

, 2015
Maria Carolina Salomé Marquezin, Bruna Raquel Zancopé, Larissa Ferreira Pacheco, Maria Beatriz Duarte Gavião, Fernanda Miori Pascon   +4 more
openalex   +1 more source

Identification of a novel homozygous <i>SLC13A5</i> nonstop mutation in a Chinese family with epileptic encephalopathy and developmental delay. [PDF]

Front Genet
He H, Long L, Tang M, Xu Q, Duan S, Chen G, Zhao Y, Wu Q, Chen J.   +8 more
europepmc   +1 more source