Results 141 to 150 of about 6,417 (245)

Phenotypic variability in LAMA3-associated amelogenesis imperfecta. [PDF]

Oral Dis, 2023
Wang SK, Zhang H, Wang YL, Seymen F, Koruyucu M, Simmer JP, Hu JC.   +6 more
europepmc   +1 more source

The transitional treatment of permanent teeth in a young patient affected by amelogenesis imperfecta : A case report

, 2002
Bangon Jirakiat
openalex   +2 more sources

The dental management and prosthodontic reconstruction of patients with amelogenesis imperfecta: A narrative review

Dentistry Review
Amelogenesis imperfecta (AI) is a rare genetic condition that affects normal enamel formation of both the primary and permanent dentition. Patients with AI not only present with restorative challenges, but also suffer from extreme hypersensitivity ...
Christina I. Wang, Naif Sinada, Todd R. Schoenbaum   +2 more
doaj  

Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta. [PDF]

Eur J Hum Genet, 2023
Resende KKM, Riou MC, Yamaguti PM, Fournier B, Rondeau S, Pacot L, Berdal A, Felizardo R, Mazzeu JF, Cormier-Daire V, Gaucher C, Acevedo AC, de La Dure-Molla M.   +12 more
europepmc   +1 more source

Amelogenesis imperfecta and nephrocalcinosis syndrome

Indian Journal of Nephrology, 2014
G Aparna, B Varalaxmi, V Chaitanya, P Sandeep, A. V. S. S. N. Sridhar, B Sangeetha, Rapur Ram, M Venkateswarlu, V. Kumar   +8 more
openaire   +3 more sources

Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification. [PDF]

Front Physiol, 2023
Bloch-Zupan A, Rey T, Jimenez-Armijo A, Kawczynski M, Kharouf N, O-Rare consortium, Dure-Molla M, Noirrit E, Hernandez M, Joseph-Beaudin C, Lopez S, Tardieu C, Thivichon-Prince B, ERN Cranio Consortium, Dostalova T, Macek M, International Consortium, Alloussi ME, Qebibo L, Morkmued S, Pungchanchaikul P, Orellana BU, Manière MC, Gérard B, Bugueno IM, Laugel-Haushalter V.   +25 more
europepmc   +1 more source

Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion. [PDF]

Intractable Rare Dis Res, 2023
Leite LDR, Resende KKM, Rosa LDS, Mazzeu JF, de Oliveira LC, Scher MDCSD, Acevedo AC, Yamaguti PM.   +7 more
europepmc   +1 more source

The Use of Mouse Models to Investigate Shear Bond Strength in Amelogenesis Imperfecta [PDF]

, 2011
Megan K. Pugach, Füsun Özer, Y. Li, K. Sheth, R. Beasley, Andrew S. Resnick, L. Daneshmehr, Ashok B. Kulkarni, John D. Bartlett, Carolyn W. Gibson, Rochelle G. Lindemeyer   +10 more
openalex   +1 more source

Pankey Mann Schuyler Philosophy-Based Prosthetic Rehabilitation for an Amelogenesis Imperfecta Patient: A Case Report. [PDF]

Cureus, 2023
Kumar A, Chirom B, Ningthoujam I, Nongthombam RS, Kumar Singh NS.   +4 more
europepmc   +1 more source

Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. [PDF]

J Pers Med, 2023
Kim YJ, Zhang H, Lee Y, Seymen F, Koruyucu M, Kasimoglu Y, Simmer JP, Hu JC, Kim JW.   +8 more
europepmc   +1 more source