Results 121 to 130 of about 15,266 (165)

Early Ceramic Crown Intervention in Adolescents With Severe Amelogenesis Imperfecta: A Clinical Case Series. [PDF]

Clin Case Rep
Das R, Børstad E, Jullumstrø Feuerherm A, Skeie MS, Lundgren GP, Dahllöf G.   +5 more
europepmc   +1 more source

Integrating Imaging and Genomics in Amelogenesis Imperfecta: A Novel Diagnostic Approach. [PDF]

Genes (Basel)
Leban T, Fidler A, Trebušak Podkrajšek K, Pavlič A, Tesovnik T, Jenko Bizjan B, Vrhovšek B, Šket R, Kovač J.   +8 more
europepmc   +1 more source

Opciones de rehabilitación al paciente joven con Amelogénesis imperfecta

The patient with Amelogenesis imperfecta (AI) has a genetic condition that affects their tooth enamel from the primary dentition in many cases, presenting complaints in its aesthetics, function and sensitivity.
Acosta de Camargo, María Gabriela, Rodríguez, Douglas   +1 more
core  

Distinctive Amelogenesis Imperfecta in Loeys-Dietz Syndrome Type II. [PDF]

J Dent Res
Duverger O, Wang SK, Liu QN, Wang Y, Martin D, NIDCD/NIDCR Genomics and Computational Biology Core, Baena V, Syed ZA, Mendoza F, Nguyen TT, Frischmeyer-Guerrerio PA, Jani PH, Lee JS.   +12 more
europepmc   +1 more source

When teeth and kidneys fail together: a case series of amelogenesis imperfecta-renal syndromes in childhood. [PDF]

Pan Afr Med J
Nouir S, Boukadida R, Hannachi S, Harbi A, Mokni H, Ajmi H, Mabrouk S.   +6 more
europepmc   +1 more source

Understanding the Real Needs and Expectations of French Patients with Amelogenesis Imperfecta Through Facebook Content: A Qualitative Thematic Analysis. [PDF]

Healthcare (Basel)
Mailloux A, Dinet J, Filloux J, Lanuel Y.   +3 more
europepmc   +1 more source

Using computer-generated protein models to analyze mutations linked to Amelogenesis Imperfecta. [PDF]

PLoS One
Sharmin N, Yuan J, Chow AK.
europepmc   +1 more source

Kohlschütter-Tönz Syndrome: A Rare Clinical Entity with Amelogenesis Imperfecta in Two Siblings, Dental Management and Scoping Review. [PDF]

Turk Arch Pediatr
Şivet EA, Akbeyaz İH, Berkel G, Yeşilyurt A, Sezer B, Menteş A, Menteş A.   +6 more
europepmc   +1 more source

Identifying a Novel Causal FAM83H Variant for Autosomal Dominant Amelogenesis Imperfecta Using Exome-Sequencing. [PDF]

Mol Genet Genomic Med
Kamps R, Martens H, de Koning B, Smeets B, van Geel M.   +4 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