Results 121 to 130 of about 4,289 (165)

Pretreatments to bonding on enamel and dentin disorders: a systematic review. [PDF]

Evid Based Dent
Voinot J, Bedez M.
europepmc   +1 more source

Orofacial Anomalies in Kindler Epidermolysis Bullosa.

JAMA Dermatol
Krämer S, Hillebrecht AL, Wang Y, Badea MA, Barrios JI, Danescu S, Fuentes I, Kartal D, Klausegger A, Ponce de León E, Schilke R, Yordanova I, Bloch-Zupan A, Has C.   +13 more
europepmc   +1 more source

IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta. [PDF]

PLoS Genet
Hytönen MK, Rönkkö J, Hundi S, Jokinen TS, Suonto E, Teräväinen E, Donner J, La Rovere R, Bultynck G, Ylikallio E, Tyynismaa H, Lohi H.   +11 more
europepmc   +1 more source

A unique case report of mulberry second molar in a non-syphilitic patient. [PDF]

Medicine (Baltimore)
Harizanova Z, Popova F, Peycheva M.
europepmc   +1 more source

Prevalence of Dental Anomalies in Pediatric Patients at King Saud University Dental Hospital, Riyadh, Saudi Arabia-A Radiographic Analysis. [PDF]

Children (Basel)
Aldowsari MK, Sulimany AM, Alkhathlan A, Alfhaed N, Aldosari M, Alayed S, Bin Saleh S, Alshami AA.   +7 more
europepmc   +1 more source

Early Neonatal Epilepsy Caused by Homozygous Mutation in the SLC13A5 Gene: A Case Report From India. [PDF]

Cureus
Saifullah KM, Samanta S, Ranjan A, Kumar R.   +3 more
europepmc   +1 more source

Interdisciplinary full mouth rehabilitation of a patient with amelogenesis imperfecta from childhood to young adult-hood: A 12-year case report. [PDF]

Clin Case Rep
Caussin É, Courson F, Dursun E, Brukarz Y, Dot D, Chaussain C, Attal JP, François P.   +7 more
europepmc   +1 more source

The ROGDI protein mutated in Kohlschutter-Tonz syndrome is a novel subunit of the Rabconnectin-3 complex implicated in V-ATPase assembly. [PDF]

J Biol Chem
Winkley SR, Kane PM.
europepmc   +1 more source

Prevalence and predictors of molar-incisor hypomineralization among Egyptian children: a cross-sectional study. [PDF]

Eur Oral Res
Etman AM, Aboubakr RM, Alkhadragy D.
europepmc   +1 more source

Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. [PDF]

J Med Genet
Hany U, Watson CM, Liu L, Smith CEL, Harfoush A, Poulter JA, Nikolopoulos G, Balmer R, Brown CJ, Patel A, Simmonds J, Charlton R, Acosta de Camargo MG, Rodd HD, Jafri H, Antanaviciute A, Moffat M, Al-Jawad M, Inglehearn CF, Mighell AJ.   +19 more
europepmc   +1 more source