Results 111 to 120 of about 5,523 (171)

Dentinogenesis imperfecta: A review and case report of a family over four generations

, 2008
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin.
Bhandari Sudhir, Pannu Karneev
core  

Phenotypic Variability and Diagnostic Characteristics of Pediatric Osteogenesis Imperfecta: A 10-Year Multicenter Cohort Study from Three Tertiary Pediatric Hospitals in Bucharest, Romania. [PDF]

Diagnostics (Basel)
Dinulescu A, Stăiculescu ME, Dijmărescu I, Pavelescu ML, Păcurar D, Ulici A.   +5 more
europepmc   +1 more source

Single-Cell Virtual Perturbation Screening Identifies STAT3 as a Key Regulator of Dentinogenesis. [PDF]

Cell Prolif
Zhu Y, Xu H, Zhang Z, Sun S, Huang Z, Gao X, Pan H, Huang X, Liu Y, Wang X, Jia H, Dai Q, Jiang L.   +12 more
europepmc   +1 more source

Anaesthetic Considerations for Twin Delivery in a Patient With Osteogenesis Imperfecta Type III: A Case Report. [PDF]

Cureus
Eapen SE, Jong BBT, Loh LWW.
europepmc   +1 more source

Developmental defects of enamel and dentin in individuals born preterm: a scoping review of evidence and mechanisms. [PDF]

Front Dent Med
B S, R M, Uchil S, D R, Saha S.
europepmc   +1 more source

Bilateral Lower Limb Deformity Correction in Osteogenesis Imperfecta Using a Non-elongating Rush Rod: A Pragmatic Approach. [PDF]

Cureus
Mk T, Harshavardhan G, Tavfiq M, Suriyakumar S, S S.   +4 more
europepmc   +1 more source

Diagnosis complexity of dentinogenesis imperfecta involving <i>DSPP</i> genetic variants. [PDF]

J Med Genet
Caravello G, Jiménez-Armijo A, Kawczynski M, Rey T, O-Rares Consortium, Antin M, Roth A, Lamouche JB, Gouronc A, Alioua A, Schluth-Bolard C, Bloch-Zupan A.   +11 more
europepmc   +1 more source

Elevated periostin level in serum of adults with osteogenesis imperfecta is associated with disease severity.

J Clin Endocrinol Metab
Mercier-Guery A, Auroux M, Gineyts E, Borel O, Szulc P, Sornay-Rendu E, Fontanges E, Croset M, Rousseau JC, Chapurlat R.   +9 more
europepmc   +1 more source

Genotype and Phenotype of 198 Korean Patients With Nonlethal Osteogenesis Imperfecta: A Retrospective Cohort Study. [PDF]

Hum Mutat
Lee J, Lee HR, Ko JM, Shin CH, Lee W, Song MH, Cho TJ.   +6 more
europepmc   +1 more source

Tissue response in hemisectioned primary mandibular second molars. [PDF]

Acta Odontol Scand
Öhman J, Rughwani V, Naoumova J.
europepmc   +1 more source